Jürg Ott

Q: What Schools Are Affiliated With Jürg Ott

Jürg Ott is affiliated with the following schools: Quaid-i-Azam University, University of Szeged, Rockefeller University, Columbia University, University of Washington, University of Geneva, University of Zurich

Jürg Ott's AcademicInfluence.com Rankings

Jürg Ott

Biology

#3959

World Rank

#5979

Historical Rank

Genetics

#301

World Rank

#354

Historical Rank

biology Degrees

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Biology

Jürg Ott's Degrees

PhD Genetics University of Geneva
Doctorate Medicine University of Geneva

Why Is Jürg Ott Influential?

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According to Wikipedia, Jürg Ott is Emeritus Professor of statistical genetics at Rockefeller University, New York. Awards In 2008, Ott received the Ming Tsuang Lifetime Achievement Award Lifetime Achievement Award from the International Society of Psychiatric Genetics. In 2010 he won the William Allan Award at the American Society of Human Genetics.

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Jürg Ott's Published Works

Number of citations in a given year to any of this author's works

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

Complement Factor H Polymorphism in Age-Related Macular Degeneration (2005) (4562)
Strategies for multilocus linkage analysis in humans. (1984) (2612)
Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis. (2009) (1704)
Analysis of Human Genetic Linkage (1985) (1178)
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. (1985) (1099)
Handbook of Human Genetic Linkage (1994) (1062)
Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. (1974) (1035)
Genetic data analysis II (1997) (997)
Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome (1989) (864)
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.213.3 (1990) (556)
A haplotype-based 'haplotype relative risk' approach to detecting allelic associations. (1992) (520)
Computer-simulation methods in human linkage analysis. (1989) (518)
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene (1993) (464)
Alopecia universalis associated with a mutation in the human hairless gene. (1998) (413)
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia (2005) (370)
Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration. (2005) (365)
An allele of COL9A2 associated with intervertebral disc disease. (1999) (363)
Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion Evidence from Inherited Hypotrichosis and Acquired Pemphigus Vulgaris (2003) (337)
A genomewide screen for autism susceptibility loci. (2001) (336)
Trimming, weighting, and grouping SNPs in human case-control association studies. (2001) (328)
Distribution and characterization of regulatory elements in the human genome. (2002) (314)
Genetic homogeneity between acute and chronic forms of spinal muscular atrophy (1990) (313)
A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3 (1994) (309)
The p53MH algorithm and its application in detecting p53-responsive genes (2002) (307)
Mathematical multi-locus approaches to localizing complex human trait genes (2003) (306)
Power and Sample Size Calculations for Case-Control Genetic Association Tests when Errors Are Present: Application to Single Nucleotide Polymorphisms (2002) (302)
A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis (2003) (297)
A computer program for linkage analysis of general human pedigrees. (1976) (295)
Family-based designs for genome-wide association studies (2011) (277)
Identification of a novel common genetic risk factor for lumbar disk disease. (2001) (272)
Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder (1999) (262)
Exposing the human nude phenotype (1999) (258)
Strategies for characterizing highly polymorphic markers in human gene mapping. (1992) (257)
Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q. (1998) (248)
Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests. (1990) (236)
Dysfunctional nitric oxide signalling increases risk of myocardial infarction (2013) (234)
Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1. (1982) (232)
First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q (1998) (231)
Schizophrenia and oxidative stress: glutamate cysteine ligase modifier as a susceptibility gene. (2006) (227)
Increased Attributable Risk Related to a Functional μ-Opioid Receptor Gene Polymorphism in Association with Alcohol Dependence in Central Sweden (2005) (227)
Genetic linkage analysis in the age of whole-genome sequencing (2015) (224)
Age-related macular degeneration--a genome scan in extended families. (2003) (216)
Genetic susceptibility to heroin addiction: a candidate gene association study (2008) (187)
Linkage analysis and family classification under heterogeneity (1983) (187)
Statistical properties of the haplotype relative risk (1989) (180)
Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits. (1993) (178)
CFH and LOC387715/ARMS2 genotypes and treatment with antioxidants and zinc for age-related macular degeneration. (2008) (175)
Substantial attributable risk related to a functional mu-opioid receptor gene polymorphism in association with heroin addiction in central Sweden (2004) (175)
Genomic analysis defines a cancer-specific gene expression signature for human squamous cell carcinoma and distinguishes malignant hyperproliferation from benign hyperplasia. (2006) (175)
Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8. (1996) (175)
A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish (1996) (172)
A susceptibility locus for migraine with aura, on chromosome 4q24. (2002) (172)
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23 (2013) (169)
Diminished support for linkage between manic depressive illness and X–chromosome markers in three Israeli pedigrees (1993) (156)
A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data. (2001) (155)
The TRP2 Allele of COL9A2 is an Age-Dependent Risk Factor for the Development and Severity of Intervertebral Disc Degeneration (2005) (154)
PREDISPOSITION TO FAMILIAL OSTEOARTHROSIS LINKED TO TYPE II COLLAGEN GENE (1989) (154)
TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa (1998) (151)
Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12 (1996) (150)
Genetic variations in IL6 associate with intervertebral disc disease characterized by sciatica (2005) (150)
ABCB1 (MDR1) genetic variants are associated with methadone doses required for effective treatment of heroin dependence. (2008) (147)
Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata. (2007) (145)
Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosis (2003) (143)
Increased OPRM1 DNA Methylation in Lymphocytes of Methadone-Maintained Former Heroin Addicts (2009) (141)
Association of the Taq I Allele in Vitamin D Receptor With Degenerative Disc Disease and Disc Bulge in a Chinese Population (2006) (140)
PDE3A mutations cause autosomal dominant hypertension with brachydactyly (2015) (139)
Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis (1990) (138)
Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7. (1991) (137)
The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative cases. (1997) (135)
Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual loss (2008) (135)
Evidence for a putative bipolar disorder locus on 2p13–16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21–24, 13q32, 14q21 and 17q11–12 (2003) (131)
GT repeats are associated with recombination on human chromosome 22. (2000) (129)
Schizophrenia susceptibility and chromosome 6p24–22 (1995) (127)
A microsatellite genetic linkage map of human chromosome 18. (1993) (124)
Cigarette smoking, CFH, APOE, ELOVL4, and risk of neovascular age-related macular degeneration. (2007) (124)
Chromosome‐based method for rapid computer simulation in human genetic linkage analysis (1993) (124)
Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosa. (1993) (117)
Relationship Estimation in Affected Sib Pair Analysis of Late-Onset Diseases (1997) (112)
Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa families. (1990) (111)
CpG Island Methylator Phenotype Associates with Low-Degree Chromosomal Abnormalities in Colorectal Cancer (2008) (109)
Associations of Six Single Nucleotide Polymorphisms in Obesity-Related Genes With BMI and Risk of Obesity in Chinese Children (2010) (107)
Selecting SNPs in two‐stage analysis of disease association data: a model‐free approach (2000) (104)
Sometimes it's hot, sometimes it's not (1998) (104)
Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD). (1993) (104)
Occupational and Genetic Risk Factors Associated With Intervertebral Disc Disease (2007) (104)
Significant linkage for Tourette syndrome in a large French Canadian family. (2000) (103)
Estimating rates of alternative splicing in mammals and invertebrates (2004) (101)
Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory (2012) (101)
Redefinition of the human kappa opioid receptor gene (OPRK1) structure and association of haplotypes with opiate addiction. (2004) (101)
Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study (2011) (100)
Scan statistics to scan markers for susceptibility genes. (2000) (99)
Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele. (1997) (99)
Alleles in the HtrA serine peptidase 1 gene alter the risk of neovascular age-related macular degeneration. (2008) (98)
Nucleotide frequency variation across human genes. (2003) (97)
Heroin addiction in African Americans: a hypothesis‐driven association study (2009) (97)
Rhesus monkeys and humans share common susceptibility genes for age-related macular disease. (2008) (96)
Mapping of a gene for severe pediatric gastroesophageal reflux to chromosome 13q14. (2000) (96)
Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis. (1992) (95)
Errors and Linkage Disequilibrium Interact Multiplicatively When Computing Sample Sizes for Genetic Case-Control Association Studies (2002) (95)
Adrenoleukodystrophy: Phenotypic variability and implications for therapy (1992) (94)
Angiotensinogen Gene Polymorphism at −217 Affects Basal Promoter Activity and Is Associated with Hypertension in African-Americans* (2002) (93)
Maximum likelihood estimation by counting methods under polygenic and mixed models in human pedigrees. (1979) (93)
The LOC387715 Gene, Smoking, Body Mass Index, Environmental Associations with Advanced Age-Related Macular Degeneration (2007) (91)
Genotype patterns that contribute to increased risk for or protection from developing heroin addiction (2008) (91)
Molecular and statistical approaches to the detection and correction of errors in genotype databases. (1993) (91)
KRAS Mutation and Microsatellite Instability: Two Genetic Markers of Early Tumor Development That Influence the Prognosis of Colorectal Cancer (2010) (89)
Estimating the frequency of nonpaternity in Switzerland. (1994) (89)
A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1. (1998) (87)
Epidemiology and Factor Analysis of Obesity, Type II Diabetes, Hypertension, and Dyslipidemia (Syndrome X) on the Island of Kosrae, Federated States of Micronesia (2000) (86)
Genetic linkage evidence for heterogeneity in Charcot‐Marie‐Tooth neuropathy (HMSN type I) (1983) (84)
Lack of an association of apolipoprotein E gene polymorphisms with familial age-related macular degeneration. (2003) (84)
True Pedigree Errors More Frequent Than Apparent Errors for Single Nucleotide Polymorphisms (1999) (84)
Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population. (1998) (83)
A Principal-Components Approach Based on Heritability for Combining Phenotype Information (1999) (83)
Joint Identification of Multiple Genetic Variants via Elastic‐Net Variable Selection in a Genome‐Wide Association Analysis (2010) (82)
Linkage probability and its approximate confidence interval under possible heterogeneity (1986) (81)
Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p. (1994) (79)
A simple scheme for the analysis of HLA linkages in pedigrees (1978) (79)
Effects of stratification in the analysis of affected-sib-pair data: benefits and costs. (2000) (78)
Neural network analysis of complex traits (1997) (78)
Genetic and phenotypic heterogeneity in pattern dystrophy (2005) (77)
A microsatellite genetic linkage map of human chromosome 13. (1993) (77)
