Rita Shiang

8.5k citations
44 papers · 3.8k · 1 hit paper · h-index 24

Impact in

Papers in

    • dental development and anomalies 5
    • Ion channel regulation and function 5
    • Craniofacial Disorders and Treatments 9
    • Cleft Lip and Palate Research 8
    • Genetics and Neurodevelopmental Disorders 5
    • Genomic variations and chromosomal abnormalities 4
    • Connective tissue disorders research 4

Rita Shiang

43 papers receiving 3.7k citations

Hit Papers

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia 1994 · 988 citations
9880+10+21Years since publication250500750

Peers

Rita Shiang
Comparison fields: 5 of 114
  • Genetics 1.8k
  • Cellular and Molecular Neuroscience 662
  • Molecular Biology 2.4k
  • Rheumatology 383
  • Cell Biology 340
Replace Uwe Kornak with:
Uwe Kornak Germany
Stephen P. Robertson New Zealand
Bernd Wollnik Germany
Andreas Janecke Austria
Hélène Dollfus France
Patrick Edery France
E. Schwinger Germany
Han G. Brunner Netherlands
Andreas Winterpacht Germany
Anita Farhi United States
Rita Shiang relative to Uwe Kornak Germany Uwe Kornak's profile →
Citations per field
00.5×1.6×
Uwe Kornak · 1×
Citations per year

Countries citing papers authored by Rita Shiang

Since Specialization
Citations

This map shows the geographic impact of Rita Shiang'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 Rita Shiang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rita Shiang more than expected).

Fields of papers citing papers by Rita Shiang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rita Shiang. 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 Rita Shiang. The network helps show where Rita Shiang may publish in the future.

Co-authors

The 25 scholars most cited alongside Rita Shiang, 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 Rita Shiang Line = papers co-authored together Rita Shiang links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 44 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
Hit paper breakdown →
1994988
2 1995466
3 1993384
4 2007207
5 2006174
6 2002161
7 1994146
8 2001145
9 1997122
10 1993106
11 1995100
12 199585
13
Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO).
199373
14 198969
15 199768
16 199862
17
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates.
199158
18 199542
19 199738
20
Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q.
199238

About Rita Shiang

Rita Shiang is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Public Health, Environmental and Occupational Health and Immunology, having authored 44 papers that have together received 3.8k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (9 papers), Cleft Lip and Palate Research (8 papers), dental development and anomalies (5 papers), Ion channel regulation and function (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Neuroscience and Neuropharmacology Research (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Connective tissue disorders research (4 papers). The work is most often cited by research in Genetics (1.8k citations), Cellular and Molecular Neuroscience (662 citations), Molecular Biology (2.4k citations), Rheumatology (383 citations) and Cell Biology (340 citations). Rita Shiang has collaborated with scholars based in United States, United Kingdom and Japan. Frequent co-authors include John J. Wasmuth, Yazhen Zhu, Leslie M. Thompson, Sara T. Winokur, Thomas J. Fielder, Maureen Bocian, Deanna M. Church, P. O’Connell, Stephen G. Ryan and Angelika F. Hahn. Their work appears in journals such as Nature Genetics, Human Molecular Genetics, The American Journal of Human Genetics, Genomics and Cytogenetic and Genome Research.

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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