The scientist’s investigation covers issues in Genetics, Single-nucleotide polymorphism, Genome-wide association study, Cancer and Genetic association. His study explores the link between Genetics and topics such as Internal medicine that cross with problems in Endocrinology. The various areas that Meredith Yeager examines in his Single-nucleotide polymorphism study include Genotyping, Case-control study, Haplotype and Candidate gene.
His Genome-wide association study study integrates concerns from other disciplines, such as Genome, Allele, Oncology and Bioinformatics. Meredith Yeager interconnects TOX3 and Polymorphism in the investigation of issues within Cancer. His studies deal with areas such as Human Phenotype Ontology, Genetic predisposition, Allele frequency and Medical genetics as well as Genetic association.
His primary areas of study are Genetics, Single-nucleotide polymorphism, Internal medicine, Genome-wide association study and Oncology. Genetic association, Gene, Locus, Linkage disequilibrium and Genetic variation are among the areas of Genetics where the researcher is concentrating his efforts. His study in Single-nucleotide polymorphism is interdisciplinary in nature, drawing from both Odds ratio, Prostate cancer and Haplotype.
His work carried out in the field of Internal medicine brings together such families of science as Gastroenterology and Endocrinology. His Genome-wide association study research incorporates themes from Genetic predisposition, International HapMap Project, Genotyping, Allele and 1000 Genomes Project. His work carried out in the field of Cancer brings together such families of science as Cancer research and Disease.
Meredith Yeager mostly deals with Oncology, Internal medicine, Genome-wide association study, Cancer and Genetics. His Oncology research is multidisciplinary, incorporating elements of Germline mutation, Proportional hazards model, MEDLINE and Lymphoblastic Leukemia. His Genome-wide association study study deals with the bigger picture of Single-nucleotide polymorphism.
He has included themes like Genetic architecture, Genome and Hazard ratio in his Single-nucleotide polymorphism study. His research in Cancer intersects with topics in Y chromosome, Chromosome, Demography and Disease. Gene is the focus of his Genetics research.
Meredith Yeager spends much of his time researching Cancer, Cervical cancer, Epidemiology, Demography and Genotyping. Meredith Yeager has researched Cancer in several fields, including Chromosome, Y chromosome and Somatic cell. Meredith Yeager combines subjects such as Odds ratio, Lineage, Biological dispersal, Genetic variation and Adenocarcinoma with his study of Epidemiology.
Meredith Yeager focuses mostly in the field of Genotype, narrowing it down to matters related to Whole Genome Amplification and, in some cases, Single-nucleotide polymorphism. His Single-nucleotide polymorphism course of study focuses on Osteosarcoma and Locus, Oncology, Internal medicine and Genome-wide association study. Mutation is a subfield of Genetics that Meredith Yeager studies.
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A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
David J Hunter;David J Hunter;Peter Kraft;Kevin B Jacobs;David G Cox.
Nature Genetics (2007)
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24
Meredith Yeager;Nick Orr;Richard B Hayes;Kevin B Jacobs.
Nature Genetics (2007)
Multiple loci identified in a genome-wide association study of prostate cancer
Gilles Thomas;Kevin B Jacobs;Meredith Yeager;Meredith Yeager;Peter Kraft.
Nature Genetics (2008)
Natural selection at major histocompatibility complex loci of vertebrates
Austin L. Hughes;Meredith Yeager.
Annual Review of Genetics (1998)
NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses.
Montserrat García-Closas;Núria Malats;Debra Silverman;Mustafa Dosemeci.
The Lancet (2005)
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).
Gilles Thomas;Kevin B Jacobs;Kevin B Jacobs;Peter Kraft;Meredith Yeager;Meredith Yeager.
Nature Genetics (2009)
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
Rosalind A. Eeles;Ali Amin Al Olama;Sara Benlloch;Edward J. Saunders.
Nature Genetics (2013)
A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma.
Maria Teresa Landi;Nilanjan Chatterjee;Kai Yu;Lynn R. Goldin.
American Journal of Human Genetics (2009)
Detectable clonal mosaicism and its relationship to aging and cancer
Kevin B. Jacobs;Kevin B. Jacobs;Meredith Yeager;Meredith Yeager;Weiyin Zhou;Weiyin Zhou;Sholom Wacholder.
Nature Genetics (2012)
A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma
Christian C. Abnet;Neal D. Freedman;Nan Hu;Zhaoming Wang;Zhaoming Wang.
Nature Genetics (2010)
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