Peter Propping

Q: What Schools Are Affiliated With Peter Propping

Peter Propping is affiliated with the following schools: Vrije Universiteit Amsterdam, University of Cologne, University of Melbourne, University of Szeged, Free University of Berlin, University of Hamburg, RWTH Aachen University, Maastricht University, University of Bonn, Radboud University Nijmegen

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Peter Propping

Biology

#4791

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#7102

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Genetics

#432

World Rank

#499

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Biology

Peter Propping's Degrees

PhD Genetics University of Cologne
Doctorate Medicine University of Cologne

Why Is Peter Propping Influential?

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According to Wikipedia, Peter Propping was a German human geneticist. The scientific work of Propping spans genetically complex diseases, especially affecting brain function such as alcoholism, manic depressive disorders, schizophrenia, epilepsy, and in addition hereditary cancer predispositions. He also studied the history of human genetics and eugenics. From 1984 to 2008 he was director of the Institute of Human Genetics of the University of Bonn.

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Peter Propping's Published Works

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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
Identification of loci associated with schizophrenia by genome-wide association and follow-up (2008) (1069)
A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy (1995) (1063)
A potassium channel mutation in neonatal human epilepsy. (1998) (1022)
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (2011) (929)
Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers (1999) (733)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder (2008) (675)
Excess of high activity monoamine oxidase A gene promoter alleles in female patients with panic disorder. (1999) (615)
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. (2003) (592)
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 (2009) (430)
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database (2013) (419)
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate (2010) (391)
An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy. (1997) (347)
Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder (2004) (326)
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci (2012) (316)
Genome-wide association study reveals two new risk loci for bipolar disorder (2014) (311)
Expanded extracolonic tumor spectrum in MUTYH-associated polyposis. (2009) (309)
Evidence for a Relationship Between Genetic Variants at the Brain-Derived Neurotrophic Factor (BDNF) Locus and Major Depression (2005) (305)
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. (2011) (286)
Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families (2001) (285)
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies (2003) (271)
Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. (1996) (264)
Risks of less common cancers in proven mutation carriers with lynch syndrome. (2012) (258)
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. (2006) (254)
High proportion of large genomic STK11 deletions in Peutz‐Jeghers syndrome (2005) (246)
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q. (2005) (235)
A similarity-based method for genome-wide prediction of disease-relevant human genes (2002) (232)
Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria. (1998) (231)
Familial adenomatous polyposis: mutation at codon 1309 and early onset of colon cancer (1994) (226)
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B (2000) (222)
High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome (2007) (222)
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia. (2005) (211)
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease. (2003) (199)
MUTYH‐associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype (2006) (197)
Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder (2008) (195)
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease (2001) (187)
Evidence for linkage of spelling disability to chromosome 15. (1998) (178)
Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer. (2010) (172)
Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers (2002) (169)
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 (1998) (164)
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 (2002) (159)
Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium. (2006) (158)
An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics (1996) (154)
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. (2016) (153)
The power of sample size and homogenous sampling: Association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder (2005) (152)
Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis (2004) (151)
Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia. (1998) (150)
The electroencephalogram (EEG) as a research tool in human behavior genetics: Psychological examinations in healthy males with various inherited EEG variants (1979) (146)
A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q. (2001) (145)
Lack of evidence for allelic association between personality traits and the dopamine D4 receptor gene polymorphisms. (1997) (140)
Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP) (2007) (138)
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. (2005) (137)
Association between the 5' UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder. (2001) (133)
Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families (1999) (133)
A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome (2004) (130)
Nonreplication of association between mu-opioid-receptor gene (OPRM1) A118G polymorphism and substance dependence. (2001) (129)
Susceptibility variants for male-pattern baldness on chromosome 20p11 (2008) (122)
Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain. (1998) (121)
Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder. (2007) (120)
Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer (2005) (120)
Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63. (2002) (119)
Systematic search for variation in the human norepinephrine transporter gene: identification of five naturally occurring missense mutations and study of association with major psychiatric disorders. (1996) (118)
PRENATAL DIAGNOSIS OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE WITH A DNA PROBE (1986) (118)
[S3-Guidelines Conference "Colorectal Carcinoma" 2004]. (2004) (117)
Genetic Contribution to Variation in Cognitive Function: An fMRI Study in Twins (2009) (115)
Efficacy and side‐effects of clozapine not associated with variation in the 5‐HT2C receptor (1997) (115)
Hereditary nonpolyposis colorectal cancer: Frequent occurrence of large genomic deletions in MSH2 and MLH1 genes (2003) (114)
Chromocolonoscopy detects more adenomas than white light colonoscopy or narrow band imaging colonoscopy in hereditary nonpolyposis colorectal cancer screening. (2009) (114)
Association Between TAS2R38 Gene Polymorphisms and Colorectal Cancer Risk: A Case-Control Study in Two Independent Populations of Caucasian Origin (2011) (113)
Familial adenomatous polyposis: Aberrant splicing due to missense or silent mutations in the APC gene (2004) (112)
Frequent 4‐bp deletion in exon 9 of the SMAD4/MADH4 gene in familial juvenile polyposis patients (1999) (110)
Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1. (1995) (109)
Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations? (2006) (109)
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 (1996) (105)
S3 guidelines for colorectal carcinoma: results of an evidence-based consensus conference on February 6/7, 2004 and June 8/9, 2007 (for the topics IV, VI and VII). (2010) (104)
Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1) (2000) (104)
Cystic sebaceous tumors as marker lesions for the Muir-Torre syndrome: a histopathologic and molecular genetic study. (1999) (103)
Genetic aspects of the EEG: an investigation into the within-pair similarity of monozygotic and dizygotic twins with a new method of analysis. (1987) (103)
Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationships to monoamine metabolite concentrations in CSF of healthy volunteers (1998) (101)
Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining (2005) (99)
Genetic variation of the 5-HT2A receptor and response to clozapine (1995) (98)
DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation (2007) (94)
Microsatellite instability—a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer (1999) (93)
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations. (2009) (92)
Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants (2006) (92)
Attenuated familial adenomatous polyposis due to a mutation in the 3′ part of the APC gene. A clue for understanding the function of the APC protein (1996) (91)
Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis (2005) (89)
Retraction: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies (2003) (88)
Different familial transmission patterns in bipolar I disorder with onset before and after age 25. (2001) (88)
Efficacy and Side-Effects of Clozapine: Testing for Association with Allelic Variation in the Dopamine D4 Receptor Gene (1996) (87)
Frequency of microsatellite instability in unselected sebaceous gland neoplasias and hyperplasias. (2003) (87)
Metabotropic glutamate receptor 3 (GRM3) gene variation is not associated with schizophrenia or bipolar affective disorder in the German population. (2002) (86)
Hereditary nonpolyposis colorectal cancer (HNPCC)/Lynch syndrome. (2013) (86)
Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach (2001) (85)
Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder (2012) (85)
Association between a promoter polymorphism in the dopamine D2 receptor gene and schizophrenia (1999) (85)
Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease. (2008) (81)
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 (2006) (77)
Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population. (2003) (76)
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. (1996) (75)
Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2 (2009) (75)
Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1). (1994) (74)
Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene? (1996) (73)
Consensus paper of the WFSBP Task Force on Genetics: Genetics, epigenetics and gene expression markers of major depressive disorder and antidepressant response (2017) (73)
Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association study (2001) (73)
Investigation of the human serotonin 6 [5-HT6] receptor gene in bipolar affective disorder and schizophrenia. (2000) (72)
Lack of association between dopamine D1 and D2 receptor genes and bipolar affective disorder. (1992) (72)
ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia. (1993) (69)
S3-Guidelines Colorectal Cancer 2004 (2005) (68)
Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies. (1997) (67)
Dopamine D3 receptor variant and tardive dyskinesia (2000) (67)
No association between serotonin transporter gene polymorphisms and personality traits. (1999) (67)
Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposis. (1994) (67)
Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients (2004) (67)
5HT2a receptor T102C polymorphism and schizophrenia (1996) (65)
Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome (2008) (65)
Novel Hairless mutations in two kindreds with autosomal recessive papular atrichia. (1999) (64)
Activating ERBB2/HER2 mutations indicate susceptibility to pan-HER inhibitors in Lynch and Lynch-like colorectal cancer (2015) (63)
Effect of alcohol on genetically determined variants of the normal electroencephalogram (1980) (63)
Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patients. (2001) (63)
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 (1993) (62)
