Debra Abrams
Impact in
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- BRCA gene mutations in cancer
- Inflammatory Bowel Disease
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 3
- BRCA gene mutations in cancer 1
- Genetic Syndromes and Imprinting 1
- Co-authors
- Mark R. Geier (2 shared papers)Håkon Håkonarson (7 shared papers)Lisa G. Shaffer (1 shared paper)Sue Ann Berend (1 shared paper)Benjamin B. Roa (1 shared paper)Marcella Devoto (4 shared papers)Joseph Glessner (3 shared papers)Rosetta Chiavacci (4 shared papers)
- Journals
- Frontiers in Genetics (1 paper)BMC Urology (1 paper)The Journal of Immunology (1 paper)Blood (1 paper)Clinical Gastroenterology and Hepatology (1 paper)
- Partner nations
- United StatesItalyGermany
In The Last Decade
Debra Abrams
11 papers receiving 184 citations
Peers
Comparison fields: 5 of 51
- Genetics 82
- Pediatrics, Perinatology and Child Health 35
- Reproductive Medicine 11
- Public Health, Environmental and Occupational Health 36
- Immunology 26
Countries citing papers authored by Debra Abrams
This map shows the geographic impact of Debra Abrams'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 Debra Abrams with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Debra Abrams more than expected).
Fields of papers citing papers by Debra Abrams
This network shows the impact of papers produced by Debra Abrams. 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 Debra Abrams. The network helps show where Debra Abrams may publish in the future.
Co-authors
The 25 scholars most cited alongside Debra Abrams, 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 | 2006 | 73 | |
| 2 | 2007 | 51 | |
| 3 | 2001 | 35 | |
| 4 | 2015 | 20 | |
| 5 | 2022 | 16 | |
| 6 | 2014 | 14 | |
| 7 | 2016 | 4 | |
| 8 | 2020 | 2 | |
| 9 | 2022 | 2 | |
| 10 | 2023 | 1 | |
| 11 | 2016 | 1 |
About Debra Abrams
Debra Abrams is a scholar working on Genetics, Immunology, Pediatrics, Perinatology and Child Health, Infectious Diseases and Surgery, having authored 11 papers that have together received 219 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (2 papers), Ferroptosis and cancer prognosis (1 paper), Cancer Genomics and Diagnostics (1 paper), Family and Disability Support Research (1 paper), BRCA gene mutations in cancer (1 paper), Virology and Viral Diseases (1 paper), Genetic Syndromes and Imprinting (1 paper) and Pregnancy-related medical research (1 paper). The work is most often cited by research in Genetics (82 citations), Pediatrics, Perinatology and Child Health (35 citations), Reproductive Medicine (11 citations), Public Health, Environmental and Occupational Health (36 citations) and Immunology (26 citations). Debra Abrams has collaborated with scholars based in United States, Italy and Germany. Frequent co-authors include Mark R. Geier, Håkon Håkonarson, Lisa G. Shaffer, Sue Ann Berend, Benjamin B. Roa, Marcella Devoto, Joseph Glessner, Rosetta Chiavacci, Robert Skraban and Edward C. Frackelton. Their work appears in journals such as Frontiers in Genetics, BMC Urology, The Journal of Immunology, Blood and Clinical Gastroenterology and Hepatology.
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.