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List of works by Markus M Nöthen

274. MIR137 Influences White Matter Fractional Anisotropy and Cortical Surface Area in Individuals with High Genetic Risk for Psychosis

4th Pediatric Allergy and Asthma Meeting (PAAM)

scientific article (publication date: November 2016)

5-HT2A receptor and bipolar affective disorder: association studies in affected patients

scientific article

5-HT2A receptor gene polymorphisms, anorexia nervosa, and obesity

scientific article published in The Lancet

5-HTTLPR/rs25531 polymorphism and neuroticism are linked by resting state functional connectivity of amygdala and fusiform gyrus

scientific article published on 30 May 2014

A Gene for Universal Congenital Alopecia Maps to Chromosome 8p21-22 ⬇️

scientific article published on February 1, 1998

A Longitudinal Approach to Biological Psychiatric Research: The PsyCourse Study

A Neuregulin-1 schizophrenia susceptibility variant causes perihippocampal fiber tract anomalies in healthy young subjects.

scientific article published on 19 January 2014

A Novel Missense Mutation in the DNA Mismatch Repair Gene hMLH1 Present among East Asians but Not among Europeans

article

A Systematic Evaluation of Machine Learning-based Biomarkers for Major Depressive Disorder across Modalities

scientific article published on 27 February 2023

A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer

scientific article

A common Ser/Thr polymorphism in the perforin-homologous region of human complement component C7

scientific article published on 01 November 1994

A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders

scientific article

A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder

scientific article

A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.

scientific article published on 19 February 2013

A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

scientific article

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family

article

A family-based and case–control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder

article

A functional IL-6 receptor (IL6R) variant is a risk factor for persistent atopic dermatitis

scientific article

A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder

scientific article

A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q

article

A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis

scientific article published on 19 October 2015

A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

scientific article

A genome-wide association study of alcohol dependence

scientific article

A genome-wide association study of attempted suicide.

scientific article

A genome-wide supported variant in CACNA1C influences hippocampal activation during episodic memory encoding and retrieval

scientific article

A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families

article published in 2008

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

scientific article

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

scientific article

A mega-analysis of genome-wide association studies for major depressive disorder

scientific article

A new susceptibility locus for bipolar affective disorder in PAR1 on Xp22.3/Yp11.3

A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp

article

A novel Alzheimer disease locus located near the gene encoding tau protein.

scientific article

A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism

scientific article published on 21 March 2015

A novel splice site associated polymorphism in the tuberous sclerosis 2 (TSC2) gene may predispose to the development of sporadic gangliogliomas

scientific article published in July 1997

A one-degree-of-freedom test for supra-multiplicativity of SNP effects

scientific article

A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25–q26

article by Sven Cichon et al published 27 April 2001 in Molecular Psychiatry

A putative high risk diplotype of the G72 gene is in healthy individuals associated with better performance in working memory functions and altered brain activity in the medial temporal lobe

scientific article

A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry

scientific article

A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: No role in the genetic predisposition to bipolar affective disorder

scientific article published on 01 March 1993

A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci

scientific article

A systematic association mapping on chromosome 6q in bipolar affective disorder--evidence for the melanin-concentrating-hormone-receptor-2 gene as a risk factor for bipolar affective disorder

scientific article published in June 2010

A systematic eQTL study of cis-trans epistasis in 210 HapMap individuals

scientific article published on 17 August 2011

A systems medicine research approach for studying alcohol addiction

scientific article published in November 2013

Achalasia: will genetic studies provide insights?

scientific article published on 11 August 2010

Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature

scientific article

Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies

article

Affective symptomatology in schizophrenia: a risk factor for tardive dyskinesia?

scientific article published on 01 February 2001

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.

scientific article published on 09 April 2013

Allelic variants of dopamine receptor D4 (DRD4) and serotonin receptor 5HT2c (HTR2c) and temperament factors: replication tests

scientific article published in April 1999

Altered Functional Subnetwork During Emotional Face Processing: A Potential Intermediate Phenotype for Schizophrenia

scientific article published on 4 May 2016

Alzheimer's disease risk variants modulate endophenotypes in mild cognitive impairment

scientific article

An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

scientific article published on 8 December 2016

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

scientific article published on 31 May 2017

An association study of a neurotrophic3 (NT-3) gene polymorphism with schizophrenia

article

An association study of debrisoquine hydroxylase (CYP2D6) polymorphisms in schizophrenia

scientific article published on 01 January 1994

An integrated genome research network for studying the genetics of alcohol addiction

scientific article published on October 2010

An interstitial deletion of chromosome 7 at band q21: a case report and review

scientific article published in April 2005

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.

scientific article

Analysis of Rare Variants in the Alcohol Dependence Candidate Gene GATA4

scientific article published on 04 July 2016

Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder

scientific article

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sample

article

Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder.

scientific article published on 31 May 2018

Analysis of the TSC2 gene in human medulloblastoma

scientific article

Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology

article

Androgenetic alopecia. Current aspects of a common phenotype

scientific article published in August 2003

Apolipoprotein E genotype distribution in schizophrenia.

scientific article published in January 1996

Apolipoprotein E ɛ4 and clinical phenotype in schizophrenia

scientific article published in The Lancet

Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees

scientific article published on 01 March 1996

Assignment of the human serotonin 1F receptor gene (HTR1F) to the short arm of chromosome 3 (3p13-p14.1) ⬇️

scientific article published on July 1, 1997

Assignment of the human serotonin 4 receptor gene (HTR4) to the long arm of chromosome 5 (5q31–q33) ⬇️

scientific article published on April 1, 1998

Association Study of Nonsynonymous Single Nucleotide Polymorphisms in Schizophrenia

article by Noa Carrera et al published January 2012 in Biological Psychiatry

Association analyses identify 31 new risk loci for colorectal cancer susceptibility

scientific article published on 14 May 2019

Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder

article

Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method

article

Association analysis of the monoamine oxidase A gene in bipolar affective disorder by using family-based internal controls

scientific article published on October 1995

Association and linkage studies in bipolar affective disorder

scientific article published on January 1992

Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study

scientific article published in June 2005

Association between a polymorphism in the pseudoautosomal X-linked gene SYBL1 and bipolar affective disorder

scientific article (publication date: 8 January 2002)

Association between a promoter dopamine D2 receptor gene variant and the personality trait detachment

scientific article published in April 2003

Association between a promoter polymorphism in the dopamine D2 receptor gene and schizophrenia

article

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample

scientific article

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

scientific article

Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder

scientific article published on 31 August 2016

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder

scientific article published on 11 April 2012

Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies

scientific article published on 25 April 2013

Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells

scientific article published on 20 April 2015

Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study.

