List of works by Peter Holmans

A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs

article

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

scientific article published on February 1996

A comparison of four clustering methods for brain expression microarray data

scientific article published on 25 November 2008

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

A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter.

scientific article published on January 1998

A flexible model for association analysis in sibships with missing genotype data

scientific article

A full genome scan for late onset Alzheimer's disease.

scientific article published in February 1999

A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis

article

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk

scientific article published on 11 November 2012

A genomewide linkage study of age at onset in schizophrenia

article

A linkage study of chromosome 22q in sib-pairs with schizophrenia

A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia.

scientific article published in March 1998

A modifier of Huntington's disease onset at the MLH1 locus

scientific article published in October 2017

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

scientific article

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

scientific article published on 7 December 2012

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

scientific article published on 13 November 2013

A polygenic resilience score moderates the genetic risk for schizophrenia

scientific article published on 06 September 2019

A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin

scientific article published on 25 September 2015

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease

scientific article

A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies

scientific article

A survey of genetic human cortical gene expression

article

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

scientific article published on 18 November 2003

A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease

scientific article

ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure

scientific article

Allowing for genotyping error in analysis of unmatched case-control studies.

scientific article

Alpha-2 macroglobulin gene and Alzheimer disease.

scientific article published in May 1999

Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease

scientific article published on January 2004

An examination of single nucleotide polymorphism selection prioritization strategies for tests of gene-gene interaction

scientific article published on 9 April 2011

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

scientific article

Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.

scientific article published on 21 July 2015

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

Analysis of shared heritability in common disorders of the brain

Association between a PS-1 intronic polymorphism and late onset Alzheimer's disease

scholarly article by P Kehoe et al published 2 September 1996 in NeuroReport

Association of ABCA1 with late-onset Alzheimer's disease is not observed in a case-control study.

scientific article

Association of Elevated Urinary miR-126, miR-155, and miR-29b with Diabetic Kidney Disease

Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family

scientific article

Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease

scientific article published in October 1997

Association of the angiotensin I converting enzyme gene deletion polymorphism with early onset of ESRF in PKD1 adult polycystic kidney disease

article

Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme.

scientific article

Association studies in psychiatric genetics

article

Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT).

scientific article published in September 1997

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

Autosome search for schizophrenia susceptibility genes in multiply affected families

article

Bayesian trio models for association in the presence of genotyping errors.

scientific article published in January 2004

Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants

scientific article

Bipolar affective puerperal psychosis: genome-wide significant evidence for linkage to chromosome 16.

scientific article published in July 2007

Brain Regions Showing White Matter Loss in Huntington's Disease Are Enriched for Synaptic and Metabolic Genes

scientific article

Brain gene expression correlates with changes in behavior in the R6/1 mouse model of Huntington's disease.

scientific article published on 13 August 2007

Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder ⬇️

scientific article published on August 5, 2010

Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1.

scientific article published on 8 January 2008

Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants

scientific article

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

scientific article

Common alleles contribute to schizophrenia in CNV carriers.

scientific article published on 22 September 2015

Common polygenic variation enhances risk prediction for Alzheimer's disease

scientific article published on 21 October 2015

Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

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 on chromosome 6p22.1 are associated with schizophrenia

scientific article

Comparison of Methods for Combining Case-Control and Family-Based Association Studies

Conservation of regional gene expression in mouse and human brain

scientific article published on April 2007

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

scientific article

Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia

scientific article

Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease

scientific article published on 12 March 2012

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

scientific article

Correction: ACSL6 Is Associated with the Number of Cigarettes Smoked and Its Expression Is Altered by Chronic Nicotine Exposure

scientific article published on 14 August 2012

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

scientific article published on 11 February 2011

Covariate linkage analysis of GAW14 simulated data incorporating subclinical phenotype, sex, population, parent-of-origin, and interaction

scientific article

DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases

scientific article published on 04 April 2016

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.

scientific article

De novo CNVs in bipolar affective disorder and schizophrenia

scientific article

De novo mutations in schizophrenia implicate synaptic networks

scientific article

Design of Case-controls Studies with Unscreened Controls

article by V. Moskvina et al published September 2005 in Annals of Human Genetics

Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease

scientific article published in January 2000

Detecting Gene-Gene Interactions Using Affected Sib Pair Analysis with Covariates

article

Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13?

