Miriam Regev
0009-0001-8854-8948
Publication & Citation Trends
Publications
0 total
Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria OA
Cited by 25
Semantic Scholar
Orbital Lymphatic-Venous Malformation Accompanied by an Intraocular Vascular Malformation: A Rare Case Study OA
Cited by 0
Semantic Scholar
A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies OA
Cited by 15
Semantic Scholar
A founder mutation in TCTN2 causes Meckel‐Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin
Cited by 4
Semantic Scholar
Phenotype variability in Hajdu-Cheney syndrome.
Cited by 12
Semantic Scholar
Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families OA
Cited by 35
Semantic Scholar
Fishing for Genes in Autoimmunity.
Cited by 2
Semantic Scholar
Involvement of Rho GAP GRAF1 in maintenance of epithelial phenotype OA
Cited by 8
Semantic Scholar
Congenital myopathy is caused by mutation of HACD1 OA
Cited by 56
Semantic Scholar
Research Topics
Genomic variations and chromosomal abnormalities
(4)
Genomics and Rare Diseases
(4)
Genetics and Neurodevelopmental Disorders
(4)
Prenatal Screening and Diagnostics
(3)
Diverse Scientific and Economic Studies
(3)
Affiliations
Tel Aviv University
Sheba Medical Center
Assaf Harofeh Medical Center
Institute of Genetics
Research Network (United States)