Robin L. Bennett
Impact in
- Genetics top 0.5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
- Ethics and Legal Issues in Pediatric Healthcare
Papers in
- Genetics 46
- BRCA gene mutations in cancer 38
- Genomics and Rare Diseases 11
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 5
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- Prenatal Screening and Diagnostics 10
- Co-authors
- Robert G. Resta (10 shared papers)Susan Hahn (2 shared papers)Sandra Blum (1 shared paper)Barbara B. Biesecker (1 shared paper)Michelle N. Strecker (1 shared paper)Janet L. Williams (1 shared paper)Heather Hampel (1 shared paper)Rachel Pearlman (1 shared paper)
- Journals
- Genetics in Medicine (10 papers)Journal of Clinical Investigation (4 papers)The American Journal of Human Genetics (4 papers)Journal of Genetic Counseling (28 papers)Gynecologic Oncology (3 papers)
- Partner nations
- United StatesCanadaAustralia
In The Last Decade
Robin L. Bennett
75 papers receiving 4.1k citations
Robin L. Bennett's Hit Papers
Peers
Comparison fields: 5 of 136
- Genetics 2.1k
- Pediatrics, Perinatology and Child Health 676
- Pathology and Forensic Medicine 512
- Cancer Research 357
- Neurology 299
Countries citing papers authored by Robin L. Bennett
This map shows the geographic impact of Robin L. Bennett'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 Robin L. Bennett with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robin L. Bennett more than expected).
Fields of papers citing papers by Robin L. Bennett
This network shows the impact of papers produced by Robin L. Bennett. 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 Robin L. Bennett. The network helps show where Robin L. Bennett may publish in the future.
Co-authors
The 25 scholars most cited alongside Robin L. Bennett, 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 79 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A New Definition of Genetic Counseling: National Society of Genetic Counselors’ Task Force Report Hit paper breakdown → | 2006 | 571 |
| 2 | A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment Hit paper breakdown → | 2014 | 380 |
| 3 | 2011 | 248 | |
| 4 | 2017 | 243 | |
| 5 | 2013 | 217 | |
| 6 | 2008 | 169 | |
| 7 | 2012 | 151 | |
| 8 | 2002 | 141 | |
| 9 | Deletions spanning the neurofibromatosis 1 gene: identification and phenotype of five patients. | 1994 | 140 |
| 10 | 1998 | 126 | |
| 11 | Recommendations for standardized human pedigree nomenclature. Pedigree Standardization Task Force of the National Society of Genetic Counselors. | 1995 | 126 |
| 12 | 1995 | 118 | |
| 13 | 2011 | 110 | |
| 14 | 2007 | 91 | |
| 15 | Predisposition genetic testing for late-onset disorders in adults. A position paper of the National Society of Genetic Counselors. | 1997 | 86 |
| 16 | 2005 | 85 | |
| 17 | 1996 | 75 | |
| 18 | 2013 | 72 | |
| 19 | 2020 | 63 | |
| 20 | 2012 | 56 |
About Robin L. Bennett
Robin L. Bennett is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine, Molecular Biology and Public Health, Environmental and Occupational Health, having authored 79 papers that have together received 4.3k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (38 papers), Genetic factors in colorectal cancer (12 papers), Genomics and Rare Diseases (11 papers), Prenatal Screening and Diagnostics (10 papers), Genetics and Neurodevelopmental Disorders (7 papers), Cancer Genomics and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Family and Disability Support Research (5 papers). The work is most often cited by research in Genetics (2.1k citations), Pediatrics, Perinatology and Child Health (676 citations), Pathology and Forensic Medicine (512 citations), Cancer Research (357 citations) and Neurology (299 citations). Robin L. Bennett has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Robert G. Resta, Susan Hahn, Sandra Blum, Barbara B. Biesecker, Michelle N. Strecker, Janet L. Williams, Heather Hampel, Rachel Pearlman, Georgia L. Wiesner and Adam H. Buchanan. Their work appears in journals such as Genetics in Medicine, Journal of Clinical Investigation, The American Journal of Human Genetics, Journal of Genetic Counseling and Gynecologic Oncology.
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.