Nurit Magal

Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in Israel

Hagit Toledano‐Alhadef, Lina Basel‐Vanagaite, Nurit Magal et al. · The American Journal of Human Genetics · 2001 · 228 citations · Full text

Genetic Testing, Mendelian Disorder, Genetic Disorder +10

Phenotype–genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis

Mordechai Shohat, Nurit Magal, Tami Shohat et al. · European Journal of Human Genetics · 1999 · 210 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +9

Autosomal Recessive Ichthyosis with Hypotrichosis Caused by a Mutation in ST14, Encoding Type II Transmembrane Serine Protease Matriptase

Lina Basel‐Vanagaite, Revital Attia, Akemi Ishida‐Yamamoto et al. · The American Journal of Human Genetics · 2007 · 188 citations · Full text

Autosomal Recessive Ichthyosis, Medicine, Genetics +5

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

Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups

Nava Stoffman, Nurit Magal, Tamy Shohat et al. · European Journal of Human Genetics · 2000 · 146 citations

Healthcare-associated Infection, Genetic Epidemiology, Disease Outbreak +5