Bella Davidov

Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in Israel

Hagit Toledano‐Alhadef, Lina Basel‐Vanagaite, Nurit Magal et al. · The American Journal of Human Genetics · 2001 · 228 citations · Full text

Genetic Testing, Mendelian Disorder, Genetic Disorder +10

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families

Zippora Brownstein, Lilach M. Friedman, Hashem Shahin et al. · Genome biology · 2011 · 201 citations · Full text

Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel

Jun Shen, Andrea M. Oza, Ignacio del Castillo et al. · Genetics in Medicine · 2019 · 98 citations · Full text

Genetics, P.val37ile Variants, Genetic Epidemiology +5

Amniotic trisomy 11 mosaicism—is it a benign finding?

Lina Basel‐Vanagaite, Bella Davidov, J. Friedman et al. · Prenatal Diagnosis · 2006 · 80 citations

Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis

Pamela Magini, Daphne J. Smits, Laura Vandervore et al. · The American Journal of Human Genetics · 2019 · 79 citations · Full text

Developmental Anomaly, Developmental Disorder Characterized, Developmental Biology +6