scientific article published on 9 November 2017

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Association of a functional 1019C>G 5-HT1A receptor gene polymorphism with panic disorder with agoraphobia

scientific article published on 25 February 2004

Association of major depression with rare functional variants in norepinephrine transporter and serotonin1A receptor genes

scientific article

Association of polygenic score for major depression with response to lithium in patients with bipolar disorder

scientific article published on 16 March 2020

Association of rs1006737 in CACNA1C with alterations in prefrontal activation and fronto-hippocampal connectivity

scientific article

Association of the DTNBP1 genotype with cognition and personality traits in healthy subjects

scientific article published in April 2009

Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

scientific article

Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women

scientific article published on 5 March 2004

Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder

article

Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder

scientific article published in August 2008

Association study between two variants in the DOPA decarboxylase gene in bipolar and unipolar affective disorder

scientific article

Association study of 20 genetic variants at the D-amino acid oxidase gene in schizophrenia

article

Association study of a functional promoter polymorphism in theXBP1 gene and schizophrenia

article

Association study of dopamine D2, D3, D4 receptor and serotonin transporter gene polymorphisms with sleep attacks in Parkinson's disease

scientific article published in June 2004

Association study of schizophrenia and the histidase gene

article

Association study of the GRIA1 and CLINT1 (Epsin 4) genes in a German schizophrenia sample

article

Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach

scientific article published in January 2001

Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls

article

Association versus linkage studies in psychosis genetics

scientific article published on August 1993

At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia

scientific article published on 16 March 2011

Atopic dermatitis is associated with an increased risk for rheumatoid arthritis and inflammatory bowel disease, and a decreased risk for type 1 diabetes

scientific article published on 4 August 2015

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Author Correction: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

scientific article published in Nature Communications

Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature

scientific article

Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits

scientific article published in 2022

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Brain function in carriers of a genome-wide supported bipolar disorder variant

scientific article

Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder

scientific article

Breakthroughs in the genetics of orofacial clefting

scientific article published on 30 August 2011

Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin

scientific article published on 13 May 2008

CNTF and psychiatric disorders

CNV analysis in 169 patients with bladder exstrophy-epispadias complex

scientific article

CNV analysis in monozygotic twin pairs discordant for urorectal malformations

scientific article published on 9 May 2013

Campomelic dysplasia without overt campomelia.

scientific article published in April 1993

Can long-range microsatellite data be used to predict short-range linkage disequilibrium?

scientific article

Caspase recruitment domain 15 gene haplotypes in sarcoidosis

article

Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios

scientific article published in May 2001

Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

scientific article

Characterizing the genetic basis of innate immune response in TLR4-activated human monocytes

scientific article published on 20 October 2014

Cholecystokinin- and cholecystokinin-B-receptor gene polymorphisms in panic disorder

article

Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region

article

Clinical evidence for genomic imprinting in bipolar I disorder

scientific article published in November 1995

Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia

scientific article

Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q

scientific article

Common and rare variant analysis in early-onset bipolar disorder vulnerability

scientific article published on 11 August 2014

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

preprint

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

scholarly article

Common genetic variants and gene-expression changes associated with bipolar disorder are over-represented in brain signaling pathway genes

scientific article published on 12 April 2012

Common genetic variants influence human subcortical brain structures

scientific article

Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder.

scientific article published on 26 March 2013

Common variant at 16p11.2 conferring risk of psychosis.

scientific article

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

scientific article (publication date: May 2011)

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

scientific article published on 26 July 2011

Common variants conferring risk of schizophrenia

scientific article

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

scientific article published on 7 June 2021

Common variants in KCNN3 are associated with lone atrial fibrillation

scientific article

Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia.

scientific article

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

scientific article published on 30 October 2011

Common variation at 10p12.31 near MLLT10 influences meningioma risk

scientific article

Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk

scientific journal article

Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk

scientific journal article

Common variation in NCAN, a risk factor for bipolar disorder and schizophrenia, influences local cortical folding in schizophrenia

scientific article published in March 2014

Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German families

scientific article published on 6 November 2015

Comprehensive epidemiological and genotype-phenotype analyses in a large European sample with idiopathic achalasia

scientific article

Computer-assisted phenotype characterization for genetic research in psychiatry

scientific article

Consensus paper of the WFSBP Task Force on Genetics: Genetics, epigenetics and gene expression markers of major depressive disorder and antidepressant response

scientific article published on 7 September 2016

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

scientific article

Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis

scientific article published on 4 December 2015

Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene

scientific article

Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder

scientific article published on 17 May 2013

Copy number variants in German patients with schizophrenia

scientific article

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

scientific article published on 29 September 2009

Coronary Artery Calcification and Its Relationship to Validated Genetic Variants for Diabetes Mellitus Assessed in the Heinz Nixdorf Recall Cohort

Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease.

scientific article published on 11 February 2011

Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

scientific article published in June 2015

Cortical surface area alterations shaped by genetic load for neuroticism

scientific article published on 5 September 2018

Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease

scientific article published on 20 January 2022

DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder

scientific article

DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations

scientific article published on 28 July 2015

DRD4 exon 3 variants are not associated with symptomatology of major psychoses in a German population

scientific article published in September 2004

DRD4 exon III VNTR polymorphism—susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach

scientific article published on 01 January 2000

De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL-like association and analysis ofEFNB2in patients with anorectal malformations

article

De novo Partial Trisomy 18p and Partial Monosomy 18q in a Patient with Anorectal Malformation

scientific article published on 29 June 2011

De novo duplication of 18p11.21-18q12.1 in a female with anorectal malformation

article published in 2011

De novo microduplication at 22q11.21 in a patient with VACTERL association

De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association

scientific article published on 03 April 2013

Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis.

scientific article

Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III

scientific article published on 20 July 2015

Defective removal of ribonucleotides from DNA promotes systemic autoimmunity.

scientific article

Defective removal of ribonucleotides from DNA promotes systemic lupus erythematosus.

scientific article published on 28 September 2015

Defining the role of common variation in the genomic and biological architecture of adult human height

scientific article

Delineation of marker chromosomes by reverse chromosome painting using only a small number of DOP-PCR amplified microdissected chromosomes

scientific article published on June 1994

Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.

scientific article

Desbuquois syndrome: three further cases and review of the literature.

scientific article

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics

article

Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1)

article

Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair design

scientific article published on 2 May 2005

Different familial transmission patterns in bipolar I disorder with onset before and after age 25.

scientific article published on December 2001

Differential Expression between Human Dermal Papilla Cells from Balding and Non-Balding Scalps Reveals New Candidate Genes for Androgenetic Alopecia.