Haplotypes in the Complement Factor H (CFH) Gene: Associations with Drusen and Advanced Age-Related Macular Degeneration (2007) (76)
Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners. (2001) (75)
Brain-derived neurotrophic factor gene C-270T and Val66Met functional polymorphisms and risk of schizophrenia: A moderate-scale population-based study and meta-analysis (2007) (75)
Multi-Locus Nonparametric Linkage Analysis of Complex Trait Loci with Neural Networks (1998) (74)
Cutting a Gordian knot in the linkage analysis of complex human traits. (1990) (73)
ADHDgene: a genetic database for attention deficit hyperactivity disorder (2011) (72)
Early-onset osteoarthritis linked to the type II procollagen gene. Detailed clinical phenotype and further analyses of the gene. (1993) (71)
Pharmacogenetic analysis of adverse drug effect reveals genetic variant for susceptibility to liver toxicity (2002) (70)
Ethnic diversity of DNA methylation in the OPRM1 promoter region in lymphocytes of heroin addicts (2010) (70)
Genome‐wide autozygosity mapping in human populations (2009) (70)
Progression of geographic atrophy and genotype in age-related macular degeneration. (2010) (70)
Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR (2005) (70)
A Functional Haplotype Implicated in Vulnerability to Develop Cocaine Dependence is Associated with Reduced PDYN Expression in Human Brain (2009) (69)
Predicting the range of linkage disequilibrium. (2000) (69)
Counting methods (EM algorithm) in human pedigree analysis: Linkage and segregation analysis (1977) (67)
Use of a Combined Ex Vivo/In Vivo Population Approach for Screening of Human Genes Involved in the Human Immunodeficiency Virus Type 1 Life Cycle for Variants Influencing Disease Progression (2005) (66)
Sum statistics for the joint detection of multiple disease loci in case‐control association studies with SNP markers (2003) (66)
A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents (2004) (65)
Two-locus linkage analysis in multiple sclerosis (MS). (1994) (63)
Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA (2003) (63)
Multi-locus interactions predict risk for post-PTCA restenosis: an approach to the genetic analysis of common complex disease (2002) (63)
Association analysis of polymorphisms in serotonin 1B receptor (HTR1B) gene with heroin addiction: a comparison of molecular and statistically estimated haplotypes (2006) (63)
A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27. (1998) (63)
Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22-Xp11.3. (1991) (62)
Assessment and management of single nucleotide polymorphism genotype errors in genetic association analysis. (2000) (61)
Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16. (1999) (61)
Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: incorporation of linkage disequilibrium in multipoint analysis. (1993) (60)
Extremely discordant sib-pair study design to determine risk factors for neovascular age-related macular degeneration. (2004) (58)
Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus. (1990) (58)
Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration. (1999) (58)
Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis (2014) (57)
Linkage evidence for genetic heterogeneity among kinships with hereditary motor and sensory neuropathy, type I. (1983) (57)
Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers. (1988) (57)
Cold-induced sweating syndrome is caused by mutations in the CRLF1 gene. (2003) (55)
Genome-wide association study identifies genes that may contribute to risk for developing heroin addiction (2010) (54)
Genetic dissection of diseases: design and methods. (2004) (54)
An Examination of Linkage of Schizophrenia and Schizoaffective Disorder to the Pseudoautosomal Region (Xp22.3) (1994) (54)
Significant evidence for linkage disequilibrium over a 5-cM region among Afrikaners. (2000) (54)
TPH2 and TPH1: Association of Variants and Interactions with Heroin Addiction (2008) (52)
Linkage of Autosomal Recessive Primary Congenital Glaucoma to the GLC3A Locus in Roms (Gypsies) from Slovakia (1998) (52)
Drug Addiction and Stress‐Response Genetic Variability: Association Study in African Americans (2014) (51)
The signatures of autozygosity among patients with colorectal cancer. (2008) (51)
Neuronal Genes for Subcutaneous Fat Thickness in Human and Pig Are Identified by Local Genomic Sequencing and Combined SNP Association Study (2011) (50)
Familial juvenile hyperuricemic nephropathy: localization of the gene on chromosome 16p11.2-and evidence for genetic heterogeneity. (2000) (49)
Linkage analysis with misclassification at one locus (1977) (48)
GENETIC STUDY: Prodynorphin gene promoter repeat associated with cocaine/alcohol codependence (2007) (48)
Linkage studies in a large kindred with familial hypercholesterolemia. (1974) (48)
Genetic Linkage in Mental Illness (1990) (48)
Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis. (1989) (48)
The effect of marker heterozygosity on the power to detect linkage disequilibrium. (1997) (46)
Extended access oxycodone self-administration and neurotransmitter receptor gene expression in the dorsal striatum of adult C57BL/6 J mice (2014) (46)
Association of common variants in/near six genes (ATP2B1, CSK, MTHFR, CYP17A1, STK39 and FGF5) with blood pressure/hypertension risk in Chinese children (2014) (46)
Association of polymorphisms of the cannabinoid receptor (CNR1) and fatty acid amide hydrolase (FAAH) genes with heroin addiction: impact of long repeats of CNR1 (2010) (46)
Linkage analyses of chromosome 18 markers do not identify a major susceptibility locus for bipolar affective disorder in the Old Order Amish. (1995) (46)
Candidate genes involved in cardiovascular risk factors by a family-based association study on the island of Kosrae, Federated States of Micronesia. (2002) (46)
Genetic predisposition for femoral neck stress fractures in military conscripts (2010) (45)
A chi‐square test to distinguish allelic association from other causes of phenotypic association between two loci (1985) (45)
Set association analysis of SNP case-control and microarray data (2002) (44)
