Robin M. Winter
Impact in
- Genetics top 0.2%
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Developmental Biology top 1%
Papers in
- Genetics 37
- Craniofacial Disorders and Treatments 13
- Genomic variations and chromosomal abnormalities 10
- Cleft Lip and Palate Research 8
- Connective tissue disorders research 7
- Genetics and Neurodevelopmental Disorders 6
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- Congenital heart defects research 5
- Co-authors
- William Reardon (8 shared papers)Louise J. Pulleyn (4 shared papers)Paul Rutland (4 shared papers)Sue Malcolm (6 shared papers)Andrew O.M. Wilkie (4 shared papers)Barry M. Jones (4 shared papers)Jonathan Flint (3 shared papers)Sarah F. Slaney (5 shared papers)
- Journals
- Nature Genetics (9 papers)Journal of Medical Genetics (2 papers)American Journal of Medical Genetics (16 papers)Human Molecular Genetics (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Robin M. Winter
60 papers receiving 5.4k citations
Robin M. Winter's Hit Papers
Peers
Comparison fields: 5 of 124
- Genetics 3.7k
- Developmental Biology 226
- Molecular Biology 2.8k
- Pediatrics, Perinatology and Child Health 546
- Genetics 250
Countries citing papers authored by Robin M. Winter
This map shows the geographic impact of Robin M. Winter'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 Robin M. Winter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robin M. Winter more than expected).
Fields of papers citing papers by Robin M. Winter
This network shows the impact of papers produced by Robin M. Winter. 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 Robin M. Winter. The network helps show where Robin M. Winter may publish in the future.
Co-authors
The 25 scholars most cited alongside Robin M. Winter, 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 61 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome Hit paper breakdown → | 1995 | 739 |
| 2 | Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome Hit paper breakdown → | 1994 | 623 |
| 3 | A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome Hit paper breakdown → | 1994 | 517 |
| 4 | 2004 | 429 | |
| 5 | 1995 | 409 | |
| 6 | 1995 | 375 | |
| 7 | 1999 | 343 | |
| 8 | 1998 | 259 | |
| 9 | 1997 | 224 | |
| 10 | 2004 | 197 | |
| 11 | 1998 | 142 | |
| 12 | 2003 | 119 | |
| 13 | 1994 | 118 | |
| 14 | 2002 | 94 | |
| 15 | 1998 | 84 | |
| 16 | 1993 | 59 | |
| 17 | 1996 | 58 | |
| 18 | 1999 | 53 | |
| 19 | 2003 | 50 | |
| 20 | 1988 | 49 |
About Robin M. Winter
Robin M. Winter is a scholar working on Genetics, Molecular Biology, Surgery, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 61 papers that have together received 5.7k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (13 papers), Genomic variations and chromosomal abnormalities (10 papers), Congenital limb and hand anomalies (9 papers), Cleft Lip and Palate Research (8 papers), Connective tissue disorders research (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), Congenital heart defects research (5 papers) and Prenatal Screening and Diagnostics (5 papers). The work is most often cited by research in Genetics (3.7k citations), Developmental Biology (226 citations), Molecular Biology (2.8k citations), Pediatrics, Perinatology and Child Health (546 citations) and Genetics (250 citations). Robin M. Winter has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include William Reardon, Louise J. Pulleyn, Paul Rutland, Sue Malcolm, Andrew O.M. Wilkie, Barry M. Jones, Jonathan Flint, Sarah F. Slaney, Richard Hayward and Michael Oldridge. Their work appears in journals such as Nature Genetics, Journal of Medical Genetics, American Journal of Medical Genetics, Human Molecular Genetics and The American Journal of 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.