Joan Bailey-Wilson
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American statistical geneticist
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Why Is Joan Bailey-Wilson Influential?
(Suggest an Edit or Addition)According to Wikipedia, Joan Ellen Bailey-Wilson is an American statistical geneticist. She is a senior investigator and co-chief of the Computational and Statistical Genomic Branch of the National Human Genome Research Institute.
Joan Bailey-Wilson'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
- Replicating genotype–phenotype associations (2007) (1367)
- REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants. (2016) (1110)
- Major Susceptibility Locus for Prostate Cancer on Chromosome 1 Suggested by a Genome-Wide Search (1996) (801)
- HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome (2002) (658)
- Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases. (1998) (632)
- Evidence for a prostate cancer susceptibility locus on the X chromosome. (1998) (620)
- Germline mutations in the ribonuclease L gene in families showing linkage with HPC1 (2002) (523)
- Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk (2002) (395)
- Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). I. Clinical description of resource (1985) (384)
- Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (2013) (379)
- Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis. (2004) (346)
- Genes, environment and the value of prospective cohort studies (2006) (305)
- A major lung cancer susceptibility locus maps to chromosome 6q23-25. (2004) (292)
- Evidence for mendelian inheritance in the pathogenesis of lung cancer. (1990) (278)
- Increased familial risk for lung cancer. (1986) (263)
- Establishing an adjusted p-value threshold to control the family-wide type 1 error in genome wide association studies (2008) (241)
- Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer. (2002) (231)
- Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. (2004) (218)
- Genome-wide analysis of multiethnic cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma (2014) (212)
- Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin gene. (1999) (212)
- Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11. (2004) (207)
- Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus. (2000) (197)
- HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG) (2012) (186)
- High Incidence of Unrecognized Visceral/Neurological Late-onset Niemann-Pick Disease, type C1 Predicted by Analysis of Massively Parallel Sequencing Data Sets (2015) (170)
- A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics. (2005) (161)
- Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). II. Biomarker studies (1985) (157)
- Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer. (2008) (157)
- Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12. (2004) (148)
- Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error (2018) (147)
- Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. (2013) (143)
- EPHA2 Is Associated with Age-Related Cortical Cataract in Mice and Humans (2009) (140)
- DNA Identifications After the 9/11 World Trade Center Attack (2005) (133)
- Localization of a novel melanoma susceptibility locus to 1p22. (2003) (124)
- A more powerful robust sib‐pair test of linkage for quantitative traits (1989) (116)
- Evaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancer. (2001) (114)
- Genetic epidemiology of breast cancer and associated cancers in high-risk families. I. Segregation analysis. (1983) (111)
- Genome-Wide Association Study of Intracranial Aneurysms Confirms Role of Anril and SOX17 in Disease Risk (2012) (109)
- Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36 (2006) (104)
- Linkage Analysis in the Next-Generation Sequencing Era (2011) (103)
- Localization of a gene for Duane retraction syndrome to chromosome 2q31. (1999) (102)
- EGFR-T790M is a rare lung cancer susceptibility allele with enhanced kinase activity. (2007) (99)
- A genetic epidemiological study of hereditary prostate cancer (HPC) in Finland: frequent HPCX linkage in families with late-onset disease. (2000) (98)
- Brief review of regression‐based and machine learning methods in genetic epidemiology: the Genetic Analysis Workshop 17 experience (2011) (98)
- Fine Mapping of Chromosome 6q23-25 Region in Familial Lung Cancer Families Reveals RGS17 as a Likely Candidate Gene (2009) (96)
- Heritability analysis of spherical equivalent, axial length, corneal curvature, and anterior chamber depth in the Beaver Dam Eye Study. (2009) (96)
