Laura Kühlewein

ORCID: 0000-0003-1906-8681

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 6 papers. Top paper: “De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa”.

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

Nature Genetics(2026)10.1038/s41588-025-02451-4

N/A

0.370DataRank · unranked

8 citations

Kim Rodenburg, Zuzana Cvackova, Karolina Kaminska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +212 more

CNGB1 ‐related rod‐cone dystrophy: A mutation review and update

Human Mutation(2021)10.1002/humu.24205

N/A

0DataRank · unranked

24 citations

Vasily Smirnov, Cyntia Solis Hernandez, Saddek Mohand‐Saïd, Christel Condroyer, Aline Antonio +28 more

Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study

British Journal of Ophthalmology(2024)10.1136/bjo-2023-323747

N/A

0DataRank · unranked

7 citations

Elizabeth White, Alaa Tayyib, Lesley Everett, Ajoy Vincent, Elise Héon +52 more

Comparison of Full-Field Stimulus Threshold Measurements in Patients With Retinitis Pigmentosa and Healthy Subjects With Dilated and Nondilated Pupil

Translational Vision Science & Technology(2024)10.1167/tvst.13.4.23

N/A

0DataRank · unranked

3 citations

Katarína Štingl, Katarina Stingl, Laura Kühlewein, Melanie Kempf, Krunoslav Stingl +2 more

Bi-allelic loss-of-function variants in POC5 cause a syndromic retinal, endocrine, and neuromuscular ciliopathy

Genetics in Medicine(2025)10.1016/j.gim.2025.101513

N/A

0DataRank · unranked

1 citations

Ingrid M. Jazet, Suzanne Yzer, Jeroen Pas, Serwet Demirdas, Elisabeth F. C. van Rossum +39 more

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa

medRxiv(2025)10.1101/2025.01.06.24317169

N/A

0DataRank · unranked

15 citations

Kim Rodenburg, Zuzana Cvačková, Karolina Kamińska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +95 more