Kenneth Offit
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Reproductive Medicine top 5%
- Ovarian cancer diagnosis and treatment
Papers in
- Genetics 8
- BRCA gene mutations in cancer 7
- Genetic Syndromes and Imprinting 1
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- Cancer Genomics and Diagnostics 4
- Co-authors
- Jeffery P. StruewingPatrick I. BorgenLarry NortonSuresh C. JhanwarDavid E. GoldgarBruce R. HaasMichael M. KabackHarry Ostrer
- Journals
- Human Mutation (1 paper)Nature Genetics (1 paper)JNCI Journal of the National Cancer Institute (1 paper)Hematology/Oncology Clinics of North America (1 paper)Familial Cancer (1 paper)
- Partner nations
- United StatesCanadaSpain
In The Last Decade
Kenneth Offit
14 papers receiving 814 citations
Peers
Comparison fields: 5 of 65
- Genetics 488
- Reproductive Medicine 143
- Cancer Research 223
- Pathology and Forensic Medicine 187
- Oncology 274
Countries citing papers authored by Kenneth Offit
This map shows the geographic impact of Kenneth Offit'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 Kenneth Offit with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kenneth Offit more than expected).
Fields of papers citing papers by Kenneth Offit
This network shows the impact of papers produced by Kenneth Offit. 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 Kenneth Offit. The network helps show where Kenneth Offit may publish in the future.
Co-authors
The 25 scholars most cited alongside Kenneth Offit, 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 | 2019 | 18 | |
| 2 | 2013 | 23 | |
| 3 | 2010 | 91 | |
| 4 | 2010 | 29 | |
| 5 | 2009 | 26 | |
| 6 | 2009 | 56 | |
| 7 | 2005 | 19 | |
| 8 | 2004 | 69 | |
| 9 | Rare variants of ATM and risk for Hodgkin's disease and radiation-associated breast cancers. | 2002 | 29 |
| 10 | 2002 | 53 | |
| 11 | A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers. | 2001 | 118 |
| 12 | 2000 | 9 | |
| 13 | 1997 | 5 | |
| 14 | 1996 | 298 |
About Kenneth Offit
Kenneth Offit is a scholar working on Genetics, Cancer Research, Oncology, Reproductive Medicine and Molecular Biology, having authored 14 papers that have together received 843 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (7 papers), DNA Repair Mechanisms (4 papers), Cancer Genomics and Diagnostics (4 papers), Cancer-related Molecular Pathways (3 papers), Epigenetics and DNA Methylation (2 papers), Pancreatic and Hepatic Oncology Research (1 paper), Ethics in Clinical Research (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (488 citations), Reproductive Medicine (143 citations), Cancer Research (223 citations), Pathology and Forensic Medicine (187 citations) and Oncology (274 citations). Kenneth Offit has collaborated with scholars based in United States, Canada and Spain. Frequent co-authors include Jeffery P. Struewing, Patrick I. Borgen, Larry Norton, Suresh C. Jhanwar, David E. Goldgar, Bruce R. Haas, Michael M. Kaback, Harry Ostrer, Lawrence C. Brody and Susan L. Neuhausen. Their work appears in journals such as Human Mutation, Nature Genetics, JNCI Journal of the National Cancer Institute, Hematology/Oncology Clinics of North America and Familial Cancer.
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.