Angela Brooks-Wilson mainly focuses on Genetics, Genome-wide association study, Single-nucleotide polymorphism, Locus and Lymphoma. As part of her studies on Genetics, she often connects relevant subjects like Tangier disease. Her Genome-wide association study study incorporates themes from Genetic predisposition, Ovarian cancer, Genetic association, Heritability and Chronic lymphocytic leukemia.
Her studies deal with areas such as Estrogen receptor and Case-control study as well as Single-nucleotide polymorphism. Follicular lymphoma and Diffuse large B-cell lymphoma are among the areas of Lymphoma where Angela Brooks-Wilson concentrates her study. The study incorporates disciplines such as Mutation and Germline mutation in addition to Cancer research.
Angela Brooks-Wilson focuses on Genetics, Single-nucleotide polymorphism, Genome-wide association study, Internal medicine and Oncology. Genetic association, Locus, Genotype, Gene and Allele are the primary areas of interest in her Genetics study. She interconnects Haplotype, Bioinformatics and Candidate gene in the investigation of issues within Single-nucleotide polymorphism.
Her research integrates issues of Genotyping, Ovarian cancer, Follicular lymphoma and Genetic predisposition in her study of Genome-wide association study. Her research on Ovarian cancer also deals with topics like
Angela Brooks-Wilson mainly investigates Internal medicine, Oncology, Single-nucleotide polymorphism, Genome-wide association study and Odds ratio. The study incorporates disciplines such as Genotyping and Genetic predisposition in addition to Single-nucleotide polymorphism. Her Genome-wide association study study is concerned with the field of Genetics as a whole.
Her Odds ratio study incorporates themes from Cancer and Cancer prevention. Angela Brooks-Wilson has researched Cancer in several fields, including Hygiene hypothesis, Family aggregation, Case-control study and Genotype, Gene–environment interaction. Genetic variation, Multiple sclerosis, Autoimmune disease, Disease and Confounding is closely connected to Chronic lymphocytic leukemia in her research, which is encompassed under the umbrella topic of Lymphoma.
Angela Brooks-Wilson mostly deals with Linkage disequilibrium, Genome-wide association study, Gene, Internal medicine and Oncology. The Linkage disequilibrium portion of her research involves studies in Genetics and Single-nucleotide polymorphism. Her work on Ovarian cancer, Genotyping, Minor allele frequency and Diffuse large B-cell lymphoma is typically connected to Scaffold/matrix attachment region as part of general Genetics study, connecting several disciplines of science.
Her Genome-wide association study research is multidisciplinary, incorporating perspectives in Autoimmune disease, Disease and Follicular lymphoma, Lymphoma. Her Internal medicine study integrates concerns from other disciplines, such as Multiple sclerosis and Genetic variation. Her biological study spans a wide range of topics, including Breast cancer, Stepwise regression, Prostate cancer and Cancer prevention.
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The Genome Sequence of the SARS-associated Coronavirus
Marco A. Marra;Steven J. M. Jones;Caroline R. Astell;Robert A. Holt.
Science (2003)
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
A. Brooks-Wilson;M. Marcil;S. M. Clee;L.-H. Zhang.
Nature Genetics (1999)
Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma
Ryan D Morin;María Méndez-Lago;Andrew J Mungall;Rodrigo Goya.
Nature (2011)
Association analysis identifies 65 new breast cancer risk loci
Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley.
Nature (2017)
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 independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Stig E. Bojesen;Stig E. Bojesen;Karen A. Pooley;Sharon E. Johnatty;Jonathan Beesley.
Nature Genetics (2013)
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Nasim Mavaddat;Kyriaki Michailidou;Kyriaki Michailidou;Joe Dennis;Michael Lush.
American Journal of Human Genetics (2019)
Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria
A R Brooks-Wilson;P Kaurah;G Suriano;S Leach.
Journal of Medical Genetics (2004)
Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium
Nathaniel Rothman;Christine F Skibola;Sophia S Wang;Gareth Morgan.
Lancet Oncology (2006)
Gender and telomere length : systematic review and meta-analysis
Michael Gardner;David Bann;Laura Wiley;Rachel Cooper.
Experimental Gerontology (2014)
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