Excess of homozygosity at the dopamine D3 receptor gene in schizophrenia not confirmed. (1993) (61)
Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder (2015) (61)
Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia. (2001) (60)
No evidence of association between dopamine D3 receptor gene and bipolar affective disorder. (1997) (60)
Identification of Genetic Variation in the Human Serotonin 1Dβ Receptor Gene (1994) (60)
Human δ‐opioid receptor gene and susceptibility to heroin and alcohol dependence (1999) (59)
Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility. (2010) (59)
G72 and its association with major depression and neuroticism in large population-based groups from Germany. (2008) (59)
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. (2005) (58)
Association versus linkage studies in psychosis genetics. (1993) (58)
A gene for universal congenital alopecia maps to chromosome 8p21-22. (1998) (57)
A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25–q26 (2001) (56)
Developmental Dyslexia – Recurrence Risk Estimates from a German Bi-Center Study Using the Single Proband Sib Pair Design (2005) (56)
Association between a promoter dopamine D2 receptor gene variant and the personality trait detachment (2003) (55)
Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin (2004) (55)
The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders (2017) (54)
The kinetics of ethanol absorption and elimination in twins and supplementary repetitive experiments in singleton subjects (2004) (54)
Association analysis between the human interleukin 1β (−511) gene polymorphism and susceptibility to febrile convulsions (2002) (53)
5-HT2A receptor and bipolar affective disorder: association studies in affected patients (1997) (52)
Lack of association between dopamine D4 receptor gene and personality traits (1998) (52)
Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease. (1993) (52)
Twins as a tool of behavioral genetics. (1993) (52)
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3. (2000) (52)
Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples (2009) (52)
The human serotonin 7 (5-HT7) receptor gene: genomic organization and systematic mutation screening in schizophrenia and bipolar affective disorder. (1996) (51)
"Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivation. (2001) (51)
Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26–q26.1 (1993) (50)
Towards mapping phenotypical traits in 18p− syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation (2007) (50)
Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics (2017) (50)
Further evidence for age of onset being an indicator for severity in bipolar disorder. (2002) (49)
Exon–Intron Structure of the Human Neuronal Nicotinic Acetylcholine Receptor α4 Subunit (CHRNA4) (1996) (48)
RFLP alleles at the tyrosine hydroxylase locus: No association found to affective disorders (1990) (48)
Mutagenic activity of isoniazid and hydrazine in mammalian test systems. (1972) (47)
Association of major depression with rare functional variants in norepinephrine transporter and serotonin1A receptor genes (2009) (47)
Monoamine related functional gene variants and relationships to monoamine metabolite concentrations in CSF of healthy volunteers (2004) (47)
Interrelationship and Familiality of Dyslexia Related Quantitative Measures (2007) (46)
Compound heterozygosity for two MSH6 mutations in a patient with early onset colorectal cancer, vitiligo and systemic lupus erythematosus (2008) (46)
MSH6 mutation in Muir–Torre syndrome: could this be a rare finding? (2007) (46)
Nonreplication of linkage disequilibrium between the dopamine D4 receptor locus and Tourette syndrome. (1997) (46)
Genetic disposition to alcoholism. An EEG study in alcoholics and their relatives (1981) (46)
No Association Between the Putative Functional ZDHHC8 Single Nucleotide Polymorphism rs175174 and Schizophrenia in Large European Samples (2005) (45)
Tourette syndrome and the norepinephrine transporter gene: results of a systematic mutation screening. (1999) (45)
Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene (1995) (45)
Comparative investigations on the mutagenicity of pesticides in mammalian test systems (1973) (45)
Genetic control of ethanol action on the central nervous system (1977) (45)
Genetic determination of the human EEG (1988) (44)
Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder (2008) (44)
DRD4 exon III VNTR polymorphism—susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach (2000) (43)
CLCN2 variants in idiopathic generalized epilepsy (2009) (43)
Neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) and panic disorder: an association study. (1997) (43)
Dopamine D2 receptor molecular variant and schizophrenia (1994) (42)
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36. (2000) (42)
Genetic Counseling in a Patient with XXY/XXXY/XY Mosaic Klinefelter’s Syndrome: Estimate of Sex Chromosome Aberrations in Sperm Before Intracytoplasmic Sperm Injection (1998) (41)
Genetic variation of CNS receptors--a new perspective for pharmacogenetics. (1995) (41)
Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample (2007) (41)
Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region (1997) (40)
Clinical evidence for genomic imprinting in bipolar I disorder (1995) (39)
Lack of association between schizophrenia and alleles of the dopamine D1, D2, D3 and D4 receptor loci1 (1993) (39)
Modified ligand binding to the naturally occurring Cys-124 variant of the human serotonin 5-HT1B receptor. (1999) (39)
Pharmacological properties of naturally occurring variants of the human norepinephrine transporter. (2000) (38)
Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes (2005) (38)
A modified multiplex PCR assay for detection of large deletions in MSH2 and MLH1 (2002) (38)
Tyrosine hydroxylase polymorphisms and manic-depressive illness (1990) (38)
Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15 (2009) (38)
Deciphering the genetics of hereditary non-syndromic colorectal cancer (2008) (37)
