His main research concerns Genome-wide association study, Genetics, Single-nucleotide polymorphism, Breast cancer and Genotype. The Genome-wide association study study combines topics in areas such as Odds ratio, Genetic predisposition, Case-control study, Genotyping and Genetic association. His work in Allele, Locus, Linkage disequilibrium, Cancer and Genetic variation are all subfields of Genetics research.
His Cancer research includes themes of Lung cancer, Incidence, Immunology and Physiology. His Single-nucleotide polymorphism research incorporates themes from Meta-analysis, Haplotype, Allele frequency and Bioinformatics. Breast cancer is the subject of his research, which falls under Internal medicine.
The scientist’s investigation covers issues in Internal medicine, Genome-wide association study, Oncology, Genetics and Single-nucleotide polymorphism. Internal medicine is represented through his Breast cancer, Prostate cancer, Cancer, Odds ratio and Case-control study research. In his research, Epidemiology is intimately related to Body mass index, which falls under the overarching field of Breast cancer.
His Genome-wide association study study is related to the wider topic of Genotype. His research in Oncology intersects with topics in Cohort study, Gynecology, Prospective cohort study, Cohort and Risk factor. His research integrates issues of Haplotype and Bioinformatics in his study of Single-nucleotide polymorphism.
His primary areas of investigation include Internal medicine, Oncology, Breast cancer, Genome-wide association study and Prostate cancer. Christopher A. Haiman focuses mostly in the field of Internal medicine, narrowing it down to matters related to Single-nucleotide polymorphism and, in some cases, Genetic variation and Transplantation. His study on Oncology also encompasses disciplines like
His work on Estrogen receptor as part of general Breast cancer research is often related to Risk assessment, thus linking different fields of science. His Genome-wide association study research is classified as research in Genetics. His Prostate cancer study combines topics from a wide range of disciplines, such as Prostate and Multiethnic population.
His primary scientific interests are in Internal medicine, Oncology, Breast cancer, Genome-wide association study and Odds ratio. Christopher A. Haiman has included themes like Germline mutation, PALB2, Genetic predisposition, Mendelian Randomization Analysis and Family history in his Oncology study. His Breast cancer study incorporates themes from CHEK2, Germline, Ovarian cancer and Bioinformatics.
His Genome-wide association study research is multidisciplinary, incorporating perspectives in Genetic association and Medical genetics. His Odds ratio research is multidisciplinary, incorporating elements of Mendelian randomization, Logistic regression, Case-control study and Cancer prevention. His research in Cancer tackles topics such as Lung cancer which are related to areas like Vitamin B12.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Genome-wide association study identifies novel breast cancer susceptibility loci
Douglas F. Easton;Karen A. Pooley;Alison M. Dunning;Paul D. P. Pharoah.
Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes
Siddhartha Jaiswal;Pierre Fontanillas;Jason Flannick;Jason Flannick;Alisa Manning.
The New England Journal of Medicine (2014)
Defining the role of common variation in the genomic and biological architecture of adult human height
Andrew R. Wood;Tonu Esko;Jian Yang;Sailaja Vedantam.
Nature Genetics (2014)
Genetic studies of body mass index yield new insights for obesity biology
Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice.
Faculty of Health; Institute of Health and Biomedical Innovation (2015)
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Kyriaki Michailidou;Per Hall;Anna Gonzalez-Neira;Maya Ghoussaini.
Nature Genetics (2013)
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.
Simon N Stacey;Andrei Manolescu;Patrick Sulem;Thorunn Rafnar.
Nature Genetics (2007)
Associations of Breast Cancer Risk Factors With Tumor Subtypes: A Pooled Analysis From the Breast Cancer Association Consortium Studies
Xiaohong R. Yang;Jenny Chang-Claude;Ellen L. Goode;Fergus J. Couch.
Journal of the National Cancer Institute (2011)
Multiple regions within 8q24 independently affect risk for prostate cancer.
Christopher A Haiman;Nick Patterson;Matthew L Freedman;Matthew L Freedman;Simon R Myers.
Nature Genetics (2007)
The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer.
Mark M. Pomerantz;Nasim Ahmadiyeh;Nasim Ahmadiyeh;Li Jia;Paula Herman.
Nature Genetics (2009)
Association analysis identifies 65 new breast cancer risk loci
Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley.
Profile was last updated on December 6th, 2021.
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