Hannie Kremer

19PUBLICATIONS
77CO-AUTHORS
Translation and interpretation studiesGene expression (incl. microarray and other genome-wide approaches)Other European languagesEpigenetics (incl. genome methylation and epigenomics)Gene mapping
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Publications (19)

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

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

|Mar 04, 2025
Deciphering the largest disease-associated transcript isoforms in the human neural retina with advanced long-read sequencing approaches.

Merel Stemerdink, Tabea Riepe, Nick Zomer

|Sep 27, 2024
Uncovering recessive alleles in rare Mendelian disorders by genome sequencing of 174 individuals with monoallelic pathogenic variants.

Gaby Schobers, Maartje Pennings, Juliette de Vries

|Jun 28, 2023
Generation and Characterization of a Zebrafish Model for ADGRV1-Associated Retinal Dysfunction Using CRISPR/Cas9 Genome Editing Technology.

Merel Stemerdink, Sanne Broekman, Theo Peters

|May 23, 2023
Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment.

Laurence Jonard, Davide Brotto, Miguel A Moreno-Pelayo

|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

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Frequent Collaborators

8 joint publications

Ronald Pennings

7 joint publications

Erwin van Wijk

6 joint publications

Susanne Roosing

6 joint publications

Cris P Lanting