Graeme Suthers
Impact in
- Genetics top 1%
- BRCA gene mutations in cancer
- Genetics and Neurodevelopmental Disorders
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- Genetic factors in colorectal cancer
Papers in
- Genetics 36
- BRCA gene mutations in cancer 23
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 5
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- DNA Repair Mechanisms 7
- Co-authors
- Bettina Meiser (8 shared papers)Robyn L. Ward (3 shared papers)Nicholas J. Hawkins (2 shared papers)David I. K. Martin (2 shared papers)Megan P. Hitchins (2 shared papers)Catherine M. Suter (2 shared papers)Kathy Tucker (6 shared papers)Phyllis Butow (5 shared papers)
- Journals
- Familial Cancer (3 papers)Nucleic Acids Research (2 papers)Gastroenterology (2 papers)British Journal of Cancer (2 papers)Human Genetics (2 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Graeme Suthers
55 papers receiving 2.4k citations
Peers
Comparison fields: 5 of 111
- Genetics 1.2k
- Pathology and Forensic Medicine 718
- Cancer Research 429
- Oncology 597
- Molecular Biology 981
Countries citing papers authored by Graeme Suthers
This map shows the geographic impact of Graeme Suthers'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 Graeme Suthers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Graeme Suthers more than expected).
Fields of papers citing papers by Graeme Suthers
This network shows the impact of papers produced by Graeme Suthers. 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 Graeme Suthers. The network helps show where Graeme Suthers may publish in the future.
Co-authors
The 25 scholars most cited alongside Graeme Suthers, 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 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 290 | |
| 2 | Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident. | 1997 | 213 |
| 3 | 2011 | 171 | |
| 4 | 2005 | 145 | |
| 5 | 2005 | 134 | |
| 6 | A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers. | 2001 | 118 |
| 7 | 2004 | 116 | |
| 8 | 2014 | 115 | |
| 9 | 2000 | 101 | |
| 10 | 1992 | 84 | |
| 11 | 2002 | 76 | |
| 12 | 2001 | 75 | |
| 13 | 1999 | 60 | |
| 14 | 2005 | 56 | |
| 15 | 2002 | 56 | |
| 16 | Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines. | 1990 | 55 |
| 17 | 1988 | 50 | |
| 18 | 1997 | 40 | |
| 19 | Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome. | 1991 | 38 |
| 20 | 2008 | 34 |
About Graeme Suthers
Graeme Suthers is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health and Oncology, having authored 57 papers that have together received 2.5k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (23 papers), Genetic factors in colorectal cancer (14 papers), Cancer Genomics and Diagnostics (7 papers), DNA Repair Mechanisms (7 papers), Genomics and Rare Diseases (6 papers), Family Support in Illness (5 papers), Prenatal Screening and Diagnostics (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Genetics (1.2k citations), Pathology and Forensic Medicine (718 citations), Cancer Research (429 citations), Oncology (597 citations) and Molecular Biology (981 citations). Graeme Suthers has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Bettina Meiser, Robyn L. Ward, Nicholas J. Hawkins, David I. K. Martin, Megan P. Hitchins, Catherine M. Suter, Kathy Tucker, Phyllis Butow, Justin Wong and Judy Kirk. Their work appears in journals such as Familial Cancer, Nucleic Acids Research, Gastroenterology, British Journal of Cancer and 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.