Dr Joan Ellen Bailey-Wilson
Current affiliation: NHGRI/NIH
Subject: Health Sciences
Primary location: United States
Lung Cancer Susceptibility Genes
Published in:Lung Cancer
Publication date:Not available
Segregation analysis of cutaneous melanoma in Queensland
Published in:Genetic Epidemiology
Publication date:1998-01-01
Parametric and Nonparametric Linkage Analysis
Published in:Encyclopedia of Life Sciences
Publication date:2006-01-27
Segregation analysis of cutaneous melanoma in Queensland
Published in:Genetic Epidemiology
Publication date:1998-01-01
A Comprehensive Method for Genome Scans
Published in:Human Heredity
Publication date:2002-01-01
Estimation of Linkage and Association from Allele Transmission Data
Published in:Biometrical Journal
Publication date:2003-04-01
Risk estimation using probability machines
Published in:BioData Mining
Publication date:2014-03-01
VARIABLE SELECTION METHOD FOR THE IDENTIFIC ATION OF EPISTATIC MODELS
Published in:Biocomputing 2015
Publication date:2014-11-01
Performance of random forests and logic regression methods using mini-exome sequence data
Published in:BMC Proceedings
Publication date:2011-01-01
Evaluation of random forests performance for genome-wide association studies in the presence of interaction effects
Published in:BMC Proceedings
Publication date:2009-01-01
Brief review of regression-based and machine learning methods in genetic epidemiology: the Genetic Analysis Workshop 17 experience
Published in:Genetic Epidemiology
Publication date:2011-01-01
High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequenci...
Published in:Genetics in Medicine
Publication date:2015-03-12
Gene-Gene Interaction AmongWNTGenes for Oral Cleft in Trios
Published in:Genetic Epidemiology
Publication date:2015-02-06Gene-Gene Interaction Among WNT Genes
Linkage Analysis in the Next-Generation Sequencing Era
Published in:Human Heredity
Publication date:2011-01-01
Sib-pair linkage analyses of Alzheimer's disease
Published in:Genetic Epidemiology
Publication date:1993-01-01Sib-pair Linkage of Alzheimer's Disease
The HGAR1 familial hypercholesterolemia pedigree
Published in:Genetic Epidemiology
Publication date:1993-01-01The HGAR1 Pedigree
Parametric versus nonparametric and two-point versus multipoint: controversies in gene mapping
Published in:Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics
Publication date:2005-07-15
Critique of a published analysis of the Jacobsen data
Published in:Genetic Epidemiology
Publication date:1986-01-01
George Bonney (1947-2013) Remembered
Published in:Genetic Epidemiology
Publication date:2013-12-23
Linkage analysis in a large pedigree ascertained due to essential familial hypercholesterolemia
Published in:Genetic Epidemiology
Publication date:1993-01-01Sib-pair Linkage in a Large Pedigree
Comparison of sib-pair and variance-components methods for genomic screening
Published in:Genetic Epidemiology
Publication date:1997-01-01
Comparison of sib‐pair and variance‐components methods for genomic screening
Published in:Genetic Epidemiology
Publication date:1997-01-01
Genes, environment and the value of prospective cohort studies
Published in:Nature Reviews Genetics
Publication date:2006-10-01
The number of STR markers necessary to resolve relationships in deficiency paternity cases
Published in:International Congress Series
Publication date:2004-04-01
Model-free association analysis of a rare Disease
Published in:Genetic Epidemiology
Publication date:1995-01-01Association Study of a Rare Disease
Genomewide scan of ocular refraction in African‐American families shows significant linkage to chromosome 7p15
Published in:Genetic Epidemiology
Publication date:2008-07-01
Comparison of selected methods used to analyze bipolar disorder
Published in:Genetic Epidemiology
Publication date:1997-01-01
Evidence for a major gene influencing risk of pancreatic cancer
Published in:Genetic Epidemiology
Publication date:2002-08-01
Discrimination of heterozygotes for phenylketonuria, persistent hyperphenylalaninemia and controls by phenylalanine loading
Published in:Clinica Chimica Acta
Publication date:1986-12-01
Discrimination of phenylketonurics from persistent hyperphenylalaninemia patients using a simple phenylalanine loading test
Published in:Clinica Chimica Acta
Publication date:1985-12-01
Haplotypes and haplotype-tagging single-nucleotide polymorphism: Presentation Group 8 of Genetic Analysis Workshop 14
