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Author Details

Faezeh Mojahedi
Blood Borne Infections Research Center, Academic Center for Education
2007
16
10
Trey Ideker (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36844688Adverse events following immunisation with the first dose of sputnik V among Iranian health care providers.Clin Exp Vaccine Res2023
29302074Genetics of intellectual disability in consanguineous families.Mol Psychiatry2019
30950035Identification of disease-causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families.Clin Genet2019
30315573Effect of inbreeding on intellectual disability revisited by trio sequencing.Clin Genet2019
30013181Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration.Nat Genet2018
28294978Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica.Int J Mol Sci2017
25555641Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of hearing loss in Iranian population.Int J Pediatr Otorhinolaryngol2015
25848753Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.Nat Genet2015
24482476Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.Science2014
24979557Investigation of microdeletions in syndromic intellectual disability by MLPA in Iranian population.Arch Iran Med2014
22695344The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.Int J Pediatr Otorhinolaryngol2012
21529108Gene dosage analysis of proximal spinal muscular atrophy carriers using real-time PCR.Arch Iran Med2011
22291774Chromosome abnormality rate among Iranian patients with idiopathic mental retardation from consanguineous marriages.Arch Med Sci2011
21937992Deep sequencing reveals 50 novel genes for recessive cognitive disorders.Nature2011
21686705Sensorineural deafness and male infertility: a contiguous gene deletion syndrome.BMJ Case Rep2009
17098888Sensorineural deafness and male infertility: a contiguous gene deletion syndrome.J Med Genet2007
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Collaborators

Ariana Kariminejad
Clinical Genetics Deaprtment
Co-authored papers 5
Joseph G Gleeson
University of California
Co-authored papers 3
Eric Scott
Rady Children's Institute for Genomic Medicine, University of California
Co-authored papers 3
Rasim O Rosti
University of Virginia
Co-authored papers 3
Murat Gunel
Yale School of Medicine
Co-authored papers 3
H??lya Kayserili
Istanbul University
Co-authored papers 3
Jennifer L Silhavy
University of California
Co-authored papers 3
Maha S Zaki
Human Genetics and Genome Research Institute, National Research Centre
Co-authored papers 3
Ahmet Okay Caglayan
Yale School of Medicine
Co-authored papers 2
Tawfeg Ben-Omran
Hamad Medical Corporation.
Co-authored papers 2
Majdi Kara
University of Tripoli, Tripoli Children's Hospital
Co-authored papers 2
Jana Schroth
University of California
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Keith K Vaux
university of california san diego Health Physician Network
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Lobna Mansour
Cairo University Children Hospital
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Hisham Megahed
Clinical Genetics Department, National Research Centre
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Brett Copeland
University of California
Co-authored papers 2
Amira Masri
The University of Jordan
Co-authored papers 2
B??lent Kara
Kocaeli University Faculty of Medicine
Co-authored papers 2
Matloob Azam
Wah Medical College
Co-authored papers 2
Kaya Bilguvar
Acibadem Mehmet Ali Aydinlar University
Co-authored papers 2
Basak Rosti
Howard Hughes Medical Institute, The Rockefeller University
Co-authored papers 2
Naiara Akizu
University of Pennsylvania
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Laila Selim
Cairo University
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Stacey Gabriel
Broad Institute of MIT and Harvard
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Ghada M H Abdel-Salam
Human Genetics and Genome Research Institute, National Research Centre
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Sylvie Forlani
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Release 1.2