Strong Association of the Y 402 H Variant in Complement Factor H at 1 q 32 with Susceptibility to Age-Related Macular Degeneration (2005) (44)
Comprehensive analysis of CRP, CFH Y402H and environmental risk factors on risk of neovascular age-related macular degeneration (2008) (43)
Detecting marker inconsistencies in human gene mapping. (1993) (42)
The impact of phenotypic variation on genetic analysis: application to X‐linkage in manic‐depressive illness (1990) (41)
Osteopenia in 37 Members of Seven Families: Analysis Based on a Model of Dominant Inheritance (1996) (41)
The number of families required to detect or exclude linkage heterogeneity. (1986) (41)
Association of genetic variation in pharmacodynamic factors with methadone dose required for effective treatment of opioid addiction. (2013) (41)
Common Regulatory Variants of CYFIP1 Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism (2015) (40)
Complex traits on the map (1996) (40)
No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees. (1998) (40)
20 Applications of neural networks for gene finding (2001) (40)
Overlapping Dopaminergic Pathway Genetic Susceptibility to Heroin and Cocaine Addictions in African Americans (2015) (40)
Statistical approaches to gene mapping. (2000) (39)
A genome-wide association study reveals ARL15, a novel non-HLA susceptibility gene for rheumatoid arthritis in North Indians. (2013) (39)
A novel polylocus method for linkage analysis using the lod‐score or affected sib‐pair method (1993) (39)
Chromosomes 4q28.3 and 7q31.2 as new susceptibility loci for comitant strabismus. (2009) (38)
Statistical significance for hierarchical clustering in genetic association and microarray expression studies (2003) (38)
Linkage analysis of spinal muscular atrophy. (1992) (38)
The Ising model in physics and statistical genetics. (2001) (37)
Catechol‐O‐methyltransferase (COMT) gene variants: Possible association of the Val158Met variant with opiate addiction in hispanic women (2008) (36)
Fine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communities (2001) (36)
Amino acid substitutions in the human genome: evolutionary implications of single nucleotide polymorphisms. (2003) (36)
Neural networks and disease association studies. (2001) (36)
Insights into gene modulation by therapeutic TNF and IFNgamma antibodies: TNF regulates IFNgamma production by T cells and TNF-regulated genes linked to psoriasis transcriptome. (2008) (36)
On the relative importance of marker heterozygosity and intermarker distance in gene mapping. (1992) (35)
Genetic risk factors for diabetic nephropathy on chromosomes 6p and 7q identified by the set-association approach (2007) (34)
Estimating distances from the centromere by means of benign ovarian teratomas in man (1976) (34)
Methods of analysis and resources available for genetic trait mapping. (1999) (33)
The ADAMTS1 Gene Is Associated with Familial Mandibular Prognathism (2015) (33)
Multipoint mapping under genetic interference. (1993) (33)
Association of polymorphisms in the melanocortin receptor type 2 (MC2R, ACTH receptor) gene with heroin addiction (2008) (32)
AprioriGWAS, a New Pattern Mining Strategy for Detecting Genetic Variants Associated with Disease through Interaction Effects (2014) (32)
Familial rheumatoid arthritis: linkage of HLA to disease susceptibility locus in four families where proband presented with juvenile rheumatoid arthritis. (1980) (32)
An analytic solution to single nucleotide polymorphism error-detection rates in nuclear families: implications for study design. (1999) (31)
Power loss for multiallelic transmission/disequilibrium test when errors introduced: GAW11 simulated data (1999) (30)
Analysis of multiple phenotypes in genome-wide genetic mapping studies (2013) (30)
Genetic linkage and complex diseases: A comment (1990) (30)
Genome-wide examination of genetic variants associated with response to platinum-based chemotherapy in patients with small-cell lung cancer (2010) (30)
Applications of neural networks for gene finding. (2001) (30)
Multiple cutaneous and uterine leiomyomas: refinement of the genetic locus for multiple cutaneous and uterine leiomyomas on chromosome 1q42.3-43. (2002) (29)
Extensive Ethnogenomic Diversity of Endothelial Nitric Oxide Synthase (eNOS) Polymorphisms (2013) (28)
Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6. (1992) (28)
Detection of genetic interference: simulation studies and mouse data. (1994) (27)
Detecting disease-associated genotype patterns (2009) (27)
Are Molecular Haplotypes Worth the Time and Expense? A Cost-Effective Method for Applying Molecular Haplotypes (2006) (27)
Methodological issues in linkage analyses for psychiatric disorders: secular trends, assortative mating, bilineal pedigrees. Report of the MacArthur Foundation Network I Task Force on Methodological Issues. (1993) (26)
Heterogeneity for Multiple Disease Loci in Linkage Analysis (1999) (25)
Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndrome. (1992) (25)
Association of Angiotensinogen Gene Polymorphisms with Essential Hypertension in African-Americans and Caucasians (2005) (25)
ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies (2002) (24)
Heterogeneity analysis of breast cancer families by using age at onset as a covariate. (1992) (24)
Dopaminergic pathway polymorphisms and heroin addiction: further support for association of CSNK1E variants. (2014) (23)
Statistical multilocus methods for disequilibrium analysis in complex traits (2001) (23)
Familial juvenile hyperuricaemic nephropathy (FJHN): linkage analysis in 15 families, physical and transcriptional characterisation of the FJHN critical region on chromosome 16p11.2 and the analysis of seven candidate genes (2003) (23)
Genetic linkage studies in alopecia areata. (2003) (23)
Statistical Methods for Analyzing Microarray Feature Data with Replications (2003) (23)
Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease. (1994) (23)
A multisample bootstrap approach to the estimation of maximized-over-models lod score distributions. (1992) (22)
Linkage analysis of two-locus diseases under single-locus and two-locus analysis models. (1992) (21)
Issues in Association Analysis: Error Control in Case-Control Association Studies for Disease Gene Discovery (2005) (21)
