Eric T. Rush

Also affiliated with Kansas City Research Institute, University of Missouri–Kansas City

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 4 papers. Top paper: “Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling”.

Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling

EMBO Molecular Medicine(2020)10.15252/emmm.201911739

N/A

0DataRank · unranked

28 citations

Sara P. Abraham, Alexandru Niţă, Eva Hrubá, Marcela Buchtová, S. Paige Taylor +19 more

Jansen‐de Vries syndrome: Expansion of the PPM1D clinical and phenotypic spectrum in 34 families

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63226

N/A

0DataRank · unranked

10 citations

Siddharth Srivastava, Pankaj B. Agrawal, Tuğçe B. Balcı, Bert Callewaert, Pier Luigi Calvo +35 more

De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.02.016

N/A

0DataRank · unranked

5 citations

Kaitlyn Kiernan, Erin Torti, Ethan Pavlovsky, Nicholas Tilton, Austin Sekula +35 more

X-Linked Hypophosphatemia Management in Children: An International Working Group Clinical Practice Guideline

The Journal of Clinical Endocrinology & Metabolism(2025)10.1210/clinem/dgaf093

N/A

0DataRank · unranked

19 citations

Thomas O. Carpenter, Erik A. Imel, Leanne M. Ward, Natasha M. Appelman‐Dijkstra, Catherine Chaussain +39 more