Published in:Genetic Epidemiology
Publication date:2005-01-01
Suggestive evidence of linkage identified at chromosomes 12q24 and 2p16 in African American prostate cancer families from louisiana
Published in:The Prostate
Publication date:2011-10-05
Matrix Metalloproteinases and Educational Attainment in Refractive Error
Published in:Ophthalmology
Publication date:2013-02-01
Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder
Published in:BMC Genetics
Publication date:2015-03-15
Genetic analysis of human breast cancer: A synthesis of contributions to Gaw IV
Published in:Genetic Epidemiology
Publication date:1986-01-01
Application of sex-specific single-nucleotide polymorphism filters in genome-wide association data
Published in:BMC Proceedings
Publication date:2009-01-01
Bipolar disorder: Evidence for a major locus
Published in:American Journal of Medical Genetics
Publication date:1995-10-09
Comparison of selected methods used to analyze bipolar disorder
Published in:Genetic Epidemiology
Publication date:1997-01-01
The Transmission/Disequilibrium Test for Linkage on the X Chromosome
Published in:The American Journal of Human Genetics
Publication date:2000-03-01
False-positive rates in two-point parametric linkage analysis
Published in:BMC Proceedings
Publication date:2014-01-01
High carrier frequency for recessive OI in West Africans
Published in:Matrix Biology
Publication date:2008-12-01
Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression
Published in:BMC Proceedings
Publication date:2011-01-01
Possible linkage of alcoholism, monoamine oxidase activity and P300 amplitude to markers on chromosome 12q24
Published in:Genetic Epidemiology
Publication date:1999-01-01Possible Linkage of Alcoholism, MAO and P300
Environmental covariates: Effects on the power of sib-pair linkage methods
Published in:Genetic Epidemiology
Publication date:1999-01-01Environmental Covariates and Power
Effects of Misspecification of Allele Frequencies on the Type I Error Rate of Model-Free Linkage Analysis
Published in:Human Heredity
Publication date:1999-11-24
Generalized Functional Linear Models for Gene-Based Case-Control Association Studies
Published in:Genetic Epidemiology
Publication date:2014-09-09
Genome-wide Linkage Analysis of Multiple Metabolic Factors: Evidence of Genetic Heterogeneity
Published in:Obesity
Publication date:2010-01-01
Admixture Mapping of Obesity-related Traits in African Americans: The Atherosclerosis Risk in Communities (ARIC) Study*
Published in:Obesity
Publication date:2009-08-20
Effects of misspecification of allele frequencies on the power of Haseman-Elston sib-pair linkage method for quantitative traits
Published in:American Journal of Medical Genetics
Publication date:2001-01-01
Effects of misspecification of allele frequencies on the power of Haseman‐Elston sib‐pair linkage method for quantitative traits
Published in:American Journal of Medical Genetics
Publication date:2001-11-01
Functional Linear Models for Association Analysis of Quantitative Traits
Published in:Genetic Epidemiology
Publication date:2013-10-15Functional Linear Models for Association Analysis of Quantitative Traits
Pleiotropy Analysis of Quantitative Traits at Gene Level by Multivariate Functional Linear Models
Published in:Genetic Epidemiology
Publication date:2015-03-23
Identifying rare variants from exome scans: the GAW17 experience
Published in:BMC Proceedings
Publication date:2011-01-01
A founder mutation in LEPRE1 carried by 1.5% of West Africans and 0.4% of African Americans causes lethal recessive osteogenesis imperfecta
Published in:Genetics in Medicine
Publication date:2012-01-26
Segregation analysis of 389 Icelandic pedigrees with Breast and prostate cancer
Published in:Genetic Epidemiology
Publication date:2002-11-01Breast-Prostate Cancer Phenotype
Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). II. Biomarker studies
Published in:Cancer
Publication date:1985-08-15
Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). I. Clinical description of resource
Published in:Cancer
Publication date:1985-08-15
Establishing an adjusted p-value threshold to control the family-wide type 1 error in genome wide association studies
Published in:BMC Genomics
Publication date:2008-01-01
Inheritance of Total Serum IgE in the Isolated Tangier Island Population from Virginia: Complexities Associated with Genealogical Depth of Pedigree...
