List of works by Peter Propping

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

article

A complex rearrangement in the APC gene uncovered by multiplex ligation-dependent probe amplification

scientific article published on February 2007

A modified multiplex PCR assay for detection of large deletions in MSH2 and MLH1

scientific article published on 01 March 2002

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

Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants.

scientific article

Activating ERBB2/HER2 mutations indicate susceptibility to pan-HER inhibitors in Lynch and Lynch-like colorectal cancer

scientific article

Analysis of rare APC variants at the mRNA level: six pathogenic mutations and literature review

scientific article published on 05 February 2009

Arylamine N-acetyltransferase type 2 and glutathione S-transferases M1 and T1 polymorphisms in familial adenomatous polyposis

scientific article published in January 2002

Assisted reproduction: an important review of the literature on the risk of malformation after in vitro fertilization and intracytoplasmic sperm injection

scientific article published on 7 January 2008

Association analysis between the human interleukin 1beta (-511) gene polymorphism and susceptibility to febrile convulsions

scientific article published on 01 December 2002

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

article

Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin

scientific article (publication date: 2011)

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

scientific article

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

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

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

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

scientific article

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

scientific article

Compound heterozygosity for twoMSH6 mutations in a patient with early onset colorectal cancer, vitiligo and systemic lupus erythematosus

scientific article published on 01 May 2008

Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation.

scientific article published in September 2003

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

Deciphering the genetics of hereditary non-syndromic colorectal cancer

scientific article published on 16 July 2008

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

Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer

scientific article published on 14 October 2009

Embryo screening: update German view of genetic testing

scientific article

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

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

Expanded extracolonic tumor spectrum in MUTYH-associated polyposis

scientific article

FHL2 expression in peritumoural fibroblasts correlates with lymphatic metastasis in sporadic but not in HNPCC-associated colon cancer

scientific article

Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.

scientific article

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

Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis ⬇️

scientific article published on January 1, 2004

Frequency of Microsatellite Instability in Unselected Sebaceous Gland Neoplasias and Hyperplasias ⬇️

scientific article published on May 1, 2003

Friedrich Vogel 1925–2006

From degeneration to genetic susceptibility, from eugenics to genethics, from Bezugsziffer to LOD score: the history of psychiatric genetics

scientific article

Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations

scientific article

Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1).

scientific article published in November 2005

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

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

scientific article published on 17 March 2008

Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63

scientific article published on 01 April 2002

Genetic analysis for early diagnosis of otorhinolaryngeal diseases.

scientific article

Genetic contribution to variation in cognitive function: an FMRI study in twins

scientific article published in March 2009

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

scientific article

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

scientific article

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

scientific article

Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.

scientific article published on 14 October 2013

Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.

scientific article

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

scientific article

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

scientific article

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

article

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

scientific article

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

scientific article (publication date: 11 March 2014)

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

scientific journal article

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.

scientific article

Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium.

scientific article published on 14 August 2006

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

Hereditary nonpolyposis colorectal cancer (HNPCC)/Lynch syndrome

scientific article

Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes

scientific article

Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes

scientific article

High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome

scientific article

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

scientific article

Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease

scientific article

ISPG Lifetime Achievement Award 2004.

scientific article published in July 2005

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

scientific article

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

scientific article published in May 2013

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

article

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

scientific article published in November 2004

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

Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers

scientific article published on 13 June 2002

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 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 genomic aberrations in MSH2 and MLH1 genes are frequent in Chinese colorectal cancer.

scientific article

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

article

Loss of DNA mismatch repair proteins in skin tumors from patients with Muir-Torre syndrome and MSH2 or MLH1 germline mutations: establishment of immunohistochemical analysis as a screening test

scientific article published on 01 March 2002

MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype

scientific article published on 01 August 2006

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

article

Maternal uniparental disomy 14 in a 15-year-old boy with normal karyotype and no evidence of precocious puberty

scientific article published on 01 June 2005

May the APC gene somatic mutations in tumor tissues influence the clinical features of Chinese sporadic colorectal cancers?

scientific article published on 01 January 2007

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

scientific article

Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies

scientific article published in June 2011

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

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

article

Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

scientific article (publication date: April 2003)

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

scientific article published on 01 April 1997

Nine novel pathogenic germline mutations in MLH1, MSH2, MSH6 and PMS2 in families with Lynch syndrome

scientific article published on 01 January 2007

No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients

scientific article published on 27 February 2008

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 genetic variants at the ASCT1 gene and schizophrenia or bipolar disorder in a German sample

article

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 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 association between NOTCH4 and schizophrenia in a large family-based and case???control association analysis

article

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

article

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

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 de novo mutation of MADH4/SMAD4 in a patient with juvenile polyposis

scientific article published on 01 July 2002

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

article

Polymorphisms in CTNNBL1 in relation to colorectal cancer with evolutionary implications

scientific article

Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study

scientific article

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

Primary immunodeficiency in combination with transverse upper limb defect and anal atresia in a 34-year-old patient with Jacobsen syndrome.

scientific article published in April 2004

Prodynorphin gene promoter polymorphism and temporal lobe epilepsy

scientific article published on 01 February 2003

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer ⬇️

scientific article

Response

Risks of less common cancers in proven mutation carriers with lynch syndrome

scientific article published on 22 October 2012

Role of the oxidative DNA damage repair gene OGG1 in colorectal tumorigenesis

scientific article published on 12 July 2013

Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?

scientific article

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

scientific article

Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP).

scientific article published in October 2007

Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer

scientific article published on 01 September 2005

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

scientific article

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

scientific 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-HT 2A ) receptor gene: identification of two naturally occurring receptor variants and association analysis in schizophrenia

article

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

article

Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families

article

The Andalusian Bipolar Family (ABiF) Study: Protocol and sample description

scientific article published on 12 June 2017

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 biography of psychiatric genetics: from early achievements to historical burden, from an anxious society to critical geneticists

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 impact of genetics on psychiatric nosology.

scientific article published in December 2006

The optimization of polar body diagnosis: a consequence of the german embryo protection act.

scientific article published on 14 March 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

Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.

scientific article published on 4 October 2006

Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining

scientific article published on 01 December 2005

Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples

scientific article

“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)

article

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