PHG Foundation
Impact in
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- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 77
- BRCA gene mutations in cancer 51
- Genomics and Rare Diseases 23
- Nutrition, Genetics, and Disease 15
- Genetic Associations and Epidemiology 12
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- Ethics in Clinical Research 32
- Top scholars
- Simon G. ThompsonStephen BurgessFelix FranksPaul D.P. PharoahCaroline F. WrightTom DentAlison HallCarlos Caldas
- Journals
- Genetics in Medicine (9 papers)Public Health Genomics (9 papers)European Journal of Human Genetics (6 papers)Journal of Public Health (5 papers)Journal of Medical Ethics (4 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
PHG Foundation
206 papers receiving 8.0k citations
Peers
Comparison fields: 5 of 199
- Genetics 2.6k
- Cancer Research 970
- Pediatrics, Perinatology and Child Health 1.1k
- Pathology and Forensic Medicine 679
- Rheumatology 535
Countries citing scholars working at PHG Foundation
This map shows the geographic impact of research produced by authors working at PHG Foundation. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by papers produced at PHG Foundation with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites PHG Foundation more than expected).
Fields of papers published by authors at PHG Foundation
This network shows the impact of papers affiliated with PHG Foundation at the time of their publication. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers affiliated with PHG Foundation at the time of their publication.
About PHG Foundation
In recent decades, authors affiliated with PHG Foundation have published 249 papers, which have received a total of 10.1k indexed citations . Scholars at this organization have produced 77 papers in Genetics, 60 papers in Public Health, Environmental and Occupational Health, 3 papers in Health Informatics, 29 papers in Pediatrics, Perinatology and Child Health and 23 papers in Cancer Research on the topics of BRCA gene mutations in cancer (51 papers), Ethics in Clinical Research (32 papers), Genomics and Rare Diseases (23 papers), Prenatal Screening and Diagnostics (20 papers), Cancer Genomics and Diagnostics (17 papers), Nutrition, Genetics, and Disease (15 papers), Genetic Associations and Epidemiology (12 papers) and Biomedical Ethics and Regulation (11 papers). Their work is cited by papers focused on Genetics (2.6k citations), Cancer Research (970 citations), Pediatrics, Perinatology and Child Health (1.1k citations), Pathology and Forensic Medicine (679 citations) and Rheumatology (535 citations). Authors at PHG Foundation collaborate with scholars in United Kingdom, United States and Australia and have published in prestigious journals including Genetics in Medicine, Public Health Genomics, European Journal of Human Genetics, Journal of Public Health and Journal of Medical Ethics. Some of PHG Foundation's most productive authors include Simon G. Thompson, Stephen Burgess, Felix Franks, Paul D.P. Pharoah, Caroline F. Wright, Tom Dent, Alison Hall, Carlos Caldas, H. Burton and A. John Barrett.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.