Shamir Zenvirt

A Deleterious Mutation in DNAJC6 Encoding the Neuronal-Specific Clathrin-Uncoating Co-Chaperone Auxilin, Is Associated with Juvenile Parkinsonism

Simon Edvardson, Yuval Cinnamon, Asaf Ta‐Shma et al. · PLoS ONE · 2012 · 319 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Exome sequencing and disease-network analysis of a single family implicate a mutation in <i>KIF1A</i> in hereditary spastic paraparesis

Yaniv Erlich, Simon Edvardson, Emily Hodges et al. · Genome Research · 2011 · 197 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy

Yoram Nevo, Bruria Ben‐Zeev, Adi Tabib et al. · Blood · 2012 · 166 citations

Life Sciences, Immunology, Neurology +10

Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia

Esther Maor‐Sagie, Yuval Cinnamon, Yaacov Barak et al. · Journal of Assisted Reproduction and Genetics · 2015 · 122 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

An <i>SNX10</i> mutation causes malignant osteopetrosis of infancy

Memet Aker, Alex Rouvinski, Saar Hashavia et al. · Journal of Medical Genetics · 2012 · 121 citations · Full text

Medicine, Genetics, Molecular Genetics +17