Bas P. Hartel

Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation

Radulfus WN Slijkerman, Christel Vaché, Margo Dona et al. · Molecular Therapy — Nucleic Acids · 2016 · 134 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis Pigmentosa

Laurence Pierrache, Bas P. Hartel, Erwin van Wijk et al. · Ophthalmology · 2016 · 105 citations

Medicine, Dermatology, Ophthalmology +12

A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIa

Bas P. Hartel, Maria Löfgren, P.L.M. Huygen et al. · Hearing Research · 2016 · 63 citations

Life Sciences, Genetics, Molecular Genetics +12

MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse

Mieke Wesdorp, Silvia Murillo‐Cuesta, Theo Peters et al. · The American Journal of Human Genetics · 2018 · 49 citations · Full text

Life Sciences, Neurobiology, Neuroscience +10

Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction

Mieke Wesdorp, Pia A. M. de Koning Gans, Margit Schraders et al. · Human Genetics · 2018 · 39 citations · Full text

Medicine, Genetics, Molecular Genetics +17