2023 - Research.com Medicine in Australia Leader Award
2022 - Research.com Best Female Scientist Award
Melissa C. Southey focuses on Breast cancer, Genome-wide association study, Internal medicine, Oncology and Genetics. Her Breast cancer research entails a greater understanding of Cancer. Melissa C. Southey interconnects Germline mutation and PALB2 in the investigation of issues within Cancer.
Her Genome-wide association study study combines topics in areas such as Genotyping, Prostate cancer and Genetic association. Her Internal medicine research includes themes of Penetrance, Gene mutation and Pathology. Melissa C. Southey has researched Oncology in several fields, including Cohort study, Case-control study, Ovarian cancer, Hazard ratio and Risk factor.
Breast cancer, Internal medicine, Oncology, Genetics and Genome-wide association study are her primary areas of study. Her work carried out in the field of Breast cancer brings together such families of science as Germline mutation, Family history, Genotype and Bioinformatics. Her study looks at the relationship between Internal medicine and topics such as DNA methylation, which overlap with Epigenetics and Confounding.
Melissa C. Southey has included themes like Methylation, Cohort study, Hazard ratio, Colorectal cancer and Prostate cancer in her Oncology study. In her research, Carcinogenesis is intimately related to Cancer research, which falls under the overarching field of Genetics. Her Genome-wide association study study is focused on Single-nucleotide polymorphism in general.
Melissa C. Southey mostly deals with Internal medicine, Oncology, Breast cancer, DNA methylation and Cancer. Her biological study spans a wide range of topics, including Logistic regression, Biomarker, Penetrance, Single-nucleotide polymorphism and Prostate cancer. The various areas that Melissa C. Southey examines in her Breast cancer study include Genome-wide association study, Epidemiology, CHEK2, Germline and Family history.
Her Genome-wide association study research includes elements of Genetic variation, Human genetics, Bioinformatics and Longevity. Her DNA methylation research is multidisciplinary, relying on both Colorectal cancer, Methylation and Epigenetics. Her Cancer course of study focuses on Lung cancer and Anthropometry and Biomarkers of aging.
Melissa C. Southey mainly focuses on Internal medicine, Oncology, Breast cancer, Cohort study and DNA methylation. Her study in Internal medicine is interdisciplinary in nature, drawing from both Gene sequence and Allele frequency. Her research in Oncology intersects with topics in Germline mutation, PALB2, Colorectal cancer, Prostate cancer and Risk factor.
Her study in the field of Estrogen receptor also crosses realms of FANCM GENE. Her DNA methylation research is multidisciplinary, incorporating perspectives in Methylation and Epigenetics. Her work investigates the relationship between Disease and topics such as Bioinformatics that intersect with problems in Genome-wide association study.
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.
Nature (2007)
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.
JAMA (2017)
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)
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Kyriaki Michailidou;Per Hall;Anna Gonzalez-Neira;Maya Ghoussaini.
Nature Genetics (2013)
RAD51B in Familial Breast Cancer
Liisa M. Pelttari;Sofia Khan;Mikko Vuorela;Johanna I. Kiiski.
PLOS ONE (2016)
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)
Association analysis identifies 65 new breast cancer risk loci
Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley.
Nature (2017)
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
Bjarni J. Vilhjálmsson;Jian Yang;Hilary K. Finucane;Alexander Gusev.
American Journal of Human Genetics (2015)
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)
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)
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