S E Rowell
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Nutrition, Genetics, and Disease
- Reproductive Medicine top 10%
- Ovarian cancer diagnosis and treatment
Papers in
- Genetics 5
- BRCA gene mutations in cancer 5
- Genomic variations and chromosomal abnormalities 4
- Nutrition, Genetics, and Disease 1
-
- DNA Repair Mechanisms 2
- CRISPR and Genetic Engineering 1
- Co-authors
- Lori S. Friedman (6 shared papers)Mary‐Claire King (6 shared papers)Patrick J. Dowd (5 shared papers)Elizabeth Ostermeyer (5 shared papers)Csilla I. Szabo (5 shared papers)Eric D. Lynch (2 shared papers)Ming K. Lee (3 shared papers)Lee Anderson (3 shared papers)
- Journals
- Diabetes Care (1 paper)Cold Spring Harbor Symposia on Quantitative Biology (1 paper)Nature Genetics (1 paper)Genomics (1 paper)PubMed (3 papers)
- Partner nations
- United States
In The Last Decade
S E Rowell
8 papers receiving 878 citations
Peers
Comparison fields: 5 of 64
- Genetics 592
- Reproductive Medicine 85
- Cancer Research 101
- Molecular Biology 490
- Pathology and Forensic Medicine 105
Countries citing papers authored by S E Rowell
This map shows the geographic impact of S E Rowell'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 S E Rowell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S E Rowell more than expected).
Fields of papers citing papers by S E Rowell
This network shows the impact of papers produced by S E Rowell. 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 S E Rowell. The network helps show where S E Rowell may publish in the future.
Co-authors
The 25 scholars most cited alongside S E Rowell, 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 | 1994 | 495 | |
| 2 | Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families. | 1995 | 149 |
| 3 | 1999 | 100 | |
| 4 | THRA1 and D17S183 flank an interval of < 4 cM for the breast-ovarian cancer gene (BRCA1) on chromosome 17q21. | 1993 | 69 |
| 5 | The search for BRCA1. | 1994 | 49 |
| 6 | 1995 | 41 | |
| 7 | 1994 | 1 | |
| 8 | EXCESS MATERNAL TRANSMISSION OF TYPE II DIABETES | 1999 | 1 |
About S E Rowell
S E Rowell is a scholar working on Genetics, Molecular Biology, Public Health, Environmental and Occupational Health, Reproductive Medicine and Plant Science, having authored 8 papers that have together received 905 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Genomic variations and chromosomal abnormalities (4 papers), DNA Repair Mechanisms (2 papers), Cancer Genomics and Diagnostics (1 paper), Biotechnology and Related Fields (1 paper), Genetically Modified Organisms Research (1 paper), Nutrition, Genetics, and Disease (1 paper) and CRISPR and Genetic Engineering (1 paper). The work is most often cited by research in Genetics (592 citations), Reproductive Medicine (85 citations), Cancer Research (101 citations), Molecular Biology (490 citations) and Pathology and Forensic Medicine (105 citations). S E Rowell has collaborated with scholars based in United States. Frequent co-authors include Lori S. Friedman, Mary‐Claire King, Patrick J. Dowd, Elizabeth Ostermeyer, Csilla I. Szabo, Eric D. Lynch, Ming K. Lee, Lee Anderson, Andrew J. Karter and Lesley M. Butler. Their work appears in journals such as Diabetes Care, Cold Spring Harbor Symposia on Quantitative Biology, Nature Genetics, Genomics and PubMed.
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.