Marieke De Bruyne

HOGENT University of Applied Sciences and Arts

Also affiliated with Ghent University Hospital, Ghent University

Biochemistry, Genetics and Molecular BiologyImmunology and MicrobiologyMedicine

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: “GTF3A mutations predispose to herpes simplex encephalitis by disrupting biogenesis of the host-derived RIG-I ligand RNA5SP141”.

GTF3A mutations predispose to herpes simplex encephalitis by disrupting biogenesis of the host-derived RIG-I ligand RNA5SP141

Science Immunology(2022)10.1126/sciimmunol.abq4531

N/A

0.550DataRank · unranked

38 citations

Santoshi Muppala, Dhiraj Acharya, Josephine Nemegeer, Delfien Bogaert, Jung‐Hyun Lee +16 more

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

Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variants

Clinical Genetics(2024)10.1111/cge.14614

N/A

0DataRank · unranked

11 citations

Vincent De Man, Isabelle Audo, Irina Balikova, Wadih M. Zein, Vasily Smirnov +20 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

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

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

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

The Journal of Experimental Medicine(2020)10.1084/jem.20191804

N/A

0DataRank · unranked

113 citations

Simon J. Tavernier, Yin‐Huai Chen, S. Cindy, Marie Materna, Arian Laurence +55 more