Publications by authors named "Parham Nejati"

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A case study of a novel homozygous EDAR splice site variant in hypohidrotic ectodermal dysplasia with tooth agenesis: molecular dynamics insights.
Parham Nejati, Teymoor Khosravi, Saba Lorestani, Morteza Oladnabi

BMC Med Genomics· December 2025

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A novel Bi-Allelic pathogenic MCOLN1 variant underlying mucolipidosis type IV in an Iranian family: clinical, genetic, and molecular dynamics-based structural analysis.
Mohaddese Mohsenipour, Parham Nejati, Teymoor Khosravi, Elham Alimoradi, Mohammad Salehi

BMC Med Genomics· December 2025

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A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy.
Parham Nejati, Nafiseh Falsafi, Elham Alimoradi, Teymoor Khosravi, Mohana Kamari

BMC Med Genomics· November 2025

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Contribution of chromosomal aberrations to the pathogenesis of primary and secondary amenorrhea: A study from Western Iran.
Azam Azimi, Matin Heidari, Reza Alibakhshi, Sara Hamani, Negar Salimi, Parham Nejati

Clin Exp Reprod Med· March 2025

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Cytogenetic Analysis of 570 Couples with Recurrent Pregnancy Loss: Reporting 11 Years of Experience.
Reza Alibakhshi, Parham Nejati, Sara Hamani, Narges Mir-Ahadi, Nazanin Jalilian

J Hum Reprod Sci· October 2020

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Severe α-Thalassemia Due to Compound Heterozygosity for Hb Adana (α59 Gly>Asp) (: c.179G > A) and Codon 127 (A > T) (: c.382A > T) in an Iranian Family.
Azam Azimi, Susan Tahmasebi, Keivan Moradi, Parham Nejati, Reza Alibakhshi

Hemoglobin· March 2020

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Characterization of the IVS-II-821 (A>C) (: c.316-30A>C) Mutation in a β-Thalassemia Phenotype in Iran.
Azam Azimi, Parham Nejati, Soosan Tahmasebi, Sasan Alimoradi, Reza Alibakhshi

Hemoglobin· January 2019

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Combination of Myelin Basic Protein Gene Polymorphisms with HLA-DRB1*1501 in Iranian Patients with Multiple Sclerosis.
Parham Nejati, Marzieh Attar, Maryam Rahimian, Davood Fathi, Majid Shahbazi

Iran J Immunol· September 2017

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