Steven Alexander Narod
Impact in
- Genetics top 0.01%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Reproductive Medicine top 0.01%
- Ovarian cancer diagnosis and treatment
Papers in
- Genetics 490
- BRCA gene mutations in cancer 464
- Genomic variations and chromosomal abnormalities 69
- Nutrition, Genetics, and Disease 61
- Cancer Research 145
- Cancer Genomics and Diagnostics 71
- Breast Cancer Treatment Studies 57
- Co-authors
- Ping Sun (117 shared papers)William David Foulkes (94 shared papers)Henry T. Lynch (92 shared papers)Wedad M. Hanna (20 shared papers)Barry P. Rosen (73 shared papers)Rebecca Alexandra Dent (10 shared papers)Ellen Rawlinson (7 shared papers)Jan Lubiński (137 shared papers)
- Journals
- Breast Cancer Research and Treatment (99 papers)Gynecologic Oncology (39 papers)British Journal of Cancer (38 papers)Journal of Clinical Oncology (34 papers)International Journal of Cancer (28 papers)
- Partner nations
- CanadaUnited StatesPoland
In The Last Decade
Steven Alexander Narod
836 papers receiving 66.1k citations
Steven Alexander Narod's Hit Papers
Peers
Comparison fields: 5 of 191
- Genetics 35.4k
- Reproductive Medicine 8.5k
- Cancer Research 14.5k
- Oncology 15.3k
- Pathology and Forensic Medicine 9.2k
Countries citing papers authored by Steven Alexander Narod
This map shows the geographic impact of Steven Alexander Narod'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 Steven Alexander Narod with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Steven Alexander Narod more than expected).
Fields of papers citing papers by Steven Alexander Narod
This network shows the impact of papers produced by Steven Alexander Narod. 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 Steven Alexander Narod. The network helps show where Steven Alexander Narod may publish in the future.
Co-authors
The 25 scholars most cited alongside Steven Alexander Narod, 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 846 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A Strong Candidate for the Breast and Ovarian Cancer Susceptibility Gene BRCA1 Hit paper breakdown → | 1994 | 4987 |
| 2 | Triple-Negative Breast Cancer: Clinical Features and Patterns of Recurrence Hit paper breakdown → | 2007 | 4069 |
| 3 | Identification of the breast cancer susceptibility gene BRCA2 Hit paper breakdown → | 1995 | 2921 |
| 4 | Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies Hit paper breakdown → | 2003 | 2866 |
| 5 | Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families Hit paper breakdown → | 1998 | 2460 |
| 6 | Localization of a Breast Cancer Susceptibility Gene, BRCA2 , to Chromosome 13q12-13 Hit paper breakdown → | 1994 | 1528 |
| 7 | Prophylactic Oophorectomy in Carriers of BRCA1 or BRCA2 Mutations Hit paper breakdown → | 2002 | 1188 |
| 8 | Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations Hit paper breakdown → | 2002 | 904 |
| 9 | Bilateral Prophylactic Mastectomy Reduces Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers: The PROSE Study Group Hit paper breakdown → | 2004 | 897 |
| 10 | Prevalence and Penetrance of Germline BRCA1 and BRCA2 Mutations in a Population Series of 649 Women with Ovarian Cancer Hit paper breakdown → | 2001 | 810 |
| 11 | BRCA1 and BRCA2: 1994 and beyond Hit paper breakdown → | 2004 | 772 |
| 12 | 2006 | 545 | |
| 13 | 1999 | 539 | |
| 14 | 2015 | 527 | |
| 15 | Impact of Oophorectomy on Cancer Incidence and Mortality in Women With a BRCA1 or BRCA2 Mutation Hit paper breakdown → | 2014 | 517 |
| 16 | 2004 | 495 | |
| 17 | 1998 | 471 | |
| 18 | 2015 | 471 | |
| 19 | Pattern of metastatic spread in triple-negative breast cancer Hit paper breakdown → | 2008 | 460 |
| 20 | Increasing Hospital Admission Rates for Urological Complications After Transrectal Ultrasound Guided Prostate Biopsy Hit paper breakdown → | 2012 | 450 |
About Steven Alexander Narod
Steven Alexander Narod is a scholar working on Genetics, Cancer Research, Reproductive Medicine, Oncology and Pathology and Forensic Medicine, having authored 846 papers that have together received 68.9k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (464 papers), Ovarian cancer diagnosis and treatment (106 papers), DNA Repair Mechanisms (99 papers), Genetic factors in colorectal cancer (83 papers), Cancer Genomics and Diagnostics (71 papers), Genomic variations and chromosomal abnormalities (69 papers), Nutrition, Genetics, and Disease (61 papers) and Breast Cancer Treatment Studies (57 papers). The work is most often cited by research in Genetics (35.4k citations), Reproductive Medicine (8.5k citations), Cancer Research (14.5k citations), Oncology (15.3k citations) and Pathology and Forensic Medicine (9.2k citations). Steven Alexander Narod has collaborated with scholars based in Canada, United States and Poland. Frequent co-authors include Ping Sun, William David Foulkes, Henry T. Lynch, Wedad M. Hanna, Barry P. Rosen, Rebecca Alexandra Dent, Ellen Rawlinson, Jan Lubiński, Maureen Trudeau and Susan L. Neuhausen. Their work appears in journals such as Breast Cancer Research and Treatment, Gynecologic Oncology, British Journal of Cancer, Journal of Clinical Oncology and International Journal of 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.