scientific article published on 06 April 2016

Dinucleotide repeat polymorphism at the D18S365 locus

scientific article

Dinucleotide repeat polymorphism at the D18S99 locus

scientific article published on 01 January 1993

Dinucleotide repeat polymorphism at the human CD59 locus

scientific article published on 01 March 1995

Direct conversion of fibroblasts into stably expandable neural stem cells

scientific article

Disruption of the neurexin 1 gene is associated with schizophrenia

scientific article

Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter

scientific article

Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking

scientific article

Distribution of a novel mutation in the first exon of the human dopamine D4 receptor gene in psychotic patients.

scientific article

Dopamine D2 receptor molecular variant and schizophrenia

scientific article published in The Lancet

Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial cases

article

Dopamine D3 receptor variant and tardive dyskinesia

scientific article published on 01 January 2000

Dopamine D4 receptor gene (DRD4) variants and schizophrenia: meta-analyses

scientific article published in May 2003

Dual association of a TRKA polymorphism with schizophrenia.

scientific article

Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets.

scientific article

Dysfunctional nitric oxide signalling increases risk of myocardial infarction

scientific article published on 10 November 2013

Effect of copy number variant burden on Global Assessment of Functioning in schizophrenia

scientific article

Effect of the G72 (DAOA) putative risk haplotype on cognitive functions in healthy subjects

scientific article published on 24 September 2009

Effects of BDNF Val66Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans

article published in 2018

Effects of BDNF ValMet genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans

Effects of a CACNA1C genotype on attention networks in healthy individuals

scientific article

Effects of a genome-wide supported psychosis risk variant on neural activation during a theory-of-mind task

scientific article published on 16 March 2010

Effects of a neurodevelopmental genes based polygenic risk score for schizophrenia and single gene variants on brain structure in non-clinical subjects: A preliminary report

scientific article published on 06 August 2019

Efficacy and side-effects of clozapine not associated with variation in the 5-HT2C receptor

scientific article published in May 1997

Efficacy and side-effects of clozapine: testing for association with allelic variation in the dopamine D4 receptor gene

scientific article

Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder

scientific article published on 29 November 2018

Efficient strategy for detecting gene × gene joint action and its application in schizophrenia

scientific article

Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance

scientific article published on 06 November 2019

Embryonic expression of the cysteine rich protein 61 (CYR61) gene: A candidate for the development of human epispadias

scientific article published on July 2010

Epigenetic alteration of the dopamine transporter gene in alcohol-dependent patients is associated with age.

scientific article published on 16 April 2012

Epigenome-wide association study of alcohol use disorder in five brain regions

scientific article published on 13 November 2021

Erratum: Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function and bipolar disorder susceptibility

scholarly article published in Molecular Psychiatry

Erratum: Genetic risk prediction and neurobiological understanding of alcoholism

scholarly article published in Translational Psychiatry

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

scholarly article published in Nature Genetics

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

article

Erratum: Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder

article

Erratum: Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients

scientific article published on 14 April 2015

Estrogen receptor 1 gene (ESR1) variants in panic disorder

article

Etiopathological aspects of achalasia: lessons learned with Hirschsprung's disease

scientific article

European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset

article

Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate

scientific article published on 24 August 2012

Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population

scientific article published on 31 December 2013

Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families

article

Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome

scientific article

Evidence for PTGER4, PSCA, and MBOAT7 as risk genes for gastric cancer on the genome and transcriptome level

article

Evidence for a polygenic contribution to androgenetic alopecia

article

Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depression

scientific article published in August 2005

Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family

scientific article published in September 2010

Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder

scientific article published in February 2004

Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder

article

Excess of homozygosity at the dopamine D3 receptor gene in schizophrenia not confirmed

scientific article published on August 1993

Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

scientific article published on 27 July 2016

Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis

scientific article published on 16 January 2016

Expanding the range of ZNF804A variants conferring risk of psychosis

scientific article published on 5 January 2010

Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population: comparison of a clinical interview and a self-administered checklist

scientific article published on 20 July 2017

Exploring genetic variants predisposing to diabetes mellitus and their association with indicators of socioeconomic status

scientific article

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish

scientific article

FARVAT: a family-based rare variant association test

scientific article published on 29 July 2014

Factor Analysis of Mania

article

Familial Cosegregation of Affective Disorder and Hailey-Hailey Disease

scientific article published on 01 July 1993

Familial aggregation of alopecia areata

Familial occurrence of primary premature ejaculation

scientific article published on 01 January 1998

Familial occurrence of systemic mast cell activation disease

scientific article

Familial occurrence of tardive dyskinesia

scientific article published on 01 November 2001

Familial occurrence of the VATER/VACTERL association

scientific article published on 16 March 2012

Family history influences age of onset in bipolar I disorder in females but not in males

scientific article published in February 2005

Family-based association studies of alpha-adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder

scientific article published in April 2004

Family-based association study of theMTHFR polymorphism C677T in the bladder-exstrophy-epispadias-complex

article published in 2006

Feasible and Successful: Genome-Wide Interaction Analysis Involving All 1.9 × 1011 Pair-Wise Interaction Tests

article

Fine mapping of the human AR/EDA2R locus in androgenetic alopecia

scientific article published on 01 March 2010

First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children

scientific article published on 29 September 2009

First genotype-phenotype study reveals HLA-DQβ1 insertion heterogeneity in high-resolution manometry achalasia subtypes

scientific article published on 03 October 2018

First report of a FXII gene mutation in a Brazilian family with hereditary angio-oedema with normal C1 inhibitor.

scientific article

Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene

scientific article

Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance

scientific article

Functional analysis of splice site mutations in the human hairless (HR) gene using a minigene assay

article

Functional and genetic characterization of the non-lysosomal glucosylceramidase 2 as a modifier for Gaucher disease

scientific article published on 26 September 2013

Functional impact of a recently identified quantitative trait locus for hippocampal volume with genome-wide support

scientific article published on 23 July 2013

Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains

scientific article published on 10 January 2017

Further evidence for DYX1C1 as a susceptibility factor for dyslexia

scientific article

Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21.

scientific article published in June 2008

Further evidence for age of onset being an indicator for severity in bipolar disorder

article

Further evidence for the impact of a genome-wide-supported psychosis risk variant in ZNF804A on the Theory of Mind Network

scientific article

Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate

scientific article published in April 2009

G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

scientific article

G72 and its association with major depression and neuroticism in large population-based groups from Germany

scientific article published on 17 March 2008

GLRB allelic variation associated with agoraphobic cognitions, increased startle response and fear network activation: a potential neurogenetic pathway to panic disorder.

scientific article

GNB3 gene 825 TT variant predicts hard coronary events in the population-based Heinz Nixdorf Recall study

scientific article published on 28 August 2014

GWAS for executive function and processing speed suggests involvement of the CADM2 gene.

