Standout Papers

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism... 1994 2026 2004 2015 975
  1. Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia (1994)
    Rita Shiang, Leslie M. Thompson et al. Cell

Immediate Impact

11 by Nobel laureates 30 from Science/Nature 66 standout
Sub-graph 1 of 19

Citing Papers

Autoantibodies to Synaptic Receptors and Neuronal Cell Surface Proteins in Autoimmune Diseases of the Central Nervous System
2017 Standout
SWELL1, a Plasma Membrane Protein, Is an Essential Component of Volume-Regulated Anion Channel
2014 StandoutNobel
59 intermediate papers

Works of Rita Shiang being referenced

A missense mutation in the gene encoding the α1 subunit of the inhibitory glycine receptor in the spasmodic mouse
1994
Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia
1993
and 4 more

Author Peers

Author Last Decade Papers Cites
Rita Shiang 2403 1792 657 43 3.7k
Nathalie Drouot 1837 1400 524 36 3.4k
Colette Dib 3087 2484 476 21 5.9k
Mark Carlton 4286 1544 635 44 7.4k
Alfons Meindl 3400 2006 545 76 5.6k
Michael A. Patton 3992 1260 533 80 5.8k
Nick Thomas 3115 1303 227 41 4.5k
Tayfun Özçelık 1781 917 676 66 3.5k
Angeliki Louvi 2372 1087 515 43 3.9k
Han G. Brunner 3015 1778 456 56 4.4k
Carol A. Wise 2706 1224 727 85 5.6k

All Works

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2026