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. (2007) (37)
Genetic variation of the 5-HT2A receptor and response to clozapine. (1995) (37)
The voltage-gated sodium channel gene SCN2A and idiopathic generalized epilepsy (2001) (37)
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy (2003) (37)
Probable metachromatic leukodystrophy/pseudodeficiency compound heterozygote at the arylsulfatase A locus with neurological and psychiatric symptomatology. (1988) (36)
Pharmacogenetics of schizophrenia. (2000) (36)
Human adenosine A2a receptor (A2aAR) gene: systematic mutation screening in patients with schizophrenia (2005) (36)
Investigation of the DAOA/G30 locus in panic disorder (2005) (36)
Tourette's syndrome and homozygosity for the dopamine D3 receptor gene (1993) (35)
Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German‐British sample of manic depressive patients and controls (1994) (35)
An association study of a neurotrophic3 (NT‐3) gene polymorphism with schizophrenia (1995) (35)
Frequency of Hereditary Non-Polyposis Colorectal Cancer among Unselected Patients with Colorectal Cancer in Germany (2006) (34)
Genetic Variation in Human 5‐HT Receptors: Potential Pathogenetic and Pharmacological Role a (1998) (34)
Association between a polymorphism in the pseudoautosomal X-linked gene SYBL1 and bipolar affective disorder. (2002) (33)
Novel 5'-regulatory region polymorphisms of the 5-HT2C receptor gene: association study with panic disorder. (2000) (33)
No association between dopamine D4 receptor gene variants and Novelty Seeking (2002) (33)
Single-strand conformation analysis (SSCA) of the dopamine D1 receptor gene (DRD1) reveals no significant mutation in patients with schizophrenia and manic depression (1994) (32)
Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study (2010) (32)
Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial cases (1996) (32)
FHL2 expression in peritumoural fibroblasts correlates with lymphatic metastasis in sporadic but not in HNPCC-associated colon cancer (2011) (32)
ADULT syndrome allelic to limb mammary syndrome (LMS)? (2000) (31)
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family (2000) (31)
A family-based and case–control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder (2005) (31)
Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families (2014) (30)
Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21 (2011) (30)
5HT 2a receptor T102C polymorphism and schizophrenia. (1996) (30)
Ileorectal anastomosis is appropriate for a subset of patients with familial adenomatous polyposis. (2001) (29)
Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios. (2001) (29)
Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3. (2014) (28)
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer (2015) (28)
Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31. (2009) (28)
Detection of APC and k-ras mutations in the serum of patients with colorectal cancer. (2001) (28)
Patterns of parental transmission and familial aggregation models in bipolar affective disorder. (1998) (28)
Genetic counseling in a patient with XXY/XXXY/XY mosaic Klinefelter's syndrome: estimate of sex chromosome aberrations in sperm before intracytoplasmic sperm injection. (1998) (28)
From degeneration to genetic susceptibility, from eugenics to genethics, from Bezugsziffer to LOD score: the history of psychiatric genetics (2004) (27)
Muir‐Torre syndrome: clinical features and molecular genetic analysis (1997) (27)
Apolipoprotein E genotype distribution in schizophrenia (1996) (27)
Human delta-opioid receptor gene and susceptibility to heroin and alcohol dependence. (1999) (27)
Small bowel cancer risk in Lynch syndrome (2008) (26)
Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations. (2002) (26)
Is there an increase of reproductive rates in schizophrenics? (1983) (26)
The biography of psychiatric genetics: From early achievements to historical burden, from an anxious society to critical geneticists (2005) (25)
Predictive diagnosis in familial adenomatous polyposis: evaluation of molecular genetic and ophthalmologic methods. (1993) (24)
Phylogenetic conservation of the benzodiazepine binding sites: Pharmacological evidence (1988) (24)
A Novel Missense Mutation in the DNA Mismatch Repair Gene hMLH1 Present among East Asians but Not among Europeans (1998) (24)
Polymorphic MAO-A and 5-HT-Transporter Genes: Analysis of Interactions in Panic Disorder (2000) (24)
No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients (2008) (23)
3H-imipramine binding in human platelets: A study in normal twins (1984) (23)
Qualitative variation of photolabelled benzodiazepine receptors in different species (1986) (23)
Early ontogeny of the central benzodiazepine receptor in human embryos and fetuses. (1988) (23)
Identification of genetic variation in the human serotonin 1D beta receptor gene. (1994) (23)
Primary immunodeficiency in combination with transverse upper limb defect and anal atresia in a 34‐year‐old patient with Jacobsen syndrome (2004) (23)
Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes. (1997) (23)
Can long-range microsatellite data be used to predict short-range linkage disequilibrium? (2002) (23)
Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation (2003) (23)
Investigation of complement C4B deficiency in schizophrenia. (1997) (23)
Lack of genetically determined structural variants of the human serotonin-1E (5-HT1E) receptor protein points to its evolutionary conservation. (1995) (22)
No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach (2003) (22)
Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implications (1989) (22)
Schizophrenia: genetic tools for unraveling the nature of a complex disorder. (1995) (22)
Comparative investigations on the chemical induction of point mutations and dominant lethal mutations in mice (2004) (22)
Association study between two variants in the DOPA decarboxylase gene in bipolar and unipolar affective disorder. (2002) (22)
Role of the oxidative DNA damage repair gene OGG1 in colorectal tumorigenesis. (2013) (21)
