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Publications by Bernd Wissinger
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
American Journal of Human Genetics
Genetics
ABCA4-associated Disease as a Model for Missing Heritability in Autosomal Recessive Disorders: Novel Noncoding Splice, Cis-Regulatory, Structural, and Recurrent Hypomorphic Variants
Genetics in Medicine
Medicine
Genetics
Electrophysiological and Histologic Assessment of Retinal Ganglion Cell Fate in a Mouse Model forOPA1-Associated Autosomal Dominant Optic Atrophy
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Molecular and Clinical Analysis of 27 German Patients With Leber Congenital Amaurosis
PLoS ONE
Multidisciplinary
Imaging Ca2+ Dynamics in Cone Photoreceptor Axon Terminals of the Mouse Retina
Journal of Visualized Experiments
Immunology
Molecular Biology
Biochemistry
Microbiology
Chemical Engineering
Neuroscience
Genetics
Ribosomal Protein S14 Transcripts Are Edited inOenotheramitochondria
Nucleic Acids Research
Genetics
Functional Consequences of Disease-Associated Mutations in the Pore Region of Human Cone Photoreceptor CNG Channels
Biophysical Journal
Biophysics
Identification of a Locus on Chromosome 2q11 at Which Recessive Amelogenesis Imperfecta and Cone-Rod Dystrophy Cosegregate
European Journal of Human Genetics
Genetics
Cone Dystrophy With Supernormal Rod Response Is Strictly Associated With Mutations inKCNV2
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
