Elfride De Baere

HOGENT University of Applied Sciences and Arts

Also affiliated with Ghent University Hospital, Ghent University

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 8 papers. Top paper: “Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development”.

Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development

Nature Communications(2024)10.1038/s41467-024-53553-2

N/A

0.306DataRank · unranked

6 citations

Munevver Burcu Cicekdal, Richard Holt, Елена А. Сорокина, Nicolas Chassaing, Samuel Clokie +15 more

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

0DataRank · unranked

37 citations

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

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

Juggling offsets unlocks RNA-seq tools for fast and Scalable differential usage, Aberrant Splicing and Expression Retrieval

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.29.547014

N/A

0DataRank · unranked

5 citations

Jeroen Gilis, Mattias Van Heetvelde, Davide Risso, Elfride De Baere, Lieven Clement +1 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

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

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