scientific article

GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.

scientific article

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

scientific article

Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders

scientific article

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

scientific article

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017

Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis

scientific article published on 17 July 2017

Genetic Variation in Human 5-HT Receptors: Potential Pathogenetic and Pharmacological Rolea

scientific article published on 01 December 1998

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

scientific article published on 11 September 2013

Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019

Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case???control study

article

Genetic association in psychiatric diseases. Concepts and findings

scientific article published in November 1994

Genetic association signal near NTN4 in Tourette syndrome

scientific article

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

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Genetic associations with valvular calcification and aortic stenosis

scientific article published on February 2013

Genetic counseling in psychiatric diseases

scientific article published in January 1996

Genetic determination of human facial morphology: links between cleft-lips and normal variation

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Genetic effects influencing risk for major depressive disorder in China and Europe

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Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

scientific article (publication date: 15 November 2010)

Genetic evidence of assortative mating in humans

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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

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Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.

scientific article published in January 1999

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 28 February 2019

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

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Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25.

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Genetic risk prediction and neurobiological understanding of alcoholism

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Genetic studies of body mass index yield new insights for obesity biology

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Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study

scientific article published on 21 January 2016

Genetic variants in CTLA4 are strongly associated with alopecia areata

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Genetic variants of lipase activity in chronic pancreatitis

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Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia

scientific article published on 24 September 2012

Genetic variation in G72 correlates with brain activation in the right middle temporal gyrus in a verbal fluency task in healthy individuals

scientific article

Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individuals

scientific article published on June 2009

Genetic variation in the G72 gene is associated with increased frontotemporal fiber tract integrity

scientific article published on 17 July 2014

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia

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Genetic variation in the lymphotoxin-α (LTA)/tumour necrosis factor-α (TNFα) locus as a risk factor for idiopathic achalasia

scientific article published on 20 November 2013

Genetic variation in the schizophrenia-risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals

scientific article published on October 2009

Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with differences in frontal brain activation in a working memory task in healthy individuals

scientific article published on 12 June 2008

Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with personality traits in healthy individuals

scientific article published in May 2008

Genetic variation of CNS receptors--a new perspective for pharmacogenetics.

scientific article published on October 1995

Genetic variation of the 5-HT2A receptor and response to clozapine

scientific article published in The Lancet

Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder.

scientific article published on 16 October 2007

Genetics of bipolar affective disorders. Current status of research for identification of susceptibility genes

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Genetics of dyslexia: the evolving landscape

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Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics

scientific article published on 23 January 2017

Geneties of Schizophrenia and Bipolar Affective Disorder

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

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Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture

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Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis

scientific article published on 30 September 2014

Genome-wide Comparative Analysis of Atopic Dermatitis and Psoriasis Gives Insight into Opposing Genetic Mechanisms.

scientific article published on 3 December 2015

Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder

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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

scientific article published on 26 April 2018

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

scientific article published on 25 July 2016

Genome-wide association analysis identifies a meningioma risk locus at 11p15.5

Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder

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Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder

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Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

scientific article published on 09 December 2008

Genome-wide association of mood-incongruent psychotic bipolar disorder

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Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis ⬇️

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Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy

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Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.

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Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

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Genome-wide association study identifies 30 loci associated with bipolar disorder.

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Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

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Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis

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Genome-wide association study identifies multiple susceptibility loci for glioma ⬇️

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Genome-wide association study identifies multiple susceptibility loci for multiple myeloma ⬇️

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Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia ⬇️

scientific article published on 9 April 2018

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

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Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

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Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder

scientific article published on January 2013

Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma

scientific article published on 07 September 2018

Genome-wide association study in German patients with attention deficit/hyperactivity disorder

scientific article published on 19 October 2011

Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder

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Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

scientific article

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

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Genome-wide association study of alcohol dependence

scientific journal article

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

scientific article published on 20 June 2017

Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility

scientific article published in December 2017

Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts.

scientific article published on 4 July 2017

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

scientific article published on 27 March 2017

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

scientific article published in June 2021

Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

scientific article published on 11 November 2019

Genome-wide association study of pathological gambling

scientific article published on 14 June 2016

Genome-wide association study of suicide attempts in mood disorder patients

scientific article

Genome-wide association study reveals two new risk loci for bipolar disorder

scientific article (publication date: 11 March 2014)

Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression

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Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms

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Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European origin

Genome-wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalities

scientific article published on 24 September 2014

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

scientific journal article

Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci

scientific article published on 22 January 2015

Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata

scientific article published on 26 October 2011

Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26

scientific article

Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14

scientific article

Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1.

scientific article published on 25 September 2012

Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster

scientific article published on 18 October 2011

Genome-wide significant risk factors for Alzheimer's disease: role in progression to dementia due to Alzheimer's disease among subjects with mild cognitive impairment

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Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium

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Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci

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Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

scientific article published in March 2011

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

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Genome-wide transcriptome induced by Porphyromonas gingivalis LPS supports the notion of host-derived periodontal destruction and its association with systemic diseases

scientific article published on 24 November 2015

Genome-wide transcriptome induced by nickel in human monocytes

scientific article published on 28 July 2016

Genomewide Association Study of Alcohol Dependence Identifies Risk Loci Altering Ethanol-Response Behaviors in Model Organisms

scientific article published on 22 February 2017

Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2.

scientific article published on 16 June 2016

Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.

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Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

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Genotype-phenotype association mining in bipolar disorder: market research meets complex genetics

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Genotype-phenotype studies in bipolar disorder showing association between the DAOA/G30 locus and persecutory delusions: a first step toward a molecular genetic classification of psychiatric phenotypes

scientific article published in November 2005

Germline variation in the insulin-like growth factor pathway and risk of Barrett's esophagus and esophageal adenocarcinoma

scientific article published on 10 December 2020

GestaltMatcher facilitates rare disease matching using facial phenotype descriptors

scientific article published on 10 February 2022

Glutamate receptor δ 1 (GRID1) genetic variation and brain structure in schizophrenia

scientific article published on 25 September 2012

HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study

scientific article published in September 2007

Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes

scientific article published on 10 November 2017

Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder.

scientific article

Hereditary angioedema with normal C1 inhibitor gene in a family with affected women and men is associated with the p.Thr328Lys mutation in the F12 gene

article

Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies

scientific article published on 8 August 2014

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

scientific article published on December 2011

High incidence of the CFTR mutations 3272-26A→G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A→G, E588V, and 1671insTATCA)

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High loading of polygenic risk in cases with chronic schizophrenia

scientific article published on September 2015

High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences.

scientific article published on 10 December 2015

High-density genotyping study identifies four new susceptibility loci for atopic dermatitis

scientific article published on 02 June 2013

Hippocampal and frontolimbic function as intermediate phenotype for psychosis: evidence from healthy relatives and a common risk variant in CACNA1C.

