David E. Goldgar
- Genetics top 0.5%
- BRCA gene mutations in cancer 51
- Genomics and Rare Diseases 18
- Genomic variations and chromosomal abnormalities 15
- Genetic Associations and Epidemiology 10
- Cancer Research top 1%
- Cancer Genomics and Diagnostics 28
- Pathology and Forensic Medicine top 0.5%
- Genetic factors in colorectal cancer 24
- Oncology top 1%
- Cutaneous Melanoma Detection and Management 13
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- DNA Repair Mechanisms 17
- Co-authors
- John C. GallagherMark H. SkolnickLisa Cannon‐AlbrightJames P. KushnerSean V. TavtigianWarren T. KableLinda M. GriffenCorwin Q. Edwards
- Journals
- Human Mutation (13 papers)JNCI Journal of the National Cancer Institute (7 papers)Genomics (5 papers)
- Partner nations
- United StatesAustraliaCanada
In The Last Decade
David E. Goldgar
126 papers receiving 6.5k citations
Hit Papers
Peers
Comparison fields: 5 of 138
- Genetics 3.1k
- Cancer Research 1.3k
- Pathology and Forensic Medicine 1.3k
- Oncology 1.7k
- Orthopedics and Sports Medicine 528
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2022 | 4 | |
| 2 | 2022 | 7 | |
| 3 | 2022 | 8 | |
| 4 | 2018 | 3 | |
| 5 | 2017 | 5 | |
| 6 | 2013 | 61 | |
| 7 | 2012 | 35 | |
| 8 | 2010 | 132 | |
| 9 | 2009 | 90 | |
| 10 | 2008 | 159 | |
| 11 | 1996 | 219 | |
| 12 | 1995 | 2 | |
| 13 | Test of linkage between candidate loci and a prostate cancer susceptibility locus in a set of high risk kindreds | 1994 | 1 |
| 14 | 1994 | 76 | |
| 15 | 1992 | 4 | |
| 16 | 1991 | 153 | |
| 17 | 1989 | 98 | |
| 18 | 1989 | 7 | |
| 19 | 1989 | 91 | |
| 20 | 1985 | 5 |
About David E. Goldgar
David E. Goldgar is a scholar working on Genetics, Cancer Research, Pathology and Forensic Medicine, Oncology and Orthopedics and Sports Medicine, having authored 128 papers that have together received 6.7k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (51 papers), Cancer Genomics and Diagnostics (28 papers), Genetic factors in colorectal cancer (24 papers), Genomics and Rare Diseases (18 papers), DNA Repair Mechanisms (17 papers), Genomic variations and chromosomal abnormalities (15 papers), Cutaneous Melanoma Detection and Management (13 papers) and Genetic Associations and Epidemiology (10 papers). The work is most often cited by research in Genetics (3.1k citations), Cancer Research (1.3k citations), Pathology and Forensic Medicine (1.3k citations), Oncology (1.7k citations) and Orthopedics and Sports Medicine (528 citations). David E. Goldgar has collaborated with scholars based in United States, Australia and Canada. Frequent co-authors include John C. Gallagher, Mark H. Skolnick, Lisa Cannon‐Albright, James P. Kushner, Sean V. Tavtigian, Warren T. Kable, Linda M. Griffen, Corwin Q. Edwards, Fergus J. Couch and Bing Feng. Their work appears in journals such as Human Mutation, JNCI Journal of the National Cancer Institute, Genomics, Breast Cancer Research and Treatment and Breast Cancer Research.
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.