S.A. Whitmore
Impact in
- Biochemistry top 2%
- Amino Acid Enzymes and Metabolism
-
- Biomedical Research and Pathophysiology
Papers in
-
- Genomics and Chromatin Dynamics 6
- DNA Repair Mechanisms 4
- Cancer-related gene regulation 4
- Epigenetics and DNA Methylation 3
- RNA modifications and cancer 3
- CRISPR and Genetic Engineering 3
- Genetics 9
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 5
- Co-authors
- David F. Callen (25 shared papers)Corinne Antignac (2 shared papers)Marlene Attard (1 shared paper)William van’t Hoff (1 shared paper)Margaret Town (1 shared paper)Olivier Gribouval (1 shared paper)G Jean (1 shared paper)Lionel Forestier (1 shared paper)
- Journals
- Genomics (14 papers)Human Genetics (2 papers)Biochemical and Biophysical Research Communications (1 paper)The Lancet (1 paper)Annals of Human Genetics (1 paper)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
S.A. Whitmore
26 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 77
- Biochemistry 249
- Pathology and Forensic Medicine 452
- Pediatrics, Perinatology and Child Health 278
- Genetics 253
- Molecular Biology 509
Countries citing papers authored by S.A. Whitmore
This map shows the geographic impact of S.A. Whitmore'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.A. Whitmore with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S.A. Whitmore more than expected).
Fields of papers citing papers by S.A. Whitmore
This network shows the impact of papers produced by S.A. Whitmore. 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.A. Whitmore. The network helps show where S.A. Whitmore may publish in the future.
Co-authors
The 25 scholars most cited alongside S.A. Whitmore, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 494 | |
| 2 | 1994 | 95 | |
| 3 | 1998 | 92 | |
| 4 | 1996 | 87 | |
| 5 | 1991 | 53 | |
| 6 | CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3. | 2002 | 53 |
| 7 | 1998 | 47 | |
| 8 | 1992 | 44 | |
| 9 | 1997 | 43 | |
| 10 | 2002 | 41 | |
| 11 | Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12. | 1991 | 41 |
| 12 | 1992 | 36 | |
| 13 | 1999 | 35 | |
| 14 | 1995 | 29 | |
| 15 | 1998 | 27 | |
| 16 | 1999 | 21 | |
| 17 | 1993 | 21 | |
| 18 | 1999 | 20 | |
| 19 | 1994 | 18 | |
| 20 | 1991 | 15 |
About S.A. Whitmore
S.A. Whitmore is a scholar working on Molecular Biology, Genetics, Oncology, Surgery and Pathology and Forensic Medicine, having authored 26 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Chromatin Dynamics (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), DNA Repair Mechanisms (4 papers), Cancer-related gene regulation (4 papers), Epigenetics and DNA Methylation (3 papers), RNA modifications and cancer (3 papers) and CRISPR and Genetic Engineering (3 papers). The work is most often cited by research in Biochemistry (249 citations), Pathology and Forensic Medicine (452 citations), Pediatrics, Perinatology and Child Health (278 citations), Genetics (253 citations) and Molecular Biology (509 citations). S.A. Whitmore has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include David F. Callen, Corinne Antignac, Marlene Attard, William van’t Hoff, Margaret Town, Olivier Gribouval, G Jean, Lionel Forestier, Gillian P. Bates and M. Broyer. Their work appears in journals such as Genomics, Human Genetics, Biochemical and Biophysical Research Communications, The Lancet and Annals of Human Genetics.
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.