scientific article published on 8 December 2013

Hippocampal function in healthy carriers of the CLU Alzheimer's disease risk variant

scientific article published in December 2011

Homozygosity for a factor XII mutation in one female and one male patient with hereditary angio-oedema.

scientific article published on 22 September 2015

Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity

scientific article

Hormonal regulation in male androgenetic alopecia-Sex hormones and beyond: Evidence from recent genetic studies

scientific article published on 17 June 2020

Human 5-HT5AReceptor Gene: Systematic Screening for DNA Sequence Variation and Linkage Mapping on Chromosome 7q34–q36 Using a Polymorphism in the 5′ Untranslated Region

article

Human Adenosine A1 Receptor Gene: Systematic Screening for DNA Sequence Variation and Linkage Mapping on Chromosome 1q31-32.1 Using a Silent Polymorphism in the Coding Region

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Human complement component C8

scientific article published on 01 March 1994

Human delta-opioid receptor gene and susceptibility to heroin and alcohol dependence

scientific article published in October 1999

Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity

scientific article published in December 1994

Human metabotropic glutamate receptor 2 gene (GRM2): chromosomal sublocalization (3p21.1-p21.2) and genomic organization

scientific article

Hunting the genes in male-pattern alopecia: how important are they, how close are we and what will they tell us?

scientific article published on 4 February 2016

Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability

scientific article published on April 2013

Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation--clinical report and review

scientific article published in March 2006

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

scientific article (publication date: June 2003)

IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate

scientific article published in December 2009

Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk

scientific article

Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1.

scientific article published on 25 August 2016

Identification of a keratin-associated protein with a putative role in vesicle transport

scientific article published on 29 March 2007

Identification of common variants associated with human hippocampal and intracranial volumes

scientific article published on 15 April 2012

Identification of genetic variation in the human serotonin 1D beta receptor gene.

scientific article

Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients

scientific article published on 3 June 2014

Identification of loci associated with schizophrenia by genome-wide association and follow-up

scientific article

Identification of loci of functional relevance to Barrett's esophagus and esophageal adenocarcinoma: Cross-referencing of expression quantitative trait loci data from disease-relevant tissues with genetic association data

scientific article published on 31 December 2019

Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

scientific article published in Nature Communications

Identification of mutations in the human hairless gene in two new families with congenital atrichia

scientific article

Identification of pleiotropy at the gene level between psychiatric disorders and related traits

scientific article published in 2021

Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.

scientific article published on 23 September 2016

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

scientific article

Identifying bipolar disorder susceptibility loci in a densely affected pedigree

scientific article published on 18 December 2012

Identifying genetic factors in common diseases: more helpful in relation to etiology than prediction

scientific article published in May 2013

Identifying multimodal signatures underlying the somatic comorbidity of psychosis: the COMMITMENT roadmap

scientific article published on 15 October 2020

Immunochip analysis identifies association of the RAD50/IL13 region with human longevity

scientific article published on 22 March 2016

Immunochip-based analysis: high-density genotyping of immune-related loci sheds further light on the autoimmune genetic architecture of alopecia areata

scientific article published on 22 October 2014

Immunoglobulin light-chain amyloidosis shares genetic susceptibility with multiple myeloma

scientific article published on 3 July 2014

Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance

scientific article published on 3 September 2015

Impact of atopy on risk of glioma: a Mendelian randomisation study

scientific article published on 15 March 2018

Impact of schizophrenia-risk gene dysbindin 1 on brain activation in bilateral middle frontal gyrus during a working memory task in healthy individuals

scientific article

Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation

scientific article

Implication of a rare deletion at distal 16p11.2 in schizophrenia

scientific article published on March 2013

In vitro analysis of LIPH mutations causing hypotrichosis simplex: evidence confirming the role of lipase H and lysophosphatidic acid in hair growth

scientific article published on 18 June 2009

Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III

scientific article

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

scientific article

Increased levels of glucocorticoid receptors and enhanced glucocorticoid receptor auto-regulation after hydrocortisone challenge in B-lymphoblastoids from patients with affective disorders.

scientific article published on 9 December 2004

Independent evidence for the selective influence of GABA(A) receptors on one component of the bipolar disorder phenotype

scientific article published on 15 June 2010

Influence of age and cognitive performance on resting-state brain networks of older adults in a population-based cohort

scientific article published on 23 January 2017

Influence of obesity-related risk factors in the aetiology of glioma

scientific article published on 13 March 2018

Inheritance of the VATER/VACTERL association

scientific article

Inherited genetic susceptibility to monoclonal gammopathy of unknown significance

scientific article published on 21 January 2014

Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia

scientific article

Interrelationship and familiality of dyslexia related quantitative measures

scientific article published on 13 October 2006

Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

scientific article published on 01 March 2019

Intestinal atresia, encephalocele, and cardiac malformations in infants with 47,XXX: Expansion of the phenotypic spectrum and a review of the literature

scientific article published on 16 February 2010

Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study

Investigation of Complement C4B Deficiency in Schizophrenia ⬇️

scientific article published on September 1, 1997

Investigation of SHANK3 in schizophrenia

scientific article

Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss

scientific article published on 19 December 2013

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample

scientific article published on 23 September 2008

Investigation of manic and euthymic episodes identifies state- and trait-specific gene expression and STAB1 as a new candidate gene for bipolar disorder

scientific article

Investigation of selected cytokine genes suggests thatIL2RAand theTNF/LTAlocus are risk factors for severe alopecia areata

article

Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss

scientific article published on 16 July 2013

Investigation of the DAOA/G30 locus in panic disorder.

scientific article

Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample

scientific article published in December 2008

Investigation of the HLA-DRB1 locus in alopecia areata.

scientific article

Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 (FCRL3) gene in alopecia areata.

scientific article

Investigation of the human serotonin 6 (5HT6) receptor gene in bipolar affective disorder and schizophrenia

article

Investigation of the human serotonin 6 [5-HT6] receptor gene in bipolar affective disorder and schizophrenia

scientific article published on 01 April 2000

Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients

scientific article published in November 2004

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

scientific article

Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss

scientific article published in June 2012

Investigation of the p.Ser278Arg polymorphism of the autoimmune regulator (AIRE) gene in alopecia areata

article

Investigation of the role of TCF4 rare sequence variants in schizophrenia

scientific article published on 22 May 2015

Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population

scientific article published in October 2008

Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss

scientific article published on 4 August 2011

Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T gene.

scientific article

Involvement of the atrial natriuretic peptide transcription factor GATA4 in alcohol dependence, relapse risk and treatment response to acamprosate

scientific article

Is there a phenotypic difference between probands in case-control versus family-based association studies?

Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12.

scientific article published on 29 January 2013

KID Syndrome: Report of a Scandinavian Patient with Connexin‐26 Gene Mutation

article

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

scientific article

Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia

article

Lack of association between dopamine D1 and D2 receptor genes and bipolar affective disorder

scientific article published on February 1992

Lack of association between dopamine D4 receptor gene and personality traits

article

Lack of evidence for allelic association between personality traits and the dopamine D4 receptor gene polymorphisms

scientific article published in May 1997

Lack of genetic association between the phospholipase A2 gene and bipolar mood disorder in a European multicentre case-control study

scientific article published in August 2006

Lack of genetically determined structural variants of the human serotonin-1E (5-HT1E) receptor protein points to its evolutionary conservation

scientific article

Lack of imprinting of the human dopamine D4 receptor (DRD4) gene

scientific article published in April 1996

Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin

scientific article published in August 2004

Large recurrent microdeletions associated with schizophrenia

scientific article

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

scientific article

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

scientific article

Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS.

scientific article published on 25 January 2016

Linkage analyses of chromosomal region 18p11-q12 in dyslexia

scientific article published on 03 August 2005

Linkage disequilibrium mapping at DAT1, DRD5 and DBH narrows the search for ADHD susceptibility alleles at these loci

scientific article published in March 2003

Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1

article

Linkage-disequilibrium-based binning affects the interpretation of GWASs

scientific article published on 22 March 2012

Linking single nucleotide polymorphisms

scientific article published on 01 March 2002

Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.

scientific article published on 30 June 2000

Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?

Longer telomere length in patients with schizophrenia

scientific article

Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease

article

Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease

scientific article

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

scientific article published on 4 January 2009

Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations

scientific article

Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases

scientific article published on 27 November 2015

MORC1 exhibits cross-species differential methylation in association with early life stress as well as genome-wide association with MDD.

scientific article

Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21

article

Mapping of the human adenosine A 2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region

article

Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report

Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness

scientific article

Mendelian randomisation study of the relationship between vitamin D and risk of glioma

scientific article

Meta-analysis identifies seven susceptibility loci involved in the atopic march

scientific article

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

scientific article

Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia

scientific article published in The Lancet

Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.

scientific article

Metabotropic glutamate receptor 3 (GRM3) gene variation is not associated with schizophrenia or bipolar affective disorder in the German population

scientific article

MicroRNAs as the cause of schizophrenia in 22q11.2 deletion carriers, and possible implications for idiopathic disease: a mini-review

scientific article

Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy

Microduplications of 16p11.2 are associated with schizophrenia

scientific article

Missing Heritability in the Tails of Quantitative Traits? A Simulation Study on the Impact of Slightly Altered True Genetic Models

article

Moclobemide response in depressed patients: association study with a functional polymorphism in the monoamine oxidase A promoter

scientific article published in July 2002

Modified ligand binding to the naturally occurring Cys-124 variant of the human serotonin 5-HT1B receptor

scientific article

Molecular diagnosis of trisomy 18 using DNA recovered from paraffin embedded tissues and possible implications for genetic counselling

article

Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder

scientific article

Monoamine related functional gene variants and relationships to monoamine metabolite concentrations in CSF of healthy volunteers

scientific article

Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31

article

Morbus Galli-Galli

scientific article published on 01 November 2011

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

scientific article published on 19 October 2015

Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum

scientific article published on 06 May 2022

Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.

scientific article

Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadias

scientific article published on 2 July 2012

Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors

article

Mutation in the beta amyloid precursor protein gene and schizophrenia

scientific article published in October 1993

Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease

scientific article (publication date: July 2001)

Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex

scientific article

NCAN Cross-Disorder Risk Variant Is Associated With Limbic Gray Matter Deficits in Healthy Subjects and Major Depression

scientific article

Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder

scientific article published on 25 July 2012

Neuronal nicotinic acetylcholine receptor α4 subunit (CHRNA4) and panic disorder: An association study

scientific article published on 01 April 1997

New Genetic Findings in Schizophrenia: Is there Still Room for the Dopamine Hypothesis of Schizophrenia?

scientific article

New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

scientific article

New findings in the genetics of major psychoses

scientific article

Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorder

scientific article published on 30 January 2012

No Association Between Vitamin D Status and Risk of Barrett's Esophagus or Esophageal Adenocarcinoma: A Mendelian Randomization Study

scientific article published on 01 February 2019

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

scientific article

No association between a promoter dopamine D(4) receptor gene variant and schizophrenia.

scientific article published in August 2001

No association between a putative functional promoter variant in the dopamine beta-hydroxylase gene and schizophrenia

scientific article published in September 2003

No association between dopamine D4 receptor gene variants and novelty seeking

scientific article published in January 2002

No association between genetic variants at the DGCR2 gene and schizophrenia in a German sample

article

No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia

scientific article

No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample

scientific article published in October 2006

No association between length of the (CAG)n repeat of the Huntington's disease gene and Tourette's syndrome

scientific article

No association between serotonin 2A receptor gene variants and personality traits

scientific article published in March 2001

No association between serotonin transporter gene polymorphisms and personality traits

article

No association between the D-aspartate oxidase locus and schizophrenia

scientific article published in February 2009

No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples

scientific article

No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample

scientific article published in April 2007

No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample

scientific article published in April 2007

No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.

scientific article

No evidence for an association between variants at the gamma-amino-n-butyric acid type A receptor beta2 locus and schizophrenia

scientific article published in February 2007

No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder

scientific article published in September 2005

No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder

scientific article published in February 2013

No evidence of association between dopamine D4 receptor variants and bipolar affective disorder

article

Nonreplication of association between mu-opioid-receptor gene (OPRM1) A118G polymorphism and substance dependence

scientific article

Nonreplication of linkage disequilibrium between the dopamine D4 receptor locus and Tourette syndrome

scientific article published in July 1997

Nonsyndromic cleft lip with or without cleft palate in arab populations: genetic analysis of 15 risk loci in a novel case-control sample recruited in Yemen

scientific article published on 13 March 2014

Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway

scientific article

Norepinephrine transporter (NET) promoter and 5'-UTR polymorphisms: association analysis in panic disorder

scientific article

Novel 5′-regulatory region polymorphisms of the 5-HT2C receptor gene: association study with panic disorder

article

Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

scientific article (publication date: 3 October 2016)

Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation

scientific article published on 17 June 2016

PEDIA: prioritization of exome data by image analysis

scientific article published on 05 June 2019

PLD3 in non-familial Alzheimer's disease

scientific article published in April 2015

Partial support for ZNF804A genotype-dependent alterations in prefrontal connectivity

scientific article published on 31 October 2011

Patterns of parental transmission and familial aggregation models in bipolar affective disorder

scientific article published in September 1998

Pemphigus chronicus benignus familiaris (Morbus Hailey-Hailey) und bipolare affektive Erkrankung bei drei Mitgliedern einer Familie

scientific article published on 01 May 1994

Perceived stress and hair cortisol: Differences in bipolar disorder and schizophrenia

scientific article

Pharmacogenetics of clozapine response

scientific article published in The Lancet

Pharmacological properties of naturally occurring variants of the human norepinephrine transporter

scientific article published on 01 July 2000

Phenotype severity in the bladder exstrophy-epispadias complex: analysis of genetic and nongenetic contributing factors in 441 families from North America and Europe

scientific article

Pluripotent stem cell-derived radial glia-like cells as stable intermediate for efficient generation of human oligodendrocytes

scientific article

Polymorphic MAO-A and 5-HT-Transporter Genes: Analysis of Interactions in Panic Disorder

article

Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain

scientific article published in August 1998

Polymorphism of Human Complement Component C6: An Amino Acid Substitution (GLU/ALA) within the Second Thrombospondin Repeat Differentiates between the Two Common Allotypes C6A and C6B

scientific article published on 01 July 1993

Polymorphisms in DCDC2 and S100B associate with developmental dyslexia

scientific article published on 16 April 2015

Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples

scientific article

Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers

scientific article

Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationships to monoamine metabolite concentrations in CSF of healthy volunteers

scientific article

Population-Specific Association between a Polymorphic Variant in ST18, Encoding a Pro-Apoptotic Molecule, and Pemphigus Vulgaris

Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample

scientific article published in October 2007

Possible association of Down syndrome and exstrophy-epispadias complex: report of two new cases and review of the literature

scientific article published on 16 October 2008

Possible association of different G72/G30 SNPs with mood episodes and persecutory delusions in bipolar I Romanian patients

scientific article published on 15 March 2010

Prediction of male-pattern baldness from genotypes

scientific article published on 28 October 2015

Premorbid adjustment in schizophrenia--an important aspect of phenotype definition

scientific article published on 21 March 2007

Premorbid adjustment: a phenotype highlighting a distinction rather than an overlap between schizophrenia and bipolar disorder

scientific article published on 3 April 2009

Prenatal diagnosis of Pfeiffer syndrome type II

Prevalence of incompletely penetrant Huntington's disease alleles among individuals with major depressive disorder

scientific article

Pseudoautosomal marker DXYS20 and manic depression.

scientific article published on April 1993

Publisher Correction: Mendelian randomisation study of the relationship between vitamin D and risk of glioma

scientific article published on 23 May 2019

Quantifying the heritability of glioma using genome-wide complex trait analysis

scientific article

RETRACTED: Identification of gene ontologies linked to prefrontal-hippocampal functional coupling in the human brain

retracted scientific article

Rare SHANK2 variants in schizophrenia

scientific article published on 25 August 2015

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

scientific article

Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4

scientific article published on 16 November 2021

Rare variant testing of imputed data: an analysis pipeline typified

scientific article

Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness

scientific article

Recurrent null mutation in SPG20 leads to Troyer syndrome

scientific article

Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours

scientific article

Reduced cortical thickness is associated with the glutamatergic regulatory gene risk variant DAOA Arg30Lys in schizophrenia

scientific article

Replication analysis of 15 susceptibility loci for nonsyndromic cleft lip with or without cleft palate in an italian population

scientific article published on 9 December 2015

Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families.

scientific article

Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects

scientific article

Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study

scientific article published on 17 April 2012

Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients

article published in 2009

Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder

scientific article

Reply

Reply to “Replication of association of 3p21.1 with susceptibility to bipolar disorder but not major depression”

Reproducible grey matter patterns index a multivariate, global alteration of brain structure in schizophrenia and bipolar disorder

scientific article published on 17 January 2019

Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients

Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate

scientific article published on 18 October 2012

Retraction for Dixson et al., Identification of gene ontologies linked to prefrontal-hippocampal functional coupling in the human brain

scientific article published on 2 September 2014

Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome)

scientific article published on 01 October 1993

Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study

scientific article

SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.

scientific article published on 4 January 2011

SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease

scientific article

SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: No evidence for the involvement of common or rare variants in Central European patients

article

Schizophrenia and the serotonin transporter gene

scientific article published in January 1998

Schizophrenia: genetic tools for unraveling the nature of a complex disorder

scientific article

Search for association between suicide attempt and serotonergic polymorphisms

scientific article published in March 2000

Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis ⬇️

scientific article

Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: No evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association s

article

Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples

scientific article

Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss

scientific article published on 5 November 2012

Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: no association with female pattern hair loss identified

scientific article published in May 2012

Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate

scientific article published on 22 March 2016

Serotonin subtype 2 receptor genes and clinical response to clozapine in schizophrenia patients.

scientific article published in August 1998

Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study

scientific article

Serum lipid levels, body mass index, and their role in coronary artery calcification: a polygenic analysis

scientific article published on 10 January 2015

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

scientific article

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

scientific article

Shared Genetic Etiology of Obesity-Related Traits and Barrett's Esophagus/Adenocarcinoma: Insights from Genome-Wide Association Studies

scientific article published on 20 November 2019

Shared genetic etiology between alcohol dependence and major depressive disorder.

scientific article published in August 2018

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

scientific article published on 16 February 2020

Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population

scientific article

Single-strand conformation analysis (SSCA) of the dopamine D1 receptor gene (DRD1) reveals no significant mutation in patients with schizophrenia and manic depression

article

Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases

scientific article

Smoking behaviour: investigation of the coaction of environmental and genetic risk factors

scientific article published in December 2014

Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis

scientific article

Steinfeld syndrome: report of a second family and further delineation of a rare autosomal dominant disorder

scientific article published in June 1993

Strauch et al reply

scientific article published on 01 March 2000

Striatal response to reward anticipation: evidence for a systems-level intermediate phenotype for schizophrenia

scientific article published in May 2014

Strong association of variants around FOXE1 and orofacial clefting.

scientific article

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

scientific article

Studies in humans and mice implicate neurocan in the etiology of mania

scientific article

Studying variability in human brain aging in a population-based German cohort—rationale and design of 1000BRAINS

scientific article (publication date: 14 July 2014)

Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array

scientific article published on 26 October 2015

Suicide attempts in schizophrenia and affective disorders with relation to some specific demographical and clinical characteristics

scientific article

Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families

scientific article published on 3 July 2013

Supporting evidence for LRRTM1 imprinting effects in schizophrenia.

