Claire‐Marie Dhaenens

Also affiliated with Université de Lille, Institut Pasteur de Lille, Centre Hospitalier Universitaire de Lille

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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 7 papers. Top paper: “Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability”.

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

0.396DataRank · unranked

13 citations

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

ABCA4c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease

Investigative Ophthalmology & Visual Science(2022)10.1167/iovs.63.4.20

N/A

0DataRank · unranked

7 citations

Manar Salameh, Mubeen Khan, Elise Héon, Ketan Mishra, Rebekkah J. Hitti‐Malin +12 more

Compendium of Clinical Variant Classification for 2,246 Unique ABCA4 Variants to Clarify Variant Pathogenicity in Stargardt Disease Using a Modified ACMG/AMP Framework

Human Mutation(2023)10.1155/2023/6815504

N/A

0DataRank · unranked

20 citations

Miriam Bauwens, Lonneke Haer‐Wigman, Marieke De Bruyne, Madhulatha Pantrangi, Elfride De Baere +4 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

RPE65 Variant p.(E519K) Causes a Novel Dominant Adult-Onset Maculopathy in 83 Affected Individuals

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.12.53

N/A

0DataRank · unranked

2 citations

Filip Van den Broeck, Quinten Mahieu, Eline Geens, Mattias Van Heetvelde, Marieke De Bruyne +32 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

RPE65 variant p.(E519K) causes a novel dominant adult-onset maculopathy in 83 affected individuals

Research Square(2025)10.21203/rs.3.rs-5849564/v2

N/A

0DataRank · unranked

1 citations

Filip Van den Broeck, Quinten Mahieu, Eline Geens, Mattias Van Heetvelde, Marieke De Bruyne +32 more