Sue Healey
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Genetic factors in colorectal cancer
Papers in
-
- Epigenetics and DNA Methylation 3
- Mitochondrial Function and Pathology 3
- Genetics 14
- BRCA gene mutations in cancer 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Co-authors
- Georgia Chenevix‐Trench (16 shared papers)Amanda B. Spurdle (6 shared papers)Nicholas G. Martin (13 shared papers)Sean V. Tavtigian (5 shared papers)David E. Goldgar (3 shared papers)Sunil R. Lakhani (6 shared papers)Leonard Da Silva (5 shared papers)Fergus J. Couch (4 shared papers)
- Journals
- Nucleic Acids Research (3 papers)Human Mutation (3 papers)Breast Cancer Research (2 papers)Journal of Medical Genetics (2 papers)Gastroenterology (1 paper)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Sue Healey
33 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 74
- Genetics 662
- Pathology and Forensic Medicine 241
- Cancer Research 190
- Pediatrics, Perinatology and Child Health 155
- Molecular Biology 468
Countries citing papers authored by Sue Healey
This map shows the geographic impact of Sue Healey'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 Sue Healey with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sue Healey more than expected).
Fields of papers citing papers by Sue Healey
This network shows the impact of papers produced by Sue Healey. 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 Sue Healey. The network helps show where Sue Healey may publish in the future.
Co-authors
The 25 scholars most cited alongside Sue Healey, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 196 | |
| 2 | 2011 | 196 | |
| 3 | 2011 | 163 | |
| 4 | 1994 | 63 | |
| 5 | 2015 | 57 | |
| 6 | 2008 | 56 | |
| 7 | 2010 | 55 | |
| 8 | 2007 | 47 | |
| 9 | Evidence for an association between nonsyndromic cleft lip with or without cleft palate and a gene located on the long arm of chromosome 4. | 1995 | 46 |
| 10 | 1996 | 44 | |
| 11 | 2002 | 40 | |
| 12 | 2010 | 40 | |
| 13 | 2011 | 32 | |
| 14 | 2004 | 29 | |
| 15 | 2010 | 27 | |
| 16 | 1993 | 22 | |
| 17 | 2001 | 20 | |
| 18 | 2001 | 19 | |
| 19 | 2003 | 12 | |
| 20 | 1999 | 9 |
About Sue Healey
Sue Healey is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Cellular and Molecular Neuroscience, having authored 33 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (6 papers), BRCA gene mutations in cancer (5 papers), Assisted Reproductive Technology and Twin Pregnancy (5 papers), Genetic Neurodegenerative Diseases (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Epigenetics and DNA Methylation (3 papers), Mitochondrial Function and Pathology (3 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Genetics (662 citations), Pathology and Forensic Medicine (241 citations), Cancer Research (190 citations), Pediatrics, Perinatology and Child Health (155 citations) and Molecular Biology (468 citations). Sue Healey has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Georgia Chenevix‐Trench, Amanda B. Spurdle, Nicholas G. Martin, Sean V. Tavtigian, David E. Goldgar, Sunil R. Lakhani, Leonard Da Silva, Fergus J. Couch, Cathryn M. Lewis and Frans B.L. Hogervorst. Their work appears in journals such as Nucleic Acids Research, Human Mutation, Breast Cancer Research, Journal of Medical Genetics 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.