scientific article

Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma

scientific article

Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients

scientific article

Susceptibility variants for male-pattern baldness on chromosome 20p11.

scientific article

Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness

scientific article published in December 2011

Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function

scientific article

Systematic investigation of genetic variability in 111 human genes-implications for studying variable drug response.

scientific article published in January 2005

Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of disease

scientific article published on 01 January 1998

Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease

scientific article published on 05 March 2010

Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1)

article

Systematic screening for mutations in the 5′-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder

article

Systematic screening for mutations in the human N-methyl-D-aspartate receptor 1 gene in schizophrenic patients from the German population

scientific article published in December 2004

Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia

article

Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: identification of two naturally occurring receptor variants and association analysis in schizophrenia

scientific article published on 01 May 1996

Systematic screening for mutations in the promoter and the coding region of the 5-HT1A gene

article

Systemic mast cell activation disease: the role of molecular genetic alterations in pathogenesis, heritability and diagnostics

scientific article

TCF7L2 polymorphism rs7903146 and predisposition for type 2 diabetes mellitus in obese children

scientific article published on 10 June 2008

TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palate

scientific article published on 15 May 2008

TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies

scientific article published on 6 April 2010

Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association

scientific article

The 7p15.3 (rs4487645) association for multiple myeloma shows strong allele-specific regulation of the MYC-interacting gene CDCA7L in malignant plasma cells

scientific article published on 5 December 2014

The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A ⬇️

scientific article

The Barrett-associated variants at GDF7 and TBX5 also increase esophageal adenocarcinoma risk

scientific article published on 18 January 2016

The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma

scientific article

The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

scientific article published on 04 May 2009

The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease

scientific article

The FU gene and its possible protein isoforms

scientific article

The G72/G30 gene locus in psychiatric disorders: a challenge to diagnostic boundaries?

scientific article

The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among Europeans ⬇️

scientific article published on 6 January 2016

The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata

scientific article published on 19 November 2007

The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language

scientific article

The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: findings from a large German case-control and family-based sample

scientific article published on 19 July 2010

The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia

scientific article published on 24 March 2011

The effect of G72 genotype on neural correlates of memory encoding and retrieval

scientific article

The effect of Neuregulin 1 on neural correlates of episodic memory encoding and retrieval

scientific article published on 28 December 2009

The effect of neurogranin on neural correlates of episodic memory encoding and retrieval

scientific article

The effects of a DTNBP1 gene variant on attention networks: an fMRI study

scientific article

The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.

scientific article

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

scientific article

The genetics of panic disorder

article

The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach

scientific article (publication date: April 2002)

The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3

article

The human serotonin 7 (5-HT7) receptor gene: genomic organization and systematic mutation screening in schizophrenia and bipolar affective disorder.

scientific article published in November 1996

The impact of a Dysbindin schizophrenia susceptibility variant on fiber tract integrity in healthy individuals: a TBSS-based diffusion tensor imaging study

scientific article published on 14 October 2011

The impact of dystrobrevin-binding protein 1 (DTNBP1) on neural correlates of episodic memory encoding and retrieval

scientific article

The impact of genetics on psychiatric nosology

scientific article published in December 2006

The influence of MIR137 on white matter fractional anisotropy and cortical surface area in individuals with familial risk for psychosis

scientific article

The inverse link between genetic risk for schizophrenia and migraine through NMDA (N-methyl-D-aspartate) receptor activation via D-serine

scientific article published on 6 July 2016

The neuronal transporter gene SLC6A15 confers risk to major depression

scientific article

The oestrogen receptor 2 (ESR2) gene in female-pattern hair loss: replication of association with rs10137185 in German patients

scientific article published in April 2014

The opioid peptides enkephalin and beta-endorphin in alcohol dependence

scientific article published on 27 June 2008

The power of sample size and homogenous sampling: association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder

scientific article published in February 2005

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

scientific article published on 10 January 2017

The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease

scientific article

The two most common alleles of the coding GGN repeat in the androgen receptor gene cause differences in protein function

scientific article published in July 2007

The use of microsatellites in zygosity diagnosis of twins

scientific article published on 01 January 1993

Tourette syndrome and the norepinephrine transporter gene: Results of a systematic mutation screening

article

Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) gene

scientific article

Tourette's syndrome and homozygosity for the dopamine D3 receptor gene

scientific article published in The Lancet

Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scholarly article published 10 March 2018

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scientific article published on 26 November 2018

Transcriptome-Wide Association Study Identifies New Candidate Susceptibility Genes for Glioma

scientific article published on 01 February 2019

Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent

scientific article

Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunction

scientific article published on February 1996

Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association study

scientific article

Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups

scientific journal article

Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder

scientific article

Tyrosine hydroxylase gene and manic-depressive illness

scientific article published in The Lancet

Tyrosine hydroxylase polymorphisms and manic-depressive illness

scientific article published in September 1990

Using Network Methodology to Infer Population Substructure

scientific article published on 22 June 2015

Utilizing the Jaccard index to reveal population stratification in sequencing data: a simulation study and an application to the 1000 Genomes Project

scientific article

VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis

scientific article

VEGF Gene Haplotypes Are Associated With Sarcoidosis

article

Variant 1859G-->A (Arg620Gln) of the "hairless" gene: absence of association with papular atrichia or androgenic alopecia

scientific article published in July 2001

Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype

scientific journal article

Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma

scientific journal article

Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.

scientific article published in March 2010

Volition diminishes genetically mediated amygdala hyperreactivity

scientific article published on 5 December 2009

Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts

scientific article

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association

scientific article published on 23 October 2013

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families

scientific article published on 04 February 2020

Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases

scientific article

XRCC5 as a risk gene for alcohol dependence: evidence from a genome-wide gene-set-based analysis and follow-up studies in Drosophila and humans

scientific article

Y402H-Polymorphismus im Komplementfaktor H und altersabhängige Makuladegeneration (AMD)

scientific article published on 01 November 2005

ZNF804A and cortical structure in schizophrenia: in vivo and postmortem studies

scientific article published on 27 September 2013

ZNF804A genetic variation (rs1344706) affects brain grey but not white matter in schizophrenia and healthy subjects

scientific article published on 20 May 2014

[A unit for the care of acute headache attacks. A new experience in our milieu]

scientific article published on 01 May 1989

hSKCa3: no association of the polymorphic CAG repeat with bipolar affective disorder and schizophrenia

scientific article published on 01 December 1999

αCaMKII autophosphorylation controls the establishment of alcohol drinking behavior

scientific article published on 04 March 2013

“Association study of a functional promoter polymorphism in theXBP1 gene and schizophrenia,” American Journal Of Medical Genetics Part B (Neuropsychiatric Genetics) 141B:71–75 (2006)

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