L. Ingeborgh van den Born

Medicine

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 2 papers. Top paper: “Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration”.

Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration

Genetics in Medicine(2024)10.1016/j.gim.2024.101106

N/A

0DataRank · unranked

14 citations

Kim Rodenburg, Tamar Hayman, Giacomo Calzetti, Karolina Kamińska, Mathieu Quinodoz +20 more

Non-coding single-nucleotide and structural variants affecting the EYS putative promoter cause autosomal recessive retinitis pigmentosa

Genetics in Medicine(2025)10.1016/j.gim.2025.101427

N/A

0DataRank · unranked

3 citations

Shai Ovadia, Jaya Krishnan, Manon Bouckaert, Daan M. Panneman, Milton A. English +13 more