D-Index & Metrics Best Publications
Medicine
UK
2023

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
Medicine D-index 146 Citations 91,634 901 World Ranking 723 National Ranking 82

Research.com Recognitions

Awards & Achievements

2023 - Research.com Medicine in United Kingdom Leader Award

Overview

What is he best known for?

The fields of study he is best known for:

  • Cancer
  • Gene
  • Internal medicine

Paul D.P. Pharoah mainly focuses on Breast cancer, Internal medicine, Genetics, Oncology and Genome-wide association study. Breast cancer is a subfield of Cancer that he tackles. In most of his Internal medicine studies, his work intersects topics such as Endocrinology.

Paul D.P. Pharoah interconnects Pathology, Genetic counseling, Penetrance, Tissue microarray and Genetic testing in the investigation of issues within Oncology. His Genome-wide association study study necessitates a more in-depth grasp of Single-nucleotide polymorphism. Paul D.P. Pharoah has researched Single-nucleotide polymorphism in several fields, including Case-control study, Polymorphism and Genetic variation.

His most cited work include:

  • Genome-wide association study identifies novel breast cancer susceptibility loci (2045 citations)
  • The clonal and mutational evolution spectrum of primary triple-negative breast cancers (1368 citations)
  • Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk (951 citations)

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

Paul D.P. Pharoah mainly investigates Internal medicine, Breast cancer, Oncology, Single-nucleotide polymorphism and Genetics. His study in Internal medicine focuses on Cancer, Odds ratio, Ovarian cancer, Case-control study and Prostate cancer. His Cancer research integrates issues from Candidate gene, Endocrinology and Risk factor.

Paul D.P. Pharoah combines subjects such as Cancer research, Genetic predisposition and Bioinformatics with his study of Breast cancer. His Oncology study integrates concerns from other disciplines, such as Disease, Pathology, Gynecology, Proportional hazards model and Hazard ratio. Single-nucleotide polymorphism is a subfield of Genotype that Paul D.P. Pharoah studies.

He most often published in these fields:

  • Internal medicine (47.52%)
  • Breast cancer (44.36%)
  • Oncology (43.12%)

What were the highlights of his more recent work (between 2018-2021)?

  • Internal medicine (47.52%)
  • Oncology (43.12%)
  • Breast cancer (44.36%)

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

Paul D.P. Pharoah mostly deals with Internal medicine, Oncology, Breast cancer, Genome-wide association study and Cancer. Many of his studies involve connections with topics such as Single-nucleotide polymorphism and Internal medicine. The study incorporates disciplines such as Logistic regression, Genotyping and Gene–environment interaction in addition to Single-nucleotide polymorphism.

His Oncology research is multidisciplinary, relying on both Prostate, MEDLINE, Ovarian cancer, Disease and Genotype. His Breast cancer research incorporates elements of Cancer research, Genetic variants, Germline and Hazard ratio. His Genome-wide association study research is under the purview of Genetics.

Between 2018 and 2021, his most popular works were:

  • Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes (257 citations)
  • Collateral damage: the impact on outcomes from cancer surgery of the COVID-19 pandemic. (135 citations)
  • Discovery of common and rare genetic risk variants for colorectal cancer (131 citations)

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

  • Cancer
  • Gene
  • Internal medicine

The scientist’s investigation covers issues in Internal medicine, Oncology, Breast cancer, Cancer and Genome-wide association study. His research integrates issues of PALB2, Confidence interval, Proportional hazards model, Prostate cancer and Cohort in his study of Oncology. His research in Breast cancer intersects with topics in Germline mutation, Bioinformatics, Genetic testing and Hazard ratio.

His Cancer study combines topics in areas such as Myeloid, Cancer research, CHEK2 and MEDLINE. Genome-wide association study is the subject of his research, which falls under Single-nucleotide polymorphism. His Case-control study research includes elements of Demography and Genotype.

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

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies

A. Antoniou;P.D.P. Pharoah;S. Narod;H.A. Risch.
American Journal of Human Genetics (2003)

4309 Citations

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)

2713 Citations

The clonal and mutational evolution spectrum of primary triple-negative breast cancers

Sohrab P. Shah;Andrew Roth;Rodrigo Goya;Arusha Oloumi.
Nature (2012)

2010 Citations

Independent validation of genes and polymorphisms reported to be associated with radiation toxicity: a prospective analysis study.

Gillian C. Barnett;Gillian C. Barnett;Charlotte E. Coles;Rebecca M. Elliott;Caroline Baynes.
Lancet Oncology (2012)

1451 Citations

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)

1348 Citations

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

Kyriaki Michailidou;Per Hall;Anna Gonzalez-Neira;Maya Ghoussaini.
Nature Genetics (2013)

1179 Citations

The somatic mutation profiles of 2,433 breast cancers refines their genomic and transcriptomic landscapes

Bernard Pereira;Suet Feung Chin;Oscar M. Rueda;Hans Kristian Moen Vollan.
Nature Communications (2016)

1151 Citations

RAD51B in Familial Breast Cancer

Liisa M. Pelttari;Sofia Khan;Mikko Vuorela;Johanna I. Kiiski.
PLOS ONE (2016)

1014 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

Polygenic susceptibility to breast cancer and implications for prevention

Paul D.P. Pharoah;Antonis Antoniou;Martin Bobrow;Ron L. Zimmern.
Nature Genetics (2002)

956 Citations

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