No association between a promoter dopamine D(4) receptor gene variant and schizophrenia. (2001) (21)
Linkage analyses of chromosomal region 18p11-q12 in dyslexia (2006) (21)
Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls. (2000) (21)
Is there an increase of reproductive rates in schizophrenics? (1982) (20)
Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15–q21 (2008) (20)
Platelet MAO activity in patients with affective psychosis and their first-degree relatives. (1981) (20)
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) (2005) (20)
Genotype-phenotype relationship in various degrees of arylsulfatase A deficiency (1991) (20)
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder (2016) (20)
Pharmacogenetics of alcohol's CNS effect: Implications for the etiology of alcoholism (1983) (19)
Hereditary nonpolyposis colorectal cancer (HNPCC): Eight novel germline mutations in hMSH2 or hMLH1 genes (1997) (19)
Analysis of rare APC variants at the mRNA level: six pathogenic mutations and literature review. (2009) (19)
Direct-to-consumer genetic testing for health-related purposes in the European Union (2012) (19)
Novel de novo mutation of MADH4/SMAD4 in a patient with juvenile polyposis. (2002) (19)
European collaborative study of early‐onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset (2010) (19)
The shark GABA-benzodiazepine receptor: further evidence for a not so late phylogenetic appearance of the benzodiazepine receptor (1988) (19)
Exonic variants of the GABAB receptor gene and panic disorder (2000) (18)
Description of the Genetic Analysis Workshop 10 bipolar disorder linkage data sets (1997) (18)
The voltage-gated sodium channel beta2-subunit gene and idiopathic generalized epilepsy. (2000) (17)
Eleven novel germline mutations in the adenomatous polyposis coli (APC) gene. (1994) (17)
Familial Cosegregation of Affective Disorder and Hailey-Hailey Disease (1993) (17)
The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family‐based association approach (2002) (17)
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 (1997) (17)
Low platelet MAO activity and schizophrenia: sex differences (1981) (17)
Nine novel pathogenic germline mutations in MLH1, MSH2, MSH6 and PMS2 in families with Lynch syndrome (2007) (17)
Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia. (1996) (17)
Phenotypic consequences of low arylsulfatase A genotypes (ASAp/ASAp and ASA-/ASAp): does there exist an association with multiple sclerosis? (1991) (17)
hSKCa3: no association of the polymorphic CAG repeat with bipolar affective disorder and schizophrenia. (1999) (17)
No association between serotonin 2A receptor gene variants and personality traits (2001) (16)
Exon-intron structure of the human neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4). (1996) (16)
Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies. (1998) (15)
A somatic mutation in the adenomatous polyposis coli (APC) gene in peripheral blood cells--implications for predictive diagnosis. (1994) (15)
Genetic disorders presenting as “schizophrenia”. Karl bonhoeffer's early view of the psychoses in the light of medical genetics (2004) (15)
Low arylsulphatase A activity and choreoathetotic syndrome in three siblings: differentiation of pseudodeficiency from metachromatic leukodystrophy (1991) (15)
Alcohol effects on the percentage of beta waves in the electroencephalograms of twins (1988) (14)
Familial adenomatous polyposis: A submicroscopic deletion at the APC locus in a family with mentally normal patients (1996) (14)
Variant 1859G-->A (Arg620Gln) of the "hairless" gene: absence of association with papular atrichia or androgenic alopecia. (2001) (14)
Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families. (2008) (14)
Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder (2006) (14)
Family history influences age of onset in bipolar I disorder in females but not in males (2005) (14)
Systematic investigation of genetic variability in 111 human genes—implications for studying variable drug response (2005) (14)
Human erythrocyte transketolase: no evidence for variants. (1987) (13)
Genetic control of adrenergic receptors on human platelets. A twin study (2004) (13)
Is there an increase of reproductive rates in schizophrenics? (1983) (13)
No association between a putative functional promoter variant in the dopamine beta-hydroxylase gene and schizophrenia. (2003) (13)
[S3-guideline conference "Colorectal Cancer" 2004]. (2005) (13)
A novel germline mutation in the hMLH1 DNA mismatch repair gene in a patient with an isolated cystic sebaceous tumor. (1999) (13)
No evidence of association between dopamine D4 receptor variants and bipolar affective disorder. (1994) (13)
Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy. (2000) (13)
May the APC gene somatic mutations in tumor tissues influence the clinical features of Chinese sporadic colorectal cancers? (2007) (13)
Peutz‐Jeghers syndrome: Four novel inactivating germline mutations in the STK11 gene (1999) (13)
No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy (2000) (13)
[Genetic association in psychiatric diseases. Concepts and findings]. (1994) (13)
Large genomic aberrations in MSH2 and MLH1 genes are frequent in Chinese colorectal cancer. (2005) (13)
No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample. (2007) (13)
The use of microsatellites in zygosity diagnosis of twins. (1993) (12)
Tyrosine hydroxylase gene and manic-depressive illness (1995) (12)
Estrogen receptor 1 gene (ESR1) variants in panic disorder. (2002) (12)
Twin studies in medical genetics. (1974) (12)
No association between genetic variants at the ASCT1 gene and schizophrenia or bipolar disorder in a German sample. (2006) (12)
Genetic studies at the receptor level: investigations in human twins and experimental animals. (1986) (12)
Susceptibility for alcoholism: DRD4 exon III polymorphism: a case–control and a family‐based association approach (2000) (12)
Exonic variants of the GABA(B) receptor gene and panic disorder. (2000) (11)
A twin study on three enzymes (DBH, COMT, MAO) of catecholamine metabolism (1978) (11)