Age-related Macular Degeneration Clinical Features in a Large Family and Linkage to Chromosome 1 q (2000) (21)
Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus. (1990) (20)
Assessing the Evidence for Linkage in Psychiatric Genetics (1992) (20)
Evidence for association of two variants of the nociceptin/orphanin FQ receptor gene OPRL1 with vulnerability to develop opiate addiction in Caucasians (2010) (20)
Analysis of complex traits using neural networks (1999) (20)
Low-Order Polynomial Trends of Female-to-Male Map Distance Ratios along Human Chromosomes (1998) (19)
Putative Susceptibility Locus on Chromosome 21q for Lumbar Disc Disease (LDD) in the Finnish Population (2007) (19)
Support Vector Machines with L1 penalty for detecting gene-gene interactions (2012) (18)
Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21. (1995) (18)
Synaptic Plasticity and Signal Transduction Gene Polymorphisms and Vulnerability to Drug Addictions in Populations of European or African Ancestry (2015) (17)
Tradeoff Between No-Call Reduction in Genotyping Error Rate and Loss of Sample Size for Genetic Case/Control Association Studies (2003) (17)
EB simplex superficialis resulting from a mutation in the type VII collagen gene. (2002) (17)
Dopamine gene variants in opioid addiction: comparison of dependent patients, nondependent users and healthy controls. (2018) (17)
Variants of opioid system genes are associated with non-dependent opioid use and heroin dependence. (2016) (17)
Expression of Ephrin Receptors and Ligands in Postmortem Brains of HIV-Infected Subjects With and Without Cognitive Impairment (2013) (17)
Association of polymorphisms of the mu opioid receptor gene with the severity of HIV infection and response to HIV treatment. (2012) (17)
SNP haplotype tagging from DNA pools of two individuals (2003) (17)
MK4MDD: A Multi-Level Knowledge Base and Analysis Platform for Major Depressive Disorder (2012) (16)
No Genetic Linkage Detected for Schizophrenia to Xq27–q28 (1991) (16)
Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningocele. (1994) (16)
Failure to find a chromosome 18 pericentric linkage in families with schizophrenia. (1995) (16)
Multilocus association mapping using generalized ridge logistic regression (2011) (16)
Major strengths and weaknesses of the lod score method. (2001) (16)
Collapsing SNP Genotypes in Case-Control Genome-Wide Association Studies Increases the Type I Error Rate and Power (2008) (15)
Coordinated Conditional Simulation with SLINK and SUP of Many Markers Linked or Associated to a Trait in Large Pedigrees (2011) (15)
Susceptibility loci for heroin and cocaine addiction in the serotonergic and adrenergic pathways in populations of different ancestry. (2015) (14)
Expanded genome scan in extended families with age-related macular degeneration. (2007) (14)
Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy. (1993) (14)
MHC fine mapping of human type 1 diabetes using the T1DGC data (2009) (14)
Reifenstein's syndrome: Investigation of linkage to X‐chromosomal loci (1974) (14)
Linkage analysis with biological markers. (1995) (14)
Report of the first international workshop on human chromosome 18 mapping. (1993) (14)
A train of thoughts on gene mapping. (2001) (14)
Testing Association with Interactions by Partitioning Chi‐Squares (2009) (13)
Short tandem repeat polymorphism linkage studies in a new family with X-linked mental retardation (MRX20). (1995) (13)
Glutamatergic and GABAergic susceptibility loci for heroin and cocaine addiction in subjects of African and European ancestry (2016) (13)
Tests of gene order from three‐locus linkage data (1987) (12)
A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3. (1996) (12)
Heterogeneity in the map distance between X-linked agammaglobulinemia and a map of nine RFLP loci (1986) (12)
Y-linkage and pseudoautosomal linkage. (1986) (11)
Association of genetic loci: replication or not, that is the question. (2004) (11)
Lack of association between the apolipoprotein B gene 3‘ hypervariable region alleles and coronary artery disease in Finnish patients with angiographically documented coronary artery disease (1992) (11)
Challenging False Discovery Rate: A Partition Test Based on p Values in Human Case-Control Association Studies (2012) (11)
African-specific variability in the acetylcholine muscarinic receptor M4: association with cocaine and heroin addiction. (2016) (11)
Artificial neural networks as statistical tools in epidemiological studies: analysis of risk factors for early infant wheeze. (2004) (10)
Affective disorders: Evaluation of a three‐allele model accounting for clinical heterogeneity (1989) (10)
Targeted re-sequencing of linkage region on 2q21 identifies a novel functional variant for hip and knee osteoarthritis. (2016) (10)
Genetic Linkage Mapping (2005) (10)
Two Approaches for Consolidating Results from Genome Scans of Complex Traits: Selection Methods and Scan Statistics (2001) (10)
Goodness‐of‐fit tests for locus order in three‐point mapping (1987) (10)
Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence. (1991) (10)
Re-evaluation of the KMSK scales, rapid dimensional measures of self-exposure to specific drugs: Gender-specific features. (2018) (10)
Association of genetic loci (2004) (10)
Are trait impulsivity and exposure to cannabis or alcohol associated with the age of trajectory of cocaine use? A gender-specific dimensional analysis in humans with cocaine dependence diagnosis. (2020) (9)
Survival analysis of microarray expression data by transformation models (2005) (9)
Combining identity by descent and association in genetic case-control studies (2008) (9)
Parsimonious estimation of sex-specific map distances by stepwise maximum likelihood regression. (1995) (9)
VMAT2 gene (SLC18A2) variants associated with a greater risk for developing opioid dependence. (2019) (9)
Asthma, allergy, and airway hyperresponsiveness are not linked to the beta(2)-adrenoceptor gene. (2002) (9)
Complex Inheritance and Localizing Disease Genes (1999) (9)
Beyond Homozygosity Mapping: Family-Control analysis based on Hamming distance for prioritizing variants in exome sequencing (2015) (9)
