Robin Winter
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genetic and Kidney Cyst Diseases
- Genomic variations and chromosomal abnormalities
- Cleft Lip and Palate Research
- Developmental Biology top 5%
Papers in
-
- RNA regulation and disease 2
- Genetics 12
- Genetics and Neurodevelopmental Disorders 3
- Genomics and Rare Diseases 3
- Genetic Syndromes and Imprinting 3
- Co-authors
- William Reardon (3 shared papers)Sue Malcolm (3 shared papers)Brunella Franco (2 shared papers)Andrea Ballabio (2 shared papers)A. Roche (2 shared papers)Yutaka Nakahori (2 shared papers)R H Lindenbaum (2 shared papers)Mark C. Hirst (2 shared papers)
- Journals
- Human Genetics (2 papers)Early Human Development (2 papers)Journal of Medical Genetics (2 papers)The American Journal of Human Genetics (2 papers)Prenatal Diagnosis (1 paper)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
Robin Winter
29 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 98
- Genetics 840
- Developmental Biology 59
- Molecular Biology 859
- Cell Biology 142
- Genetics 75
Countries citing papers authored by Robin Winter
This map shows the geographic impact of Robin 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 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 Winter more than expected).
Fields of papers citing papers by Robin Winter
This network shows the impact of papers produced by Robin 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 Winter. The network helps show where Robin Winter may publish in the future.
Co-authors
The 25 scholars most cited alongside Robin 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1991 | 286 | |
| 2 | 2001 | 240 | |
| 3 | 1995 | 173 | |
| 4 | 2014 | 155 | |
| 5 | Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations. | 2000 | 97 |
| 6 | Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families. | 1995 | 87 |
| 7 | 1995 | 82 | |
| 8 | 1998 | 79 | |
| 9 | 2003 | 72 | |
| 10 | 2001 | 45 | |
| 11 | 2003 | 39 | |
| 12 | 1997 | 37 | |
| 13 | 1985 | 20 | |
| 14 | 1992 | 17 | |
| 15 | 1988 | 16 | |
| 16 | 1986 | 9 | |
| 17 | 2011 | 9 | |
| 18 | 1991 | 6 | |
| 19 | 1999 | 5 | |
| 20 | 2004 | 4 |
About Robin Winter
Robin Winter is a scholar working on Molecular Biology, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Genetics, having authored 30 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (3 papers), Infant Nutrition and Health (2 papers), Prenatal Screening and Diagnostics (2 papers), Congenital limb and hand anomalies (2 papers), RNA regulation and disease (2 papers) and Cancer-related molecular mechanisms research (2 papers). The work is most often cited by research in Genetics (840 citations), Developmental Biology (59 citations), Molecular Biology (859 citations), Cell Biology (142 citations) and Genetics (75 citations). Robin Winter has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include William Reardon, Sue Malcolm, Brunella Franco, Andrea Ballabio, A. Roche, Yutaka Nakahori, R H Lindenbaum, Mark C. Hirst, Kay E. Davies and Aleš Janka. Their work appears in journals such as Human Genetics, Early Human Development, Journal of Medical Genetics, The American Journal of Human Genetics and Prenatal Diagnosis.
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.