Published in:Human Heredity
Publication date:2005-01-01
GENETIC EPIDEMIOLOGY OF HEREDITARY PROSTATE CANCER IN FINLAND
Published in:The Journal of Urology
Publication date:1999-04-01DISCOVERY OF NOVEL SUSCEPTIBILITY LOCI
Novel region of interest in chromosome 11 and other putative regions identified in a genome-wide scan in finnish hereditary prostate cancer families
Published in:European Urology Supplements
Publication date:2002-01-01
Abstract A69: Identification of prostate cancer genes in the African American Hereditary Prostate Cancer (AAHPC) study
Published in:Cancer Epidemiology Biomarkers & Prevention
Publication date:2011-09-01
Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36
Published in:Human Genetics
Publication date:2006-02-24
Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree
Published in:Human Genetics
Publication date:2006-05-30
Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritance
Published in:Human Genetics
Publication date:2007-01-03
Segregation analysis of hereditary nonpolyposis colorectal cancer
Published in:Genetic Epidemiology
Publication date:1986-01-01Segregation Analysis of Colorectal Cancer
Effects of marker information on sib-pair linkage analysis of a rare disease
Published in:Genetic Epidemiology
Publication date:1995-01-01Marker Information Effects on Linkage Analysis
Effect of cohort differences in smoking prevalence on models of lung cancer susceptibility
Published in:Genetic Epidemiology
Publication date:1992-01-01Smoking Differences and Lung Cancer Susceptibility
Mild association between the A/G polymorphism in the promoter of the apolipoprotein A‐I gene and apolipoprotein A‐I levels: A meta‐analysis
Published in:American Journal of Medical Genetics
Publication date:1999-01-29
Genetic epidemiology of breast cancer: Segregation analysis of 389 Icelandic pedigrees
Published in:Genetic Epidemiology
Publication date:2000-01-01
Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in ...
Published in:American Journal of Medical Genetics
Publication date:1999-08-06
Survey of genetic counselors and clinical geneticists regarding recurrence risks for families with nonsyndromic cleft lip with or without cleft palate
Published in:American Journal of Medical Genetics
Publication date:1998-09-23
Application of the propensity score in a covariate-based linkage analysis of the Collaborative Study on the Genetics of Alcoholism
Published in:BMC Genetics
Publication date:2005-01-01
Identification of tag single-nucleotide polymorphisms in regions with varying linkage disequilibrium
Published in:BMC Genetics
Publication date:2005-01-01
Mild association between the A/G polymorphism in the promoter of the apolipoprotein A-I gene and apolipoprotein A-I levels: A meta-analysis
Published in:American Journal of Medical Genetics
Publication date:1999-01-29
Abstract 3648: Unraveling phenotype heterogeneity in prostate cancer susceptibility in Finland utilizing covariate-based analysis.
