| A cohort study protocol to analyze the predisposing factors to common chronic non-communicable diseases in rural areas: Fasa Cohort Study M Farjam, H Bahrami, E Bahramali, J Jamshidi, A Askari, H Zakeri, ... BMC public health 16, 1-8, 2016 | 100 | 2016 |
| 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 | 88 | 2018 |
| Association between Vitamin D Receptor Gene BsmI Polymorphism and Bone Mineral Density in A Population of 146 Iranian Women. F Pouresmaeili, J Jamshidi, E Azargashb Cell Journal 15 (1), 75-82, 2013 | 61 | 2013 |
| Association of ACE gene D polymorphism with left ventricular hypertrophy in patients with diastolic heart failure: a case–control study E Bahramali, M Rajabi, J Jamshidi, SM Mousavi, M Zarghami, A Manafi, ... BMJ open 6 (2), e010282, 2016 | 57 | 2016 |
| 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 | 49 | 2013 |
| RIT2 Polymorphisms: Is There a Differential Association? B Emamalizadeh, J Jamshidi, A Movafagh, M Ohadi, MS Khaniani, ... Molecular neurobiology 54, 2234-2240, 2017 | 39 | 2017 |
| PTRHD1 (C2orf79) mutations lead to autosomal‐recessive intellectual disability and parkinsonism H Khodadadi, LJ Azcona, V Aghamollaii, MD Omrani, M Garshasbi, ... Movement Disorders 32 (2), 287-291, 2017 | 38 | 2017 |
| Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome SG Firouzabadi, R Kariminejad, R Vameghi, H Darvish, H Ghaedi, ... Molecular neurobiology 54, 7019-7027, 2017 | 34 | 2017 |
| Association of renin–angiotensin–aldosterone system gene polymorphisms with left ventricular hypertrophy in patients with heart failure with preserved ejection fraction: a case … E Bahramali, N Firouzabadi, M Rajabi, A Manafi, M Zarghami, ... Clinical and Experimental Hypertension 39 (4), 371-376, 2017 | 33 | 2017 |
| Diverse phenotypic measurements of wellbeing: Heritability, temporal stability, and the variance explained by polygenic scores J Jamshidi, LM Williams, PR Schofield, HRP Park, A Montalto, MR Chilver, ... Genes, Brain and Behavior, e12694, 2020 | 31 | 2020 |
| 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 | 31 | 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 | 30 | 2014 |
| A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder T Dadkhah, S Rahimi-Aliabadi, J Jamshidi, H Ghaedi, S Taghavi, ... Journal of affective disorders 208, 218-222, 2017 | 29 | 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, 323-328, 2016 | 25 | 2016 |
| Biased homozygous haplotypes across the human caveolin 1 upstream purine complex in Parkinson’s disease H Darvish, A Heidari, S Hosseinkhani, A Movafagh, A Khaligh, J Jamshidi, ... Journal of Molecular Neuroscience 51, 389-393, 2013 | 23 | 2013 |
| Omentin Val109Asp polymorphism and risk of coronary artery disease J Jamshidi, M Ghanbari, A Asnaashari, N Jafari, GA Valizadeh Asian Cardiovascular and Thoracic Annals 25 (3), 199-203, 2017 | 20 | 2017 |
| 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 | 19 | 2019 |
| 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 |
| 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 | 19 | 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 | 18 | 2016 |
Hossein Darvishmedical geneticsZweryfikowany adres z sbmu.ac.ir