Bella Davidov

Rafael Advanced Defense Systems (Israel) — Israel

Neuroscience · Life Sciences

14h-index1.0kcitations27works1.02yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Hearing, Cochlea, Tinnitus, Genetics(10), Prenatal Screening and Diagnostics(5), Ear Surgery and Otitis Media(4), Hearing Loss and Rehabilitation(3), RNA and protein synthesis mechanisms(3)

Publications27 total

A multicenter study reveals a novel pathogenic splice-site founder variant in OTOF
Human Genomics·2025Open Access
Agenesis of the Ductus Venosus and Its Association With Genetic Abnormalities
Prenatal Diagnosis·2024· 2 citedOpen Access
Pathogenic variant‐based preconception carrier screening in the <scp>Israeli Jewish</scp> population
Clinical Genetics·2022· 8 cited
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing
European Journal of Human Genetics·2021· 14 citedOpen Access
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene <scp> <i>ATOH1</i> </scp>
Clinical Genetics·2020· 28 citedOpen Access
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene <i>ATOH1</i>
2020· 1 cited
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel
PMC·2019
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis
The American Journal of Human Genetics·2019· 79 citedOpen Access
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel
Genetics in Medicine·2019· 98 citedOpen Access
Consensus interpretation of the Met34Thr and Val37Ile variants in <i>GJB2</i> by the ClinGen Hearing Loss Expert Panel
2018· 1 citedOpen Access
[UTILIZATION OF WHOLE EXOME SEQUENCING IN DIAGNOSTICS OF GENETIC DISEASE: RABIN MEDICAL CENTER'S EXPERIENCE].
PubMed·2017
A founder mutation in ADAMTSL4 causes early-onset bilateral ectopia lentis among Jews of Bukharian origin
Molecular Genetics and Metabolism·2015· 18 cited
Nonvisualization of the Fetal Gallbladder: Can Levels of &amp;#947;-Glutamyl Transpeptidase in Amniotic Fluid Predict Fetal Prognosis&amp;#947;
Fetal Diagnosis and Therapy·2015· 22 cited
Founder mutation for Huntington disease in Caucasus Jews
Clinical Genetics·2014· 7 cited
The Many Faces of Sensorineural Hearing Loss: One Founder and Two Novel Mutations Affecting One Family of Mixed Jewish Ancestry
Genetic Testing and Molecular Biomarkers·2013· 13 citedOpen Access
Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing
European Journal of Human Genetics·2013· 48 citedOpen Access
Abstracts* <sup>)</sup> : Israel Society for Auditory Research (ISAR) 2013 Annual Scientific Conference
Journal of Basic and Clinical Physiology and Pharmacology·2013Open Access
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families
Genome biology·2011· 201 citedOpen Access
Diagnostic utility of array‐based comparative genomic hybridization (aCGH) in a prenatal setting
Prenatal Diagnosis·2010· 78 cited
Escroto agudo como presentación de apendicitis aguda. Presentación de un caso y revisión de la literatura
Revista Mexicana de Urología·2008· 2 citedOpen Access
page 1 of 2Next →

Frequent Co-authors

Mordechai Shohat(12), Lina Basel‐Vanagaite(11), Zippora Brownstein(11), Karen B. Avraham(10), Moshe Frydman(7), Dorit Lev(6), Nurit Magal(5), Amal Abu Rayyan(5), Yoel Hirsch(5), Tzvi Weiden(5), Moien Kanaan(4), Jun Shen(4), Andrea M. Oza(4), Margaret A. Kenna(4), Minjie Luo(4), Sami S. Amr(4), Heidi L. Rehm(4), Hanna Dar(4), Boleslaw Goldman(4), Valerie Drasinover(3)