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 75
- BRCA gene mutations in cancer 49
- Genomics and Rare Diseases 23
- Nutrition, Genetics, and Disease 14
- Genetic Associations and Epidemiology 12
- Top scholars
- Simon G. ThompsonStephen BurgessFelix FranksPaul D.P. PharoahCaroline F. WrightTom DentCarlos CaldasAlison Hall
- Journals
- Public Health Genomics (9 papers)Genetics in Medicine (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
198 papers receiving 7.5k citations
Peers
Comparison fields: 5 of 195
- Genetics 2.4k
- Cancer Research 912
- Pediatrics, Perinatology and Child Health 1.0k
- Pathology and Forensic Medicine 644
- Rheumatology 506
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 239 papers, which have received a total of 9.5k indexed citations . Scholars at this organization have produced 75 papers in Genetics, 3 papers in Health Informatics, 58 papers in Public Health, Environmental and Occupational Health, 29 papers in Pediatrics, Perinatology and Child Health and 22 papers in Cancer Research on the topics of BRCA gene mutations in cancer (49 papers), Ethics in Clinical Research (30 papers), Genomics and Rare Diseases (23 papers), Prenatal Screening and Diagnostics (20 papers), Cancer Genomics and Diagnostics (17 papers), Nutrition, Genetics, and Disease (14 papers), Genetic Associations and Epidemiology (12 papers) and Biomedical Ethics and Regulation (11 papers). Their work is cited by papers focused on Genetics (2.4k citations), Cancer Research (912 citations), Pediatrics, Perinatology and Child Health (1.0k citations), Pathology and Forensic Medicine (644 citations) and Rheumatology (506 citations). Authors at PHG Foundation collaborate with scholars in United Kingdom, United States and Australia and have published in prestigious journals including Public Health Genomics, Genetics in Medicine, 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, Carlos Caldas, Alison Hall, 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.