Pegah Ghandil
Ahvaz Jundishapur University of Medical Sciences
H-index: 14
Asia-Iran
Top articles of Pegah Ghandil
Genetic features of patients with MPS type IIIB: Description of five pathogenic gene variations
Gene
2024/6/30
Alihossein Saberi
H-Index: 13
Pegah Ghandil
H-Index: 9
بررسی پلی مورفیسم های CBS 844ins68 و RFC1 A80G و ریسک بروز سندروم داون در مادران جوان ایرانی: یک مطالعه مقطعی
International Journal of Reproductive BioMedicine
2024/2/10
Pegah Ghandil
H-Index: 9
Javad Mohammadi-Asl
H-Index: 13
Folate gene polymorphisms CBS 844ins68 and RFC1 A80G and risk of Down syndrome offspring in young Iranian women: A cross-sectional study
International Journal of Reproductive BioMedicine
2024/2
Pegah Ghandil
H-Index: 9
Javad Mohammadi-Asl
H-Index: 13
Association Study of Polymorphisms in Folate Metabolism and Mothers of Down Syndrome Offsprings in the Southwest of Iran
Jundishapur Journal of Chronic Disease Care
2024
Atefeh Heydari
H-Index: 0
Pegah Ghandil
H-Index: 9
Association of DRD2, DRD4 and COMT genes variants and their gene-gene interactions with antipsychotic treatment response in patients with schizophrenia
BMC psychiatry
2023/10/25
Mahdi Bijanzadeh
H-Index: 7
Pegah Ghandil
H-Index: 9
Association of rs1570360 and rs2010963 in VEGF and rs2279744 in the MDM2 gene with Recurrent Implantation Failure in Iranian Women
JBRA Assisted Reproduction
2023/7
Association Study of Interleukin 23 Receptor (IL-23R) Polymorphisms with Inflammatory Bowel Disease (IBD) in Khuzestan Province of Iran
2023/5/22
Clinical and molecular spectrum of muscular dystrophies (MDs) with intellectual disability (ID): A comprehensive overview
2022/1/1
Molecular diagnosis of maturity onset diabetes of the young in Iranian patients: improving management
Journal of Diabetes & Metabolic Disorders
2021/12
Utilization of whole exome sequencing in non-syndromic premature ovarian failure: ficolin-3 gene mutation in an iranian family
Iranian Biomedical Journal
2021/11
Roshan Nikbakht
H-Index: 9
Pegah Ghandil
H-Index: 9
Genetic association study of CTLA4 and FCεRIα polymorphisms in asthmatic patients in the southwestern region of Iran
Nucleosides, Nucleotides & Nucleic Acids
2021/9/2
Evaluating the distribution of (+ 2044G/A, R130Q) Rs20541 and (-1112 C/T) Rs1800925 polymorphism in IL-13 gene: An association-based study with asthma in Ahvaz, Iran
International Journal of Medical Laboratory
2021/3/9
Identification of Cytochrome b‐245, beta‐chain gene mutations, and clinical presentations in Iranian patients with X‐linked chronic granulomatous disease
Journal of Clinical Laboratory Analysis
2021/2
Atefeh Heydari
H-Index: 0
Alihossein Saberi
H-Index: 13
Ahmad Shamsizadeh
H-Index: 13
Pegah Ghandil
H-Index: 9
Effects of epigallocatechin gallate on total antioxidant capacity, biomarkers of systemic low-grade inflammation and metabolic risk factors in patients with type 2 diabetes …
Archives of Medical Science: AMS
2021
The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further …
The Journal of Gene Medicine
2020/12
Mohsen Naseri
H-Index: 8
Pegah Ghandil
H-Index: 9
A novel homozygous variant in an Iranian pedigree with cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 4
Journal of Clinical Laboratory Analysis
2020/11
Pegah Ghandil
H-Index: 9
Mohsen Naseri
H-Index: 8
Association metabolic obesity phenotypes with cardiometabolic index, atherogenic index of plasma and novel anthropometric indices: a link of FTO-rs9939609 polymorphism
Vascular Health and Risk Management
2020/6/24
Meysam Alipour
H-Index: 11
Pegah Ghandil
H-Index: 9
Características clínicas e análise genética e de cofatores de dobramento da tubulinaem pacientes iranianos com síndrome de Sanjad-Sakati
Jornal de Pediatria
2020/3/2
Pegah Ghandil
H-Index: 9
Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad-Sakati syndrome
Jornal de Pediatria
2020/3/2
Pegah Ghandil
H-Index: 9
Association of vascular endothelial growth factor A polymorphisms and aberrant expression of connexin 43 and VEGFA with idiopathic recurrent spontaneous miscarriage
Journal of Obstetrics and Gynaecology Research
2020/3