scientific article published on September 2008

Dopa-responsive dystonia: A clinical and molecular genetic study

scientific article published on 01 October 1998

Effect of Genotyping Error on Type-I Error Rate of Affected Sib Pair Studies with Genotyped Parents

scientific article published on 26 May 2005

Effects of differential genotyping error rate on the type I error probability of case-control studies

scientific article published on 06 April 2006

Effects of low birth weight, maternal smoking in pregnancy and social class on the phenotypic manifestation of Attention Deficit Hyperactivity Disorder and associated antisocial behaviour: investigation in a clinical sample

scientific article

Efficient strategies for genome scanning with affected sib pairs

scientific article published in January 1998

Erratum: A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia

article

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 significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC

scholarly article published in Molecular Psychiatry

Erratum: Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22

article

Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study

scientific article published on 17 October 2011

Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants

article

Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha.

scientific article published on 29 September 2009

Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease

scientific article

Examining pathways between genetic liability for schizophrenia and patterns of tobacco and cannabis use in adolescence

scientific article published on 09 June 2020

Exome arrays capture polygenic rare variant contributions to schizophrenia.

scientific article published on 5 January 2016

Expression profiling of Huntington's disease models suggests that brain-derived neurotrophic factor depletion plays a major role in striatal degeneration

scientific article

Factor derived sub-syndromes of schizophrenia and familial morbid risks

Factor-derived subsyndromes of schizophrenia and familial morbid risks

scientific article published on 01 February 1997

Familial phenotype differences in PKD11.

scientific article

Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder

scientific article published on 06 April 2010

Full genome screen for Alzheimer disease: Stage II analysis

article

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia.

scientific article

Gender differences in CNV burden do not confound schizophrenia CNV associations.

scientific article published on 17 May 2016

Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder

scientific article

Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease

scientific article published on 08 July 2019

Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

scientific article

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

scientific article

Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease

scientific article (publication date: March 2005)

Genetic control of human brain transcript expression in Alzheimer disease

scientific article published on April 2009

Genetic differences between five European populations

scientific article published on 08 July 2010

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

scientific article (publication date: 15 November 2010)

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 predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis

scientific article

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

scientific article

Genetic risk sum score comprised of common polygenic variation is associated with body mass index

scientific article

Genetic studies on chromosome 12 in late-onset Alzheimer disease.

scientific article published in August 1998

Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease.

scientific article published in July 1999

Genetics of Recurrent Early-Onset Major Depression (GenRED): Final Genome Scan Report

article

Genetics of recurrent early-onset depression (GenRED): design and preliminary clinical characteristics of a repository sample for genetic linkage studies

scientific article published in May 2003

Genetics of recurrent early-onset major depression (GenRED): final genome scan report

scientific article published on February 2007

Genetics of recurrent early-onset major depression (GenRED): significant linkage on chromosome 15q25-q26 after fine mapping with single nucleotide polymorphism markers.

scientific article published on February 2007

Genome scan for association and linkage

Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease.

scientific article

Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes

scientific article published on 14 October 2005

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

scientific article published on February 2012

Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci.

scientific article published on 12 April 2016

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

scientific article published in October 2013

Genome-wide association of mood-incongruent psychotic bipolar disorder

scientific article

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

scientific article

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

scientific article

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

scientific article

Genome-wide association study of Alzheimer's disease with psychotic symptoms

scientific 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 clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms ⬇️

scientific article

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 multiplex schizophrenia pedigrees.

scientific article

Genome-wide association study of recurrent early-onset major depressive disorder

scientific journal article

Genome-wide linkage and follow-up association study of postpartum mood symptoms

scientific article published on 15 September 2009

Genome-wide scan in 124 Indonesian sib-pair families with schizophrenia reveals genome-wide significant linkage to a locus on chromosome 3p26-21.

scientific article

Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12

article

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

scientific article

Genomewide Linkage Scan in Schizoaffective Disorder

scientific article published on 01 October 2005

Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample

scientific article

Genomewide significant linkage to recurrent, early-onset major depressive disorder on chromosome 15q.

scientific article

Haplotype-based stratification of Huntington's disease

scientific article

High loading of polygenic risk for ADHD in children with comorbid aggression

scientific article published on August 2013

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

scientific article

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

scientific article

Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations

scientific article

Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis.

scientific article published in October 2007

Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.

scientific article published on February 2012

Investigating the genetic architecture of general and specific psychopathology in adolescence

scientific article published on 08 August 2018

Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depression

scientific article

Likelihood-ratio affected sib-pair tests applied to multiply affected sibships: Issues of power and type I error rate

scientific article published on 01 January 2001

Linkage analyses of rheumatoid arthritis and related quantitative phenotypes: the GAW15 experience

scientific article published on 01 January 2007

Linkage disequilibrium mapping of a chromosome 15q25-26 major depression linkage region and sequencing of NTRK3.

scientific article

Linkage study of chromosome 6p in sib-pairs with schizophrenia.

scientific article published in May 1997

Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder ⬇️

scientific article published on August 1, 2010

Meta-analysis of 32 genome-wide linkage studies of schizophrenia.

