Clara Gaff
Impact in
- Genetics top 0.5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 97
- BRCA gene mutations in cancer 77
- Genomics and Rare Diseases 39
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- Ethics in Clinical Research 18
- Co-authors
- Sylvia A. Metcalfe (26 shared papers)Bettina Meiser (22 shared papers)Zornitza Stark (20 shared papers)Jane Halliday (9 shared papers)Belinda McClaren (23 shared papers)Martin B. Delatycki (7 shared papers)Amy Nisselle (16 shared papers)Melissa Martyn (29 shared papers)
- Journals
- European Journal of Human Genetics (21 papers)Genetics in Medicine (16 papers)Frontiers in Genetics (5 papers)npj Genomic Medicine (5 papers)Patient Education and Counseling (5 papers)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
Clara Gaff
148 papers receiving 3.9k citations
Peers
Comparison fields: 5 of 126
- Genetics 2.3k
- Pediatrics, Perinatology and Child Health 486
- Pathology and Forensic Medicine 352
- Public Health, Environmental and Occupational Health 480
- Genetics 165
Countries citing papers authored by Clara Gaff
This map shows the geographic impact of Clara Gaff'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 Clara Gaff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Clara Gaff more than expected).
Fields of papers citing papers by Clara Gaff
This network shows the impact of papers produced by Clara Gaff. 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 Clara Gaff. The network helps show where Clara Gaff may publish in the future.
Co-authors
The 25 scholars most cited alongside Clara Gaff, 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 152 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 196 | |
| 2 | 2010 | 164 | |
| 3 | 2017 | 150 | |
| 4 | 2018 | 126 | |
| 5 | 2004 | 117 | |
| 6 | 2007 | 113 | |
| 7 | 2008 | 94 | |
| 8 | 2005 | 91 | |
| 9 | 2018 | 88 | |
| 10 | Family communication about genetics: theory and practice | 2010 | 88 |
| 11 | 2001 | 74 | |
| 12 | 2019 | 72 | |
| 13 | 2017 | 68 | |
| 14 | 2004 | 66 | |
| 15 | 2016 | 66 | |
| 16 | 2017 | 65 | |
| 17 | 2005 | 62 | |
| 18 | 2019 | 58 | |
| 19 | 2007 | 58 | |
| 20 | 2002 | 56 |
About Clara Gaff
Clara Gaff is a scholar working on Genetics, Public Health, Environmental and Occupational Health, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Sociology and Political Science, having authored 152 papers that have together received 3.9k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (77 papers), Genomics and Rare Diseases (39 papers), Ethics in Clinical Research (18 papers), Genetic factors in colorectal cancer (16 papers), Family Support in Illness (12 papers), Prenatal Screening and Diagnostics (9 papers), Cancer Genomics and Diagnostics (9 papers) and Health Systems, Economic Evaluations, Quality of Life (8 papers). The work is most often cited by research in Genetics (2.3k citations), Pediatrics, Perinatology and Child Health (486 citations), Pathology and Forensic Medicine (352 citations), Public Health, Environmental and Occupational Health (480 citations) and Genetics (165 citations). Clara Gaff has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Sylvia A. Metcalfe, Bettina Meiser, Zornitza Stark, Jane Halliday, Belinda McClaren, Martin B. Delatycki, Amy Nisselle, Melissa Martyn, Sebastian Lunke and Susan M. White. Their work appears in journals such as European Journal of Human Genetics, Genetics in Medicine, Frontiers in Genetics, npj Genomic Medicine and Patient Education and Counseling.
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.