| 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, 3477-3489, 2018 | 77 | 2018 |
| 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 | 45 | 2013 |
| RIT2 Polymorphisms: Is There a Differential Association? B Emamalizadeh, J Jamshidi, A Movafagh, M Ohadi, MS Khaniani, ... Molecular neurobiology 54, 2234-2240, 2017 | 35 | 2017 |
| RIT2, a susceptibility gene for Parkinson’s disease in Iranian population B Emamalizadeh, A Movafagh, M Akbari, S Kazeminasab, A Fazeli, ... Neurobiol Aging 35 (12), e27-e28, 2014 | 30 | 2014 |
| 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 | 29 | 2015 |
| 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 | 29 | 2014 |
| 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, 611-617, 2017 | 21 | 2017 |
| Features, genetics and their correlation in Jalili syndrome: a systematic review Y Daneshmandpour, H Darvish, F Pashazadeh, B Emamalizadeh Journal of Medical Genetics 56 (6), 358-369, 2019 | 20 | 2019 |
| 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, 323-328, 2016 | 20 | 2016 |
| 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 | 19 | 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, ... Asian Pacific Journal of Cancer Prevention 17 (sup3), 23-26, 2016 | 18 | 2016 |
| An updated overview and classification of bioinformatics tools for MicroRNA analysis, which one to choose? SS Mortazavi, Z Bahmanpour, Y Daneshmandpour, F Roudbari, ... Computers in biology and medicine 134, 104544, 2021 | 17 | 2021 |
| RIT2: responsible and susceptible gene for neurological and psychiatric disorders Y Daneshmandpour, H Darvish, B Emamalizadeh Molecular genetics and genomics 293, 785-792, 2018 | 17 | 2018 |
| 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 | 17 | 2015 |
| 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), 1424-1432, 2016 | 16 | 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, 593-596, 2015 | 16 | 2015 |
| Macromolecular biomarkers of chronic obstructive pulmonary disease in exhaled breath condensate S Kazeminasab, B Emamalizadeh, A Jouyban, MM Shoja, ... Biomarkers in Medicine 14 (11), 1047-1063, 2020 | 15 | 2020 |
| 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, 731-736, 2016 | 15 | 2016 |
| Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy M Chapi, H Sabbaghi, F Suri, E Alehabib, S Rahimi-Aliabadi, F Jamali, ... Ophthalmic Genetics 40 (3), 259-266, 2019 | 14 | 2019 |
| 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 | 14 | 2016 |
