Search details
1.
Genetic etiology of hearing loss in Iran.
Hum Genet
; 141(3-4): 623-631, 2022 Apr.
Article
in English
| MEDLINE | ID: mdl-35050400
2.
Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.
Clin Genet
; 100(1): 59-78, 2021 07.
Article
in English
| MEDLINE | ID: mdl-33713422
3.
When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS).
J Hum Genet
; 65(7): 609-617, 2020 Jul.
Article
in English
| MEDLINE | ID: mdl-32231217
4.
C-reactive protein and complement factor H polymorphism interaction in advanced exudative age-related macular degeneration.
Int Ophthalmol
; 37(5): 1161-1168, 2017 Oct.
Article
in English
| MEDLINE | ID: mdl-27778189
5.
Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran.
J Med Genet
; 52(12): 823-9, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-26445815
6.
PDZD7 and hearing loss: More than just a modifier.
Am J Med Genet A
; 167A(12): 2957-65, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-26416264
7.
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.
NPJ Genom Med
; 9(1): 12, 2024 Feb 19.
Article
in English
| MEDLINE | ID: mdl-38374194
8.
Identification of a homozygous frameshift mutation in the FGF3 gene in a consanguineous Iranian family: First report of labyrinthine aplasia, microtia, and microdontia syndrome in Iran and literature review.
Mol Genet Genomic Med
; 11(5): e2168, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36934406
9.
Copy Number Variations in Hereditary Spastic Paraplegia-Related Genes: Evaluation of an Iranian Hereditary Spastic Paraplegia Cohort and Literature Review.
Mol Syndromol
; 14(6): 477-484, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-38058755
10.
An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene.
Arch Iran Med
; 26(3): 176-180, 2023 03 01.
Article
in English
| MEDLINE | ID: mdl-37543941
11.
A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran.
Am J Med Genet A
; 158A(10): 2485-92, 2012 Oct.
Article
in English
| MEDLINE | ID: mdl-22903915
12.
Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population.
Am J Med Genet A
; 158A(8): 1857-64, 2012 Aug.
Article
in English
| MEDLINE | ID: mdl-22736430
13.
Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population.
Ann Otol Rhinol Laryngol
; 119(12): 830-5, 2010 Dec.
Article
in English
| MEDLINE | ID: mdl-21250555
14.
G130V de novo mutation in an Iranian pedigree with nonsyndromic hearing loss without palmoplantar keratoderma.
Int J Pediatr Otorhinolaryngol
; 126: 109607, 2019 Nov.
Article
in English
| MEDLINE | ID: mdl-31419744
15.
Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases.
Mol Genet Genomic Med
; 7(8): e820, 2019 08.
Article
in English
| MEDLINE | ID: mdl-31210028
16.
SLC52A2 mutations cause SCABD2 phenotype: A second report.
Int J Pediatr Otorhinolaryngol
; 104: 195-199, 2018 Jan.
Article
in English
| MEDLINE | ID: mdl-29287867
17.
Investigating the CFH Gene Polymorphisms as a Risk Factor for Age-related Macular Degeneration in an Iranian Population.
Ophthalmic Genet
; 37(2): 144-9, 2016 06.
Article
in English
| MEDLINE | ID: mdl-25612476
18.
Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.
Arch Iran Med
; 19(10): 720-728, 2016 Oct 01.
Article
in English
| MEDLINE | ID: mdl-27743438
19.
Impact of whole exome sequencing among Iranian patients with autosomal recessive retinitis pigmentosa.
Arch Iran Med
; 18(11): 776-85, 2015 Nov.
Article
in English
| MEDLINE | ID: mdl-26497376
20.
Association of polymorphisms at LDLR locus with coronary artery disease independently from lipid profile.
Acta Med Iran
; 52(5): 352-9, 2014.
Article
in English
| MEDLINE | ID: mdl-24902015