Her main research concerns Genetics, Genetic linkage, Locus, Prostate cancer and Genome-wide association study. All of her Genetics and Gene, Genetic association, Allele, Haplotype and Germline mutation investigations are sub-components of the entire Genetics study. The various areas that Joan E. Bailey-Wilson examines in her Genetic linkage study include Genetic determinism, Genotype and Pedigree chart.
Her Locus research incorporates elements of Microsatellite, Lung cancer and Gene mapping. Her work is dedicated to discovering how Prostate cancer, Allele frequency are connected with Ensemble learning, Mutation and Exome sequencing and other disciplines. Genome-wide association study is a primary field of her research addressed under Single-nucleotide polymorphism.
Her primary scientific interests are in Genetics, Genetic linkage, Linkage, Locus and Internal medicine. Genetics is a component of her Single-nucleotide polymorphism, Genome-wide association study, Prostate cancer, Allele and Genotype studies. The Genetic linkage study which covers Haplotype that intersects with Candidate gene.
Her Linkage research integrates issues from Genetic analysis, Statistics, Type I and type II errors, Microsatellite and Computational biology. Her study in Locus is interdisciplinary in nature, drawing from both Genetic marker, Genome, Human genetics and Gene mapping. Joan E. Bailey-Wilson has included themes like Endocrinology and Oncology in her Internal medicine study.
Joan E. Bailey-Wilson mainly focuses on Genetics, Genome-wide association study, Exome, Candidate gene and Lung cancer. Her study in Genetic linkage, Exome sequencing, Gene, Haplotype and Allele frequency falls within the category of Genetics. Her research in Haplotype intersects with topics in Microsatellite and Linkage.
Her study explores the link between Genome-wide association study and topics such as Genetic association that cross with problems in Functional data analysis, Type I and type II errors, Computational biology and Statistics. Her Lung cancer research includes elements of Cancer, Disease and 1000 Genomes Project. Her research integrates issues of Germline mutation, Oncology and Germline in her study of Cancer.
Genetics, Genome-wide association study, Genetic association, Exome and Exome sequencing are her primary areas of study. The study of Genetics is intertwined with the study of Disease in a number of ways. Joan E. Bailey-Wilson usually deals with Genome-wide association study and limits it to topics linked to 1000 Genomes Project and Oncology, CDKN2A, Imputation, Squamous carcinoma and Adenocarcinoma.
In her research on the topic of Genetic association, Keratoconus, Astigmatism and Heritability is strongly related with Statistics. Her studies deal with areas such as Whole genome sequencing, Massive parallel sequencing and Mutation as well as Exome. She interconnects Allele frequency and DNA sequencing in the investigation of issues within Exome sequencing.
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Replicating genotype–phenotype associations
Stephen J. Chanock;Teri Manolio;Michael Boehnke;Eric Boerwinkle.
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants
Nilah M M. Ioannidis;Joseph H H. Rothstein;Joseph H H. Rothstein;Vikas Pejaver;Sumit Middha.
American Journal of Human Genetics (2016)
Major Susceptibility Locus for Prostate Cancer on Chromosome 1 Suggested by a Genome-Wide Search
Jeffrey R. Smith;Diha Freije;John D. Carpten;Henrik Grönberg;Henrik Grönberg.
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome
J.D. Carpten;C.M. Robbins;A. Villablanca;L. Forsberg.
Nature Genetics (2002)
Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases
Kevin G. Becker;Richard M. Simon;Joan E. Bailey-Wilson;Boris Freidlin.
Proceedings of the National Academy of Sciences of the United States of America (1998)
Germline mutations in the ribonuclease L gene in families showing linkage with HPC1.
J. Carpten;N. Nupponen;S. Isaacs;R. Sood.
Nature Genetics (2002)
Evidence for a prostate cancer susceptibility locus on the X chromosome.
Jianfeng Xu;Deborah Meyers;Diha Freije;Sarah Isaacs.
Nature Genetics (1998)
Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). I. Clinical description of resource
Henry T. Lynch;William Kimberling;William A. Albano;Jane F. Lynch.
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Virginie J M Verhoeven;Pirro G Hysi;Robert Wojciechowski;Robert Wojciechowski;Qiao Fan.
Nature Genetics (2013)
Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk
Jianfeng Xu;S. Lilly Zheng;Akira Komiya;Josyf C. Mychaleckyj.
Nature Genetics (2002)
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