- Recruitment experience in the first phase of the African American Hereditary Prostate Cancer (AAHPC) study. (2000) (95)
- Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association (2012) (92)
- A Hereditary Form of Small Intestinal Carcinoid Associated With a Germline Mutation in Inositol Polyphosphate Multikinase. (2015) (91)
- Combined genome-wide scan for prostate cancer susceptibility genes. (2004) (89)
- Evidence for a Prostate Cancer Susceptibility Locus on the X Chromosome (1999) (88)
- Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy (2017) (87)
- Consanguineous matings in an Israeli-Arab community. (1994) (86)
- Increased familial risk for non-lung cancer among relatives of lung cancer patients. (1987) (79)
- Linkage heterogeneity for the IBD1 locus in Crohn's disease pedigrees by disease onset and severity. (2000) (78)
- A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes (2002) (77)
- Attention-Deficit/Hyperactivity Disorder and Comorbid Disruptive Behavior Disorders: Evidence of Pleiotropy and New Susceptibility Loci (2007) (75)
- Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium (2012) (75)
- A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history (2005) (74)
- Mild association between the A/G polymorphism in the promoter of the apolipoprotein A-I gene and apolipoprotein A-I levels: a meta-analysis. (1999) (69)
- Whole Exome Sequencing of Distant Relatives in Multiplex Families Implicates Rare Variants in Candidate Genes for Oral Clefts (2014) (67)
- Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. (2013) (67)
- Pedigree disequilibrium test (PDT) replicates association and linkage between DRD4 and ADHD in multigenerational and extended pedigrees from a genetic isolate (2004) (66)
- Penetrances of breast and ovarian cancer in a large series of families tested for BRCA1/2 mutations (2004) (65)
- Segregation analysis of hereditary nonpolyposis colorectal cancer (1986) (64)
- A genetic contribution to intraocular pressure: the beaver dam eye study. (2005) (64)
- Segregation analysis of esophageal cancer in a moderately high-incidence area of northern China. (2000) (62)
- Genome-wide scan for myopia in the Old Order Amish. (2005) (60)
- Lung cancer detection and prevention: evidence for an interaction between smoking and genetic predisposition. (1992) (60)
- Attention-deficit/hyperactivity disorder and comorbidities in 18 Paisa Colombian multigenerational families. (2004) (59)
- Functional Linear Models for Association Analysis of Quantitative Traits (2013) (58)
- Segregation analysis of smoking-associated malignancies: evidence for Mendelian inheritance. (1994) (57)
- Hypercholesterolemia in children with Smith-Magenis syndrome: del (17)(p11.2p11.2) (2002) (57)
- Genomewide scan of ocular refraction in African‐American families shows significant linkage to chromosome 7p15 (2008) (57)
- Assessing the Genetic Predisposition of Education on Myopia: A Mendelian Randomization Study (2016) (56)
- Profiling genetic variation along the androgen biosynthesis and metabolism pathways implicates several single nucleotide polymorphisms and their combinations as prostate cancer risk factors. (2006) (56)
- Evaluation of widely used models for predicting BRCA1 and BRCA2 mutations (2004) (56)
- Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (2013) (55)
- Autosomal dominant inheritance of prostate cancer: a confirmatory study. (2001) (55)
- Identification of novel genetic loci for intraocular pressure: a genomewide scan of the Beaver Dam Eye Study. (2007) (55)
- Confirmation of linkage to ocular refraction on chromosome 22q and identification of a novel linkage region on 1q. (2007) (55)
- Bipolar disorder: evidence for a major locus. (1995) (55)
- A recurrent mutation in PARK2 is associated with familial lung cancer. (2015) (54)
- Pleiotropy Analysis of Quantitative Traits at Gene Level by Multivariate Functional Linear Models (2015) (54)
- Genome Screen to Detect Linkage to Intracranial Aneurysm Susceptibility Genes: The Familial Intracranial Aneurysm (FIA) Study (2008) (53)
- A susceptibility locus on chromosome 6q greatly increases lung cancer risk among light and never smokers. (2010) (52)
- r2VIM: A new variable selection method for random forests in genome-wide association studies (2016) (50)
- Heritability and familial aggregation of refractive error in the Old Order Amish. (2007) (50)
- The Relationship Between Smoking and Replicated Sequence Variants on Chromosomes 8 and 9 With Familial Intracranial Aneurysm (2010) (49)
