F. Mojahedi

发表

Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders

T. Ideker, J. Al-Aama, Matan Hofree, 2014, Science.

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Wei Chen, Reinhard Ullmann, Dagmar Wieczorek, 2011, Nature.

Sensorineural deafness and male infertility: a contiguous gene deletion syndrome

K. Kahrizi, H. Najmabadi, F. Mojahedi, 2006, Journal of Medical Genetics.

Identification of disease‐causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families

H. Ropers, A. Kariminejad, V. Kalscheuer, 2019, Clinical genetics.

Chromosome abnormality rate among Iranian patients with idiopathic mental retardation from consanguineous marriages

K. Kahrizi, H. Najmabadi, F. Mojahedi, 2011, Archives of medical science : AMS.

Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica

A. Kariminejad, E. Morava, F. Mojahedi, 2017, International journal of molecular sciences.

Gene dosage analysis of proximal spinal muscular atrophy carriers using real-time PCR.

F. Mojahedi, M. Abbaszadegan, F. Ashrafzadeh, 2011, Archives of Iranian medicine.

Investigation of microdeletions in syndromic intellectual disability by MLPA in Iranian population.

A. Kariminejad, H. Najmabadi, F. Mojahedi, 2014, Archives of Iranian medicine.

Effect of inbreeding on intellectual disability revisited by trio sequencing

T. Wienker, H. Ropers, V. Kalscheuer, 2018, Clinical genetics.

Genetics of intellectual disability in consanguineous families

T. Wienker, Wei Chen, R. Herwig, 2019, Molecular Psychiatry.

Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction

S. Gabriel, J. Casanova, E. Dikoglu, 2015, Nature Genetics.

Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of hearing loss in Iranian population.

K. Kahrizi, H. Najmabadi, F. Mojahedi, 2015, International journal of pediatric otorhinolaryngology.

Bi-allelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 over-activity and disordered cortical neuronal migration

Kiely N. James, Martin W. Breuss, I. Miller, 2018, Nature Genetics.

Sensorineural deafness and male infertility: a contiguous gene deletion syndrome

K. Kahrizi, H. Najmabadi, F. Mojahedi, 2009, BMJ Case Reports.

The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.

K. Kahrizi, H. Najmabadi, F. Mojahedi, 2012, International journal of pediatric otorhinolaryngology.

Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration

Kiely N. James, Martin W. Breuss, A. Caglayan, 2018, Nature Genetics.

Adverse events following immunisation with the first dose of sputnik V among Iranian health care providers

F. Mojahedi, H. Bidkhori, S. A. Shamsian, 2023, Clinical and experimental vaccine research.

A clinical and molecular genetic study of 112 Iranian families with primary microcephaly

H. Ropers, A. Tzschach, K. Kahrizi, 2010, Journal of Medical Genetics.