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Hajar aryan
Hajar aryan
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Year
Complement factor H Y402H and LOC387715 A69S polymorphisms in association with age-related macular degeneration in Iran
HN Khanamiri, KG Falavarjani, MH Sanati, H Aryan, A Irani, M Hashemi, ...
Journal of Ophthalmic & Vision Research 9 (2), 181, 2014
272014
Genetic polymorphisms in calcitonin receptor gene and risk for recurrent kidney calcium stone disease
N Shakhssalim, A Basiri, M Houshmand, H Pakmanesh, B Golestan, ...
Urologia Internationalis 92 (3), 356-362, 2014
202014
Novel imaging and clinical phenotypes of CONDSIAS disorder caused by a homozygous frameshift variant of ADPRHL2: a case report
H Aryan, E Razmara, D Farhud, M Zarif-Yeganeh, S Zokaei, SA Hassani, ...
BMC neurology 20, 1-11, 2020
192020
The Effect of TGF-β2 on MMP-2 Production and Activity in Highly Metastatic Human Bladder Carcinoma Cell Line 5637
E Dehnavi, ZS Soheili, S Samiei, Z Ataei, H Aryan
Cancer investigation 27 (5), 568-574, 2009
192009
Novel mutations in Sandhoff disease: a molecular analysis among Iranian cohort of infantile patients
H Aryan, O Aryani, K Banihashemi, T Zaman, M Houshmand
Iranian journal of public health 41 (3), 112, 2012
152012
Association of Htra1 gene polymorphisms with the risk of developing AMD in Iranian population
M Askari, AR Nikpoor, F Gorjipour, M Mazidi, MH Sanati, H Aryan, A Irani, ...
Reports of biochemistry & molecular biology 4 (1), 43, 2015
82015
A homozygote mutation in S-antigen visual arrestin SAG gene in an Iranian patient with Oguchi type one: a case report
H Aryan, A Bahadori, DD Farhud, MZ Yeganeh, H Pourkalhor
Iranian Journal of Public Health 49 (5), 995, 2020
52020
Novel phenotype and genotype spectrum of WDR62 in two patients with associated primary autosomal recessive microcephaly
H Aryan, S Zokaei, D Farhud, M Keykhaei, MR Ashrafi, M Rasulinezhad, ...
Irish Journal of Medical Science (1971-), 1-9, 2022
22022
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry
M Ashrafi, R Kameli, S Hosseinpour, E Razmara, Z Zamani, Z Rezaei, ...
neurogenetics 24 (4), 279-289, 2023
12023
Identification of PI3K Isoforms in Human Prostate Cancer Cell Lines (PC3, DU145) and Human Bladder Carcinoma Cell line (5637)
H Aryan, ZS Soheili
Journal of Cell and Molecular Research 7 (1), 3-10, 2015
12015
Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients
AZ Dehnavi, M Bemanalizadeh, SM Kahani, MR Ashrafi, M Rohani, ...
Orphanet journal of rare diseases 18 (1), 177, 2023
2023
Association of Apolipoprotein E Alleles with Susceptibility to Age-Related Macular Degeneration in Iranian Patients
M Askari, AR Nikpoor, H Aryan, H Ghaedi, J Akhtari, A Azarnejad, ...
Research in Molecular Medicine 3 (2), 22-27, 2015
2015
MUTATION SPECTRUM IN KCNQ1 AND KCNH2 GENES IN IRANIAN LONG QT SYNDROME PATIENTS: O053
K Banihashemi, S Saber, M Houshmand, Z Moradmand, H Aryan, ...
Pacing and Clinical Electrophysiology 34 (11), 2011
2011
A COMPREHENSIVE GENETIC STUDY ON CALCIUM SENSING RECEPTOR, CALCITONIN RECEPTOR, VITAMIN D RECEPTOR AND ANDROGEN RECEPTOR IN RELATIONSHIP WITH RECURRENT CALCIUM KIDNEY STONE FORMERS
A Basiri, N Shakhssalim, M Houshmand, B Kazemi, H Pakmanesh, ...
JOURNAL OF ENDOUROLOGY 24, A20-A20, 2010
2010
A new pathogenic mutation in cystic fibrosis patients
M Badalzadeh, SS Hassani, S Dadgar, H Aryan, O Aryani, Z Pourpak, ...
ALLERGY 64, 415-415, 2009
2009
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AZ Dehnavi, M Bemanalizadeh, SM Kahani, MR Ashrafi, M Rohani, ...
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