Lack of imprinting of the human dopamine D4 receptor (DRD4) gene. (1996) (11)
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. (1995) (11)
No evidence for association between NOTCH4 and schizophrenia in a large family-based and case–control association analysis (2006) (11)
Arylamine N-acetyltransferase type 2 and glutathione S-transferases M1 and T1 polymorphisms in familial adenomatous polyposis. (2002) (11)
Association study of a functional promoter polymorphism in the XBP1 gene and schizophrenia (2006) (11)
Severe persistent nasolacrimal duct obstruction: a typical finding in ADULT syndrome (2006) (10)
The concept of isoreceptors: Application to the nicotinic acetylcholine receptor and the gamma-aminobutyric acidA/benzodiazepine receptor complex (2005) (10)
A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci (2006) (10)
Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder (2008) (10)
Role of the Oxidative DNA Damage Repair Gene OGG1 in Colorectal Tumorigenesis (2013) (10)
Twinning frequencies in Baden-Wurttemberg according to maternal age and parity from 1955 to 1972. (1976) (10)
396. Linkage studies of bipolar disorder to chromosome 18 markers (1996) (10)
No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder (2005) (10)
Intraindividual stability and extent of genetic determination of platelet monoamine oxidase activity. (1981) (10)
Plasma DBH, platelet MAO and proteins of red blood cell membranes in individuals with variants of the normal EEG. (1979) (10)
[Genetics of bipolar affective disorders. Current status of research for identification of susceptibility genes]. (2002) (10)
Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissue (1997) (10)
Reliable computer-assisted classification of the EEG: EEG variants in index cases and their first degree relatives. (1996) (10)
Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome) (1993) (10)
The influence of low arylsulfatase A activity on neuropsychiatric morbidity: a large-scale screening in patients (1986) (10)
Genetic aspects of alcohol action on the electroencephalogram (EEG). (1980) (9)
Polymorphisms in CTNNBL1 in relation to colorectal cancer with evolutionary implications. (2011) (9)
No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample. (2006) (9)
[The incidence of twin births]. (1976) (9)
Limited Tryptic Proteolysis of the Benzodiazepine Binding Proteins in Different Species Reveals Structural Homologies (1988) (8)
Human 5-HT5A receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 7q34-q36 using a polymorphism in the 5' untranslated region. (1997) (8)
A complex rearrangement in the APC gene uncovered by multiplex ligation-dependent probe amplification. (2007) (8)
Pseudoautosomal marker DXYS20 and manic depression. (1993) (8)
Human metabotropic glutamate receptor 2 gene (GRM2): chromosomal sublocalization (3p21.1-p21.2) and genomic organization. (2002) (8)
Maternal uniparental disomy 14 in a 15‐year‐old boy with normal karyotype and no evidence of precocious puberty (2005) (8)
Twins as a tool of behavioral genetics : report of the Dahlem Workshop on What Are the Mechanisms Mediating the Genetic and Environmental Determinants of Behavior? Twins as a Tool of Behavioral Genetics, held in Berlin , 17-22 May 1992 (1993) (8)
[Familial aggregation of psychiatric disorders and the consequences for the psychiatric diagnosis]. (1991) (8)
3H-Imipramine binding in platelets: Influence of varying proportions of intact platelets in membrane preparations on binding (2004) (8)
Autosomal dominant polycystic kidney disease in children. (1987) (7)
No evidence for an association between variants at the ??-amino-n-butyric acid type A receptor ??2 locus and schizophrenia (2007) (7)
Systematic screening for mutations in the human N-methyl-D-aspartate receptor 1 gene in schizophrenic patients from the German population. (2004) (7)
Reliability of presymptomatic test for adenomatous polyposis coli (1991) (7)
[Val384Asp in hMLH1 gene in Chinese, Japanese and German and its etiological role in colorectal cancer]. (1998) (7)
No association between genetic variants at the DGCR2 gene and schizophrenia in a German sample. (2009) (7)
P63 mutations in the EEC, Hay-Wells, ADULT syndromes and in split hand/foot malformation reveals a genotype-phenotype correlation. (2000) (7)
Association study of the GRIA1 and CLINT1 (Epsin 4) genes in a German schizophrenia sample. (2011) (7)
No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia. (2006) (7)
Familial pericentric inversion of chromosome 1 in a boy with Goldenhar's syndrome (2004) (7)
Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy (2000) (7)
Chemical constitution and mutagenic activity of three cyclophosphamides in three mammalian test systems (1973) (7)
What can twin studies contribute to the understanding of adult psychopathology (1993) (6)
Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011) (2011) (6)
CNTF and psychiatric disorders (1996) (6)
Molecular diagnosis of trisomy 18 using DNA recovered from paraffin embedded tissues and possible implications for genetic counselling. (1993) (6)
[Decrease in twin births in the german federal republic (author's transl)]. (1976) (6)
The influence of metabolism on mutagenic activity in the host-mediated assay (1971) (6)
Tourette's syndrome and homozygosity for the dopamine D3 receptor gene. German Tourette's Syndrome Collaborative Research Group. (1993) (6)
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 (2009) (6)
Genetics – Ethical Implications of Research, Diagnostics and Counseling (2010) (5)
Benign essential tremor. (2019) (5)
Family‐based association studies of α‐adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder (2004) (5)
TO JMG A genotype-phenotype correlation in HNPCC : strong predominance of msh 2 mutations in 41 patients with Muir-Torre syndrome (2004) (5)
[Genetic counseling in schizophrenia]. (2008) (5)
Family-based association studies of alpha-adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder. (2004) (5)
Abuse of genetics in Nazi Germany. (1992) (5)
