Mohammad Amin Tabatabaiefar (Mohamad Amin Tabatabaiefar)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 11

Top Topics

Duchenne Muscular Dystrophy

Molecular Dynamics

Top Venues

Molecular genetics & genomic medicine

BMC medical genomics

Journal of cellular biochemistry

This page only lists publications with an associated author ORCID identifier.

Publications

Atefeh Mir, Yongjun Song, Hane Lee, Mostafa Montazer-Zohouri, Marziyeh Reisi, Mohammad Amin Tabatabaiefar
A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature review. Molecular genetics & genomic medicine (2023)
Zahra Ataei, Zahra Nouri, Farial Tavakoli, Mohammad Reza Pourreza, Sina Narrei, Mohammad Amin Tabatabaiefar
Novel in-frame duplication variant characterization in late infantile metachromatic leukodystrophy using whole-exome sequencing and molecular dynamics simulation. PloS one 18 (2) (2023)
Zahra Ataei, Zahra Nouri, Farial Tavakoli, Mohammad Reza Pourreza, Sina Narrei, Mohammad Amin Tabatabaiefar
Novel in-frame duplication variant characterization in late infantile metachromatic leukodystrophy using whole-exome sequencing and molecular dynamics simulation. PloS one 18 (2) (2023)
Atefeh Mir, Yongjun Song, Hane Lee, Hossein Khanahmad, Erfan Khorram, Jafar Nasiri, Mohammad Amin Tabatabaiefar
Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature. BMC medical genomics 16 (1) (2023)
Zahra Ataei, Zahra Nouri, Farial Tavakoli, Mohammad Reza Pourreza, Sina Narrei, Mohammad Amin Tabatabaiefar
Novel in-frame duplication variant characterization in late infantile metachromatic leukodystrophy using whole-exome sequencing and molecular dynamics simulation. PloS one 18 (2) (2023)
Atefeh Mir, Yongjun Song, Hane Lee, Zakiye Nadeali, Mohammad Amin Tabatabaiefar
A novel de novo frameshift variant in the CHD2 gene related to intellectual and developmental disability, seizures and speech problems. Molecular genetics & genomic medicine (2023)
Roshanak S Sajjadi, Mohammad Hossein Modarressi, Fahimeh Akbarian, Mohammad Amin Tabatabaiefar
A Computational Framework to Infer Prostate Cancer-Associated Long Noncoding RNAs and Analyses for Identifying a Competing Endogenous RNA Network. Genetic testing and molecular biomarkers 25 (9) (2022)
Mehdi Khorrami, Mohammad Amin Tabatabaiefar, Erfan Khorram, Omid Yaghini, Mojgan Rezaei, Arash Hejazifar, Maryam Riahinezhad, Majid Kheirollahi
Homozygous TFG gene variants expanding the mutational and clinical spectrum of hereditary spastic paraplegia 57 and a review of literature. Journal of human genetics 66 (10) (2021)
Akram Sarmadi, Samane Nasrniya, Maryam Soleimani Farsani, Sina Narrei, Zahra Nouri, Mahsa Sepehrnejad, Mohammad Hussein Nilforoush, Hamidreza Abtahi, Mohammad Amin Tabatabaiefar
A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. BMC medical genetics 21 (1) (2020)
Minoo Sayyari, Ali Salehzadeh, Mohammad Amin Tabatabaiefar, Ali Abbasi
Profiling of 17 Y-STR loci in Mazandaran and Gilan provinces of Iran Turkish journal of medical sciences 49 (5) (2019)
Azam Ahmadi Shadmehri, Najmeh Fattahi, Mohammad Reza Pourreza, Mahboobeh Koohiyan, Shahnaz Zarifi, Mojtaba Darbouy, Reza Sharifi, Javad Tavakkoly Bazzaz, Mohammad Amin Tabatabaiefar
Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation. Journal of cellular biochemistry 120 (3) (2018)