R. Sid Wilroy

2.4k citations
53 papers · 1.3k · h-index 21

Impact in

  • Genetics top 2%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetic Syndromes and Imprinting
    • Craniofacial Disorders and Treatments

Papers in

    • Genomic variations and chromosomal abnormalities 20
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
    • Genetics and Neurodevelopmental Disorders 4
    • RNA regulation and disease 5

R. Sid Wilroy

53 papers receiving 1.2k citations

Peers

R. Sid Wilroy
Comparison fields: 5 of 74
  • Genetics 751
  • Developmental Biology 43
  • Pediatrics, Perinatology and Child Health 251
  • Molecular Biology 595
  • Urology 44
Replace Boris G. Kousseff with:
Boris G. Kousseff United States
B. Le Marec France
M.H. Breuning Netherlands
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Chiara Bacchelli United Kingdom
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Elisabeth Flori France
Sarah F. Slaney United Kingdom
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Citations per field
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Citations per year

Countries citing papers authored by R. Sid Wilroy

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with R. Sid Wilroy Line = papers co-authored together R. Sid Wilroy links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 53 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1994237
2
Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions.
199383
3 199662
4 198659
5 199557
6 199047
7 198244
8 197442
9 199440
10
Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B.
199838
11 199835
12 198331
13 198030
14
Familial gingival fibromatosis associated with progressive deafness in five generations of a family.
197730
15 199027
16 200027
17 197827
18 197123
19
A microassay for argininosuccinase in cultured cells.
197223
20 197921

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 1.3k 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 (751 citations), Developmental Biology (43 citations), Pediatrics, Perinatology and Child Health (251 citations), Molecular Biology (595 citations) and Urology (44 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, Thomas W. Glover, Jerome L. Gorski, Roger E. Stevenson, N.German Pasteris 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 European Journal of Pediatrics.

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.

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