- A founder mutation in LEPRE1 carried by 1.5% of West Africans and 0.4% of African Americans causes lethal recessive osteogenesis imperfecta (2012) (49)
- Haplotype and cell proliferation analyses of candidate lung cancer susceptibility genes on chromosome 15q24-25.1. (2009) (48)
- Therapeutic and other interventions to reduce the risk of mother‐to‐child transmission of HIV‐1 in Europe (1998) (48)
- Support for polygenic influences on ocular refractive error. (2005) (48)
- Candidate high myopia loci on chromosomes 18p and 12q do not play a major role in susceptibility to common myopia (2004) (47)
- Genetic epidemiology of breast cancer and associated cancers in high-risk families. II. Linkage analysis. (1983) (47)
- Potential role of an additive genetic component in the cause of amyotrophic lateral sclerosis and parkinsonism-dementia in the western Pacific. (1993) (46)
- Genome-Wide Meta-Analysis of Myopia and Hyperopia Provides Evidence for Replication of 11 Loci (2014) (45)
- Genetic epidemiologic studies on age-specified traits (2000) (42)
- Association of matrix metalloproteinase gene polymorphisms with refractive error in Amish and Ashkenazi families. (2010) (41)
- Genome-wide association study of familial lung cancer (2018) (40)
- A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region (2005) (39)
- Matrix metalloproteinases and educational attainment in refractive error: evidence of gene-environment interactions in the Age-Related Eye Disease Study. (2013) (39)
- Identification of a novel tumor suppressor gene p34 on human chromosome 6q25.1. (2007) (38)
- A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin. (2016) (38)
- Genome-wide scanning for linkage in Finnish breast cancer families (2004) (37)
- Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics. (2007) (37)
- Contribution of HPC1 (RNASEL) and HPCX variants to prostate cancer in a founder population (2010) (34)
- Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2 (2003) (34)
- Effect of cohort differences in smoking prevalence on models of lung cancer susceptibility (1992) (33)
- A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1 (2018) (33)
- Genomewide linkage scans for ocular refraction and meta-analysis of four populations in the Myopia Family Study. (2009) (33)
- Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer (2000) (33)
- African-American heredity prostate cancer study: a model for genetic research. (2001) (32)
- Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritance (2007) (32)
- Hereditary prostate cancer in Finland: fine-mapping validates 3p26 as a major predisposition locus (2004) (32)
- The Biology of Tobacco and Nicotine: Bench to Bedside (2005) (32)
- Segregation analysis of urothelial cell carcinoma. (2006) (31)
- Genome screen in familial intracranial aneurysm (2009) (30)
- Cumulative Effect of Multiple Loci on Genetic Susceptibility to Familial Lung Cancer (2010) (30)
- Replicating genotype – phenotype associations What constitutes replication of a genotype – phenotype association , and how best can it be achieved ? (2007) (29)
- 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 (2011) (29)
- Inferring relationships between pairs of individuals from locus heterozygosities (2002) (29)
- Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium (2014) (28)
- Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease (2014) (27)
- Generalized Functional Linear Models for Gene‐Based Case‐Control Association Studies (2014) (26)
- Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives (2014) (26)
- Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer. (2020) (25)
- Evaluation of random forests performance for genome-wide association studies in the presence of interaction effects (2009) (24)
- ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies (2002) (24)
- Genome-wide scan of additional Jewish families confirms linkage of a myopia susceptibility locus to chromosome 22q12. (2006) (24)
- Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge (2018) (23)
- Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung Cancer (2016) (23)
- Genome‐wide linkage of 77 families from the African American Hereditary Prostate Cancer Study (AAHPC) (2007) (23)
- Clinical characteristics of African-American men with hereditary prostate cancer: the AAHPC study (2004) (23)
- Segregation analysis of cutaneous melanoma in Queensland (1998) (23)
- Stepwise oligogenic segregation and linkage analysis illustrated with dopamine-beta-hydroxylase activity. (1990) (21)
