Hannie Kremer

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 20

Top Venues

International journal of molecular sciences

Human genetics

Genes

Cells

Radboud Universiteit (MSC)

This page only lists publications with an associated author ORCID identifier.

Education History

Radboud Universiteit

Netherlands

MSC

Publications

Merel Stemerdink, Sanne Broekman, Theo Peters, Hannie Kremer, Erik de Vrieze, Erwin van Wijk
Generation and Characterization of a Zebrafish Model for ADGRV1- Associated Retinal Dysfunction Using CRISPR/Cas9 Genome Editing Technology. Cells 12 (12) (2023)
Laurence Jonard, Davide Brotto, Miguel Angel Moreno-Pelayo, Ignacio Del Castillo, Hannie Kremer, Ronald J E Pennings, Helena Caria, Graça Fialho, An Boudewyns, Guy Van Camp, Monika Ołdak, Dominika Oziębło, Naïma Deggouj, Romolo Daniele De Siati, Paolo Gasparini, Giorgia Girotto, Margriet Verstreken, Silvia Dossena, Sebastian Roesch, Saba Battelino, Katarina Trebušak Podkrajšek, Athanasia Warnecke, Thomas Lenarz, Anke Lesinski-Schiedat, Michel Mondain, Anne-Françoise Roux, Françoise Denoyelle, Natalie Loundon, Margaux Serey-Gaut, Patrizia Trevisi, Elisa Rubinato, Alessandro Martini, Sandrine Marlin
Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment. Audiology research 13 (3) (2023)
Merel Stemerdink, Sanne Broekman, Theo Peters, Hannie Kremer, Erik de Vrieze, Erwin van Wijk
Generation and Characterization of a Zebrafish Model for ADGRV1- Associated Retinal Dysfunction Using CRISPR/Cas9 Genome Editing Technology. Cells 12 (12) (2023)
Hedwig M Velde, Xanne J J Huizenga, Helger G Yntema, Lonneke Haer-Wigman, Andy J Beynon, Jaap Oostrik, Sjoert A H Pegge, Hannie Kremer, Cornelis P Lanting, Ronald J E Pennings
Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38. Genes 14 (2) (2023)
Hedwig M Velde, Xanne J J Huizenga, Helger G Yntema, Lonneke Haer-Wigman, Andy J Beynon, Jaap Oostrik, Sjoert A H Pegge, Hannie Kremer, Cornelis P Lanting, Ronald J E Pennings
Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38. Genes 14 (2) (2023)
Hedwig M Velde, Xanne J J Huizenga, Helger G Yntema, Lonneke Haer-Wigman, Andy J Beynon, Jaap Oostrik, Sjoert A H Pegge, Hannie Kremer, Cornelis P Lanting, Ronald J E Pennings
Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38. Genes 14 (2) (2023)
Merel Stemerdink, Sanne Broekman, Theo Peters, Hannie Kremer, Erik de Vrieze, Erwin van Wijk
Generation and Characterization of a Zebrafish Model for ADGRV1- Associated Retinal Dysfunction Using CRISPR/Cas9 Genome Editing Technology. Cells 12 (12) (2023)
Janine Reurink, Jaap Oostrik, Marco Aben, Mariana Guimarães Ramos, Emma van Berkel, Monika Ołdak, Erwin van Wijk, Hannie Kremer, Susanne Roosing, Frans P M Cremers
Minigene-Based Splice Assays Reveal the Effect of Non-Canonical Splice Site Variants in USH2A . International journal of molecular sciences 23 (21) (2022)
Hannie Kremer, Ignacio Del Castillo
Genetics of Hearing Impairment. Genes 13 (5) (2022)
Sybren M M Robijn, Jeroen J Smits, Kadriye Sezer, Patrick L M Huygen, Andy J Beynon, Erwin van Wijk, Hannie Kremer, Erik de Vrieze, Cornelis P Lanting, Ronald J E Pennings
Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis. Biomolecules 12 (2) (2022)
Hedwig M Velde, Janine Reurink, Sebastian Held, Catherina H Z Li, Suzanne Yzer, Jaap Oostrik, Jack Weeda, Lonneke Haer-Wigman, Helger G Yntema, Susanne Roosing, Laurenz J B Pauleikhoff, Clemens A Lange, Laura Whelan, Adrian Dockery, Julia Zhu, David J Keegan, Gwyneth Jane Farrar, Hannie Kremer, Cornelis P Lanting, Markus Damme, Ronald J E Pennings
Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants. Human genetics 141 (11) (2022)
Janine Reurink, Adrian Dockery, Dominika Oziębło, Gwyneth Jane Farrar, Monika Ołdak, Jacoline B Ten Brink, Arthur A Bergen, Tuula Rinne, Helger G Yntema, Ronald J E Pennings, L Ingeborgh van den Born, Marco Aben, Jaap Oostrik, Hanka Venselaar, Astrid S Plomp, M Imran Khan, Erwin van Wijk, Frans P M Cremers, Susanne Roosing, Hannie Kremer
Molecular Inversion Probe-Based Sequencing of USH2A Exons and Splice Sites as a Cost-Effective Screening Tool in USH2 and arRP Cases. International journal of molecular sciences 22 (12) (2021)
Jeroen J Smits, Suzanne E de Bruijn, Cornelis P Lanting, Jaap Oostrik, Luke O'Gorman, Tuomo Mantere, null null, Frans P M Cremers, Susanne Roosing, Helger G Yntema, Erik de Vrieze, Ronny Derks, Alexander Hoischen, Sjoert A H Pegge, Kornelia Neveling, Ronald J E Pennings, Hannie Kremer
Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant. Human genetics (2021)
Hannie Kremer
Novel gene discovery for hearing loss and other routes to increased diagnostic rates. Human genetics (2021)
Suzanne E de Bruijn, Zeinab Fadaie, Frans P M Cremers, Hannie Kremer, Susanne Roosing
The Impact of Modern Technologies on Molecular Diagnostic Success Rates, with a Focus on Inherited Retinal Dystrophy and Hearing Loss. International journal of molecular sciences 22 (6) (2021)
Jeroen J Smits, Suzanne E de Bruijn, Cornelis P Lanting, Jaap Oostrik, Luke O'Gorman, Tuomo Mantere, null null, Frans P M Cremers, Susanne Roosing, Helger G Yntema, Erik de Vrieze, Ronny Derks, Alexander Hoischen, Sjoert A H Pegge, Kornelia Neveling, Ronald J E Pennings, Hannie Kremer
Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant. Human genetics (2021)
Erik de Vrieze, Suzanne E de Bruijn, Janine Reurink, Sanne Broekman, Vince van de Riet, Marco Aben, Hannie Kremer, Erwin van Wijk
Efficient Generation of Knock-In Zebrafish Models for Inherited Disorders Using CRISPR-Cas9 Ribonucleoprotein Complexes. International journal of molecular sciences 22 (17) (2021)
Renske Schellens, Erik de Vrieze, Pam Graave, Sanne Broekman, Kerstin Nagel-Wolfrum, Theo Peters, Hannie Kremer, Rob W J Collin, Erwin van Wijk
Zebrafish as a Model to Evaluate a CRISPR/Cas9-Based Exon Excision Approach as a Future Treatment Option for EYS-Associated Retinitis Pigmentosa. International journal of molecular sciences 22 (17) (2021)
Jeroen J Smits, Jaap Oostrik, Andy J Beynon, Sarina G Kant, Pia A M de Koning Gans, Liselotte J C Rotteveel, Jolien S Klein Wassink-Ruiter, Rolien H Free, Saskia M Maas, Jiddeke van de Kamp, Paul Merkus, null null, Wouter Koole, Ilse Feenstra, Ronald J C Admiraal, Cornelis P Lanting, Margit Schraders, Helger G Yntema, Ronald J E Pennings, Hannie Kremer
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment. Human genetics 138 (1) (2018)
Celia Zazo Seco, Anna Castells-Nobau, Seol-Hee Joo, Margit Schraders, Jia Nee Foo, Monique van der Voet, S Sendhil Velan, Bonnie Nijhof, Jaap Oostrik, Erik de Vrieze, Radoslaw Katana, Atika Mansoor, Martijn Huynen, Radek Szklarczyk, Martin Oti, Lisbeth Tranebjærg, Erwin van Wijk, Jolanda M Scheffer-de Gooyert, Saadat Siddique, Jonathan Baets, Peter de Jonghe, Syed Ali Raza Kazmi, Suresh Anand Sadananthan, Bart P van de Warrenburg, Chiea Chuen Khor, Martin C Göpfert, Raheel Qamar, Annette Schenck, Hannie Kremer, Saima Siddiqi
A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy. Disease models & mechanisms 10 (2) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Hannie Kremer