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
-
- DNA Repair Mechanisms 3
- Epigenetics and DNA Methylation 2
- Genetics 6
- BRCA gene mutations in cancer 5
- Genetic Syndromes and Imprinting 1
- Co-authors
- Jeffery P. Struewing (2 shared papers)Patrick I. Borgen (2 shared papers)Larry Norton (2 shared papers)Suresh C. Jhanwar (2 shared papers)Susan L. Neuhausen (1 shared paper)Michael M. Kaback (1 shared paper)Lawrence C. Brody (1 shared paper)Harry Ostrer (1 shared paper)
- Journals
- Journal of Clinical Oncology (1 paper)Breast Cancer Research and Treatment (1 paper)Hematology/Oncology Clinics of North America (1 paper)Blood Advances (1 paper)Annals of Oncology (1 paper)
- Partner nations
- United StatesCanadaSpain
In The Last Decade
Kenneth Offit
14 papers receiving 817 citations
Peers
Comparison fields: 5 of 58
- Genetics 428
- Reproductive Medicine 97
- Cancer Research 155
- Pathology and Forensic Medicine 151
- Oncology 220
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 | 1996 | 300 | |
| 2 | A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers. | 2001 | 118 |
| 3 | 2010 | 91 | |
| 4 | 2004 | 69 | |
| 5 | 2009 | 56 | |
| 6 | 2002 | 53 | |
| 7 | 2010 | 31 | |
| 8 | Rare variants of ATM and risk for Hodgkin's disease and radiation-associated breast cancers. | 2002 | 29 |
| 9 | 2009 | 26 | |
| 10 | 2013 | 23 | |
| 11 | 2005 | 19 | |
| 12 | 2019 | 18 | |
| 13 | 2000 | 8 | |
| 14 | 1997 | 5 |
About Kenneth Offit
Kenneth Offit is a scholar working on Molecular Biology, Genetics, Oncology, Cancer Research and Public Health, Environmental and Occupational Health, having authored 14 papers that have together received 846 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), DNA Repair Mechanisms (3 papers), Cancer Genomics and Diagnostics (3 papers), Epigenetics and DNA Methylation (2 papers), Cancer-related Molecular Pathways (2 papers), Pancreatic and Hepatic Oncology Research (1 paper), Genetic Syndromes and Imprinting (1 paper) and Acute Lymphoblastic Leukemia research (1 paper). The work is most often cited by research in Genetics (428 citations), Reproductive Medicine (97 citations), Cancer Research (155 citations), Pathology and Forensic Medicine (151 citations) and Oncology (220 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, Susan L. Neuhausen, Michael M. Kaback, Lawrence C. Brody, Harry Ostrer, Bruce R. Haas and David E. Goldgar. Their work appears in journals such as Journal of Clinical Oncology, Breast Cancer Research and Treatment, Hematology/Oncology Clinics of North America, Blood Advances and Annals of 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.