- 8q24 risk alleles and prostate cancer in African‐Barbadian men (2014) (21)
- Genetic Analysis Workshop 13: Analysis of Longitudinal Family Data for Complex Diseases and Related Risk Factors (2003) (20)
- Physical and transcript map of the hereditary prostate cancer region at xq27. (2002) (20)
- Familial aggregation of myopia in the Tehran eye study: estimation of the sibling and parent–offspring recurrence risk ratios (2007) (20)
- Polymorphisms in the neural nicotinic acetylcholine receptor α4 subunit (CHRNA4) are associated with ADHD in a genetic isolate (2009) (20)
- Common Variants at Putative Regulatory Sites of the Tissue Nonspecific Alkaline Phosphatase Gene Influence Circulating Pyridoxal 5'-Phosphate Concentration in Healthy Adults. (2015) (19)
- Polygenic effects and cigarette smoking account for a portion of the familial aggregation of nuclear sclerosis. (2005) (19)
- Linkage analysis of quantitative refraction and refractive errors in the Beaver Dam Eye Study. (2011) (19)
- Familial Lung Cancer: A Brief History from the Earliest Work to the Most Recent Studies (2017) (19)
- Regional replication of association with refractive error on 15q14 and 15q25 in the Age-Related Eye Disease Study cohort (2013) (18)
- Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error (2020) (18)
- The transmission/disequilibrium test for linkage on the X chromosome. (2000) (18)
- Effects of Misspecification of Allele Frequencies on the Type I Error Rate of Model-Free Linkage Analysis (1999) (18)
- A genome-wide association study of corneal astigmatism: The CREAM Consortium (2018) (17)
- Cellular genes in the mouse regulate in trans the expression of endogenous mouse mammary tumor viruses. (1985) (17)
- Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder (2015) (17)
- Structure-function correlations using scanning laser polarimetry in primary angle-closure glaucoma and primary open-angle glaucoma. (2008) (17)
- Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia. (2021) (16)
- Variable Selection Method for the Identification of Epistatic Models (2014) (16)
- Evidence for a major gene effect in early-onset lung cancer. (1993) (16)
- Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer (2018) (16)
- ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer (2008) (16)
- KLF6 IVS1 -27G>A variant and the risk of prostate cancer in Finland. (2007) (15)
- A Comprehensive Method for Genome Scans (2003) (15)
- Haplotypic structure of the X chromosome in the COGA population sample and the quality of its reconstruction by extant software packages (2005) (15)
- The value of molecular haplotypes in a family-based linkage study. (2006) (15)
- IMI 2021 Yearly Digest (2021) (15)
- Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect (2006) (15)
- Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p (2017) (15)
- Survey of genetic counselors and clinical geneticists regarding recurrence risks for families with nonsyndromic cleft lip with or without cleft palate. (1998) (14)
- The FUT2 secretor variant p.Trp154Ter influences serum vitamin B12 concentration via holo-haptocorrin, but not holo-transcobalamin, and is associated with haptocorrin glycosylation (2017) (14)
- Rare copy number variants in patients with congenital conotruncal heart defects. (2017) (14)
- Risk estimation using probability machines (2014) (14)
- The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population. (2018) (13)
- Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans (2005) (13)
- Fine-mapping of candidate region in Amish and Ashkenazi families confirms linkage of refractive error to a QTL on 1p34-p36 (2009) (13)
- Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3. (1999) (12)
- National Cancer Institute Prostate Cancer Genetics Workshop. (2011) (11)
- Allele frequency misspecification: effect on power and Type I error of model-dependent linkage analysis of quantitative traits under random ascertainment (2006) (11)
- Computational aspects of fittlng a mixture of two normal distributions using maximum likelihood (1992) (11)
- Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data (2011) (11)
- Effects of misspecification of allele frequencies on the power of Haseman-Elston sib-pair linkage method for quantitative traits. (2001) (11)
- Environmental covariates: Effects on the power of sib‐pair linkage methods (1999) (10)
- GeneLink: a database to facilitate genetic studies of complex traits (2004) (10)
- Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families (2017) (10)
- Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world (2015) (10)
- Familial lung cancer--correcting an error in calculation. (1986) (10)
- Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing (2019) (10)
- Ordered Subset Analysis Identifies Loci Influencing Lung Cancer Risk on Chromosomes 6q and 12q (2010) (9)
- Normalization of microarray expression data using within-pedigree pool and its effect on linkage analysis (2007) (9)
- A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits (2016) (9)
- gsSKAT: Rapid gene set analysis and multiple testing correction for rare‐variant association studies using weighted linear kernels (2017) (9)
- Identifying rare variants from exome scans: the GAW17 experience (2011) (9)
- Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33 (2019) (9)
- Covariate-based linkage analysis: application of a propensity score as the single covariate consistently improves power to detect linkage (2006) (8)
- CCR5, vertical transmission of HIV-1, and disease progression. European Collaborative Study. (1999) (8)
- Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression (2011) (8)
- Analysis of the CDKN2A Gene in FAMMM Syndrome Families Reveals Early Age of Onset for Additional Syndromic Cancers. (2019) (8)
- Rare deleterious germline variants and risk of lung cancer (2021) (8)
- Identification of tag single-nucleotide polymorphisms in regions with varying linkage disequilibrium (2005) (8)
- Genetic analysis of human breast cancer: Literature review and description of family data in workshop (1986) (8)
- Plasma deposition of metal oxide films for integrated optics (1986) (7)
- Myopia in Chinese families shows linkage to 10q26.13 (2018) (7)
- Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families (2012) (7)
- Genome-wide scanning for linkage in Finnish breast cancer families (2004) (7)
- Inheritance of Total Serum IgE in the Isolated Tangier Island Population from Virginia: Complexities Associated with Genealogical Depth of Pedigrees in Segregation Analyses (2005) (7)
- Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q (2019) (7)
- Examining the effect of linkage disequilibrium between markers on the Type I error rate and power of nonparametric multipoint linkage analysis of two‐generation and multigenerational pedigrees in the presence of missing genotype data (2008) (7)
- Application of sex-specific single-nucleotide polymorphism filters in genome-wide association data (2009) (7)
- Importance sampling method of correction for multiple testing in affected sib-pair linkage analysis (2003) (7)
- Parametric Linkage Analysis Identifies Five Novel Genome-Wide Significant Loci for Familial Lung Cancer (2017) (7)
- ComPaSS‐GWAS: A method to reduce type I error in genome‐wide association studies when replication data are not available (2018) (6)
- Increased Burden of Rare Sequence Variants in GnRH-Associated Genes in Women with Hypothalamic Amenorrhea. (2020) (6)
- Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case‐Control Sequencing Studies (2016) (6)
- Sterol and lipid analyses identifies hypolipidemia and apolipoprotein disorders in autism associated with adaptive functioning deficits (2021) (6)
- Investigation of altering single-nucleotide polymorphism density on the power to detect trait loci and frequency of false positive in nonparametric linkage analyses of qualitative traits (2005) (6)
- Application of the propensity score in a covariate-based linkage analysis of the Collaborative Study on the Genetics of Alcoholism (2005) (6)
- Inferring Disease Risk Genes from Sequencing Data in Multiplex Pedigrees Through Sharing of Rare Variants (2018) (6)
- Genome‐wide Linkage Analysis of Multiple Metabolic Factors: Evidence of Genetic Heterogeneity (2010) (6)
- Genetic Analysis Workshop 14: Introduction to Workshop Summaries (2005) (5)
- Genome-wide Meta-Analyses Of Multi-Ethnic Cohorts Identify Multiple New Susceptibility Loci For Refractive Error And Myopia (2013) (5)
- Dissecting the genetic heterogeneity of myopia susceptibility in an Ashkenazi Jewish population using ordered subset analysis (2011) (5)
- Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families (2019) (5)
- A second genetic variant on chromosome 15q24-25.1 associates with lung cancer. (2010) (5)
- Recruitment strategies and comparison of prostate cancer-specific clinical data on African-American and Caucasian males with and without family history (2008) (4)
- What makes a good prediction? Feature importance and beginning to open the black box of machine learning in genetics (2021) (4)
- Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree (2006) (4)
- On the distribution of the likelihood ratio test statistic for a mixture of two normal distributions (1996) (4)
- GENETICS OF LUNG CANCER (1998) (4)
- Genomic Wide Linkage of Familial Myopia and evidence for a locus on chromosome 22 (2004) (4)
- Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia (2022) (3)
- A comparison of some sib-pair linkage methods and multiple locus extensions. (1989) (3)
- Estimation of Linkage and Association from Allele Transmission Data (2003) (3)
- Parametric versus nonparametric and two-point versus multipoint: controversies in gene mapping (2005) (3)
- Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis (2012) (3)
- Response to Craddock et al. (1997) (3)
- Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration (2020) (2)
- Developmental expression of tyrosyl kinase activity in human serum. (1987) (2)
- Performance of random forests and logic regression methods using mini-exome sequence data (2011) (2)
- False-positive rates in two-point parametric linkage analysis (2014) (2)
- The GLC1H glaucoma locus may reflect glaucoma with elevated intraocular pressure. (2007) (2)
- Reviewer Acknowledgment (2013) (2)
- Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer (2021) (2)
- Crohn's disease diagnosis before age 22 and with greater severity of disease identifies multiplex pedigrees at greater risk for locus IBD1 (2000) (2)
- A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region (2005) (2)
- Parametric and Nonparametric Linkage Analysis (2018) (2)
- Gene‐based association analysis of survival traits via functional regression‐based mixed effect cox models for related samples (2019) (2)
- Identification of a major susceptibility locus for human prostate cancer (1997) (1)
- Genome-wide SNP Linkage Screen for Intracranial Aneurysm Susceptibility Genes (2007) (1)
- Lung Cancer Susceptibility Genes (2008) (1)
- Complex N-Linked Glycosylation: A Potential Modifier of Niemann–Pick Disease, Type C1 Pathology (2022) (1)
- The number of STR markers necessary to resolve relationships in deficiency paternity cases (2004) (1)
- Abstract 4176: Familial lung cancer exhibits multiple novel linked haplotypes within pedigrees (2019) (1)
- Tiled regression reduces type I error rates in tests of association of rare single nucleotide variants with non-normally distributed traits, compared with simple linear regression (2015) (1)
- Abstract 4268: Familial lung cancer is significantly linked to cancer-associated genes on five chromosomes (2017) (1)
- The use of therapeutic and other interventions to reduce the risk of mother-to-child transmission of HIV in Europe (1998) (1)
- Gene‐level association analysis of ordinal traits with functional ordinal logistic regressions (2022) (1)
- GENETIC EPIDEMIOLOGY OF HEREDITARY PROSTATE CANCER IN FINLAND: DISCOVERY OF NOVEL SUSCEPTIBILITY LOCI (1999) (1)
- Family-Based Association Tests of Myopia reveal a potentially hidden association signal upstream of two GABA receptor genes (2018) (1)
- High carrier frequency for recessive OI in West Africans (2008) (1)
- Erratum: A major locus for hereditary prostate cancer in Finland: Localization by linkage disequilibrium of a haplotype in the HPCX region (Human Genetics (2005) vol. 117 (307-316) 10.1007/s00439-005-1305-z) (2005) (1)
- Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 data (2016) (1)
- Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk (2021) (1)
- Abstract 2300: Deleterious germline mutations in theBRCA1gene are associated with increased risk for cancers of the female reproductive system other than breast and ovarian as well as other cancers (2020) (0)
- Chromosome 11p is Significantly Linked to Myopia in Caucasian Families (2017) (0)
- Concordant and discordant cancers in familial atypical multiple mole melanoma syndrome (FAMMM) with the CDKN2A mutation (2018) (0)
- African-American families show genome-wide significant linkage to myopia at 7p15.2-14.2 (2018) (0)
- Linkage Analysis of Common Myopia using Whole Exome Genotyping in Highly Aggregated Ashkenazi Families Replicates Loci on Chromosomes 1 and 7. (2016) (0)
- A Genome-Wide Association Study of Age-Related Cortical Cataract and Its Progression Identifies Novel Genes (2015) (0)
- Abstract PO-202: Copy number variation (CNV) analysis identifies variants in 1p36 in African American and Caucasian hereditary prostate cancer cases (2022) (0)
- Novel genes are associated with refractive error in Indo-Europeans and East Asians using rare variant aggregation tests (2021) (0)
