Mohammad Yahya Vahidi Mehrjardi
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Explore the profile of Mohammad Yahya Vahidi Mehrjardi including associated specialties, affiliations and a list of published articles.
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46
Citations
314
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Recent Articles
1.
Vincke L, Van Schil K, Ahmadieh H, Moghaddasi A, Sabbaghi H, Daftarian N, et al.
NPJ Genom Med
. 2025 Mar;
10(1):19.
PMID: 40055385
An integrated approach combining whole exome sequencing (WES) and autozygosity mapping was used to molecularly diagnose inherited retinal disease (IRD) in 192 unrelated Iranian families, 76.1% of which originate from...
2.
Kaiyrzhanov R, Thompson K, Efthymiou S, Mukushev A, Zharylkassyn A, Prasad C, et al.
Brain Commun
. 2025 Feb;
7(1):fcae453.
PMID: 39963288
Biallelic variants in NADH (nicotinamide adenine dinucleotide (NAD) + hydrogen (H))-ubiquinone oxidoreductase 1 alpha subcomplex 13 have been linked to mitochondrial complex I deficiency, nuclear type 28, based on three...
3.
Moazzami R, Vahidi Mehrjardi M, Miri A
J Diabetes Metab Disord
. 2024 Nov;
23(2):2183-2190.
PMID: 39610478
Introduction: : Metformin, an oral hypoglycemic agent, is generally used as the first-line treatment in type 2 diabetes mellitus (T2DM) patients. The response to metformin varies between patients, and its...
4.
Eslamiyeh H, Vahidi Mehrjardi M, Poursalehi N, Dehghan Tezerjani M
Acta Neurol Belg
. 2024 Oct;
125(1):241-242.
PMID: 39417910
No abstract available.
5.
Maroofian R, Pagnamenta A, Navabazam A, Schwessinger R, Roberts H, Lopopolo M, et al.
HGG Adv
. 2024 Sep;
5(4):100352.
PMID: 39257002
The aim of this work was to identify the underlying genetic cause in a four-generation family segregating an unusual phenotype comprising a severe form of skeletal Class II malocclusion with...
6.
Feizabadi M, Alerasool M, Eslahi A, Esmaeilzadeh E, Vahidi Mehrjardi M, Saket M, et al.
Biochem Genet
. 2024 Feb;
63(1):22-42.
PMID: 38407766
Bardet-Biedl syndrome (BBS) is a rare inherited ciliopathy disorder characterized by a broad spectrum of clinical symptoms such as retinal dystrophy, obesity, polydactyly, genitourinary and kidney anomalies, learning disability, and...
7.
Zaker E, Nouri N, Movahedinia M, Dadbinpour A, Vahidi Mehrjardi M
Mol Genet Genomic Med
. 2024 Feb;
12(2):e2412.
PMID: 38400608
Background: Variants in the Aristaless-related homeobox (ARX) gene lead to a variety of phenotypes, with intellectual disability being a steady feature. Other features can include severe epilepsy, spasticity, movement disorders,...
8.
Ni C, Yu L, Vona B, Park D, Wei Y, Schmitz D, et al.
bioRxiv
. 2024 Jan;
PMID: 38260472
Highlights: variants reduce ribosome levels specifically in neural progenitor cells. Inappropriately low ribosome levels cause a transient delay in radial glia fate commitment.Reduced ribosome levels impair translation of a selected...
9.
Monshizadeh K, Tajamolian M, Anbari F, Vahidi Mehrjardi M, Kalantar S, Dehghani M
BMC Med Genomics
. 2024 Jan;
17(1):24.
PMID: 38238750
Background: Polycystic ovarian syndrome (PCOS) is a common endocrine disorder that affects 6-20% of women of reproductive age. One of the symptoms of PCOS is hyperandrogenism, which can impair follicular...
10.
Darabi Z, Jambarsang S, Vahidi Mehrjardi M, Seyed Hosseini S, Sarebanhassanabadi M, Hosseinzadeh M, et al.
J Cardiovasc Thorac Res
. 2023 Nov;
15(3):161-167.
PMID: 38028716
Introduction: Genetic and environmental factors are involved in the pathogenesis of cardiovascular diseases (CVDs). The aim of the study was to investigate between the genotype of the NFKB1 gene and...