Tamar Ben‐Yosef
Technion – Israel Institute of Technology(IL)
Publications by Year
Research Areas
Retinal Development and Disorders, Retinal Diseases and Treatments, RNA regulation and disease, Connexins and lens biology, Hearing, Cochlea, Tinnitus, Genetics
Most-Cited Works
- → Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29(2001)438 cited
- → Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration(2003)335 cited
- → Development of Novel Aminoglycoside (NB54) with Reduced Toxicity and Enhanced Suppression of Disease-Causing Premature Stop Mutations(2009)185 cited
- → Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics(2020)140 cited
- → A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews(2011)138 cited
- → A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)(2019)121 cited
- → CaV1.3 L-type Ca2+ channels modulate depression-like behaviour in mice independent of deaf phenotype(2009)109 cited
- → Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis Pigmentosa(2010)103 cited
- → Syndromic Inherited Retinal Diseases: Genetic, Clinical and Diagnostic Aspects(2020)95 cited
- → A Mutation ofPCDH15among Ashkenazi Jews with the Type 1 Usher Syndrome(2003)93 cited