Mapping of a gene for nonspecific X-linked mental retardation (MRX 75) to Xq24-q26. (2000) (5)
Assignment of the human serotonin 4 receptor gene (HTR4) to the long arm of chromosome 5 (5q31-q33). (1998) (5)
Platelet MAO activity and high risk for psychopathology in a German population. (1983) (4)
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors (2012) (4)
Platelet monoamine oxidase activity in first-degree relatives of schizophrenic patients (1979) (4)
Comparative investigations on the mutagenic activity of isoniazid in mammalian test systems (1973) (4)
The NOTCH4 locus and schizophrenia: Analyses in the german and palestinian Arab population (2001) (4)
[Detection of germline mutations in the APC gene with the protein truncation test]. (2005) (4)
Assignment of the human serotonin 1F receptor gene (HTR1F) to the short arm of chromosome 3 (3p13-p14.1). (1997) (4)
Strauch et al reply (2000) (4)
No association between length of the (CAG) n repeat of the huntington's disease gene and tourette's syndrome (1995) (4)
[Heterozygous alpha-1-antitrypsin deficiency (PiMZ): risk factor in the development of primary liver carcinoma in non-cirrhotic liver?]. (2010) (4)
[Isoniazid as a mutagen (author's transl)]. (1973) (4)
“Association study of a functional promoter polymorphism in the XBP1 gene and schizophrenia,” American Journal Of Medical Genetics Part B (Neuropsychiatric Genetics) 141B:71–75 (2006) (2006) (3)
Mutation in the β amyloid precursor protein gene and schizophrenia (1993) (3)
HLA-DR2–frequencies in affective disorders (1990) (3)
Single Gene Effects in Psychiatric Disorders (1987) (3)
No association between the D-aspartate oxidase locus and schizophrenia. (2009) (3)
Ultrathin‐layer isoelectric focusing of the photoaffinity labeled benzodiazepine receptor in calf brain: A new and simple method for the study of integral membrane proteins (1986) (3)
Misleading phenotype in kindred with familial adenomatous polyposis (1992) (3)
Linkage study of bipolar affective disorder with chromosome 4p markers (1996) (3)
Supportive evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and depressive symptoms in affective disorder and schizophrenia (2004) (3)
Pharmacogenetic aspects of psychoactive drugs: Facts and fancy (1973) (3)
[Increased birth weight in psoriasis vulgaris--an evolutionary advantage?]. (1987) (3)
No association between a putative functional promoter variant in the dopamine b-hydroxylase gene and schizophrenia (2003) (3)
DRD4 polymorphisms and personality traits in a Swedish sample of healthy volunteers (1996) (3)
Genetic influences on pharmacodynamic properties of psychotropic drugs. (1979) (3)
Brief Report: No Association Between Premorbid Adjustment in Adult-Onset Schizophrenia and Genetic Variation in Dysbindin (2008) (3)
Psychophysiologic test performance in normal twins and in a pair of identical twins with essential tremor that is suppressed by alcohol (1977) (3)
Alcohol and alcoholism. (1978) (3)
S.27.02 New molecular genetic studies in affective disorders (1996) (2)
Further RFLPs at the human tyrosine hydroxylase locus. (1988) (2)
Genetic Aspects of Brain Maturation and Behavior (1990) (2)
Association study of 20 genetic variants at the (D)-amino acid oxidase gene in schizophrenia. (2010) (2)
Update German view of genetic testing (2014) (2)
No evidence for an association between variants at the gamma-amino-n-butyric acid type A receptor beta2 locus and schizophrenia. (2007) (2)
Genetic Relationship Between the Psychoses — Implications for Genetic Modeling (1990) (2)
Fine mapping of a susceptibility locus for bipolar disorder on chromosome 4P in Bulgarian families (2004) (2)
[The diagnosis of hereditary colorectal carcinomas]. (2008) (2)
No association or linkage between polymorphisms at the porphobilinogen deaminase gene locus and schizophrenia (1993) (2)
PORPHOBILINOGEN DEAMINASE GENE ALLELES IN SCHIZOPHRENIA (1992) (2)
Independent evidence for the VMP/DCDC2/KAAG1 gene locus on chromosomal region 6p22 as susceptibility factor for dyslexia (2005) (2)
HEXOSAMINIDASE-PSEUDODEFICIENCY ?. REPLY (1990) (2)
The Andalusian Bipolar Family (ABiF) Study: Protocol and sample description. (2018) (2)
Comparison of point mutation rates in different species with human mutation rates (2004) (2)
Genetics of Schizophrenia: Discussion (1990) (2)
[Genetic counseling in psychiatric diseases]. (1996) (2)
[Psychiatric genetics]. (1985) (2)
ASSOCIATION AND LINKAGE STUDIES IN BIPOLAR AFFECTIVE DISORDER (1992) (2)
Studying biological vulnerability and heterogeneity--a long way ahead. (1987) (2)
Further evidence for a correlation between EEG synchronization and plasma DBH activity in normal subjects (2005) (2)
The Andalusian Bipolar Family (ABiF) Study: Protocol and sample description (2018) (1)
Misleading phenotype in kinded with familial adenomatous polyposis (1992) (1)
Superantigens in T Cell Mediated Skin Diseases - More than a Coincidence! (1998) (1)
[Diagnosis of familial adenomatosis polyposis]. (1994) (1)
Analysis of germline mutations in the APC gene in familial adenomatous polyposis patients. (2005) (1)
Novel 5′-regulatory region polymorphism of the 5ht2c-receptor gene: no association with clozapine-response (2000) (1)
Investigation of the serotonin 2A receptor gene in schizophrenia (1996) (1)
Molecular Studies in Hereditary Nonpolyposis Colorectal Cancer: Microsatellite Instability and Germline Mutations (1996) (1)
APC Mutations in German Families with Polyposis coli: Phenotype-Genotype Relationships (1996) (1)
Genetic influences on CNS diseases secondary to alcoholism. (1987) (1)
The optimization of polar body diagnosis: a consequence of the german embryo protection act. (2008) (1)
Assisted reproduction: an important review of the literature on the risk of malformation after in vitro fertilization and intracytoplasmic sperm injection. (2008) (1)
No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample. (2007) (1)
Non-genetic pathologic developments of brain-wave patterns in MZ twins (2000) (1)
