Her primary areas of investigation include Breast cancer, Genome-wide association study, Internal medicine, Genetics and Oncology. Her Breast cancer research entails a greater understanding of Cancer. Her study looks at the relationship between Cancer and topics such as Germline mutation, which overlap with Pathology.
Her study in Genome-wide association study is interdisciplinary in nature, drawing from both Genotyping, Prostate cancer and Genetic association. Her Internal medicine research integrates issues from Penetrance and Gene mutation. Her Oncology study incorporates themes from Surgery, Cohort study, Case-control study and Hazard ratio, Confidence interval.
Melissa C. Southey mainly focuses on Breast cancer, Internal medicine, Oncology, Genetics and Cancer. Her studies in Breast cancer integrate themes in fields like Germline mutation, Genome-wide association study, Family history and Genotype. Her Genome-wide association study research focuses on Bioinformatics and how it connects with Disease.
Her research investigates the connection between Internal medicine and topics such as DNA methylation that intersect with issues in Epigenetics and Confounding. The study incorporates disciplines such as Cohort study, Ovarian cancer, Gynecology, Hazard ratio and Colorectal cancer in addition to Oncology. Her studies deal with areas such as Lung cancer and Risk factor as well as Cancer.
Melissa C. Southey mostly deals with Internal medicine, Oncology, Breast cancer, DNA methylation and Cancer. Her Oncology study combines topics from a wide range of disciplines, such as Prostate, Gene, Germline, Colorectal cancer and Prostate cancer. Her Breast cancer research is classified as research in Genetics.
Her biological study deals with issues like Lung cancer, which deal with fields such as Biomarkers of aging and Anthropometry. Her work in Hazard ratio tackles topics such as Single-nucleotide polymorphism which are related to areas like Ovarian cancer. The various areas that she examines in her Genome-wide association study study include Genetic variation and Genetic association.
Her primary areas of study are Internal medicine, Oncology, Breast cancer, Cohort study and DNA methylation. Her Cancer and Confidence interval study, which is part of a larger body of work in Internal medicine, is frequently linked to Clinical decision making, bridging the gap between disciplines. She has researched Oncology in several fields, including Germline mutation, PALB2, Colorectal cancer, Prostate cancer and Risk factor.
Her study focuses on the intersection of Prostate cancer and fields such as Disease with connections in the field of Genome-wide association study. The Breast cancer study combines topics in areas such as Odds ratio, Germline, Family history and Bioinformatics. Her Cohort study research is multidisciplinary, relying on both Body mass index, Prospective cohort study and Cohort.
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.
Subtyping of breast cancer by immunohistochemistry to investigate a relationship between subtype and short and long term survival: a collaborative analysis of data for 10,159 cases from 12 studies
Fiona M. Blows;Kristy E. Driver;Marjanka K. Schmidt;Annegien Broeks.
PLOS Medicine (2010)
Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
Karoline B. Kuchenbaecker;Karoline B. Kuchenbaecker;John L. Hopper;Daniel R. Barnes;Kelly-Anne Phillips.
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 Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk
Ganna Chornokur;Hui-Yi Lin;Jonathan P. Tyrer;Kate Lawrenson.
PLOS ONE (2015)
Multiple newly identified loci associated with prostate cancer susceptibility.
Rosalind A Eeles;Rosalind A Eeles;Zsofia Kote-Jarai;Graham G Giles;Graham G Giles;Ali Amin Al Olama.
Nature Genetics (2008)
Breast-Cancer Risk in Families with Mutations in PALB2
A. C. Antoniou;S. Casadei;T. Heikkinen;D. Barrowdale.
The New England Journal of Medicine (2014)
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)
Iron-overload-related Disease in HFE Hereditary Hemochromatosis
Katrina J. Allen;Lyle C. Gurrin;Clare C. Constantine;Nicholas J. Osborne.
The New England Journal of Medicine (2008)
Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk
Douglas Frederick Easton;Paul David Pharoah;Antonis C. Antoniou;Marc Derek Tischkowitz.
The New England Journal of Medicine (2015)
Profile was last updated on December 6th, 2021.
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