Heidi Stöhr

Biochemistry, Genetics and Molecular BiologyMedicine

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: “CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis”.

CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.23.469779

N/A

0DataRank · unranked

0 citations

Kristof Van Schil, Sandra Liakopoulos, Miriam Bauwens, Alfredo Dueñas Rey, Stephan Käseberg +28 more

CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis

Journal of Clinical Investigation(2023)10.1172/jci161156

N/A

0DataRank · unranked

12 citations

Kristof Van Schil, Sandra Liakopoulos, Miriam Bauwens, Alfredo Dueñas Rey, Stephan Käseberg +28 more

Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100237

N/A

0DataRank · unranked

13 citations

Mubeen Khan, Rebekkah J. Hitti‐Malin, Ketan Mishra, Laura Whelan, Stéphanie S. Cornelis +14 more