Sue Healey
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
Papers in
-
- DNA Repair Mechanisms 4
- Genetics 16
- BRCA gene mutations in cancer 5
- Genomic variations and chromosomal abnormalities 4
- 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)David E. Goldgar (3 shared papers)Sean V. Tavtigian (5 shared papers)Nicholas G. Martin (13 shared papers)Sunil R. Lakhani (6 shared papers)Leonard Da Silva (5 shared papers)Fergus J. Couch (4 shared papers)
- Journals
- Human Mutation (3 papers)Nucleic Acids Research (3 papers)Breast Cancer Research (2 papers)Journal of Medical Genetics (2 papers)Human Reproduction (1 paper)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Sue Healey
33 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 78
- Genetics 656
- Cancer Research 241
- Pathology and Forensic Medicine 271
- Molecular Biology 522
- Pediatrics, Perinatology and Child Health 140
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 | 184 | |
| 2 | 2011 | 171 | |
| 3 | 2011 | 158 | |
| 4 | 1994 | 56 | |
| 5 | 2010 | 54 | |
| 6 | 2015 | 53 | |
| 7 | 2008 | 53 | |
| 8 | 2007 | 46 | |
| 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 | 45 |
| 10 | 1996 | 40 | |
| 11 | 2010 | 40 | |
| 12 | 2011 | 32 | |
| 13 | 2004 | 28 | |
| 14 | 2002 | 23 | |
| 15 | 2010 | 21 | |
| 16 | 1993 | 20 | |
| 17 | 2001 | 18 | |
| 18 | 2001 | 16 | |
| 19 | 2003 | 12 | |
| 20 | 1999 | 7 |
About Sue Healey
Sue Healey is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Oncology, having authored 33 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (8 papers), BRCA gene mutations in cancer (5 papers), Assisted Reproductive Technology and Twin Pregnancy (5 papers), DNA Repair Mechanisms (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Colorectal Cancer Treatments and Studies (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Genetics (656 citations), Cancer Research (241 citations), Pathology and Forensic Medicine (271 citations), Molecular Biology (522 citations) and Pediatrics, Perinatology and Child Health (140 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, David E. Goldgar, Sean V. Tavtigian, Nicholas G. Martin, Sunil R. Lakhani, Leonard Da Silva, Fergus J. Couch, Cathryn M. Lewis and Laura E. Mitchell. Their work appears in journals such as Human Mutation, Nucleic Acids Research, Breast Cancer Research, Journal of Medical Genetics and Human Reproduction.
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.