Lonneke Haer-Wigman

5PUBLICATIONS
173CO-AUTHORS
Translation and interpretation studiesGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|Apr 23, 2025
Cochlear Implantation Outcomes in Genotyped Subjects with Sensorineural Hearing Loss.

M L A Fehrmann, L Haer-Wigman, H Kremer

|Apr 14, 2025
Compendium of Clinical Variant Classification for 2,246 Unique ABCA4 Variants to Clarify Variant Pathogenicity in Stargardt Disease Using a Modified ACMG/AMP Framework.

Stéphanie S Cornelis, Miriam Bauwens, Lonneke Haer-Wigman

|Jan 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Feb 25, 2023
Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38.

Hedwig M Velde, Xanne J J Huizenga, Helger G Yntema

|Feb 28, 2022
Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants.

Hedwig M Velde, Janine Reurink, Sebastian Held

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Frequent Collaborators

3 joint publications

Hannie Kremer

3 joint publications

Cris P Lanting

3 joint publications

Ronald J E Pennings

2 joint publications

Elfride De Baere