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Farshid Parvini
Farshid Parvini
Assistant Professor, Faculty of Basic Sciences, Department of Genetics, Semnan University
Verified email at semnan.ac.ir
Title
Cited by
Cited by
Year
Dengue viruses and promising envelope protein domain III-based vaccines
H Fahimi, M Mohammadipour, H Haddad Kashani, F Parvini, ...
Applied microbiology and biotechnology 102, 2977-2996, 2018
622018
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
F Parvini, MD Sicardo, M Hosseini-Mazinani, JM Martinez-Rivas, ...
Journal of agricultural and food chemistry 64 (41), 7770-7781, 2016
332016
A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature
S Noavar, S Behroozi, T Tatarcheh, F Parvini, M Foroutan, H Fahimi
BMC medical genetics 20, 1-7, 2019
292019
Intra-specific morphological and molecular diversity in brown olive (Olea cuspidata) of Iran
M Sheidai, Z Noormohammadi, A Dehghani, F Parvini, H Hoshiar-Parsian, ...
Sci Asia 36, 187-193, 2010
242010
Differential expression of fatty acid desaturases in Mari and Shengeh olive cultivars during fruit development and ripening
F Parvini, AA Zeinanloo, E Ebrahimie, S Tahmasebi‐Enferadi, ...
European Journal of Lipid Science and Technology 117 (4), 523-531, 2015
232015
Association of IL-10 gene promoter polymorphisms with susceptibility to pseudoexfoliation syndrome, pseudoexfoliative and primary open-angle glaucoma
G Fakhraie, F Parvini, J Ghanavi, S Saif, P Farnia
BMC Medical Genetics 21, 1-8, 2020
152020
TNFα −857 C/T and TNFR2 +587 T/G polymorphisms are associated with cystic fibrosis in Iranian patients
M Hassanzad, P Farnia, J Ghanavi, F Parvini, S Saif, AA Velayati
European Journal of Medical Genetics 62 (11), 103584, 2019
142019
Inter-population genetic diversity in Olea cuspidata subsp. cuspidata revealed by SSR and ISSR markers
Z Noormohammadi, M Sheidai, A Dehghani, F Parvini, ...
Acta Biologica Szegediensis 56 (2), 155-163, 2012
112012
A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss
H Fahimi, S Behroozi, S Noavar, F Parvini
BMC Medical Genomics 14, 1-8, 2021
102021
A Homozygous Truncating Mutation in NALCN Causing IHPRF1: Detailed Clinical Manifestations and a Review of Literature
AH Karimi, MR Karimi, P Farnia, F Parvini, M Foroutan
The Application of Clinical Genetics, 151-157, 2020
102020
Further study of morphological and molecular diversity in 18 pomegranate landraces of Iran.
Z Noormohammadi, F Parvini, M Sheidai, MR Vazifeshenas
Gene Conserve 9 (38), 2010
82010
Functional foods and antioxidant effects: Emphasizing the role of probiotics
A Heydari, F Parvini, NA Fard
Current Topics in Functional Food, 2022
62022
A novel de novo nonsense mutation in SALL4 causing duane radial ray syndrome: a case report and expanding the phenotypic spectrum
M Ajam-Hosseini, F Parvini, A Angaji
BMC Medical Genomics 16 (1), 33, 2023
42023
Sequence characterization and temporal expression analysis of different SADs and FAD2-2 genes in two Iranian olive cultivars
F Razeghi-Jahromi, F Parvini, A Zarei, M Hosseini-Mazinani
Scientia Horticulturae 305, 111415, 2022
42022
Effect of Fruit Harvesting Time on Oil Content and Fatty Acid Profile of Two Endemic Olive Cultivars ‘Mari’ and ‘Shengeh’
F Parvini, M Hosseini Mazinani, S Tahmasbi Enferadi, AA Zeinanlooali
Iranian Journal of Horticultural Science and Technology 14 (3), 343-356, 2013
32013
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
F Razeghi‐Jahromi, A Zarei, F Parvini, M Hosseini‐Mazinani
European Journal of Lipid Science and Technology 124 (12), 2200079, 2022
22022
Study of frequency and spectrum of GJB2 gene mutations in non-syndromic hearing loss patients of Semnan province
F Parvini, S Noavar, H Fahimi
Armaghane Danesh 28 (1), 112-121, 2023
12023
Study of genes and mutations spectrum causing non-syndromic hearing loss in Iran: A review study
M Ajam-Hossieni, F Parvini, A Angaji
Feyz Medical Sciences Journal 26 (6), 722-738, 2022
12022
Cohen syndrome due to a novel stop-gain mutation in VPS13B gene: A case report and comparative study in affected siblings worldwide
M Saeediye, F Parvini
2024
Identification of novel gene variants causing autosomal recessive non-syndromic hearing loss in Iranian families
M Ajam-Hosseini, F Parvini, A Angaji
2024
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