David V. Conti spends much of his time researching Genetics, Genome-wide association study, Single-nucleotide polymorphism, Genetic association and Internal medicine. His studies link Odds ratio with Genetics. His work deals with themes such as Polymorphism, Case-control study, Meta-analysis, Colorectal cancer and Genetic architecture, which intersect with Genome-wide association study.
His work focuses on many connections between Single-nucleotide polymorphism and other disciplines, such as Candidate gene, that overlap with his field of interest in Genetic testing, Oxidative Stress Pathway, Epistasis, Multifactor dimensionality reduction and Genetic determinism. His research in Internal medicine intersects with topics in Endocrinology, Bupropion, Smoking cessation and Oncology. His Oncology research is multidisciplinary, relying on both Relative risk, Cancer, Ovarian cancer and Germline.
Internal medicine, Genome-wide association study, Genetics, Single-nucleotide polymorphism and Oncology are his primary areas of study. His study ties his expertise on Genotype together with the subject of Internal medicine. His research in Genome-wide association study tackles topics such as Genetic association which are related to areas like Genetic predisposition, Computational biology and Bayes' theorem.
His study in Linkage disequilibrium, Locus, Allele, Gene and Allele frequency is done as part of Genetics. His Single-nucleotide polymorphism study combines topics from a wide range of disciplines, such as Haplotype and Candidate gene. David V. Conti has researched Oncology in several fields, including Endocrinology, Genetic variation, Germline, Prostate cancer and Risk factor.
His scientific interests lie mostly in Internal medicine, Oncology, Genome-wide association study, Colorectal cancer and Prostate cancer. His Oncology research incorporates themes from Cancer, Cohort study, Prostate cancer screening, Allele and Prostate cancer risk. His Genome-wide association study study incorporates themes from Meta-analysis, Genetic association and Locus.
His Colorectal cancer study results in a more complete grasp of Genetics. His Prostate cancer research includes themes of Multiethnic population and Gene, DNA repair, Germline. In the subject of general Single-nucleotide polymorphism, his work in Linkage disequilibrium, Expression quantitative trait loci and SNP is often linked to Risk assessment, thereby combining diverse domains of study.
His primary areas of study are Internal medicine, Genome-wide association study, Oncology, Odds ratio and Prostate cancer. He has included themes like Linoleic acid and Genetic admixture in his Internal medicine study. To a larger extent, David V. Conti studies Single-nucleotide polymorphism with the aim of understanding Genome-wide association study.
His work deals with themes such as Autoimmune disease, Prostate cancer screening, Allele and Genetic predisposition, which intersect with Oncology. His research integrates issues of Breast cancer, Gene and Multiethnic population in his study of Prostate cancer. His Linkage disequilibrium study is concerned with the field of Genetics as a whole.
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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
Shaun M. Purcell;Shaun M. Purcell;Naomi R. Wray;Jennifer L. Stone;Jennifer L. Stone;Peter M. Visscher.
Rare chromosomal deletions and duplications increase risk of schizophrenia
Jennifer L. Stone;Jennifer L. Stone;Jennifer L. Stone;Michael C. O’Donovan;Hugh Gurling;George K. Kirov.
Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations
Dara G. Torgerson;Dara G. Torgerson;Elizabeth J. Ampleford;Grace Y. Chiu;W. James Gauderman.
Nature Genetics (2011)
Time to first cigarette in the morning as an index of ability to quit smoking: Implications for nicotine dependence
Timothy B. Baker;Megan E. Piper;Danielle E. McCarthy;Daniel M. Bolt.
Nicotine & Tobacco Research (2007)
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer
Ali Amin Al Olama;Zsofia Kote-Jarai;Sonja I. Berndt;David V. Conti.
Nature Genetics (2014)
Genetic Dissection of Complex Traits with Chromosome Substitution Strains of Mice
Jonathan B. Singer;Jonathan B. Singer;Annie E. Hill;Lindsay C. Burrage;Keith R. Olszens.
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Fredrick R. Schumacher;Ali Amin Al Olama;Sonja I. Berndt;Sara Benlloch.
Nature Genetics (2018)
Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis
Ulrike Peters;Ulrike Peters;Shuo Jiao;Fredrick R. Schumacher;Carolyn M. Hutter;Carolyn M. Hutter.
Genome-wide association study of obsessive-compulsive disorder.
S. E. Stewart;D. Yu;J. M. Scharf;B. M. Neale.
Molecular Psychiatry (2013)
Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer
Susan J. Ramus;Honglin Song;Ed Dicks;Jonathan P. Tyrer.
Journal of the National Cancer Institute (2015)
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