David E. Goldgar
Impact in
- Genetics top 0.2%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cancer Research top 1%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 62
- BRCA gene mutations in cancer 48
- Genomic variations and chromosomal abnormalities 16
- Genetic Associations and Epidemiology 13
- Nutrition, Genetics, and Disease 6
- Genetic Mapping and Diversity in Plants and Animals 5
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- DNA Repair Mechanisms 17
- Co-authors
- Douglas F. Easton (12 shared papers)Rosalind A. Eeles (7 shared papers)Fergus J. Couch (6 shared papers)Antonis C. Antoniou (9 shared papers)Sean V. Tavtigian (6 shared papers)Georgia Chenevix‐Trench (10 shared papers)Katherine L. Nathanson (6 shared papers)William D. Foulkes (6 shared papers)
- Journals
- Human Mutation (7 papers)Cancer Research (5 papers)British Journal of Cancer (5 papers)Breast Cancer Research (4 papers)Familial Cancer (3 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
David E. Goldgar
72 papers receiving 4.8k citations
David E. Goldgar's Hit Papers
Peers
Comparison fields: 5 of 121
- Genetics 3.2k
- Cancer Research 1.1k
- Pathology and Forensic Medicine 820
- Oncology 1.1k
- Molecular Biology 2.1k
Countries citing papers authored by David E. Goldgar
This map shows the geographic impact of David E. Goldgar's research. 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 David E. Goldgar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David E. Goldgar more than expected).
Fields of papers citing papers by David E. Goldgar
This network shows the impact of papers produced by David E. Goldgar. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by David E. Goldgar. The network helps show where David E. Goldgar may publish in the future.
Co-authors
The 25 scholars most cited alongside David E. Goldgar, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 72 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk Hit paper breakdown → | 2015 | 579 |
| 2 | Li-Fraumeni and related syndromes: correlation between tumor type, family structure, and TP53 genotype. | 2003 | 331 |
| 3 | 1996 | 298 | |
| 4 | 2011 | 256 | |
| 5 | Multipoint analysis of human quantitative genetic variation. | 1990 | 227 |
| 6 | 2012 | 201 | |
| 7 | 2011 | 184 | |
| 8 | 1988 | 162 | |
| 9 | 1997 | 160 | |
| 10 | 2011 | 158 | |
| 11 | 2006 | 136 | |
| 12 | 2006 | 121 | |
| 13 | 1987 | 102 | |
| 14 | 2001 | 102 | |
| 15 | 2007 | 95 | |
| 16 | 2005 | 94 | |
| 17 | 2012 | 89 | |
| 18 | 2010 | 89 | |
| 19 | 1998 | 88 | |
| 20 | 2003 | 81 |
About David E. Goldgar
David E. Goldgar is a scholar working on Genetics, Molecular Biology, Cancer Research, Oncology and Pathology and Forensic Medicine, having authored 72 papers that have together received 4.9k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (48 papers), DNA Repair Mechanisms (17 papers), Genomic variations and chromosomal abnormalities (16 papers), Cancer Genomics and Diagnostics (14 papers), Genetic Associations and Epidemiology (13 papers), Genetic factors in colorectal cancer (8 papers), Nutrition, Genetics, and Disease (6 papers) and Genetic Mapping and Diversity in Plants and Animals (5 papers). The work is most often cited by research in Genetics (3.2k citations), Cancer Research (1.1k citations), Pathology and Forensic Medicine (820 citations), Oncology (1.1k citations) and Molecular Biology (2.1k citations). David E. Goldgar has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Douglas F. Easton, Rosalind A. Eeles, Fergus J. Couch, Antonis C. Antoniou, Sean V. Tavtigian, Georgia Chenevix‐Trench, Katherine L. Nathanson, William D. Foulkes, Melissa C. Southey and Deborah J. Thompson. Their work appears in journals such as Human Mutation, Cancer Research, British Journal of Cancer, Breast Cancer Research and Familial Cancer.
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.