David B. Berman
Impact in
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Reproductive Medicine top 10%
- Ovarian cancer diagnosis and treatment
Papers in
- Genetics 3
- BRCA gene mutations in cancer 3
- Genomic variations and chromosomal abnormalities 2
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- DNA Repair Mechanisms 3
- RNA modifications and cancer 1
- Co-authors
- D. Schultz (3 shared papers)A K Godwin (2 shared papers)Lisa Vanderveer (1 shared paper)Thomas C. Hamilton (1 shared paper)Andrew K. Godwin (1 shared paper)Albert J. Wong (1 shared paper)Generosa Grana (1 shared paper)Josephine Wagner Costalas (1 shared paper)
- Journals
- Human Immunology (2 papers)Nature Medicine (1 paper)PubMed (3 papers)European Journal of Immunogenetics (1 paper)International Linear Collider (1 paper)
- Partner nations
- United StatesFranceCanada
In The Last Decade
David B. Berman
10 papers receiving 578 citations
Peers
Comparison fields: 5 of 66
- Genetics 375
- Reproductive Medicine 74
- Cancer Research 107
- Pathology and Forensic Medicine 120
- Oncology 113
Countries citing papers authored by David B. Berman
This map shows the geographic impact of David B. Berman'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 B. Berman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David B. Berman more than expected).
Fields of papers citing papers by David B. Berman
This network shows the impact of papers produced by David B. Berman. 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 B. Berman. The network helps show where David B. Berman may publish in the future.
Co-authors
The 25 scholars most cited alongside David B. Berman, 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 | 1996 | 265 | |
| 2 | Identification of two candidate tumor suppressor genes on chromosome 17p13.3. | 1996 | 127 |
| 3 | A common mutation in BRCA2 that predisposes to a variety of cancers is found in both Jewish Ashkenazi and non-Jewish individuals. | 1996 | 87 |
| 4 | Two distinct origins of a common BRCA1 mutation in breast-ovarian cancer families: a genetic study of 15 185delAG-mutation kindreds. | 1996 | 83 |
| 5 | 2017 | 22 | |
| 6 | 2019 | 19 | |
| 7 | Do good : how designers can change the world | 2009 | 12 |
| 8 | A new reverse SSO HLA DNA typing method using fluoresecent microspheres and flow analyzer | 2002 | 1 |
| 9 | 2014 | 1 | |
| 10 | 2015 | 1 |
About David B. Berman
David B. Berman is a scholar working on Genetics, Molecular Biology, Microbiology, Hardware and Architecture and Epidemiology, having authored 10 papers that have together received 618 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (3 papers), BRCA gene mutations in cancer (3 papers), Advanced Memory and Neural Computing (2 papers), Cytomegalovirus and herpesvirus research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Biosensors and Analytical Detection (2 papers), Advanced Neural Network Applications (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Genetics (375 citations), Reproductive Medicine (74 citations), Cancer Research (107 citations), Pathology and Forensic Medicine (120 citations) and Oncology (113 citations). David B. Berman has collaborated with scholars based in United States, France and Canada. Frequent co-authors include D. Schultz, A K Godwin, Lisa Vanderveer, Thomas C. Hamilton, Andrew K. Godwin, Albert J. Wong, Generosa Grana, Josephine Wagner Costalas, Mary B. Daly and M. Daly. Their work appears in journals such as Human Immunology, Nature Medicine, PubMed, European Journal of Immunogenetics and International Linear Collider.
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.