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» Authors » Mahdiyeh Moudi

Mahdiyeh Moudi

Explore the profile of Mahdiyeh Moudi including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 17
Citations 93
Followers 0
Related Specialties
General Medicine
Biochemistry
Gynecology & Obstetrics
Top 10 Co-Authors
Ramin Saravani
Saman Sargazi
Milad Heidari Nia
Shekoufeh Mirinejad
Mansoor Shakiba
Mohammadreza Dehghani
Mohammad Yahya Vahidi Mehrjardi
Hamidreza Galavi
Mahdieh Jafari Shahroudi
Mohsen Taheri
Published In
Iran J Public Health
Curr Med Mycol
Iran Biomed J
Iran J Pharm Res
Iran J Psychiatry
Affiliations
Soon will be listed here.
Recent Articles
1.
Association between Mir-499, Mir-27a, and Mir-146a polymorphisms and their susceptibility to recurrent spontaneous abortion; analysis
Bahari G, Taheri M, Mokhtari M, Moudi M, Majidpour M, Ghadimi H
Turk J Obstet Gynecol . 2024 Sep; 21(3):158-165. PMID: 39228203
Objective: Recurrent spontaneous abortion (RSA) is defined as two or more pregnancy losses before 24 gestational weeks, accounting for 1-3% of fertile couples. A vast majority of single-nucleotide polymorphisms (SNPs)...
2.
Detection of trisomy 9 mosaicism in the second trimester screening by abnormal level of biochemical markers
Salari Z, Moradi A, Moudi M, Mousavi Z
Obstet Gynecol Sci . 2024 Aug; 67(5):506-510. PMID: 39191388
Trisomy 9 is a rare chromosomal abnormality that occurs in both mosaic and non-mosaic states. The present study reports a case of mosaic trisomy 9 detected during pregnancy in a...
3.
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder
Christensen M, Levy A, Mohammadi N, Niceta M, Kaiyrzhanov R, Dentici M, et al.
Clin Genet . 2022 May; 102(2):98-109. PMID: 35616059
Biallelic variants of the gene encoding for the zinc-finger protein 142 (ZNF142) have recently been associated with intellectual disability (ID), speech impairment, seizures, and movement disorders in nine individuals from...
4.
Association of TMPRSS2 Gene Polymorphisms with COVID-19 Severity and Mortality: a Case-Control Study with Computational Analyses
Rokni M, Heidari Nia M, Sarhadi M, Mirinejad S, Sargazi S, Moudi M, et al.
Appl Biochem Biotechnol . 2022 Apr; 194(8):3507-3526. PMID: 35386063
Coronavirus disease 2019 (COVID-19) is a severe disease caused by a new variant of beta-coronavirus that first appeared in China. Human genetic factors, including polymorphisms, serve pivotal roles in the...
5.
Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families
Moudi M, Vahidi Mehrjardi M, Hozhabri H, Metanat Z, Kalantar S, Taheri M, et al.
J Clin Lab Anal . 2022 Jan; 36(2):e24241. PMID: 35019165
Background: Intellectual disability (ID) is a heterogeneous group of neurodevelopmental disorders that is characterized by significant impairment in intellectual and adaptive functioning with onset during the developmental period. Whole-exome sequencing...
6.
Relationship between Gene Variants and the Risk of Schizophrenia in South-East of Iran: A Preliminary Case-Control Study and in Silico Analysis
Heidari Nia M, Shahroudi M, Saravani R, Sargazi S, Moudi M, Mojahed A
Iran J Public Health . 2021 Jun; 50(5):978-989. PMID: 34183956
Background: Schizophrenia (SZN) is a heterogeneous disorder. Recently, the role of purinergic receptor's signaling in mental disorders has implicated. There is no evidence regarding the association of single nucleotide polymorphisms...
7.
Association of a Novel Gene Polymorphism with Susceptibility to Schizophrenia and Breast Cancer: A Case-Control Study
Sargazi S, Heidari Nia M, Mirinejad S, Moudi M, Jafari Shahroudi M, Saravani R, et al.
Iran J Public Health . 2021 Mar; 50(2):397-406. PMID: 33748005
Background: gene is found to play essential roles in regulating different aspects of cell proliferation and development of the nervous system. We aimed to determine if rs12407427 T/C polymorphism could...
8.
Impact of Proliferator-Activated Receptor γ Gene Polymorphisms on Risk of Schizophrenia: A Case-Control Study and Computational Analyses
Sargazi S, Mirani Sargazi F, Moudi M, Heidari Nia M, Saravani R, Mirinejad S, et al.
Iran J Psychiatry . 2020 Nov; 15(4):286-296. PMID: 33240378
Schizophrenia (SCZ) is a common psychiatric disorder characterized by a complex mode of inheritance. Peroxisome proliferator-activated receptor-γ (PPARG) mainly regulates lipid and glucose metabolisms while it is constitutively expressed in...
9.
Hydro-alcoholic Extract of C. Koch Reduces the Expression of Cell Death-Associated Genes while Inducing DNA Damage in HeLa Cervical Cancer Cells
Sargazi S, Moudi M, Kooshkaki O, Mirinejad S, Saravani R
Iran J Med Sci . 2020 Oct; 45(5):359-367. PMID: 33060879
Background: C. Koch hydroalcoholic extract (AWHE) is proven to induce cell death. Previous studies suggested that AWHE is an effective inhibitor against the proliferation of prostate cancer cells. The present...
10.
Relationship between Single Nucleotide Polymorphisms of and Schizophrenia Susceptibility: A Preliminary Case-Control Study and Bioinformatics Analysis
Sargazi S, Heidari Nia M, Sheervalilou R, Mirinejad S, Harati-Sadegh M, Moudi M, et al.
Int J Mol Cell Med . 2020 Sep; 9(2):154-164. PMID: 32934953
Grainyhead-like (GRHL) transcription factors were recently linked to the etiology of neural tube defects (NTDs). Overlapping patterns in the variation of schizophrenia (SCZ) incidence with that of NTDs suggests the...