|Detection of copy number changes in genes associated with Parkinson's disease in Iranian patients|
H Darvish, A Movafagh, MD Omrani, SG Firouzabadi, E Azargashb, ...
Neuroscience letters 551, 75-78, 2013
|A clinical and molecular genetic study of 50 families with autosomal recessive parkinsonism revealed known and novel gene mutations|
S Taghavi, R Chaouni, A Tafakhori, LJ Azcona, SG Firouzabadi, ...
Molecular neurobiology 55 (4), 3477-3489, 2018
|Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population|
L Haghnejad, B Emamalizadeh, J Jamshidi, AZ Bidoki, H Ghaedi, ...
Journal of the neurological sciences 355 (1-2), 72-74, 2015
|RIT2, a susceptibility gene for Parkinson's disease in Iranian population.|
B Emamalizadeh, A Movafagh, M Akbari, S Kazeminasab, A Fazeli, ...
Neurobiology of aging 35 (12), e27, 2014
|HLA‐DRA is associated with Parkinson's disease in Iranian population|
J Jamshidi, A Movafagh, B Emamalizadeh, A Zare Bidoki, A Manafi, ...
International journal of immunogenetics 41 (6), 508-511, 2014
|RIT2 Polymorphisms: Is There a Differential Association?|
B Emamalizadeh, J Jamshidi, A Movafagh, M Ohadi, S Kazeminasab, ...
Molecular neurobiology 54 (3), 2234-2240, 2017
|Analysis of CYP17, CYP19 and CYP1A1 gene polymorphisms in Iranian women with breast cancer|
F Farzaneh, G Noghabaei, E Barouti, F Pouresmaili, J Jamshidi, A Fazeli, ...
Age 52 (52.5), 0.18, 2016
|The human RIT2 core promoter short tandem repeat predominant allele is species-specific in length: a selective advantage for human evolution?|
B Emamalizadeh, A Movafagh, H Darvish, S Kazeminasab, M Andarva, ...
Molecular genetics and genomics 292 (3), 611-617, 2017
|Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population|
F Madadi, MS Khaniani, EE Shandiz, H Ayromlou, S Najmi, ...
Genetic testing and molecular biomarkers 20 (10), 629-632, 2016
|Dominant and protective role of the CYTH4 primate-specific GTTT-repeat longer alleles against neurodegeneration|
M Rezazadeh, J Gharesouran, A Movafagh, M Taheri, H Darvish, ...
Journal of Molecular Neuroscience 56 (3), 593-596, 2015
|The rs1572931 polymorphism of the RAB7L1 gene promoter is associated with reduced risk of Parkinson's disease|
M Goudarzian, A Khaligh, R Fourozan, S Jamal Mirmoosavi, H Darvish, ...
Neurological research 37 (11), 1029-1031, 2015
|RAB7L1 promoter polymorphism and risk of Parkinson’s disease; a case-control study|
A Khaligh, M Goudarzian, A Moslem, A Mehrtash, J Jamshidi, H Darvish, ...
Neurological research 39 (5), 468-471, 2017
|A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder|
M Atakhorrami, S Rahimi-Aliabadi, J Jamshidi, E Moslemi, A Movafagh, ...
Journal of Neural Transmission 123 (3), 323-328, 2016
|Hepatitis B virus infection in patients with blood disorders: a concise review in pediatric study|
N Mansouri, A Movafagh, A Sayad, S Ghafouri-Fard, H Darvish, ...
Iranian journal of pediatric hematology and oncology 4 (4), 178, 2014
|A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome|
S Rahimi-Aliabadi, N Daftarian, H Ahmadieh, B Emamalizadeh, ...
Eye 30 (11), 1424, 2016
|SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control study|
T Safaralizadeh, J Jamshidi, EE Shandiz, A Movafagh, A Fazeli, ...
Journal of the neurological sciences 369, 1-4, 2016
|The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson’s disease in Iranian population|
N Shahmohammadibeni, S Rahimi-Aliabadi, J Jamshidi, ...
Neurological Sciences 37 (5), 731-736, 2016
|Monoamine oxidase a gene polymorphisms and bipolar disorder in Iranian population|
MRE Amirabadi, SR Esfahani, R Davari-Ashtiani, M Khademi, ...
Iranian Red Crescent Medical Journal 17 (2), 2015
|Functional Genetic Variants of FOXP3 and Risk of Multiple Sclerosis|
M Gholami, H Darvish, H Ahmadi, S Rahimi-Aliabadi, B Emamalizadeh, ...
Iranian Red Crescent Medical Journal 19 (1), 2017
|c. 376G> A mutation in WFS1 gene causes Wolfram syndrome without deafness|
BS Lima, H Ghaedi, N Daftarian, H Ahmadieh, J Jamshidi, M Khorrami, ...
European journal of medical genetics 59 (2), 65-69, 2016