Increased OPRM1 DNA Methylation in Lymphocytes of Methadone (2009) (9)
Linkage analysis in heterogeneous and complex traits (2009) (9)
Ascertainment and Anticipation in Family Studies (2000) (8)
Establishing appropriate genome-wide significance levels for canine linkage analyses. (2003) (8)
HDR: a statistical two-step approach successfully identifies disease genes in autosomal recessive families (2016) (8)
Polygenic Models for Risk Prediction in Human Genetics (2016) (8)
Statistical methods in genetic mapping. (1994) (8)
A likelihood approach to calculating risk support intervals. (1994) (8)
Genetic linkage studies in man. (1979) (8)
Erratum: Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16 (Genomics (1999) 62: 1 (1)) (2000) (8)
Detecting gene-gene interactions using support vector machines with L1 penalty (2010) (8)
Multiple phenotypes in genome-wide genetic mapping studies (2011) (8)
Expanded Genome Scan in Extended Families with Age-Related Macular Degeneration (2006) (7)
Estimating Crossover Frequencies and Testing for Numerical Interference with Highly Polymorphic Markers (1996) (7)
Systematic Removal of Outliers to Reduce Heterogeneity in Case-Control Association Studies (2010) (7)
Pilot Study on Schizophrenia in Sardinia (2010) (7)
A 3’ UTR SNP rs885863, a cis-eQTL for the circadian gene VIPR2 and lincRNA 689, is associated with opioid addiction (2019) (7)
Genome-Wide Conditional Search for Epistatic Disease-Predisposing Variants in Human Association Studies (2010) (7)
Bipolar disorder and linkage to Xq28 (1994) (7)
Autosomal dominant spondyloarthropathy: no linkage to the type II collagen gene. (1990) (6)
Polymorphisms of the Kappa Opioid Receptor and Prodynorphin Genes: HIV Risk and HIV Natural History (2013) (6)
Genetic Variant in the CRH-binding Protein Gene (CRHBP) is Associated With Cessation of Cocaine Use in Methadone Maintenance Patients With Opioid Addiction. (2019) (6)
Association of variants of prodynorphin promoter 68-bp repeats in caucasians with opioid dependence diagnosis: Effect on age trajectory of heroin use (2019) (6)
X-linked agammaglobulinemia and the red blood cell determinants Xg and 12E7 are not closely linked (2004) (6)
Haplotype and multipoint linkage analysis in Finnish choroideremia families (1989) (6)
Epistatic association and linkage analysis in human families (2004) (6)
Multiple Comparisons/Testing Issues (2009) (6)
Statistical gene mapping of traits in humans--hypertension as a complex trait: is it amenable to genetic analysis? (2002) (5)
Testing linkage disequilibrium from pooled DNA: A contingency table perspective (2008) (5)
Linkage investigation of a large family with Reifenstein's syndrome (1975) (5)
Testing for interference in human genetic maps (1997) (5)
Addendum: The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia (2005) (5)
The future of multilocus linkage analysis. (1992) (5)
How do you compute a lod score? (1995) (5)
Scan statistics in human gene mapping. (2012) (4)
Heterozygosity mapping for human dominant trait variants (2019) (4)
Genotype Pattern Mining for Pairs of Interacting Variants Underlying Digenic Traits (2021) (4)
Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3. (1998) (4)
Late onset autosomal dominant cerebellar ataxia. A family description and linkage analysis with the HLA system. (1991) (4)
A bootstrap approach to estimating power for linkage heterogeneity (1993) (4)
Variants of opioid genes and response to treatment of opioid use disorder with buprenorphine-naloxone versus extended-release naltrexone in Caucasians (2020) (4)
A novel association of rs13334070 in the RPGRIP1L gene with adiposity factors discovered by joint linkage and linkage disequilibrium analysis in Iranian pedigrees: Tehran Cardiometabolic Genetic Study (TCGS) (2018) (4)
Novel etiological hypotheses imply new analysis methods for schizophrenia genetics (1996) (4)
Some statistical properties of the lod method and the method of scoring known recombination events in linkage analysis. (1978) (4)
HDR‐del: A tool based on Hamming distance for prioritizing pathogenic chromosomal deletions in exome sequencing (2017) (4)
Estimating parental relationship in linkage analysis of recessive traits. (1996) (3)
Scan Statistics in Genome-Wide Scan for Complex Trait Loci (2009) (3)
The combined effects of cardiovascular disease related SNPs on ischemic stroke (2018) (3)
Recent advances in genetic epidemiology (2000) (3)
Implication of Melanocortin Receptor Genes in the Familial Comorbidity of Type 2 Diabetes and Depression (2022) (3)
Self-administration of oxycodone by adolescent and adult mice differentially affects hypothalamic mitochondrial metabolism gene expression (2015) (3)
Age-related Macular Degeneration: A Genome-wide Scan in Extended Families (2003) (3)
Analyses of polymorphisms of intron 2 of OPRK1 (kappa-opioid receptor gene) in association with opioid and cocaine dependence diagnoses in an African-American population (2021) (3)
P-value distribution in case-control association studies (2010) (3)
Writings on Genetic Linkage in the Annals (2011) (2)
Further evidence for association of GAL, GALR1 and NPY1R variants with opioid dependence. (2020) (2)
Comorbidity of Novel CRHR2 Gene Variants in Type 2 Diabetes and Depression (2022) (2)
Absence of linkage between transcobalamin II and ABO (2004) (2)
Is there heterogeneity of age at onset for breast cancer? (1993) (2)
Adjusting for HLA-DRβ1 in a genome-wide association analysis of rheumatoid arthritis and related biomarkers (2009) (2)
Interpreting nonsignificant outcomes of heterogeneity tests in gene mapping. (1991) (2)
A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q. (2020) (2)
Note on the prior probability of autosomal linkage (1976) (2)
Leveling the Playing Field in Homozygosity Mapping Using Map Distances (2015) (2)
Presymptomatic exclusion of myotonic dystrophy in a one-generation pedigree of half-siblings. (1990) (2)
Multilocus association analysis under polygenic models (2010) (2)
Title Association study of PHOX 2 B as a candidate gene forHirschsprung ' s disease (2003) (2)
Association Studies Trimming , Weighting , and Grouping SNPs in Human Case-Control (2001) (2)
