Adina Quint

Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi Jewish Patients With Autosomal Recessive Nonsyndromic Hearing Loss

D. Corey, J. Ekstein, K. Booth, 2021, Frontiers in Genetics.

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

H. Rehm, D. Kolbe, C. Morton, 2021, European Journal of Human Genetics.

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

H. Rehm, D. Kolbe, C. Morton, 2021, European Journal of Human Genetics.

An Ashkenazi founder mutation in the PKHD1 gene.

S. Carmi, H. Daum, I. Lerer, 2016, European journal of medical genetics.

Mutation spectrum in Jewish cystic fibrosis patients in Israel: Implication to carrier screening

I. Lerer, D. Abeliovich, M. Sagi, 2005, American journal of medical genetics. Part A.

Cystic Fibrosis Heterozygote Screening in the Orthodox Community of Ashkenazi Jews: The Dor Yesharim Approach and Heterozygote Frequency

I. Lerer, D. Abeliovich, J. Ekstein, 1996, European journal of human genetics : EJHG.