Author

Mohammad Yahya Vahidi Mehrjardi

Observed names: M Y Vahidi Mehrjardi, Mehrjardi MYV, Mehrjardi, M, Mehrjardi, Mohammad Yahya Vahidi, Mohamah yahya Vahidi Mehrjardi, Mohammad Y. V. Mehrjardi, Mohammad Y.V. Mehrjardi, Mohammad YV Mehrjardi, Mohammad Yahya Mohammad Yahya Vahidi Mehrjardi, Mohammad Yahya Vahidi Mehrjerdi, Mohammad Yahya Vahidi Mehrjardi, Mohammad Yayha Vahidi Mehrjardi, Mohammad yahya Vahidi Mehjardi, Vahidi Mehrjardi MY, Vahidi Mehrjardi, Mohammad, Vahidi Mehrjardi, Mohammad Y., Vahidi Mehrjardi, Mohammad Yahya

Institution: Shahid Sadoughi University of Medical Sciences and Health Services

Observed institutions: Duke University, Shahid Sadoughi University of Medical Sciences and Health Services, Istituto Superiore di Sanità, Islamic Azad University, Marvdasht, Centre Hospitalier Universitaire de Montpellier, Bambino Gesù Children's Hospital, Institut Universitaire de Recherche Clinique, Diabetes Research Center

ORCID: 0000-0003-0535-1590

Observed ORCID: 0000-0003-0535-1590

OpenAlex ID: A5086321960

Circulating microRNA-122, microRNA-126-3p and microRNA-146a are associated with inflammation in patients with pre-diabetes and type 2 diabetes mellitus: A case control study

2021 · Fahime Zeinali, Seyed Mohsen Aghaei Zarch, et al. · PLoS ONE · 77

Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases

2019 · Elena Perenthaler, Anita Nikoncuk, et al. · Acta Neuropathologica · 70

Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration

2018 · Valentina Muto, Elisabetta Flex, et al. · Neurology · 52

The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations

2019 · Pedro M. Rodríguez Cruz, Judith Cossins, et al. · Brain · 51

Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder

2019 · Caroline M. Dias, Jaya Punetha, et al. · The American Journal of Human Genetics · 50

Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

2018 · Hugh J. McMillan, Aida Telegrafi, et al. · Orphanet Journal of Rare Diseases · 46

Molecular biomarkers in diabetes mellitus (DM)

2020 · Seyed Mohsen Aghaei Zarch, Masoud Dehghan Tezerjani, et al. · Medical Journal of the Islamic Republic of Iran · 41

Testicular expression of TDRD1, TDRD5, TDRD9 and TDRD12 in azoospermia

2020 · Emad Babakhanzadeh, Ali Khodadadian, et al. · BMC Medical Genetics · 33

Evaluation of miR-181b and miR-126-5p expression levels in T2DM patients compared to healthy individuals: Relationship with NF-κB gene expression

2020 · Mohammadreza Dehghani, Seyed Mohsen Aghaei Zarch, et al. · Endocrinología Diabetes y Nutrición · 32

Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant

2018 · Mayada Helal, Neda Mazaheri, et al. · Neurological Sciences · 30

Pontocerebellar hypoplasia due to bi-allelic variants in MINPP1

2020 · Bart Appelhof, Matias Wagner, et al. · European Journal of Human Genetics · 29

Circulating miR-15a and miR-222 as Potential Biomarkers of Type 2 Diabetes

2020 · Salman Sadeghzadeh, Mahmood Dehghani Ashkezari, et al. · Diabetes Metabolic Syndrome and Obesity · 28

Effects of synbiotic supplementation on gut microbiome, serum level of TNF-α, and expression of microRNA-126 and microRNA-146a in patients with type 2 diabetes mellitus: study protocol for a double-blind controlled randomized clinical trial

2020 · Fahime Zeinali, Seyed Mohsen Aghaei Zarch, et al. · Trials · 28

Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum

2020 · Rauan Kaiyrzhanov, Saskia Wortmann, et al. · Brain · 25

Plasma miR‐21 as a potential predictor in prediabetic individuals with a positive family history of type 2 diabetes mellitus

2022 · Zakieh Yazdanpanah, Nasrin Kazemipour, et al. · Physiological Reports · 24

Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder

2016 · Maria M Alves, Danny Halim, et al. · European Journal of Human Genetics · 24

Potential role of gender specific effect of leptin receptor deficiency in an extended consanguineous family with severe early-onset obesity

2018 · Mohammad Reza Dehghani, Mohammad Yahya Vahidi Mehrjardi, et al. · European Journal of Medical Genetics · 20

Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorder

2021 · Holger Hengel, Shabab B. Hannan, et al. · The American Journal of Human Genetics · 19

A programmed decline in ribosome levels governs human early neurodevelopment

2025 · Chunyang Ni, Yudong Wei, et al. · Nature Cell Biology · 17

Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder

2022 · Maria B. Christensen, Amanda M. Levy, et al. · Clinical Genetics · 16

Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from Iran

2020 · Hossein Hozhabri, Mehrdad Talebi, et al. · American Journal of Medical Genetics Part A · 16

MiR-181b Expression Levels as Molecular Biomarker for Type 2 Diabetes

2019 · Seyed Mohsen Aghaei Zarch, Mohammad Yahya Vahidi Mehrjardi, et al. · DOAJ (DOAJ: Directory of Open Access Journals) · 16

B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype–phenotype associations in the muscular dystrophy-dystroglycanopathies

2017 · Reza Maroofian, Moniek Riemersma, et al. · Genome Medicine · 14

Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families

2022 · Mahdiyeh Moudi, Mohammad Yahya Vahidi Mehrjardi, et al. · Journal of Clinical Laboratory Analysis · 12

GGPS1 ‐associated muscular dystrophy with and without hearing loss

2022 · Rauan Kaiyrzhanov, Luke Perry, et al. · Annals of Clinical and Translational Neurology · 11

Works count: 102

Citation count: 926

H-index: 18

I10-index: 26