Israela Lerer

The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women.

Dvorah Abeliovich, Luna Kaduri, Israela Lerer et al. · PubMed · 1997 · 359 citations

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration

Giovanni Stévanin, Hamid Azzedine, Paola S. Denora et al. · Brain · 2007 · 246 citations

A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews

Israela Lerer, Michal Sagi, Ziva Ben‐Neriah et al. · Human Mutation · 2001 · 220 citations · Full text

Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis

Karin Buiting, Bärbel Dittrich, Stephanie Groß et al. · The American Journal of Human Genetics · 1998 · 215 citations · Full text

Developmental Anomaly, Genetic Disorder, Genetics +8

The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3

Vered Molho‐Pessach, Israela Lerer, Dvorah Abeliovich et al. · The American Journal of Human Genetics · 2008 · 202 citations · Full text

Molecular Physiology, Disease Mechanism, Mendelian Disorder +8