S. Seal
Impact in
- Genetics top 2%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Nutrition, Genetics, and Disease
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
-
- Cancer Genomics and Diagnostics 3
- Genetics 7
- BRCA gene mutations in cancer 7
- Genomic variations and chromosomal abnormalities 3
- Nutrition, Genetics, and Disease 2
- Co-authors
- Nadine CollinsMichael R. StrattonRita BarfootWilliam WarrenNazneen RahmanJudith DeaconDF EastonJulian Peto
- Journals
- British Journal of Cancer (2 papers)Psycho-Oncology (2 papers)The American Journal of Human Genetics (1 paper)JNCI Journal of the National Cancer Institute (1 paper)Journal of Clinical Oncology (1 paper)
- Partner nations
- United KingdomIrelandIndia
In The Last Decade
S. Seal
13 papers receiving 1.2k citations
Hit Papers
Peers
Comparison fields: 5 of 71
- Genetics 909
- Cancer Research 398
- Pathology and Forensic Medicine 309
- Oncology 359
- Reproductive Medicine 102
Countries citing papers authored by S. Seal
This map shows the geographic impact of S. Seal'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. Seal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. Seal more than expected).
Fields of papers citing papers by S. Seal
This network shows the impact of papers produced by S. Seal. 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. Seal. The network helps show where S. Seal may publish in the future.
Co-authorship network
The 25 scholars most cited alongside S. Seal, 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 | 2012 | 79 | |
| 2 | Metastasis--an unusual cause of retroperitoneal fibrosis. | 2006 | 2 |
| 3 | 2001 | 64 | |
| 4 | BRCA1 and BRCA2 mutations in breast cancer families with multiple primary cancers. | 2000 | 52 |
| 5 | Prevalence of BRCA1 and BRCA2 Gene Mutations in Patients With Early-Onset Breast Cancer Hit paper breakdown → | 1999 | 662 |
| 6 | 1998 | 50 | |
| 7 | Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer. | 1998 | 84 |
| 8 | 1996 | 36 | |
| 9 | 1996 | 1 | |
| 10 | 1995 | 4 | |
| 11 | Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13. | 1995 | 189 |
| 12 | The incidence of germline p53 mutations in 53 Li-Fraumeni-like families and in individuals with multiple primary tumors | 1994 | 1 |
| 13 | 1994 | 74 |
About S. Seal
S. Seal is a scholar working on Cancer Research, Genetics, Biotechnology, Pathology and Forensic Medicine and Oncology, having authored 13 papers that have together received 1.3k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (7 papers), Cancer Genomics and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Nutrition, Genetics, and Disease (2 papers), Ethics in Clinical Research (2 papers), DNA Repair Mechanisms (2 papers), Health Systems, Economic Evaluations, Quality of Life (2 papers) and Cancer-related Molecular Pathways (2 papers). The work is most often cited by research in Genetics (909 citations), Cancer Research (398 citations), Pathology and Forensic Medicine (309 citations), Oncology (359 citations) and Reproductive Medicine (102 citations). S. Seal has collaborated with scholars based in United Kingdom, Ireland and India. Frequent co-authors include Nadine Collins, Michael R. Stratton, Rita Barfoot, William Warren, Nazneen Rahman, Judith Deacon, DF Easton, Julian Peto, Chris Evans and W. Ormiston. Their work appears in journals such as British Journal of Cancer, Psycho-Oncology, The American Journal of Human Genetics, JNCI Journal of the National Cancer Institute and Journal of Clinical 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.