Idit Maya

Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in <i>PIGN</i>

G. Maydan, Iris Noyman, Adi Har‐Zahav et al. · Journal of Medical Genetics · 2011 · 149 citations

RIN2 Deficiency Results in Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis: MACS Syndrome

Lina Basel‐Vanagaite, Ofer Sarig, Dov Hershkovitz et al. · The American Journal of Human Genetics · 2009 · 97 citations · Full text

Cutis Laxa, Pathology, Dermatology +4

Diagnostic utility of array‐based comparative genomic hybridization (aCGH) in a prenatal setting

Idit Maya, Bella Davidov, Liron Gershovitz et al. · Prenatal Diagnosis · 2010 · 78 citations

Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies

Lena Sagi‐Dain, Lital Cohen Vig, Sarit Kahana et al. · Genetics in Medicine · 2019 · 66 citations · Full text

When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations

Idit Maya, Reuven Sharony, Shiri Yacobson et al. · Genetics in Medicine · 2017 · 61 citations · Full text

Reproductive Genetic Counseling, Counseling, Genetic Testing +8