babak emamalizadeh
babak emamalizadeh
Assistant Proffessor, Department of Medical Genetics, Tabriz University of Medical Sciences, Tabriz
Verified email at tbzmed.ac.ir
TitleCited byYear
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
252013
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
212018
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
192015
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
162014
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
142014
RIT2 Polymorphisms: Is There a Differential Association?
B Emamalizadeh, J Jamshidi, A Movafagh, M Ohadi, S Kazeminasab, ...
Molecular neurobiology 54 (3), 2234-2240, 2017
122017
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
112016
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
92017
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
92016
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
92015
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
82015
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
72017
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
72016
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
72014
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
62016
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
62016
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
62016
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
62015
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
52017
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
42016
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