D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics D-index 58 Citations 20,107 174 World Ranking 2491 National Ranking 87

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Cancer
  • Mutation

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.

Her most cited work include:

  • The Genome Sequence of the SARS-associated Coronavirus (1741 citations)
  • Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency (1545 citations)
  • Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma (1155 citations)

What are the main themes of her work throughout her whole career to date?

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

  • Serous fluid, which have a strong connection to Clear cell carcinoma,
  • Cancer research which is related to area like Mutation. Her work in the fields of Breast cancer, such as Estrogen receptor, overlaps with other areas such as Risk assessment.

She most often published in these fields:

  • Genetics (69.20%)
  • Single-nucleotide polymorphism (59.86%)
  • Genome-wide association study (57.44%)

What were the highlights of her more recent work (between 2018-2020)?

  • Internal medicine (49.83%)
  • Oncology (39.45%)
  • Single-nucleotide polymorphism (59.86%)

In recent papers she was focusing on the following fields of study:

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.

Between 2018 and 2020, her most popular works were:

  • Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes (257 citations)
  • Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes (257 citations)
  • Ovarian Carcinoma Histotype: Strengths and Limitations of Integrating Morphology With Immunohistochemical Predictions. (14 citations)

In her most recent research, the most cited papers focused on:

  • Gene
  • Cancer
  • Mutation

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.

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.

Best Publications

The Genome Sequence of the SARS-associated Coronavirus

Marco A. Marra;Steven J. M. Jones;Caroline R. Astell;Robert A. Holt.
Science (2003)

2857 Citations

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)

2070 Citations

Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma

Ryan D Morin;María Méndez-Lago;Andrew J Mungall;Rodrigo Goya.
Nature (2011)

1645 Citations

Association analysis identifies 65 new breast cancer risk loci

Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley.
Nature (2017)

969 Citations

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)

891 Citations

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)

604 Citations

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)

571 Citations

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)

469 Citations

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)

439 Citations

Gender and telomere length : systematic review and meta-analysis

Michael Gardner;David Bann;Laura Wiley;Rachel Cooper.
Experimental Gerontology (2014)

429 Citations

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