Publications by authors named "Bella Davidov"

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A multicenter study reveals a novel pathogenic splice-site founder variant in OTOF.
Zippora Brownstein, Lara Kamal, Shir Mishan-Montefiori, Yael Hoffman, Dina Fine, Bella Davidov

Hum Genomics· October 2025

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Agenesis of the Ductus Venosus and Its Association With Genetic Abnormalities.
Yarin Mash, Ron Bardin, Yinon Gilboa, Yossi Geron, Asaf Romano, Bella Davidov

Prenat Diagn· December 2024

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Pathogenic variant-based preconception carrier screening in the Israeli Jewish population.
Bella Davidov, Amit Levon, Hadas Volkov, Naama Orenstein, Racheli Karo

Clin Genet· May 2022

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A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing.
Yoel Hirsch, Chayada Tangshewinsirikul, Kevin T Booth, Hela Azaiez, Devorah Yefet, Bella Davidov

Eur J Hum Genet· June 2021

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Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.
Zippora Brownstein, Suleyman Gulsuner, Tom Walsh, Fábio T A Martins, Shahar Taiber, Bella Davidov

Clin Genet· October 2020

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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, Hatice Duzkale, Tatsuo Matsunaga, Bella Davidov

Genet Med· November 2019

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Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis.
Pamela Magini, Daphne J Smits, Laura Vandervore, Rachel Schot, Marta Columbaro, Bella Davidov

Am J Hum Genet· October 2019

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[UTILIZATION OF WHOLE EXOME SEQUENCING IN DIAGNOSTICS OF GENETIC DISEASE: RABIN MEDICAL CENTER'S EXPERIENCE].
Lior Cohen, Naama Orenstein, Monica Weisz-Hubshman, Lily Bazak, Bella Davidov

Harefuah· April 2017

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Nonvisualization of the Fetal Gallbladder: Can Levels of Gamma-Glutamyl Transpeptidase in Amniotic Fluid Predict Fetal Prognosis?
Ron Bardin, Eran Ashwal, Bella Davidov, David Danon, Mordechai Shohat

Fetal Diagn Ther· November 2016

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A founder mutation in ADAMTSL4 causes early-onset bilateral ectopia lentis among Jews of Bukharian origin.
Eyal Reinstein, Pola Smirin-Yosef, Irina Lagovsky, Bella Davidov, Gabriela Peretz Amit

Mol Genet Metab· January 2016

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Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing.
Zippora Brownstein, Amal Abu-Rayyan, Daphne Karfunkel-Doron, Serena Sirigu, Bella Davidov

Eur J Hum Genet· June 2014

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The many faces of sensorineural hearing loss: one founder and two novel mutations affecting one family of mixed Jewish ancestry.
Doron M Behar, Bella Davidov, Zippora Brownstein, Tamar Ben-Yosef, Karen B Avraham

Genet Test Mol Biomarkers· February 2014

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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, Varda Oron-Karni, Nitzan Kol, Bella Davidov

Genome Biol· September 2011

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Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.
Idit Maya, Bella Davidov, Liron Gershovitz, Yael Zalzstein, Ellen Taub

Prenat Diagn· December 2010

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Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in Israel.
Lina Basel-Vanagaite, Ellen Taub, Gabrielle J Halpern, Valerie Drasinover, Nurit Magal, Bella Davidov

Eur J Hum Genet· February 2007

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Amniotic trisomy 11 mosaicism--is it a benign finding?
Lina Basel-Vanagaite, Bella Davidov, Jane Friedman, Yosefa Yeshaya, Nurit Magal

Prenat Diagn· September 2006

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Chromosome aberration and environmental physical activity: Down syndrome and solar and cosmic ray activity, Israel, 1990-2000.
Eliahu G Stoupel, Helena Frimer, Zvi Appelman, Ziva Ben-Neriah, Hanna Dar, Bella Davidov

Int J Biometeorol· September 2005

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Prenatal diagnosis of Down syndrome: ten year experience in the Israeli population.
Mordechai Shohat, Helena Frimer, Vered Shohat-Levy, Hormoz Esmailzadeh, Zvi Appelman, Bella Davidov

Am J Med Genet A· October 2003

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