- Abstract 4599: Somatic mutation profile differences of “driver” mutations in 26 oncogenic lung cancer genes between African American and European American non-small cell lung cancer patients (2015) (0)
- Abstract 2757: Evaluation ofEYA4as a candidate risk locus in familial lung cancer families linked to 6q (2015) (0)
- Abstract 4240: Rare candidate variants shared among affected family members in the African American Hereditary Prostate Cancer Study families (2019) (0)
- Abstract 4290: A study in locus heterogeneity: Targeted sequencing analysis of 6q reveals multiple significant loci as the source of a previous linkage peak in familial lung cancer (2017) (0)
- 6.8 Sterol and Lipid Analyses Identify Hypolipidemia and Apolipoprotein Disorders in Autism Spectrum Disorder Associated With Adaptive Functioning Deficits (2021) (0)
- Rare Variant Analysis of Refractive Error in the AREDS Cohort (2012) (0)
- Han Chinese families show significant linkage for myopia on 10q26 and suggestive linkage on 9q33. (2017) (0)
- Contents Vol. 72, 2011 (2011) (0)
- Sib-pair linkage analysis applied to pedigrees with melanoma and dysplastic nevi. (1992) (0)
- Abstract A106: Optimal strategies for selecting samples for sequencing families with a common cancer: The Genetic Epidemiology of Lung Cancer Consortium. (2012) (0)
- ' s response to reviews Title : Genome Screen in Familial Intracranial Aneurysm (2008) (0)
- Rare variant analyses across multiethnic cohorts identify novel genes for refractive error (2021) (0)
- Contributors and Participants (1982) (0)
- Case-Control Genome-Wide Association Study for Refractive Astigmatism: The CREAM Consortium (2014) (0)
- Abstract A61: Analysis of 8q prostate cancer risk locus in the Afro-Barbadian population (2009) (0)
- Contents Vol. 59, 2005 (2005) (0)
- Subject Index Vol. 54, 2002 (2003) (0)
- Genome-Wide LinkageAnalysis of 1 , 233 Prostate Cancer Pedigrees Fromthe International Consortium for ProstateCancerGeneticsUsingNovel sumLINKandsumLODAnalyses (2010) (0)
- Genetic epidemiology of prostate cancer: Segregation analysis of 1,546 Finnish pedigrees (2006) (0)
- Myopia in African Americans Is Significantly Linked to Chromosome 7p15.2-14.2 (2021) (0)
- A genome wide screen in an unusually large inflammatory bowel disease pedigree: Suggestive evidence for linkage on chromosomes 18p, 7p and 15q; No evidence for IBD1 or IBD2 loci (2001) (0)
- Abstract A69: Identification of prostate cancer genes in the African American Hereditary Prostate Cancer (AAHPC) study (2011) (0)
- OR11-6 Rare Sequence Variants in GnRH-Associated Genes May Contribute to Variable Susceptibility to Environmental Stressors in Functional Hypothalamic Amenorrhea (2019) (0)
- Subject Index Vol. 59, 2005 (2005) (0)
- Tribute to Lodewijk Sandkuijl (2003) (0)
- Gene‐based analysis of bi‐variate survival traits via functional regressions with applications to eye diseases (2021) (0)
- Multiple novel loci for corneal curvature identified through genome-wide association studies: The CREAM Consortium (2015) (0)
- Fine-mapping Of Linkage Region Shows A Novel Association Of Refractive Error To a Polymorphism In CSMD2 (2011) (0)
- Exome-focused Rare and Common Variant Analyses of Ocular Traits in a Sardinian Cohort (2017) (0)
- Abstract PO-190: Health disparities in high-risk lung cancer families and their association with smoking, environmental exposures, and other etiological factors (2022) (0)
- Abstract LB-053: Familial studies identify variants in the E2A transcription factor as putative risk factors for lung cancer (2019) (0)
- Abstract 4600: Target exome sequencing for disease-causing rare mutations in familial and sporadic lung cancer (2015) (0)
- Screening for AMD in the Amish Population (2003) (0)
- Abstract 37: Highly aggregated lung cancer families reveal a heterogeneous cause for a previous linkage signal on 6q (2020) (0)
- Meta-analysis of functional enrichment results from five GWAS studies reveals biological processes involved in human refractive variation (2013) (0)
- Acknowledgement to the Reviewers (2003) (0)
- Genomewide Screen for Intracranial Aneurysm Susceptibility Genes (2006) (0)
- Identification of susceptibility loci in hereditary prostate cancer families using copy number variation and linkage analysis. (2015) (0)
- Cellular Genes in T H E Mouse Regulate in Trans T H E Expression of Endogenous Mouse Mammary T U M O R Viruses (0)
- George Bonney (1947–2013) Remembered (2014) (0)
- Identification of BRCA1 and BRCA2 genetic modifiers. (2009) (0)