Published in:Cancer Research
Publication date:2013-04-15
Autosomal dominant inheritance of prostate cancer: a confirmatory study
Published in:Urology
Publication date:2001-01-01
Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer
Published in:Human Genetics
Publication date:2000-10-27
Potential role of an additive genetic component in the cause of amyotrophic lateral sclerosis and parkinsonism-dementia in the western Pacific
Published in:American Journal of Medical Genetics
Publication date:1993-01-01
Genetic analysis of human breast cancer: Literature review and description of family data in workshop
Published in:Genetic Epidemiology
Publication date:1986-01-01
Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis
Published in:European Journal of Human Genetics
Publication date:2012-09-05
Contribution of HPC1 (RNASEL) and HPCX variants to prostate cancer in a founder population
Published in:The Prostate
Publication date:2010-06-16
Examining the effect of linkage disequilibrium between markers on the Type I error rate and power of nonparametric multipoint linkage analysis of t...
Published in:Genetic Epidemiology
Publication date:2008-01-01
Haplotypic structure of the X chromosome in the COGA population sample and the quality of its reconstruction by extant software packages
Published in:BMC Genetics
Publication date:2005-01-01
Transmission/disequilibrium tests of androgen receptor and glutathione S-transferase pi variants in prostate cancer families
Published in:International Journal of Cancer
Publication date:2002-03-29
Normalization of microarray expression data using within-pedigree pool and its effect on linkage analysis
Published in:BMC Proceedings
Publication date:2007-01-01
Genetic epidemiology of breast cancer: Segregation analysis of 389 Icelandic pedigrees
Published in:Genetic Epidemiology
Publication date:2000-01-01
Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller‐Dieker syndrome (MDS) critical region in ...
Published in:American Journal of Medical Genetics
Publication date:1999-08-06
Hypercholesterolemia in children with Smith-Magenis syndrome: del (17)(p11.2p11.2)
Published in:Genetics in Medicine
Publication date:2002-06-01
Covariate-based linkage analysis: application of a propensity score as the single covariate consistently improves power to detect linkage
Published in:European Journal of Human Genetics
Publication date:2006-05-31
Genetic Analysis Workshop 14: Introduction to Workshop Summaries
Published in:Genetic Epidemiology
Publication date:2005-01-01
Segregation analysis of smoking-associated malignancies: Evidence for mendelian inheritance
Published in:American Journal of Medical Genetics
Publication date:1994-09-01
Segregation Analysis of Esophageal Cancer in a Moderately High–Incidence Area of Northern China
Published in:The American Journal of Human Genetics
Publication date:2000-07-01
Genomewide Linkage Scan for Myopia Susceptibility Loci among Ashkenazi Jewish Families Shows Evidence of Linkage on Chromosome 22q12
Published in:The American Journal of Human Genetics
Publication date:2004-09-01
Attention-Deficit/Hyperactivity Disorder in a Population Isolate: Linkage to Loci at 4q13.2, 5q33.3, 11q22, and 17p11
Published in:The American Journal of Human Genetics
Publication date:2004-12-01
Segregation analysis of urothelial cell carcinoma
Published in:European Journal of Cancer
Publication date:2006-07-01
Attention-Deficit/Hyperactivity Disorder and Comorbid Disruptive Behavior Disorders: Evidence of Pleiotropy and New Susceptibility Loci
Published in:Biological Psychiatry
Publication date:2007-06-01
Genome-wide Scan for Myopia in the Old Order Amish
Published in:American Journal of Ophthalmology
Publication date:2005-09-01
Linkage heterogeneity for the IBD1 locus in Crohn's disease pedigrees by disease onset and severity
Published in:Gastroenterology
Publication date:2000-12-01
KLF6 IVS1 -27G>A Variant and the Risk of Prostate Cancer in Finland
Published in:European Urology
Publication date:2007-10-01
Genome-wide Scan of African-American and White Families for Linkage to Myopia
Published in:American Journal of Ophthalmology
Publication date:2009-03-01
Structure–Function Correlations Using Scanning Laser Polarimetry in Primary Angle-Closure Glaucoma and Primary Open-Angle Glaucoma
Published in:American Journal of Ophthalmology
Publication date:2010-05-01
Crohn's disease diagnosis before age 22 and with greater severity of disease identifies multiplex pedigrees at greater risk for locus IBD1
Published in:Gastroenterology
Publication date:2000-04-01
MP66-10 CHARACTERIZATION OF SUSCEPTIBILITY LOCI IN HEREDITARY PROSTATE CANCER FAMILIES USING COPY NUMBER VARIATION AND LINKAGE ANALYSIS
Published in:The Journal of Urology
Publication date:2015-04-01
Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Work...
