Rina Leibu

Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin

Eli Sprecher, Gabriele Richard, Raziel Lurie et al. · Nature Genetics · 2001 · 184 citations

Ocular Disease, Ophthalmology, Pathology +5

A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)

Dror Sharon, Tamar Ben‐Yosef, Nitza Goldenberg‐Cohen et al. · Human Mutation · 2019 · 119 citations

Ocular Disease, Genetics, Genetic Epidemiology +17

Haptoglobin phenotype and diabetic nephropathy

Farid Nakhoul, Roaa Zoabi, Y Kanter et al. · Diabetologia · 2001 · 90 citations · Full text

Medicine, Physiology, Haptoglobin Phenotype +5

Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT)

Lonneke Haer‐Wigman, Horatio Hackett Newman, Rina Leibu et al. · Human Molecular Genetics · 2015 · 75 citations · Full text

Ocular Disease, Genetics, Glycobiology +17

A Missense Mutation in CDH3, Encoding P-Cadherin, Causes Hypotrichosis with Juvenile Macular Dystrophy

Margarita Indelman, Danny Petronius, Dan Ciubutaro et al. · Journal of Investigative Dermatology · 2002 · 67 citations · Full text

Ocular Disease, Encoding P-cadherin, Ophthalmology +8