Publications by authors named "Ranit Jaron"

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N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder.
Asier Iturrate, Nurit Assia Batzir, Ranit Jaron, David Garcia-Valentin, Julian Nevado

Eur J Hum Genet· September 2025

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High frequency of MEFV disease-causing variants in children with very-early-onset inflammatory bowel disease.
Aasem Abu Shtaya, Naama Orenstein, Lily Bazak, Gabriel Lidzbarsky, Marina Lifshitc Kalis, Ranit Jaron

Pediatr Res· January 2025

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Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection.
Adi Aran, Nuphar Rosenfeld, Ranit Jaron, Paul Renbaum, Shachar Zuckerman

Neurology· May 2016

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Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene.
Paul Renbaum, Efrat Kellerman, Ranit Jaron, Dan Geiger, Reeval Segel

Am J Hum Genet· August 2009

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Nasal potential difference in non-classic cystic fibrosis-long term follow up.
Ranit Jaron, Yasmin Yaakov, Joseph Rivlin, Hannah Blau, Lea Bentur

Pediatr Pulmonol· June 2008

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