Published in:BMC Proceedings
Publication date:2011-01-01
Importance sampling method of correction for multiple testing in affected sib-pair linkage analysis
Published in:BMC Genetics
Publication date:2003-01-01
ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer
Published in:European Journal of Human Genetics
Publication date:2008-03-12
Regression and data mining methods for analyses of multiple rare variants in the Genetic Analysis Workshop 17 mini-exome data
Published in:Genetic Epidemiology
Publication date:2011-01-01
Polymorphisms in the neural nicotinic acetylcholine receptor α4 subunit (CHRNA4) are associated with ADHD in a genetic isolate
Published in:ADHD Attention Deficit and Hyperactivity Disorders
Publication date:2009-04-25
A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region
Published in:Human Genetics
Publication date:2005-10-22
EPHA2 Is Associated with Age-Related Cortical Cataract in Mice and Humans
Published in:PLoS Genetics
Publication date:2009-07-31
Genome-wide scanning for linkage in Finnish breast cancer families
Published in:European Journal of Human Genetics
Publication date:2004-03-01
Genome screen in familial intracranial aneurysm
Published in:BMC Medical Genetics
Publication date:2009-01-01
Investigation of altering single-nucleotide polymorphism density on the power to detect trait loci and frequency of false positive in nonparametric...
Published in:BMC Genetics
Publication date:2005-01-01
Penetrances of breast and ovarian cancer in a large series of families tested for BRCA1/2 mutations
Published in:European Journal of Human Genetics
Publication date:2004-09-01
Genome-wide scanning for linkage in Finnish breast cancer families
Published in:European Journal of Human Genetics
Publication date:2003-10-15
Genome-wide scan for linkage in finnish hereditary prostate cancer (HPC) families identifies novel susceptibility loci at 11q14 and 3p25-26
Published in:The Prostate
Publication date:2003-10-29
A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region
Published in:Human Genetics
Publication date:2005-05-20
Hereditary prostate cancer in Finland: fine-mapping validates 3p26 as a major predisposition locus
Published in:Human Genetics
Publication date:2004-11-11
8q24 risk alleles and prostate cancer in African-Barbadian men
Published in:The Prostate
Publication date:2014-09-228q24 Risk Alleles and Prostate Cancer in AB Men
A Hereditary Form of Small Intestinal Carcinoid Associated With a Germline Mutation in Inositol Polyphosphate Multikinase
Published in:Gastroenterology
Publication date:2015-07-01
Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2
Published in:European Journal of Human Genetics
Publication date:2003-11-01
A genome-wide scan for loci predisposing to non-syndromic cleft lip with or without cleft palate in two large Syrian families
Published in:American Journal of Medical Genetics
Publication date:2003-10-29
A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes
Published in:Human Genetics
Publication date:2001-12-14
Genome-wide linkage scan for prostate cancer susceptibility in Finland: Evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22
Published in:International Journal of Cancer
Publication date:2011-04-20
Genetic Analysis Workshop 13: Analysis of Longitudinal Family Data for Complex Diseases and Related Risk Factors
Published in:BMC Genetics
Publication date:2003-01-01
Localization of a Gene for Duane Retraction Syndrome to Chromosome 2q31
Published in:The American Journal of Human Genetics
Publication date:1999-12-01
Germline Alterations of the RNASEL Gene, a Candidate HPC1 Gene at 1q25, in Patients and Families with Prostate Cancer
Published in:The American Journal of Human Genetics
Publication date:2002-05-01
A Recurrent Mutation in PARK2 Is Associated with Familial Lung Cancer
Published in:The American Journal of Human Genetics
Publication date:2015-02-01
A novel NFKB1 promoter polymorphism shows altered binding to nuclear proteins and increases risk for ulcerative colitis
Published in:Gastroenterology
Publication date:2003-04-01
Attention-Deficit/Hyperactivity Disorder and Comorbidities in 18 Paisa Colombian Multigenerational Families
Published in:Journal of the American Academy of Child & Adolescent Psychiatry
Publication date:2004-12-01
A genome wide screen in an unusually large inflammatory bowel disease pedigree: Suggestive evidence for linkage on chromosomes 18p, 7p and 15q; No ...