Receptor variation as a source of differential response to centrally acting agents: phylogenetic evidence. (1986) (1)
CNTF AND PSYCHIATRIC DISORDERS. AUTHORS' REPLY (1996) (1)
Genetic analysis for early diagnosis of otorhinolaryngeal diseases (2010) (1)
The impact of genetics on psychiatric nosology. (2006) (1)
Considerations of the problem of environment-induced mutations in man. (1973) (1)
Is there a phenotypic difference between probands in case‐control versus family‐based association studies? (2003) (1)
Pharmacogenetics of alcohol and its CNS effects—a digest (1983) (1)
[Hereditary colorectal carcinoma: predictive diagnosis and genetic counseling]. (2001) (1)
Introduction to the Symposium on Psychobiological Genetics (1987) (1)
[Germline mutation analysis in hMLH 1 and hMSH 2 genes in hereditary nonpolyposis colorectal cancer and colorectal cancer patients with familial history]. (1998) (1)
ISPG lifetime achievement award 2004 (2005) (1)
Examination of a possible influence of genetic variation at the DYX1C1 locus in the development of dyslexia (2004) (0)
Increased birth weight in psoriasis —Another expression of a “thrifty genotype”? (2004) (0)
[Genetic screening for early detection of ENT diseases]. (2008) (0)
[Progress in molecular genetic diagnosis]. (1993) (0)
[Genetic analysis in oncology--contra]. (2008) (0)
Challenges in defining genetic risks for familial colorectal cancer (2006) (0)
Identifying genetic factors in common diseases: more helpful in relation to etiology than prediction. (2013) (0)
Twinning Frequencies in Baden-Württemberg According to Parental Age And Birth Order. Comparison between 1955-59 and 1968-72 (1974) (0)
Peter McGuffin, Michael J. Owen, Irving I. Gottesman (editors) Psychiatric genetics and genomics (2003) (0)
Mutation in the beta amyloid precursor protein gene and schizophrenia. (1993) (0)
S-49-3 Molecular genetic studies of variation in dopamine and serotonin receptor genes (1996) (0)
Phenotypic and genetic heterogeneity in schizophrenia: pharmacogenetic studies (2004) (0)
Identifying Genetic Factors in Common Diseases (2013) (0)
Promoter polymorphisms of the 5-HT2C receptor gene: Association study with panic disorder in two independent samples (2000) (0)
Association between TAS2R38 gene polymorphisms and colorectal cancer risk (2011) (0)
The voltage‐gated sodium channel β2‐subunit gene and idiopathic generalized epilepsy (2000) (0)
Genetic Counseling in a Patient With XXYKXXYKY Mosaic Minefelter's Syndrome: Estimate of (1998) (0)
Erratum: Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia (Human Molecular Genetics (1998) 7 (1671-1679)) (1998) (0)
DOPAMINE D1, D2, D3, D4 RECEPTOR GENE POLYMORPHISMS AND SCHIZOPHRENIA (1992) (0)
Regeneration der Niere nach tubulärer Schädigung durch Pteridinderivate / Regeneration of the Kidney after Tubular Damage by Pteridine Derivatives (1969) (0)
Consultations in Molecular Diagnostics A Complex Rearrangement in the APC Gene Uncovered by Multiplex Ligation-Dependent Probe Amplification (2007) (0)
141 Linkage studies in schizophrenia and affecfive disorders in European populations (1997) (0)
Subject Index Vol. 5, 1979 (1979) (0)
[Regeneration of the kidney after tubular damage by pteridine derivatives]. (1969) (0)
3236 Familial adenomatous polyposis: Congenital hypertrophy of the retinal pigment epithelium and distribution of mutations in the adenomatous polyposis coli gene (1995) (0)
[Acute renal failure after pteridine administration]. (1970) (0)
Editorial help (2004) (0)
Correspondence (reply): In reply. (2013) (0)
Barrett's syndrome? (1966) (0)
Erratum: A genome screen for genes predisposing to bipolar affecting disorder detects a new susceptibility locus on 8q (Human Molecular Genetics (2001) vol. 10 (2933-2944)) (2002) (0)
[Cytogenetic paternity demonstration in a case of father-daughter-incest]. (1978) (0)
[The genetic revolution-impact on therapy and prevention]. (2004) (0)
[Not Available]. (1991) (0)
Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1 (2016) (0)
Genotype-phenotype correlations in familial adenomatous polyposis (FAP) and its influence on therapeutic decisions (2000) (0)
Large Deletions in the BRCA1 Gene Are Not Common in a Set of Familial German Breast Cancer Patients (2002) (0)
[Skin diseases and genetic instability. I: Basic principles of genetic instability]. (1998) (0)
CompoundHeterozygosity forMetachromatic Leukodystrophy andArylsulfatase A Pseudodeficiency Alleles IsNotAssociated withProgressive Neurological Disease (1993) (0)
Functional genetic polymorphisms in N-acetyltransferase type 2 and glutathione S-transferases M1 and T1 in Gardner syndrome (2001) (0)
p63 mutations account for a range of congenital anomaly syndromes with a clear genotype phenotype correlation (2000) (0)
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors (2011) (0)
[Modern genetic research and the human psyche]. (2008) (0)
[Genetic control of the ethanol effect on the human EEG]. (1977) (0)
Genetic variation in brain physiology (EEG) and behavior. (1982) (0)
Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in familial cases (1996) (0)
No association between a putative functional promoter variant in the dopamine &bgr;-hydroxylase gene and schizophrenia (2003) (0)
[Hereditary gastrointestinal tumors]. (1999) (0)
[Skin diseases and genetic instability. II. Genetic dermatoses with genetic instability]. (1998) (0)
The impact of genetics on psychiatric nosology. Author's reply (2006) (0)
No support for association of the DTNBP1 gene with schizophrenia in large samples from Germany, Poland, and Sweden (2003) (0)
No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients. Commentary (2008) (0)
Polymorphic monoamine oxidase a and 5-HT-transporter genes: Analysis of interactions with panic disorder (2000) (0)
1998 6th World Congress on Psychiatric Genetics, Bonn, Germany, October 6–10, 1998 sponsored by the International Society of Psychiatric Genetics (1998) (0)
[Critical view on intra-animal culture of microorganisms, a method for the detection of chemically-induced mutations]. (1973) (0)

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