Editorial: Multi-Omics Study in Revealing Underlying Pathogenesis of Complex Diseases: A Translational Perspective (2021) (1)
The Number of Families Required to Detect or Exclude Linkage Heterogeneity (2006) (1)
Chromosome 18 markers: Linked or not linked to bipolar affective disorders in the Old Order Amish? A reply to Gershon et al. (1996) (1)
William Allan Award Address: On the role and soul of a statistical geneticist. (2011) (1)
Assignment of autosomal dominant spinocerebellar ataxia centromeric to HLA using multilocus linkage analysis (1988) (1)
Linkage analysis on familial early-onset degenerative disc disease (2007) (1)
Unknown Parental Phase – Lod Score Versus Information A Comment to Prof. Edwards' Note (2006) (1)
Important findings regarding the pseudoautosomal region of the human X and Y chromosomes. (1988) (1)
Polymorphisms in Stress-Related Genes Are Associated with Reduced Cocaine Abuse and Longer Retention in Methadone Maintenance Treatment for Opioid Use Disorder (2020) (1)
Meeting report. Statistical methods in genetic mapping. (1996) (1)
Models and Methods for the Genetic Analysis of Pedigree Data (1992) (1)
Reanalysis of a Genome Scan for Schizophrenia Loci Using Multigenic Methods (2004) (1)
Assessment and Management of Single Nucleotide Polymorphism Genotype Errors in Genetic Association (2001) (1)
Gene variants of the opioid system – Relationship to heroin self-exposure, addiction, and treatment (2015) (1)
Population genetics: past, present, and future (2020) (1)
Maximal Segmental Score Method for Localizing Recessive Disease Variants Based on Sequence Data (2020) (1)
Genetic vulnerability factor for schizophrenia: association with glutamate cysteine ligase modifier gene and abnormal enzyme activity (2006) (1)
Linkage analysis for a disease with a complex mode of inheritance in a simulated data set. (1989) (1)
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27 (1991) (1)
Variability of genotype‐specific penetrance probabilities in the calculation of risk support intervals (1995) (1)
Stress-related genes and heroin addiction: A role for functional fkbp5 variants (2015) (1)
Faculty Opinions recommendation of Haplotype tagging for the identification of common disease genes. (2001) (1)
Analysis of two‐locus traits under heterogeneity for recessive versus dominant inheritance (1997) (1)
Overview of frequent pattern mining (2022) (1)
Medical statistics : current developments in statistical methodology for genetic architecture of complex diseases ; meeting at the "Mathematisches Foschungsinstitut Oberwolfach", Germany, February 2-8, 2003 (2003) (1)
Age dependent association of the COL9A2 Trp2 allele with intervertebral disc degeneration, annular tears and end-plate herniations (2003) (1)
Two new approaches toward linkage heterogeneity of FAD: Two‐locus models and age of onset as a discriminator (1993) (1)
Determining informativity of marker typing for genetic counseling in a pedigree (1989) (1)
ASSOCIATION STUDIES FOR HUMAN TRAIT GENES (2002) (1)
Human gene mapping by postreduction and recombination frequencies under complete interference (1979) (1)
Data mining for high throughput data from genome-wide association studies. (2012) (1)
A protocol of genome-wide association study in Han Chinese for primary Sjögren’s syndrome (2013) (0)
Are Molecular Haplotypes Worth the Time and Expense? A Cost-Effective Method for Treating Misclassification in Haplotype-Based Association (2005) (0)
Shared genomic segment analysis with equivalence testing (2020) (0)
Complex traits on the map. (1996) (0)
Association studies of intervertebral disc disease with genes in the aggrecan degradation pathway (2005) (0)
The Genetics of intervertebral disc degenertation (2005) (0)
Title Analysis of multiple phenotypes in genome-wide geneticmapping studies (2013) (0)
Faculty Opinions recommendation of High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs. (2006) (0)
Lecture 12 : Topics in Association Analysis : Permutation tests ; collapsing rare variants (2013) (0)
Mutations in collagen IX as genetic predisposing factors for degenerative disc disease in Southern Chinese (2002) (0)
A (CA)n Repeat Polymorphism in Enkephalin Gene: Association with Opiate Addiction (2004) (0)
Pilot application of multi-locus and time-to-event analysis to ascertain genetic risk factors for diabetic nephropathy and related adverse outcomes of diabetes mellitus (2011) (0)
Linkage analysis (2019) (0)
INVITED EDITORIAL Statistical Approaches to Gene Mapping (2000) (0)
Genetic analysis workshop III: Combining two‐point analyses under the constraints of a linear map and a constant female/male distance ratio (1985) (0)
A14520 The joint effects of cardiovascular disease related SNPs on ischemic stroke (2018) (0)
Presentation_1_Maximal Segmental Score Method for Localizing Recessive Disease Variants Based on Sequence Data.zip (2020) (0)
The Retinoic Acid Receptor-Related Orphan Receptor Gene (RORA), A Potential Anti-Angiogenic Therapeutic Target for Age-Related Macular Degeneration (2009) (0)
Methods of Analysis and Resources Available for Genetic Trait Mapping (1999) (0)
Molecular genetics and genetic epidemiology of cardiovascular disease and diabetes. Introductory remarks: genetic models and statistical approaches. (1992) (0)
Risk of schizophrenia and the glutathione related genes (2005) (0)
GLM: A relational database system for linkage mapping on PC compatibles (1994) (0)
Log-Linear Models for Gene Mapping with Affected Sib Pair Data (2002) (0)
Endothelin-1 but not endothelial nitric oxide synthase polymorphisms are implicated in sickle cell disease (P3311) (2013) (0)
Allelic variation of collagen IX as genetic predispositing factors for degenerative disc disease in Southern Chinese (2002) (0)
The analysis of four candidate chromosomal regions in two schizophrenia datasets from Fiji (2002) (0)
Introductory Remarks: Genetic Models and Statistical Approaches (1992) (0)
Multilocus approach to the identification of genetic riskfactors for diabetic nephropathy in type 2 diabetes (2004) (0)
Maximum Likelihood Estimation by Counting Methods Under Polygenic and Mixed Models in Human Pedigrees (2006) (0)
