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 22
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 5
- Nutrition, Genetics, and Disease 3
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- Genetic factors in colorectal cancer 12
- Co-authors
- Robyn Lynne Ward (3 shared papers)Bettina Meiser (8 shared papers)Nicholas John Hawkins (2 shared papers)Catherine M. Suter (2 shared papers)Megan Philippa Hitchins (2 shared papers)David I. K. Martin (2 shared papers)Kathy Tucker (6 shared papers)J Y Wong (1 shared paper)
- Journals
- The Medical Journal of Australia (3 papers)Familial Cancer (3 papers)Human Genetics (2 papers)The Lancet (2 papers)Gastroenterology (2 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Graeme Suthers
63 papers receiving 2.7k citations
Peers
Comparison fields: 5 of 114
- Genetics 1.2k
- Pathology and Forensic Medicine 674
- Cancer Research 353
- Oncology 497
- Molecular Biology 957
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 65 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 319 | |
| 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 | 227 |
| 3 | 2011 | 202 | |
| 4 | 2005 | 150 | |
| 5 | 2005 | 147 | |
| 6 | 2014 | 126 | |
| 7 | A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers. | 2001 | 123 |
| 8 | 2004 | 118 | |
| 9 | 2000 | 105 | |
| 10 | 1992 | 95 | |
| 11 | 2002 | 77 | |
| 12 | 2001 | 75 | |
| 13 | 1999 | 71 | |
| 14 | 2005 | 66 | |
| 15 | 2002 | 58 | |
| 16 | Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines. | 1990 | 56 |
| 17 | 1988 | 48 | |
| 18 | 1997 | 46 | |
| 19 | 1994 | 44 | |
| 20 | 1998 | 42 |
About Graeme Suthers
Graeme Suthers is a scholar working on Genetics, Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health, Molecular Biology and Cancer Research, having authored 65 papers that have together received 2.8k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (22 papers), Genetic factors in colorectal cancer (12 papers), Genomics and Rare Diseases (7 papers), DNA Repair Mechanisms (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Cancer Genomics and Diagnostics (4 papers), Nutrition, Genetics, and Disease (3 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Genetics (1.2k citations), Pathology and Forensic Medicine (674 citations), Cancer Research (353 citations), Oncology (497 citations) and Molecular Biology (957 citations). Graeme Suthers has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Robyn Lynne Ward, Bettina Meiser, Nicholas John Hawkins, Catherine M. Suter, Megan Philippa Hitchins, David I. K. Martin, Kathy Tucker, J Y Wong, Phyllis Noemi Butow and Judy Kirk. Their work appears in journals such as The Medical Journal of Australia, Familial Cancer, Human Genetics, The Lancet and Gastroenterology.
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.