Michal Macarov

Deletions of VCX‐A and NLGN4: a variable phenotype including normal intellect

Michal Macarov, M. Zeigler, J. P. Newman et al. · Journal of Intellectual Disability Research · 2006 · 67 citations

Universal chromosomal microarray analysis reveals high proportion of copy‐number variants in low‐risk pregnancies

Shira Stern, Nuphar Hacohen, Vardiella Meiner et al. · Ultrasound in Obstetrics and Gynecology · 2020 · 46 citations · Full text

Novel and Recurrent FERMT1 Gene Mutations in Kindler Syndrome

Tanasit Techanukul, Gomathy Sethuraman, Abraham Zlotogorski et al. · Acta Dermato Venereologica · 2011 · 29 citations · Full text

Genetics, Pathology, Integrin Signalling +17

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene <scp> <i>ATOH1</i> </scp>

Zippora Brownstein, Süleyman Gülsüner, Tom Walsh et al. · Clinical Genetics · 2020 · 28 citations · Full text

Preimplantation genetic diagnosis as a strategy to prevent having a child born with an heritable eye disease

Claudia Yahalom, Michal Macarov, Galit Lazer-Derbeko et al. · Ophthalmic Genetics · 2018 · 26 citations