David E. Goldgar
Impact in
- Genetics top 0.5%
- 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 72
- BRCA gene mutations in cancer 49
- Genomics and Rare Diseases 15
- Genomic variations and chromosomal abnormalities 14
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- DNA Repair Mechanisms 10
- CRISPR and Genetic Engineering 8
- Co-authors
- John C. Gallagher (8 shared papers)Mark H. Skolnick (23 shared papers)Lisa Cannon‐Albright (23 shared papers)James P. Kushner (2 shared papers)Warren T. Kable (3 shared papers)Sean V. Tavtigian (19 shared papers)Corwin Q. Edwards (1 shared paper)Linda M. Griffen (1 shared paper)
- Journals
- Human Mutation (13 papers)JNCI Journal of the National Cancer Institute (8 papers)Breast Cancer Research and Treatment (5 papers)Genomics (5 papers)Journal of the American Academy of Dermatology (4 papers)
- Partner nations
- United StatesAustraliaFrance
In The Last Decade
David E. Goldgar
132 papers receiving 6.9k citations
David E. Goldgar's Hit Papers
Peers
Comparison fields: 5 of 137
- Genetics 3.0k
- Cancer Research 1.1k
- Pathology and Forensic Medicine 1.2k
- Oncology 1.7k
- Orthopedics and Sports Medicine 516
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 134 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors Hit paper breakdown → | 1988 | 530 |
| 2 | 1992 | 424 | |
| 3 | Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer Hit paper breakdown → | 2017 | 408 |
| 4 | 1997 | 295 | |
| 5 | 1996 | 237 | |
| 6 | 1987 | 186 | |
| 7 | 1990 | 182 | |
| 8 | 1991 | 167 | |
| 9 | 2008 | 165 | |
| 10 | Familiality of cancer in Utah. | 1994 | 164 |
| 11 | 2010 | 143 | |
| 12 | 1985 | 138 | |
| 13 | 2008 | 136 | |
| 14 | 1995 | 131 | |
| 15 | Multipoint linkage analysis in neurofibromatosis type I: an international collaboration. | 1989 | 126 |
| 16 | 1994 | 123 | |
| 17 | 1996 | 114 | |
| 18 | 1989 | 110 | |
| 19 | 2016 | 108 | |
| 20 | 1989 | 102 |
About David E. Goldgar
David E. Goldgar is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Oncology and Cancer Research, having authored 134 papers that have together received 7.2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (49 papers), Genetic factors in colorectal cancer (19 papers), Cancer Genomics and Diagnostics (17 papers), Genomics and Rare Diseases (15 papers), Genomic variations and chromosomal abnormalities (14 papers), Cutaneous Melanoma Detection and Management (13 papers), DNA Repair Mechanisms (10 papers) and CRISPR and Genetic Engineering (8 papers). The work is most often cited by research in Genetics (3.0k citations), Cancer Research (1.1k citations), Pathology and Forensic Medicine (1.2k citations), Oncology (1.7k citations) and Orthopedics and Sports Medicine (516 citations). David E. Goldgar has collaborated with scholars based in United States, Australia and France. Frequent co-authors include John C. Gallagher, Mark H. Skolnick, Lisa Cannon‐Albright, James P. Kushner, Warren T. Kable, Sean V. Tavtigian, Corwin Q. Edwards, Linda M. Griffen, Fergus J. Couch and Laurence J. Meyer. Their work appears in journals such as Human Mutation, JNCI Journal of the National Cancer Institute, Breast Cancer Research and Treatment, Genomics and Journal of the American Academy of Dermatology.
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.