Babak Emamalizadeh

Tabriz University of Medical Sciences — IR

Medicine · Health Sciences

15h-index648citations55works0.02yr avg
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Research Topics

Parkinson's Disease Mechanisms and Treatments(12), Genetics and Neurodevelopmental Disorders(9), Nuclear Receptors and Signaling(9), Autism Spectrum Disorder Research(7), RNA regulation and disease(6)

Publications55 total

Prognostic potential of circulating cell free mitochondrial DNA levels in COVID-19 patients
Molecular Biology Reports·2023· 8 cited
Association between leukocyte telomere length and COVID-19 severity
Egyptian Journal of Medical Human Genetics·2023· 9 citedOpen Access
The study of rs324420 (C385A) polymorphism of the FAAH gene of the endocannabinoid system in patients with epilepsy and ADHD
Epilepsy Research·2023· 7 cited
A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration·2022· 4 cited
Exhaled breath condensate efficacy to identify mutations in patients with lung cancer: A pilot study
Nucleosides Nucleotides & Nucleic Acids·2022· 10 cited
An updated overview and classification of bioinformatics tools for MicroRNA analysis, which one to choose?
Computers in Biology and Medicine·2021· 29 cited
Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations
International Ophthalmology·2021· 5 cited
An interdependence between GAPVD1 gene polymorphism, expression level and response to interferon beta in patients with multiple sclerosis
Journal of Neuroimmunology·2021· 1 cited
LRP8 (rs5177) and CEP85L (rs11756438) are contributed to schizophrenia susceptibility in Iranian population
Psychiatric Genetics·2020· 1 cited
MMP9 (RS20544) and ADCY2 (RS58502974) as susceptibility factors for schizophrenia in Iranian population
Meta Gene·2020· 2 cited
A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet–Biedl syndrome
International Ophthalmology·2020· 7 cited
Macromolecular Biomarkers of Chronic Obstructive Pulmonary Disease in Exhaled Breath Condensate
Biomarkers in Medicine·2020· 18 cited
<b>Exhaled Breath Condensate: A Non-Invasive Source for Tracking of Genetic and Epigenetic Alterations in Lung Diseases</b>
Pharmaceutical Sciences·2020· 7 citedOpen Access
Analysis of polymorphism and function of GA repeat in RIT2 gene promoterAnalysis of polymorphism and function of GA repeat in RIT2 gene promoter in Parkinson’s disease
Research in Medicine·2020· 1 cited
Connection of miR-185 and miR-320a expression levels with response to interferon-beta in multiple sclerosis patients
Multiple Sclerosis and Related Disorders·2020· 7 cited
miR-504 expression level is increased in multiple sclerosis patients responder to interferon-beta
Journal of Neuroimmunology·2020· 8 cited
Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes
Scientific Reports·2020· 16 citedOpen Access
Novel <i>ABCD1</i> gene mutations in Iranian pedigrees with X-linked adrenoleukodystrophy
Journal of Pediatric Endocrinology and Metabolism·2019· 1 cited
Tips for improving the quality and quantity of the extracted DNA from exhaled breath condensate samples
Nucleosides Nucleotides & Nucleic Acids·2019· 9 cited
Genetic analysis of rs11038167, rs11038172 and rs835784 polymorphisms of the TSPAN18 gene in Iranian schizophrenia patients
Meta Gene·2019· 2 cited
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Frequent Co-authors

Hossein Darvish(35), Javad Jamshidi(25), Somayeh Kazeminasab(14), Abolfazl Movafagh(13), Elham Alehabib(12), Abbas Tafakhori(11), Shaghayegh Taghavi(10), Atena Fazeli(10), Yousef Daneshmandpour(10), Monavvar Andarva(9), Marzieh Motallebi(8), Gholam Ali Shahidi(7), Azadeh Ahmadifard(7), Neda Shahmohammadibeni(7), Minoo Atakhorrami(7), Hamid Ghaedi(7), Mehdi Khorrami(6), Zahra Bahmanpour(6), Simin Rahimi-Aliabadi(6), Amir Ehtesham Shafiei Zarneh(5)