Christian Hamel

TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness

Isabelle Audo, Susanne Kohl, Bart P. Leroy et al. · The American Journal of Human Genetics · 2009 · 262 citations · Full text

Life Sciences, Genetics, Neuroscience +10

Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness

Christina Zeitz, Samuel G. Jacobson, Christian Hamel et al. · The American Journal of Human Genetics · 2012 · 138 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness

Ajoy Vincent, Isabelle Audo, Erika Tavares et al. · The American Journal of Human Genetics · 2016 · 62 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2

Stylianos Michalakis, Lior Shaltiel, Vithiyanjali Sothilingam et al. · Human Molecular Genetics · 2013 · 41 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes

Galuh Astuti, L. van den Born, Muhammad Imran Khan et al. · Genes · 2018 · 31 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16