- Pro-oxidants and Injury Effects : Contributors to Tobacco Carcinogenesis in the Lung ? (2005) (0)
- Acknowledgement to the Reviewers (2004) (0)
- Abstract LB-189: Genetic Epidemiology of Lung Cancer Consortium: genome-wide association study of familial lung cancer cases: (2015) (0)
- Genomewide Scan of Ocular Refraction in African-Americans Shows Linkage to Chromosome 7p15 (2007) (0)
- Abstract 3648: Unraveling phenotype heterogeneity in prostate cancer susceptibility in Finland utilizing covariate-based analysis. (2013) (0)
- Novel region of interest in chromosome 11 and other putative regions identified in a genome-wide scan in finnish hereditary prostate cancer families (2002) (0)
- Abstract 1452: Analyses of whole exome sequencing (WES) data of hereditary lung cancer families identify germline copy number variations (CNVs) in multiple genes (2022) (0)
- Genome-wide linkage search for cancer susceptibility loci in a cohort of non BRCA1/2 families in Sri Lanka (2022) (0)
- A powerful new method for rare-variant analysis of quantitative traits in families (2020) (0)
- Abstract C050: Deleterious coding variants in African American Hereditary Prostate Cancer Study (AAHPC) families (2020) (0)
- Genomewide Scan Among Ashkenazi Families Shows Suggestive Evidence for Linkage of Refractive Error to a Quantitative Trait Locus on Chromosome 1p36 (2005) (0)
- Myopia in Amish Families Linked to Five Chromosomes (2018) (0)
- Association of Matrix Metalloproteinase Polymorphisms With Refractive Error in the Myopia Family Study (2010) (0)
- MP66-10 CHARACTERIZATION OF SUSCEPTIBILITY LOCI IN HEREDITARY PROSTATE CANCER FAMILIES USING COPY NUMBER VARIATION AND LINKAGE ANALYSIS (2015) (0)
- Acknowledgement to the Reviewers (2005) (0)
- Association of breast cancer with common variants in the BRCA2 gene an Afro-Barbadian population (2007) (0)
- 2 IntegratedCancerGenomicsDivision,TranslationalGenomicsResearchInstitute(TGen),Phoenix,Arizona 3 DepartmentofPreventiveMedicine,KeckSchoolofMedicine,UniversityofSouthernCalifornia, (2014) (0)
- Abstract B40: Rare variant discovery in known cancer genes from whole-exome sequencingof African American hereditary prostate cancer families (2016) (0)
- Genes Involved in the Pathogenesis of Primary Open-Angle Glaucoma (2007) (0)
- Genetic aspect of Alzheimer disease: Results of complex segregation analysis (1994) (0)
- Lung Cancer Risk among Light and Never Smokers A Susceptibility Locus on Chromosome 6 q Greatly Increases (2010) (0)
- Strong Evidence for Myopia Linkage on Chromosomes 1, 3, and 15 in Pennsylvania Amish Families (2016) (0)
- Meta-Analysis of Genomewide Linkage Scans of Ocular Refraction in Four Populations (2008) (0)
- Brief Communication ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies ILAE Genetics Commission (2002) (0)
- Evidence of linkage in MSH6-associated region exclusive to high-risk African-American families with prostate cancer. (2017) (0)
- Rare Variant TDT Association Study of Familial Myopia in Caucasian Families (2018) (0)
- Genome-wide Linkage a nalysis of Multiple Metabolic Factors: Evidence of Genetic (2010) (0)
- 240: Segregation Analysis of 1,546 Families with Prostate Cancer in Finland (2006) (0)
- Abstract A64: Genome wide linkage and finemapping studies for prostate cancer in families from the African American Hereditary Prostate Cancer Study (2009) (0)
- Genomewide Scan in Amish Families Confirms Linkage of Ocular Refraction to Chromosome 1 (2006) (0)
- ANNUAL REVIEWERS LIST (2009) (0)
- Contents Vol. 54, 2002 (2003) (0)
- 1 Title : Post-hoc Analysis for Detecting Individual Rare Variant Risk Associations using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies Running Title : Bayesian Probit Rare Variant Analysis (2017) (0)
- Abstract 3276: Whole exome sequencing identifies significantly linked regions on multiple chromosomes in families with a history of lung cancer (2018) (0)
- Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk. (2002) (0)
- Abstract 2542: Chromatin remodeling gene ARID1B is linked to familial lung cancer (2016) (0)
- Replication of known loci and suggestive linkage for Familial Myopia on three chromosomes in African-Americans (2016) (0)
- EXPERIENCE FROM A TERTIARY CENTRE FOR OPTIMAL MANAGEMENT OF PATIENTS REFERRED FOR COMPLEX ENDOSCOPIC PROCEDURES: AN ADVANCED ENDOSCOPY MULTIDISCIPLINARY TEAM MEETING (2020) (0)
- Society for Social Medicine and the International Epidemiological Association European Group (2001) (0)
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