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Abolfazl Yari
Abolfazl Yari
M.Sc. of Human Genetics, Department of Medical Genetics, Faculty of Medicine, Kerman, Iran.
Verified email at kmu.ac.ir
Title
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Cited by
Year
A Study of Associations Between rs9349379 (PHACTR1), rs2891168 (CDKN2B-AS), rs11838776 (COL4A2) and rs4880 (SOD2) Polymorphic Variants and …
A Yari, N Saleh-Gohari, M Mirzaee, F Hashemi, K Saeidi
Biochemical Genetics 60 (1), 106-126, 2022
182022
Mutation status and prognostic value of KRAS and BRAF in Southeast Iranian colorectal cancer patients: first report from Southeast of Iran
A Yari, A Samoudi, A Afzali, ZM Karam, NK Karimaldini, MFS Abadi, ...
Journal of Gastrointestinal Cancer 52, 557-568, 2021
152021
Circulatory long noncoding RNAs (circulatory-LNC-RNAs) as novel biomarkers and therapeutic targets in cardiovascular diseases: Implications for cardiovascular diseases …
SME Meybodi, N Soleimani, A Yari, A Javadifar, M Tollabi, B Karimi, ...
International Journal of Biological Macromolecules 225, 1049-1071, 2023
112023
A novel homozygous splice-site mutation in SCARB2 is associated with progressive myoclonic epilepsy with renal failure
A Yari, RM Ali-Nejad, N Saleh-Gohari
Neurological Sciences, 1-9, 2021
72021
KRAS and BRAF mutations in Iranian colorectal cancer patients: A systematic review and meta-analysis
A Yari, A Afzali, M Aalipour, M Nakheai, MJ Zahedi
Caspian Journal of Internal Medicine 11 (4), 355, 2020
72020
Clinical manifestations associated with the domain-containing protein 2 gene mutation in an Iranian family with Spastic Paraplegia 54
A Yari, S Etesam, S Zarifi, S Parvizpour, E Miri-Moghaddam
Neurodegenerative Diseases 22 (3-4), 139-150, 2022
52022
Observation period for asymptomatic penetrating chest trauma: 1 or 3 h?
L Seidzadeh Gooklan, A Yari, M Mayel, S Nazemi, M Movahedi, ...
European Journal of Trauma and Emergency Surgery 44, 829-833, 2018
52018
CDKN2B‐AS (rs2891168), SOD2 (rs4880), and PON1 (rs662) polymorphisms and susceptibility to coronary artery disease and type 2 diabetes mellitus in Iranian patients: A case …
A Yari, ZM Karam, SME Meybodi, ML Sargazi, K Saeidi
Health Science Reports 6 (11), e1717, 2023
42023
Evaluation of toll-like receptor alteration in intestinal biopsies of patients with irritable bowel syndrome: A systematic review
M Aalipour, A Yari, MJ Zahedi, MM Mohammadi
Govaresh 24 (2), 104-110, 2019
42019
Inhalation of spray-dried extract of salvia rosmarinus spenn alleviates lung inflammatory, oxidative, and remodeling changes in asthmatic rats
MA Rajizadeh, MA Bejeshk, A Aminizadeh, A Yari, F Rostamabadi, ...
Pharmacology 109 (1), 10-21, 2024
32024
Identification of a Novel ARSA Gene Mutation Through High-Throughput Molecular Diagnosis Method in Two Girls with Late Infantile Metachromatic Leukodystrophy
A Yari, F Vafaeie, ZM Karam, M Hosseini, H Hashemzade, MS Rahimi, ...
Neuromolecular Medicine 25 (4), 563-572, 2023
32023
Association of MTHFR 677C> T and 1298A> C genetic polymorphisms with colorectal cancer: genotype and haplotype analysis in a Southeast Iranian population
A Yari, SME Meybodi, ZM Karam, A Samoudi, F Hashemi, M Aalipour, ...
Gene Reports 25, 101399, 2021
32021
Lipopeptide Biosurfactant Produced by Acinetobacter junii B6 Attenuates Lung Inflammatory, Oxidative, and Histopathological Alterations due to Asthma in Rats
MA Bejeshk, MA Rajizadeh, A Yari, F Bagheri, H Najafipour, ...
International Journal of Peptide Research and Therapeutics 30 (1), 9, 2024
22024
Circular RNAs: Epigenetic regulators of PTEN expression and function in cancer
MM Farazi, S Jafarinejad-Farsangi, ZM Karam, M Gholizadeh, M Haddadi, ...
Gene, 148442, 2024
12024
Identification of a Novel Deletion Variant (c.2999_3005delTGTGTGT/p.Asn1000SerfsTer4) in NPHP4 Associated With Nephronophthisis‐4
Z Miri Karam, AK Gohari, MJR Khabaz, A Yari, SME Meybodi, R Attari, ...
Journal of Clinical Laboratory Analysis, e25077, 2024
12024
Clinical and genetic screening in a large Iranian family with Marfan syndrome: A case study
F Vafaeie, Z Miri Karam, A Yari, H Safarpour, T Kazemi, S Etesam, ...
Health Science Reports 6 (10), e1647, 2023
12023
Galloway-mowat syndrome 3 (GAMOS3): a novel disease-causing variant in OSGEP gene and expansion of the clinical spectrum
A Yari, F Vafaeie, ZM Karam, M Hosseini, E Miri-Moghaddam
Neurological Sciences, 1-16, 2024
2024
Exploring the Molecular Interaction Between NR2E3 and NR1D1 in Retinitis Pigmentosa: A Docking and Molecular Dynamics Study
F Vafaeie, M Mohammadpour, S Etesam, S Zarifi, A Yari, M Nikandish, ...
Journal of Clinical Laboratory Analysis 38 (23), e25125, 2024
2024
Association between Rotavirus Infection and Irritable Bowel Syndrome: A Case-control Study in Kerman-Iran
M Aalipour, MJ Zahedi, MR Zangouey, A Yari, M Mirzaee, ...
Journal of Kerman University of Medical Sciences 30 (6), 327-332, 2024
2024
Expanding the genotypic and phenotypic spectrum of EAST/SeSAME syndrome: identification of a novel homozygous mutation (c. 194 G> A) in KCNJ10 gene
A Yari, L Dalvand, BE Moghaddam, NN Khorasani, F Esmaeili, R Attari, ...
Neurological Sciences, 1-17, 2024
2024
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