Lack of an Association Between the SOD2 Ala/Val Polymorphism and Age-related Macular Degeneration (AMD) (2002) (0)
Gene variants of the dopaminergic system are associated with non-dependent heroin use and heroin dependence (2017) (0)
Independent Effects of CFH Genotype and Smoking History, but No Effect of APOE and ELOVL4 Genotype, on Risk for Neovascular Age–Related Macular Degeneration (2006) (0)
A powerful one degree of freedom approach to mapping genes with linkage disequilibrium (1994) (0)
Optic Atrophy in Leber Hereditary Optic Neuroretinopathy (2006) (0)
SNP-SNP interaction in intervertebral disc disease with genes in the Aggrecan Degradation Pathway (2006) (0)
Richard S. Spielman 1946–2009 (2009) (0)
Estimating Recessive Disease Allele Frequency Based on Genetic Maps (1997) (0)
Supplementary Material for: Systematic Removal of Outliers to Reduce Heterogeneity in Case-Control Association Studies (2017) (0)
Statistical Methods to Discover Susceptibility Genes for Nervous System Diseases (2001) (0)
Association test for rare variants using the hamming distance (2018) (0)
Y-Linkage and Pseudoautosomal Linkage (2006) (0)
Testing the genomic control parameter (2010) (0)
Abstract 2764: Genome-wide examination of genetic variants associated with response to platinum-based chemotherapy in patients with small-cell lung cancer (2010) (0)
Statistical Genetics Methods for Localizing Multiple Breast Cancer Genes (1996) (0)
Faculty Opinions recommendation of A global search reveals epistatic interaction between QTL for early growth in the chicken. (2003) (0)
To aggregate or not, that is the question. A commentary on single-nucleotide variant proportion in genes: a new concept to explore major depression based on DNA sequencing data (2017) (0)
Extremely Discordant Sibpair Multivariate Analyses of Apoe Alleles, Smoking, Hypertension and Hypercholesterolemia Shows That Smoking Is the Strongest Risk Factor Associated With Neovascular Age–Related Macular Degneration (2005) (0)
Two Approaches for Consolidating Results from Genome Scans of Complex Traits: Selection Methods and Scan Statistics (2017) (0)
Analysis of the 1q24-q41 Region and the Candidate Gene RGS13 in Sibling Pairs Extremely Discordant for Neovascular Age-Related Macular Degeneration (2007) (0)
Multi-allelic TDT simulation study of indigenous Fijian families with psychosis. (2000) (0)
Indication against genetic localisation of the human transcobalamin II gene (TC2) on chromosome 16 (1986) (0)
Scan statistics to scan markers for susceptibility genes (2000) (0)
Three genes in the aggrecan degradation pathway act synergistically to predispose to degenerative disc disease (2007) (0)
ODP258 CRHR1 gene shows extensive linkage to major depression and type 2 diabetes in Italian families (2022) (0)
55. Increased DNA methylation in the promoter region of the μ-opioid receptor gene (ORPM1) in lymphocytes of Caucasian methadone maintained former heroin addicts (2008) (0)
Genetics study in intervertebral disc degeneration (2002) (0)
Analysis of the TCP–1 Gene (T–Complex Polypeptide–1) in Patients With Neovascular Age–Related Macular Degeneration (2006) (0)
Strategies for Characterizing Highly Polymorphic Markers in Human Gene Mapping (2006) (0)
Faculty Opinions recommendation of Using genomic inbreeding coefficient estimates for homozygosity mapping of rare recessive traits: application to Taybi-Linder syndrome. (2006) (0)
The 22q11.2 Deletion Syndrome: Second Hit Copy Number Variants and Conotruncal Heart Defects (2011) (0)
Mapping undetected mutations within a gene-evidence for two preferential regions in the DMD gene. (1997) (0)
Computer Programs for Linkage Analysis (1991) (0)
Faculty Opinions recommendation of Comments on the entropy-based transmission/disequilibrium test. (2007) (0)
Faculty Opinions recommendation of High-resolution haplotype structure in the human genome. (2001) (0)
NG-IgAN GWAS (2015) (0)
Recent Developments in the Theoretical Aspects of Linkage Analysis (1993) (0)
LINKAGE OF HLA TO DISEASE SUSCEPTIBILITY LOCUS IN FOUR FAMILIES WHERE PROBAND PRESENTED WVITH JUVENILE RHEUMATOID ARTHRITIS (1980) (0)
DISTRIBUTION OF APOE ALLELES AMONG PATIENTS WITH NEOVASCULAR AGE–RELATED MACULAR DEGENERATION AND THEIR UNAFFECTED SIBLINGS (2004) (0)
Population genetics: past, present, and future (2020) (0)
HTRA1 Genotypes Associated With Risk of Neovascular Age-Related Macular Degeneration Independent of CFH and Smoking (2007) (0)
Faculty Opinions recommendation of Complex SNP-based haplotypes in three human helicases: implications for cancer association studies. (2002) (0)
Brief Communication ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies ILAE Genetics Commission (2002) (0)
Recent Advances in the Analysis of Genetic Traits: A Celebration of the 30th Anniversary of the Haseman-Elston Method (2003) (0)
Genetic variation in the COL9A2 gene and its association to intervertebral disc abnormalities in Southern Chinese (2003) (0)
Age-dependent association of the Trp2 allele of the COL9A2 gene with intervertebral disc degeneration in Southern Chinese (2003) (0)
Faculty Opinions recommendation of A commentary on Coronary artery disease. Genes, drugs and the agricultural connection by Ole Færgeman (ed). (2004) (0)
Faculty Opinions recommendation of Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations. (2004) (0)
Pattern dystrophy: evidence of digenic inheritance and studies of visual outcome (2004) (0)
Genetic linkage analysis of early onset degenerative disc disease in Southern Chinese (2006) (0)
A locus for autosomal recessive hypodontia maps to chromosome 16q12.1 (1998) (0)
Novel Family-control Analysis Can Highly Prioritize Sequence Variants in Familial Cardiomyopathy (2014) (0)
Evidence for a new gene associated with Hirschsprung's disease: the PHOX2B gene (2002) (0)
Colorectal Cancer The Signatures of Autozygosity among Patients with Updated (2008) (0)
Association Analysis for Human Diseases: Methods and Examples (2013) (0)
Faculty Opinions recommendation of Assessing allelic dropout and genotype reliability using maximum likelihood. (2002) (0)

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