Get started
Author

Parham Nejati

ORCID: 0000-0003-3290-5691
Observed ORCID: 0000-0003-3290-5691
OpenAlex ID: A5047642330
Cytogenetic analysis of 570 couples with recurrent pregnancy loss: Reporting 11 years of experience
2020 · Nazanin Jalilian, Reza Alibakhshi, et al. · Journal of Human Reproductive Sciences · 13
Association of tumor necrosis factor-alpha gene promoter polymorphism and its mRNA expression level in coronary artery disease
2018 · Parham Nejati, Samaneh Naeimipour, et al. · Meta Gene · 8
Combination of Myelin Basic Protein Gene Polymorphisms with HLA-DRB1*1501 in Iranian Patients with Multiple Sclerosis.
2017 · Parham Nejati, Marzieh Attar, et al. · PubMed · 4
A novel Bi-Allelic pathogenic MCOLN1 variant underlying mucolipidosis type IV in an Iranian family: clinical, genetic, and molecular dynamics-based structural analysis
2025 · Mohaddese Mohsenipour, Parham Nejati, et al. · BMC Medical Genomics · 1
PDF
Severe α-Thalassemia Due to Compound Heterozygosity for Hb Adana (α59 Gly>Asp) (HBA1: c.179G > A) and Codon 127 (A > T) (HBA2: c.382A > T) in an Iranian Family
2020 · Azam Azimi, Susan Tahmasebi, et al. · Hemoglobin · 1
Metastatic breast cancer to colon: An unusual site of metastasis with a review of literature
2019 · Parham Nejati, Masoud Sadeghi, et al. · Biomedical Research and Therapy · 1
PDF
Characterization of the IVS-II-821 (A>C) (HBB: c.316-30A>C) Mutation in a β-Thalassemia Phenotype in Iran
2019 · Azam Azimi, Parham Nejati, et al. · Hemoglobin · 1
Whole exome sequencing unveils novel pathogenic variants in an Iranian cohort with retinal dystrophies: Implications for genetic diagnosis and counseling
2026 · Elham Alimoradi, Arash Salmaninejad, et al. · Molecular and Cellular Probes
Novel SLITRK6 Nonsense Mutation in an Iranian Family with Autosomal Recessive Syndromic Hearing Loss
2026 · Elham Alimoradi, Elaheh Emadi, et al. · OBM Genetics
PDF
Identification of a novel homozygous CHST3 variant in an Iranian patient with Spondyloepiphyseal dysplasia and congenital joint dislocations
2026 · Parham Nejati, Elham Alimoradi, et al. · Human Gene
Whole-exome sequencing identifies a novel variant within the ARSB gene causing mucopolysaccharidosis type VI in an Iranian patient
2026 · Elham Alimoradi, Parham Nejati, et al. · Human Gene
A Novel Missense Variant in the CDH23 Gene is Segregated in an Iranian Family with Hearing Loss
2026 · Elham Alimoradi, Parham Nejati, et al. · OBM Genetics
PDF
Identification of a Novel Missense Homozygous Variant in LINS1 in Two Distinct Iranian Families With Consanguineous Marriage
2026 · Elham Alimoradi, Parham Nejati, et al. · Molecular Genetics & Genomic Medicine
Molecular dynamics insights into novel and nano-rare de novo mutations in the ribosomal proteins S19 and L26 causing Diamond-Blackfan anemia in Iranian patients
2025 · Teymoor Khosravi, Mohaddese Mohsenipour, et al. · Journal of Biomolecular Structure and Dynamics
A case study of a novel homozygous EDAR splice site variant in hypohidrotic ectodermal dysplasia with tooth agenesis: molecular dynamics insights
2025 · Parham Nejati, Teymoor Khosravi, et al. · BMC Medical Genomics
A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy
2025 · Parham Nejati, Nafiseh Falsafi, et al. · BMC Medical Genomics
PDF
Contribution of chromosomal aberrations to the pathogenesis of primary and secondary amenorrhea: A study from Western Iran
2024 · Azam Azimi, Matin Heidari, et al. · Daehan saengsik uihak hoeji/Clinical and experimental reproductive medicine
Solitary Fibrous Tumor of Testis: A rare Case with Review of Literature
2020 · Parham Nejati, Farhad Amirian, et al. · Iranian Journal of Blood and Cancer
Works count: 19
Citation count: 29
H-index: 3
I10-index: 1
Year
Topic
Type