| Neck pain: global epidemiology, trends and risk factors S Kazeminasab, SA Nejadghaderi, P Amiri, H Pourfathi, M Araj-Khodaei, ... BMC musculoskeletal disorders 23 (1), 1-13, 2022 | 267 | 2022 |
| Migraine: a review on its history, global epidemiology, risk factors, and comorbidities P Amiri, S Kazeminasab, SA Nejadghaderi, R Mohammadinasab, ... Frontiers in neurology, 2553, 2022 | 97 | 2022 |
| Core promoter short tandem repeats as evolutionary switch codes for primate speciation M Ohadi, E Valipour, S Ghadimi‐Haddadan, P Namdar‐Aligoodarzi, ... American journal of primatology 77 (1), 34-43, 2015 | 40 | 2015 |
| Polymorphic core promoter GA-repeats alter gene expression of the early embryonic developmental genes E Valipour, A Kowsari, H Bayat, M Banan, S Kazeminasab, ... Gene 531 (2), 175-179, 2013 | 37 | 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 |
| 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 |
| Understanding the role of telomere attrition and epigenetic signatures in COVID-19 severity A Mahmoodpoor, S Sanaie, F Roudbari, T Sabzevari, N Sohrabifar, ... Gene 811, 146069, 2022 | 25 | 2022 |
| 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 |
| Biallelic missense variants in ZBTB11 can cause intellectual disability in humans Z Fattahi, TI Sheikh, L Musante, M Rasheed, II Taskiran, R Harripaul, ... Human molecular genetics 27 (18), 3177-3188, 2018 | 20 | 2018 |
| 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 |
| Roles of mitochondrial DNA in dynamics of the immune response to COVID-19 A Mahmoodpoor, S Sanaie, Z Ostadi, M Eskandari, N Behrouzi, R Asghari, ... Gene 836, 146681, 2022 | 11 | 2022 |
| 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 | 11 | 2020 |
| CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability S Kazeminasab, II Taskiran, Z Fattahi, N Bazazzadegan, M Hosseini, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 …, 2018 | 11 | 2018 |
| Tips for improving the quality and quantity of the extracted DNA from exhaled breath condensate samples S Kazeminasab, B Emamalizadeh, V Jouyban-Gharamaleki, ... Nucleosides, Nucleotides & Nucleic Acids 39 (5), 688-698, 2020 | 9 | 2020 |
| Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations HD Babak Emamalizadeh ,Yousef Daneshmandpour ,Somayeh Kazeminasb ,Ehsan ... International Ophthalmology 41 (10), 3269-32-76, 2021 | 6 | 2021 |
| Exhaled breath condensate: a non-invasive source for tracking of genetic and epigenetic alterations in lung diseases S Kazeminasab, B Emamalizadeh, M Khoubnasabjafari, A Jouyban Pharmaceutical Sciences 27 (2), 149-161, 2020 | 6 | 2020 |
| A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet–Biedl syndrome Z Bahmanpour, Y Daneshmandpour, S Kazeminasab, S Khalil Khalili, ... International Ophthalmology 41, 389-397, 2021 | 5 | 2021 |
| A Review on Its History, Global Epidemiology, Risk Factors, and Comorbidities., 2022, 12 P Amiri, S Kazeminasab, SA Nejadghaderi, R Mohammadinasab, ... DOI: https://doi. org/10.3389/fneur, 800605, 2021 | 5 | 2021 |
| Aberrant expression of Activating Transcription Factor 6 (ATF6) in major psychiatric disorders S Kazeminasab, E Esmaeilzadeh-Gharehdaghi, M Oladnabi, M Ohadi, ... Psychiatry research 200 (2-3), 1086-1087, 2012 | 4 | 2012 |
babak emamalizadehAssistant Proffessor, Department of Medical Genetics, Tabriz University of Medical Sciences, Tabriz在 tbzmed.ac.ir 的电子邮件经过验证
