R. Sid Wilroy
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders
- Developmental Biology top 5%
Papers in
- Genetics 34
- Genomic variations and chromosomal abnormalities 20
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Craniofacial Disorders and Treatments 4
- Genetics and Neurodevelopmental Disorders 4
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- Prenatal Screening and Diagnostics 10
- Co-authors
- Avirachan T. Tharapel (21 shared papers)Robert L. Summitt (11 shared papers)Charles E. Schwartz (3 shared papers)Paula R. Martens (9 shared papers)E K Pivnick (5 shared papers)Robert E. Tipton (4 shared papers)Jerome L. Gorski (1 shared paper)Roger E. Stevenson (1 shared paper)
- Journals
- Journal of Medical Genetics (6 papers)The Journal of Pediatrics (5 papers)American Journal of Medical Genetics (19 papers)The Journal of Urology (2 papers)Cell (1 paper)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
R. Sid Wilroy
56 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 79
- Genetics 1.2k
- Developmental Biology 48
- Pediatrics, Perinatology and Child Health 328
- Molecular Biology 858
- Cell Biology 170
Countries citing papers authored by R. Sid Wilroy
This map shows the geographic impact of R. Sid Wilroy'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 R. Sid Wilroy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R. Sid Wilroy more than expected).
Fields of papers citing papers by R. Sid Wilroy
This network shows the impact of papers produced by R. Sid Wilroy. 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 R. Sid Wilroy. The network helps show where R. Sid Wilroy may publish in the future.
Co-authors
The 25 scholars most cited alongside R. Sid Wilroy, 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 56 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. | 1997 | 328 |
| 2 | 1994 | 247 | |
| 3 | Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions. | 1993 | 97 |
| 4 | 2006 | 80 | |
| 5 | 1986 | 77 | |
| 6 | 1996 | 69 | |
| 7 | 1995 | 65 | |
| 8 | 1998 | 54 | |
| 9 | 1990 | 54 | |
| 10 | 1994 | 54 | |
| 11 | 1982 | 53 | |
| 12 | 1974 | 47 | |
| 13 | 1990 | 43 | |
| 14 | Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B. | 1998 | 41 |
| 15 | 2000 | 35 | |
| 16 | 1980 | 32 | |
| 17 | Familial gingival fibromatosis associated with progressive deafness in five generations of a family. | 1977 | 31 |
| 18 | 1983 | 31 | |
| 19 | 1978 | 29 | |
| 20 | 1979 | 29 |
About R. Sid Wilroy
R. Sid Wilroy is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Urology, Molecular Biology and Developmental Biology, having authored 56 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (10 papers), Chromosomal and Genetic Variations (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Urological Disorders and Treatments (5 papers), RNA regulation and disease (5 papers), Craniofacial Disorders and Treatments (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Genetics (1.2k citations), Developmental Biology (48 citations), Pediatrics, Perinatology and Child Health (328 citations), Molecular Biology (858 citations) and Cell Biology (170 citations). R. Sid Wilroy has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Avirachan T. Tharapel, Robert L. Summitt, Charles E. Schwartz, Paula R. Martens, E K Pivnick, Robert E. Tipton, Jerome L. Gorski, Roger E. Stevenson, Thomas W. Glover and Mary E. Porteous. Their work appears in journals such as Journal of Medical Genetics, The Journal of Pediatrics, American Journal of Medical Genetics, The Journal of Urology and Cell.
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.