Published in:Gastroenterology
Publication date:2001-04-01
Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans
Published in:BMC Genetics
Publication date:2005-01-01
Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect
Published in:Human Genetics
Publication date:2005-11-23
Physical and Transcript Map of the Hereditary Prostate Cancer Region at Xq27
Published in:Genomics
Publication date:2002-01-01
Recruitment Experience in the First Phase of the African American Hereditary Prostate Cancer (AAHPC) Study
Published in:Annals of Epidemiology
Publication date:2000-11-01
Genome-wide linkage of 77 families from the African American Hereditary Prostate Cancer Study (AAHPC)
Published in:The Prostate
Publication date:2006-01-01
Replicating genotype–phenotype associations
Published in:Nature
Publication date:2007-06-07
Evaluation of Linkage and Association of HPC2/ELAC2 in Patients with Familial or Sporadic Prostate Cancer
Published in:The American Journal of Human Genetics
Publication date:2001-04-01
Localization of a Novel Melanoma Susceptibility Locus to 1p22
Published in:The American Journal of Human Genetics
Publication date:2003-08-01
Linkage analysis of Dutch families at high risk for breast cancer
Published in:Genetic Epidemiology
Publication date:1986-01-01
HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG)
Published in:Human Genetics
Publication date:2012-10-12
Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for prostate cancer Genetics using novel sumLINK ...
Published in:The Prostate
Publication date:2010-01-01
Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk
Published in:Nature Genetics
Publication date:2002-09-16
Meta-Analysis of 13 Genome Scans Reveals Multiple Cleft Lip/Palate Genes with Novel Loci on 9q21 and 2q32-35
Published in:The American Journal of Human Genetics
Publication date:2004-08-01
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
Published in:Nature Genetics
Publication date:2014-08-31
Genome-Wide Meta-Analysis of Myopia and Hyperopia Provides Evidence for Replication of 11 Loci
Published in:PLoS ONE
Publication date:2014-09-18
Segregation analysis of autosomal dominant polycystic kidney disease
Published in:Genetic Epidemiology
Publication date:1993-01-01Segregation Analysis of ADPKD
Response to Craddock et al.
Published in:American Journal of Medical Genetics
Publication date:1997-02-21
Sib-pair linkage analysis applied to pedigrees with melanoma and dysplastic nevi
Published in:Cytogenetic and Genome Research
Publication date:1992-01-01
Response
Published in:JNCI Journal of the National Cancer Institute
Publication date:1991-01-02
Identification of BRCA1 and BRCA2 genetic modifiers.
