R. Sid Wilroy
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Craniofacial Disorders and Treatments
- Developmental Biology top 5%
Papers in
- Genetics 33
- Genomic variations and chromosomal abnormalities 20
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetics and Neurodevelopmental Disorders 4
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- RNA regulation and disease 5
- Co-authors
- Avirachan T. Tharapel (21 shared papers)Robert L. Summitt (10 shared papers)Charles E. Schwartz (3 shared papers)Paula R. Martens (8 shared papers)E K Pivnick (5 shared papers)Roger E. Stevenson (1 shared paper)N.German Pasteris (1 shared paper)Thomas W. Glover (1 shared paper)
- Journals
- The Journal of Pediatrics (5 papers)Journal of Medical Genetics (5 papers)American Journal of Medical Genetics (19 papers)The Journal of Urology (2 papers)Human Molecular Genetics (1 paper)
- Partner nations
- United StatesCanadaIndia
In The Last Decade
R. Sid Wilroy
53 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 74
- Genetics 844
- Developmental Biology 43
- Pediatrics, Perinatology and Child Health 290
- Molecular Biology 635
- Urology 51
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 53 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1994 | 245 | |
| 2 | Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions. | 1993 | 95 |
| 3 | 1986 | 76 | |
| 4 | 1996 | 66 | |
| 5 | 1995 | 63 | |
| 6 | 1998 | 54 | |
| 7 | 1982 | 52 | |
| 8 | 1994 | 48 | |
| 9 | 1990 | 47 | |
| 10 | 1974 | 46 | |
| 11 | 1990 | 44 | |
| 12 | Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B. | 1998 | 40 |
| 13 | 2000 | 33 | |
| 14 | 1980 | 32 | |
| 15 | 1983 | 31 | |
| 16 | Familial gingival fibromatosis associated with progressive deafness in five generations of a family. | 1977 | 30 |
| 17 | 1978 | 29 | |
| 18 | 1971 | 26 | |
| 19 | 1966 | 25 | |
| 20 | A microassay for argininosuccinase in cultured cells. | 1972 | 25 |
About R. Sid Wilroy
R. Sid Wilroy is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 53 papers that have together received 1.4k 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), RNA regulation and disease (5 papers), Urological Disorders and Treatments (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Urologic and reproductive health conditions (3 papers). The work is most often cited by research in Genetics (844 citations), Developmental Biology (43 citations), Pediatrics, Perinatology and Child Health (290 citations), Molecular Biology (635 citations) and Urology (51 citations). R. Sid Wilroy has collaborated with scholars based in United States, Canada and India. Frequent co-authors include Avirachan T. Tharapel, Robert L. Summitt, Charles E. Schwartz, Paula R. Martens, E K Pivnick, Roger E. Stevenson, N.German Pasteris, Thomas W. Glover, Jerome L. Gorski and Mary Porteous. Their work appears in journals such as The Journal of Pediatrics, Journal of Medical Genetics, American Journal of Medical Genetics, The Journal of Urology and Human Molecular 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.