Mariela J. Nevet

Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of <i>PRCD</i> in the aetiology of retinitis pigmentosa in humans

Mariela J. Nevet, Stavit A. Shalev, Joël Zlotogora et al. · Journal of Medical Genetics · 2010 · 38 citations

Life Sciences, Genetics, Ophthalmology +16

Atrophic Skin Patches With Abnormal Elastic Fibers as a Presenting Sign of the MASS Phenotype Associated With Mutation in the Fibrillin 1 Gene

Mariela J. Nevet, Hadas Gescheidt-Shoshany, Allen L. Pimienta et al. · JAMA Dermatology · 2014 · 17 citations

Life Sciences, Dermatology, Genetics +15

PRCD is Concentrated at the Base of Photoreceptor Outer Segments and is Involved in Outer Segment Disc Formation

Gilad Allon, Irit Mann, Lital Remez et al. · Human Molecular Genetics · 2019 · 17 citations

Medicine, Neuroscience, Ophthalmology +17

Ceramide Kinase-Like (CERKL) Interacts with Neuronal Calcium Sensor Proteins in the Retina in a Cation-Dependent Manner

Mariela J. Nevet, Sharon Vekslin, Alexander M. Dizhoor et al. · Investigative Ophthalmology & Visual Science · 2012 · 15 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17