Uri Laxer

A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome

Samer Khateb, Lina Zelinger, Liliana Mizrahi‐Meissonnier et al. · Journal of Medical Genetics · 2014 · 89 citations

Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa

Alice E. Davidson, Nele Schwarz, Lina Zelinger et al. · The American Journal of Human Genetics · 2013 · 75 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +8

Characteristics of Sarcoidosis in Patients with Previous Malignancy: Causality or Coincidence?

Nissim Arish, Rottem Kuint, Eli Sapir et al. · Respiration · 2017 · 38 citations · Full text

Lymphocytic interstitial pneumonia associated with common variable immunodeficiency resolved with intravenous immunoglobulins

Nissim Arish, Roy Eldor, Yakov Fellig et al. · Thorax · 2006 · 31 citations · Full text

Primary Immunodeficiency, Autoimmune Disease, Respiratory Diseases +10

Disseminated <i>Mycobacterium kansasii</i> infection with pulmonary alveolar proteinosis in a patient with chronic myelogenous leukemia

Neta Goldschmidt, Samir Nusair, Alexander Gural et al. · American Journal of Hematology · 2003 · 23 citations · Full text