scientific article published on 30 December 2008

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

scientific article

Meta-analysis of genetic association with diagnosed Alzheimer's disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing

Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.

scientific article

Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder.

scientific article published on 18 June 2008

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

article

Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries

scientific article published on 29 October 2010

Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III

scientific article

Multicenter linkage study of schizophrenia loci on chromosome 22q.

scientific article published in August 2004

Multiple sclerosis and the HLA-D region: linkage and association studies

scientific article published on 01 May 1995

Multiple testing in the genomics era: findings from Genetic Analysis Workshop 15, Group 15.

scientific article published on January 2007

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

scientific article

No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease.

scientific article published in March 1999

No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia

scientific article

No evidence that extended tracts of homozygosity are associated with Alzheimer's disease.

scientific article published on 2 August 2011

No evidence that rare coding variants in ZNF804A confer risk of schizophrenia.

scientific article published on 22 September 2010

No linkage between multiple sclerosis and the T cell receptor alpha chain locus

scientific article published on June 1994

No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairs

scientific article published on October 1994

No major schizophrenia locus detected on chromosome 1q in a large multicenter sample

scientific article published in April 2002

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

scientific article

Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies

scientific article (publication date: February 2011)

O3-02-06 Linkage analysis of AD SIB pairs indicates evidence of interaction between genes regulating beta-amyloid degradation

article

P4-046 Association of late onset Alzheimer's disease with genetic variation in multiple members of a gene family involved in neuronal apoptosis

article

P4-070 Is APOE exclusively responsible for the AD linkage peak on chromosome 19?

P4-079 Is variation in the gene encoding insulin-degrading enzyme (IDE) a risk factor in late-onset Alzheimer's disease?

article

P4-110 A systematic scan of chromosome 10 single nucleotide polymorphisms identifies novel candidate genes showing strong association to Alzheimer's disease

article

P4-122 Genetic association of an APP binding protein gene with late onset Alzheimer's disease

article

Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23.

scientific article

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy

scientific article

Pathway analyses implicate glial cells in schizophrenia

scientific article

Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis

scientific article

Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia.

scientific article published on 29 September 2011

Phenotypic Manifestation of Genetic Risk for Schizophrenia During Adolescence in the General Population

scientific article published on 27 January 2016

Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia

scientific article

Polygenic dissection of the bipolar phenotype

scientific article

Population-specific genetic modification of Huntington's disease in Venezuela.

scientific article

Promoting Measured Genes and Measured Environments: On the Importance of Careful Statistical Analyses and Biological Relevance—Reply

article

Psychiatric gene discoveries shape evidence on ADHD's biology

scientific article published on 17 November 2015

RNA-Seq of Huntington's disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activation.

scientific article published on 11 May 2016

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

scientific article

Rare chromosomal deletions and duplications increase risk of schizophrenia

scientific article

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

scientific article

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia

scientific article published on April 2010

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

scientific article

Regional and cellular gene expression changes in human Huntington's disease brain

scientific article

Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample

scientific article published on 16 October 2012

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

scientific article

Reply to Curtis

S2-01-04 Progress toward the identification of novel genetic risk factors for late onset Alzheimer's disease

scholarly article by Alison M. Goate et al published July 2004 in Neurobiology of Aging

Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain

scientific article published on 22 February 2011

Scientific rigor and the art of motorcycle maintenance

article

Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia

scientific article published on 23 May 2013

Similar striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntington's disease are not reflected in mutant Huntingtin inclusion prevalence

scientific article published on 21 December 2015

Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22.

scientific article published on September 2005

Statistical methods for pathway analysis of genome-wide data for association with complex genetic traits

scientific article

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia

scientific article

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

scientific article published on 29 January 2009

Susceptibility locus for Alzheimer's disease on chromosome 10.

scientific article

Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region

scientific article published on 01 October 1995

Testing for gene x environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior.

scientific article published in January 2008

The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease

scientific article published on September 2015

The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease

scientific article published on February 2016

The Wellcome trust UK–Irish bipolar affective disorder sibling-pair genome screen: first stage report

article by P Bennett et al published February 2002 in Molecular Psychiatry

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

scientific article

The effect of linkage disequilibrium on linkage analysis of incomplete pedigrees

scientific article

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

scientific article

Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease.

scientific article

Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis

scientific article published in October 2003

Use of phenotypic covariates in association analysis by sequential addition of cases

scientific article published on May 2006

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

scientific article published on 13 August 2012

Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease

scientific article published on 14 February 2013

Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder

scientific article published in October 2010

Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease

article

Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD.

scientific article published in January 2004

Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule.

scientific article

Paulina is supported by:

About Paulina

Help