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somayeh kazeminasab
somayeh kazeminasab
Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz
在 tbzmed.ac.ir 的电子邮件经过验证
标题
引用次数
引用次数
年份
Neck pain: global epidemiology, trends and risk factors
S Kazeminasab, SA Nejadghaderi, P Amiri, H Pourfathi, M Araj-Khodaei, ...
BMC musculoskeletal disorders 23, 1-13, 2022
3332022
Migraine: a review on its history, global epidemiology, risk factors, and comorbidities
P Amiri, S Kazeminasab, SA Nejadghaderi, R Mohammadinasab, ...
Frontiers in neurology 12, 800605, 2022
1442022
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
422015
RIT2 Polymorphisms: Is There a Differential Association?
B Emamalizadeh, J Jamshidi, A Movafagh, M Ohadi, MS Khaniani, ...
Molecular neurobiology 54, 2234-2240, 2017
382017
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
372013
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
312014
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
292014
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
252022
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
222018
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
212017
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
182021
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
152020
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
142018
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
132022
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
82020
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
72021
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
62021
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
62020
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
52021
Association between leukocyte telomere length and COVID-19 severity
A Mahmoodpoor, S Sanaie, M Eskandari, N Behrouzi, M Taghizadeh, ...
Egyptian Journal of Medical Human Genetics 24 (1), 37, 2023
42023
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