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Farshid Parvini

Dengue viruses and promising envelope protein domain III-based vaccines
2018 · Hossein Fahimi, Mahshid Mohammadipour, et al. · Applied Microbiology and Biotechnology · 82
Transcriptional Analysis of Stearoyl-Acyl Carrier Protein Desaturase Genes from Olive (Olea europaea) in Relation to the Oleic Acid Content of the Virgin Olive Oil
2016 · Farshid Parvini, M. Dolores Sicardo, et al. · Journal of Agricultural and Food Chemistry · 36
A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature
2019 · Sadaf Noavar, Samira Behroozi, et al. · BMC Medical Genetics · 32
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Differential expression of fatty acid desaturases in Mari and Shengeh olive cultivars during fruit development and ripening
2014 · Farshid Parvini, Ali Asghar Zeinanloo, et al. · European Journal of Lipid Science and Technology · 26
Gram-negative bacterial sRNAs encapsulated in OMVs: an emerging class of therapeutic targets in diseases
2024 · Mobarakeh Ajam-Hosseini, Fatemeh Akhoondi, et al. · Frontiers in Cellular and Infection Microbiology · 20
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A Homozygous Truncating Mutation in NALCN Causing IHPRF1: Detailed Clinical Manifestations and a Review of Literature
2020 · Amir Hossein Karimi, Mohammad Reza Karimi, et al. · The Application of Clinical Genetics · 17
Association of IL-10 gene promoter polymorphisms with susceptibility to pseudoexfoliation syndrome, pseudoexfoliative and primary open-angle glaucoma
2020 · Ghasem Fakhraie, Farshid Parvini, et al. · BMC Medical Genetics · 16
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2010 · Masoud Sheidai, Zahra Noormohammadi, et al. · ScienceAsia · 15
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A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss
2021 · Hossein Fahimi, Samira Behroozi, et al. · BMC Medical Genomics · 14
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TNFα −857 C/T and TNFR2 +587 T/G polymorphisms are associated with cystic fibrosis in Iranian patients
2018 · Maryam Hassanzad, Poopak Farnia, et al. · European Journal of Medical Genetics · 13
A novel de novo nonsense mutation in SALL4 causing duane radial ray syndrome: a case report and expanding the phenotypic spectrum
2023 · Mobarakeh Ajam-Hosseini, Farshid Parvini, et al. · BMC Medical Genomics · 10
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Sequence characterization and temporal expression analysis of different SADs and FAD2-2 genes in two Iranian olive cultivars
2022 · Fateme Razeghi-Jahromi, Farshid Parvini, et al. · Scientia Horticulturae · 10
Change in Oil Composition and the Major Fatty Acids and Triacylglycerol Biosynthesis Genes in Drupe of Selected Olive Cultivars during Growing Season; A Two Years Study
2022 · Fateme Razeghi‐Jahromi, Abdolkarim Zarei, et al. · European Journal of Lipid Science and Technology · 7
Functional Foods and Antioxidant Effects: Emphasizing the Role of Probiotics
2022 · Arezu Heydari, Farshid Parvini, et al. · IntechOpen eBooks · 5
Further study of morphological and molecular diversity in 18 pomegranate landraces of Iran.
2010 · Zahra Noormohammadi, Farshid Parvini, et al. · 5
Bi‐Allelic Variants in MICU1 Cause Myopathy With Extrapyramidal Signs: Case Series, Phenotypic Spectrum, and Genotype–Phenotype Correlations From 61 Patients
2025 · Pegah Beheshti, Fahimeh Akbarian, et al. · Clinical Genetics · 3
Genetic spectrum among 2009 Iranian individuals with neuromuscular disorders using next generation sequencing and multiple ligation dependent probe amplification methods
2025 · Negar Molaei, Parnian Alagha, et al. · Scientific Reports · 2
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First report of neonatal-onset glutaric aciduria type II in the Iranian population caused by a novel deleterious ETFA variant
2025 · Farshid Parvini, Mobarakeh Ajam-Hosseini, et al. · Orphanet Journal of Rare Diseases · 2
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Identification of two novel pathogenic mutations in the SKOR2 gene linked to cerebellar hypoplasia and a broad spectrum of neurodevelopmental delay in two Iranian families
2025 · Mohammad Ali Farazi Fard, Zahra Tabatabaei, et al. · Journal of Human Genetics · 2
A novel homozygous missense mutation in the RPE65 gene in an Iranian family with retinitis pigmentosa
2024 · Hadiseh Nateghi, Farshid Parvini, et al. · Gene Reports · 1
Study of frequency and spectrum of GJB2 gene mutations in non-syndromic hearing loss patients of Semnan province
2022 · Farshid Parvini, Hossein Fahimi, et al. · Armaghane Danesh · 1
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Genetic Landscape of DMD Gene Mutations in Iranian Patients and the Applicability of Molecular Therapies
2026 · Ali Khanbazi, Farzane Zare Ashrafi, et al. · Archives of Iranian Medicine
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Mechanistic Role of Long Non-coding RNAs in Drug and Radiotherapy Resistance of Cancer Cells
2026 · Saghar Yousefnia, Farshid Parvini, et al. · Epigenetics and human health
Zygosity‐Dependent Phenotypic Spectrum of RELN ‐Related Disorders: 10 New Patients and Genotype–Phenotype Correlations Across 48 Kindreds
2026 · Sajjad Biglari, Halimeh Rezaei, et al. · Human Mutation
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Transcriptomic Analysis of Probiotic Oxidative Stress Resistance in Anti-inflammatory Pathways
2025 · Arezu Heydari, Farshid Parvini, et al. · DOAJ (DOAJ: Directory of Open Access Journals)
Works count: 32
Citation count: 319
H-index: 10
I10-index: 12
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