Published in:Cancer Research
Publication date:2009-01-15
A TWO HOUR PHENYLALANINE (P) LOAD FOR CARRIER DETECTION OF PHENYLKETONURIA (PUK)
Published in:Pediatric Research
Publication date:1984-04-01
DETERMINATION OF GENETIC SUSCEPTIBILITY TO LUNG CANCER IN FAMILIES FROM SOUTHERN LOUISIANA, AN UPDATE
Published in:Southern Medical Journal
Publication date:1999-11-01
Association of Matrix Metalloproteinase Gene Polymorphisms with Refractive Error in Amish and Ashkenazi Families
Published in:Investigative Opthalmology & Visual Science
Publication date:2010-10-01
Evidence for Mendelian Inheritance in the Pathogenesis of Lung Cancer
Published in:JNCI Journal of the National Cancer Institute
Publication date:1990-08-01
INCREASED FAMILIAL RISK FOR NON-LUNG CANCER AMONG RELATWES OF LUNG CANCER PATIENTS
Published in:American Journal of Epidemiology
Publication date:1987-08-01
A Susceptibility Locus on Chromosome 6q Greatly Increases Lung Cancer Risk among Light and Never Smokers
Published in:Cancer Research
Publication date:2010-03-09
Haplotype and Cell Proliferation Analyses of Candidate Lung Cancer Susceptibility Genes on Chromosome 15q24-25.1
Published in:Cancer Research
Publication date:2009-09-29
Identification of a Novel Tumor Suppressor Gene p34 on Human Chromosome 6q25.1
Published in:Cancer Research
Publication date:2007-01-01
EGFR-T790M Is a Rare Lung Cancer Susceptibility Allele with Enhanced Kinase Activity
Published in:Cancer Research
Publication date:2007-05-15
Familial Aggregation of Common Sequence Variants on 15q24-25.1 in Lung Cancer
Published in:JNCI Journal of the National Cancer Institute
Publication date:2008-09-09
A Major Lung Cancer Susceptibility Locus Maps to Chromosome 6q23–25
Published in:The American Journal of Human Genetics
Publication date:2004-09-01
Fine Mapping of Chromosome 6q23-25 Region in Familial Lung Cancer Families Reveals RGS17 as a Likely Candidate Gene
Published in:Clinical Cancer Research
Publication date:2009-04-07
A more powerful robust sib-pair test of linkage for quantitative traits
Published in:Genetic Epidemiology
Publication date:1989-01-01Robust Sib-Pair Tests for Linkage
Stepwise oligogenic segregation and linkage analysis illustrated with dopamine-β-hydroxylase activity
Published in:American Journal of Medical Genetics
Publication date:1990-03-01
Genomewide Linkage Scans for Ocular Refraction and Meta-analysis of Four Populations in the Myopia Family Study
Published in:Investigative Opthalmology & Visual Science
Publication date:2009-05-01
Heritability and Familial Aggregation of Refractive Error in the Old Order Amish
Published in:Investigative Opthalmology & Visual Science
Publication date:2007-09-01
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Published in:Nature Genetics
Publication date:2013-05-29
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Published in:Nature Genetics
Publication date:2013-02-10
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM con...
Published in:Human Genetics
Publication date:2014-11-04
Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium
Published in:Human Genetics
Publication date:2012-06-05
Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error
Published in:The American Journal of Human Genetics
Publication date:2013-08-01
Candidate high myopia loci on chromosomes 18p and 12q do not play a major role in susceptibility to common myopia. Ibay G, Doan B, Reider L, Dana D...
Published in:American Journal of Ophthalmology
Publication date:2004-12-01
Computational aspects of fittlng a mixture of two normal distributions using maximum likelihood
Published in:Communications in Statistics - Simulation and Computation
Publication date:1992-01-01
On the distribution of the likelihood ratio test statistic for a mixture of two normal distributions
Published in:Communications in Statistics - Simulation and Computation
Publication date:1996-01-01
Whole exome association of rare deletions in multiplex oral cleft families
Published in:Genetic Epidemiology
Publication date:2016-12-01
Rare copy number variants in patients with congenital conotruncal heart defects
Published in:Birth Defects Research
Publication date:2017-02-13CNVS in Patients with Congenital CHD
gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels
Published in:Genetic Epidemiology
Publication date:2017-02-01Larson et al .
Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families
Published in:Molecular Genetics & Genomic Medicine
Publication date:2017-08-09