|Deep sequencing reveals 50 novel genes for recessive cognitive disorders|
H Najmabadi, H Hu, M Garshasbi, T Zemojtel, SS Abedini, W Chen, ...
Nature 478 (7367), 57-63, 2011
|Genetics of intellectual disability in consanguineous families|
H Hu, K Kahrizi, L Musante, Z Fattahi, R Herwig, M Hosseini, C Oppitz, ...
Molecular psychiatry 24 (7), 1027-1039, 2019
|A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran|
M Babanejad, Z Fattahi, N Bazazzadegan, C Nishimura, N Meyer, ...
American journal of medical genetics Part A 158 (10), 2485-2492, 2012
|Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population|
Z Fattahi, AE Shearer, M Babanejad, N Bazazzadegan, SN Almadani, ...
American Journal of Medical Genetics Part A 158 (8), 1857-1864, 2012
|The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss—a twelve year study|
N Bazazzadegan, N Nikzat, Z Fattahi, C Nishimura, N Meyer, S Sahraian, ...
International journal of pediatric otorhinolaryngology 76 (8), 1164-1174, 2012
|The role of a novel TRMT1 gene mutation and rare GRM1 gene defect in intellectual disability in two Azeri families|
B Davarniya, H Hu, K Kahrizi, L Musante, Z Fattahi, M Hosseini, ...
PLoS One 10 (8), e0129631, 2015
|Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation|
MS Hildebrand, NP Thorne, CJ Bromhead, K Kahrizi, JA Webster, ...
Clinical genetics 77 (6), 563-571, 2010
|Iranome: A catalog of genomic variations in the Iranian population|
Z Fattahi, M Beheshtian, M Mohseni, H Poustchi, E Sellars, SH Nezhadi, ...
Human mutation 40 (11), 1968-1984, 2019
|A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability|
F Larti, K Kahrizi, L Musante, H Hu, E Papari, Z Fattahi, N Bazazzadegan, ...
European Journal of Human Genetics 23 (3), 331-336, 2015
|Effect of inbreeding on intellectual disability revisited by trio sequencing|
K Kahrizi, H Hu, M Hosseini, VM Kalscheuer, Z Fattahi, M Beheshtian, ...
Clinical Genetics 95 (1), 151-159, 2019
|Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss|
B Davarnia, M Babanejad, Z Fattahi, N Nikzat, N Bazazzadegan, ...
International Journal of Pediatric Otorhinolaryngology 76 (2), 268-271, 2012
|Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping|
JS Amos, L Huang, J Thevenon, A Kariminedjad, CL Beaulieu, ...
Clinical genetics 91 (1), 92-99, 2017
|Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population|
Z Fattahi, Z Kalhor, M Fadaee, R Vazehan, E Parsimehr, A Abolhassani, ...
Clinical genetics 91 (3), 386-402, 2017
|Mutation profile of BBS genes in Iranian patients with Bardet–Biedl syndrome: genetic characterization and report of nine novel mutations in five BBS genes|
Z Fattahi, P Rostami, A Najmabadi, M Mohseni, K Kahrizi, MR Akbari, ...
Journal of human genetics 59 (7), 368-375, 2014
|Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration|
Z Iqbal, L Püttmann, L Musante, A Razzaq, MY Zahoor, H Hu, TF Wienker, ...
European Journal of Human Genetics 24 (3), 392-399, 2016
|Report of a patient with limb-girdle muscular dystrophy, ptosis and ophthalmoparesis caused by plectinopathy|
Z Fattahi, K Kahrizi, S Nafissi, M Fadaee, SS Abedini, A Kariminejad, ...
Archives of Iranian medicine 18 (1), 0-0, 2015
|Prevalence of ACTN3 (the athlete gene) R577X polymorphism in Iranian population|
Z Fattahi, H Najmabadi
Iranian Red Crescent Medical Journal 14 (10), 617, 2012
|Did the GJB2 35delG mutation originate in Iran?|
V Norouzi, H Azizi, Z Fattahi, F Esteghamat, N Bazazzadegan, ...
American journal of medical genetics Part A 155 (10), 2453-2458, 2011
|Distinct genetic variation and heterogeneity of the Iranian population|
Z Mehrjoo, Z Fattahi, M Beheshtian, M Mohseni, H Poustchi, F Ardalani, ...
PLoS genetics 15 (9), e1008385, 2019
|Whole Genome Linkage Analysis Followed by Whole Exome Sequencing Identifies Nicastrin (NCSTN) as a Causative Gene in a Multiplex Family with γ-Secretase Spectrum of …|
ZM Faraji, F Sabbagh-Kermani, Z Fattahi, M Fadaee, MR Akbari, R Amiri, ...
The Journal of investigative dermatology 136 (6), 1283, 2016