Cathy Raggio

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 3 papers. Top paper: “Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice”.

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

Human Molecular Genetics(2020)10.1093/hmg/ddaa258

N/A

0DataRank · unranked

26 citations

Annabelle Enriquez, Duncan B. Sparrow, David T. Humphreys, Aideen McInerney‐Leo, Paul Leo +29 more

Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factors

Differentiation(2022)10.1016/j.diff.2022.09.002

N/A

0DataRank · unranked

18 citations

Annabelle Enriquez, Robert D. Steiner, Cathy Raggio, Megan Higgins, Di Milnes +7 more

Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis

Journal of Medical Genetics(2025)10.1136/jmg-2024-110586

N/A

0DataRank · unranked

1 citations

Gabe Haller, Julia Whittle, Momchil Nikolov, Addison Avery, José A. Morcuende +12 more