Faezeh Mojahedi
Mashhad University of Medical Sciences(IR)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Hearing, Cochlea, Tinnitus, Genetics, Genomic variations and chromosomal abnormalities, RNA regulation and disease
Most-Cited Works
- → Deep sequencing reveals 50 novel genes for recessive cognitive disorders(2011)981 cited
- → Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders(2014)537 cited
- → Genetics of intellectual disability in consanguineous families(2018)210 cited
- → Sensorineural deafness and male infertility: a contiguous gene deletion syndrome(2006)140 cited
- → Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction(2015)134 cited
- → A clinical and molecular genetic study of 112 Iranian families with primary microcephaly(2010)93 cited
- → Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration(2018)86 cited
- → Effect of inbreeding on intellectual disability revisited by trio sequencing(2018)80 cited
- → The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss—A twelve year study(2012)41 cited