Mohammad Amin Tabatabaiefar

1.2k citations

98 papers · 906 indexed · h-index 17

Co-authors: Morteza Hashemzadeh Chaleshtori Laleh Shariati Soodabeh Rostami Saeed Shoja Mohammad Reza Noori–Daloii Effat Farrokhi Ahmad Farajzadeh Sheikh Abbas Jolodar
Topics: Hearing, Cochlea, Tinnitus, Genetics (19 papers)RNA regulation and disease (10 papers)Vestibular and auditory disorders (10 papers)
Cited by: Sensory Systems Molecular Medicine Applied Microbiology and Biotechnology
Journals: SHILAP Revista de lepidopterologíaPLoS ONE Scientific Reports
Partner nations: Iran United States France

In The Last Decade

Mohammad Amin Tabatabaiefar

88 papers receiving 883 citations

Peers

Countries citing papers authored by Mohammad Amin Tabatabaiefar

Since Specialization

Citations

This map shows the geographic impact of Mohammad Amin Tabatabaiefar's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mohammad Amin Tabatabaiefar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mohammad Amin Tabatabaiefar more than expected).

Fields of papers citing papers by Mohammad Amin Tabatabaiefar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mohammad Amin Tabatabaiefar. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mohammad Amin Tabatabaiefar. The network helps show where Mohammad Amin Tabatabaiefar may publish in the future.

Co-authorship network of co-authors of Mohammad Amin Tabatabaiefar

This figure shows the co-authorship network connecting the top 25 collaborators of Mohammad Amin Tabatabaiefar. A scholar is included among the top collaborators of Mohammad Amin Tabatabaiefar based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mohammad Amin Tabatabaiefar. Mohammad Amin Tabatabaiefar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	A novel NBN germline mutation as the likely inherited etiology of various cancer types in an Iranian family 2025 ·Egyptian Journal of Medical Human Genetics ·(unknown),Samaneh Adelian,(unknown),Shaghayegh Haghjooy Javanmard,(unknown),Mohammad Amin Tabatabaiefar	0
2	Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review 2023 ·Genetics in Medicine ·Sajjad Biglari,(unknown),Mohammad Amin Tabatabaiefar,Roya Sherkat,Leila Youssefian,Amir Hossein Saeidian,(unknown),Lam C. Tsoi,Jóhann E. Guðjónsson,Håkon Håkonarson,Jean‐Laurent Casanova,Vivien Béziat,Emmanuelle Jouanguy,Hassan Vahidnezhad	1
3	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 2023 ·BMC Medical Genomics ·(unknown),Yongjun Song,Hane Lee,(unknown),(unknown),(unknown),Mohammad Amin Tabatabaiefar	5
4	Novel in-frame duplication variant characterization in late infantile metachromatic leukodystrophy using whole-exome sequencing and molecular dynamics simulation 2023 ·PLoS ONE ·(unknown),(unknown),(unknown),(unknown),(unknown),Mohammad Amin Tabatabaiefar	8
5	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 2023 ·Molecular Genetics & Genomic Medicine ·(unknown),Yongjun Song,Hane Lee,(unknown),(unknown),Mohammad Amin Tabatabaiefar	4
6	Whole exome sequencing identified a novel LAMA2 frameshift variant causing merosin-deficient congenital muscular dystrophy in a patient with cardiomyopathy, and autism-like behavior 2022 ·Neuromuscular Disorders ·(unknown),(unknown),(unknown),Mohammadreza Sehhati,Mohammad Amin Tabatabaiefar	2
7	A Versatile Biomimic Nanotemplating Fluidic Assay for Multiplex Quantitative Monitoring of Viral Respiratory Infections and Immune Responses in Saliva and Blood 2022 ·Advanced Science ·Roozbeh Siavash Moakhar,(unknown),Mahsa Jalali,(unknown),Alireza Sanati,(unknown),(unknown),Tamer AbdElFatah,Fahimeh Ghasemi,(unknown),Imman I. Hosseini,Yao Lü,(unknown),Sara Mahshid,Mohammad Amin Tabatabaiefar,Chen Liang	40
8	Genetic variant effect prediction by supervised nonnegative matrix tri-factorization 2021 ·Molecular Omics ·(unknown),Mohammadreza Sehhati,Mohammad Amin Tabatabaiefar	2
9	Homozygous TFG gene variants expanding the mutational and clinical spectrum of hereditary spastic paraplegia 57 and a review of literature 2021 ·Journal of Human Genetics ·(unknown),Mohammad Amin Tabatabaiefar,(unknown),Omid Yaghini,(unknown),(unknown),(unknown),Majid Kheirollahi	4
10	A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family 2020 ·BMC Medical Genetics ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Hamidreza Abtahi,Mohammad Amin Tabatabaiefar	5
11	New Variants in the CDH1 Gene in Iranian Families with Hereditary Diffuse Gastric Cancer 2020 ·SHILAP Revista de lepidopterología ·Majid Kheirollahi,(unknown),Mohammad Amin Tabatabaiefar,Mehrdad Zeinalian,Mohammad Minakari,Abbas Moridnia	1
12	Upregulation of MTOR, RPS6KB1, and EIF4EBP1 in the whole blood samples of Iranian patients with multiple sclerosis compared to healthy controls 2020 ·Metabolic Brain Disease ·(unknown),Mohammad Amin Tabatabaiefar,Vahid Shaygannejad,(unknown),(unknown),(unknown),(unknown),(unknown),Mohammad Reza Noori–Daloii	6
13	Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome 2019 ·Endocrine ·(unknown),Mohammad Amin Tabatabaiefar,Soudeh Ghafouri‐Fard,Asadollah Rajab,(unknown),(unknown),Abdol‐Mohammad Kajbafzadeh,Mohammad Reza Noori–Daloii	3
14	Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation 2018 ·Journal of Cellular Biochemistry ·(unknown),(unknown),(unknown),(unknown),(unknown),Mojtaba Darbouy,Reza Seyed Sharifi,Javad Tavakkoly‐Bazzaz,Mohammad Amin Tabatabaiefar	6
15	Staphylococcus aureus Isolates Carrying Panton-Valentine Leucocidin Genes: Their Frequency, Antimicrobial Patterns, and Association With Infectious Disease in Shahrekord City, Southwest Iran 2016 ·Jundishapur Journal of Microbiology ·Laleh Shariati,Majid Validi,(unknown),(unknown),(unknown),Ali Karimi,(unknown),Mohammad Amin Tabatabaiefar	8
16	Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent 2014 ·SHILAP Revista de lepidopterología ·(unknown),Mohammad Amin Tabatabaiefar,Morteza Hashemzadeh Chaleshtori,Sepideh Miraj	1
17	The Role of Epigenetics in the Induction of Fetal Hemoglobin: A Combination Therapy Approach 2014 ·SHILAP Revista de lepidopterología ·(unknown),Mehrdad Noruzinia,(unknown),(unknown),Mohammad Amin Tabatabaiefar,Masoud Soleimani,Saeid Kaviani,Saeid Abroun,(unknown),Najmaldin Saki	4
18	Large-Scale Screening of Mitochondrial DNA Mutations Among Iranian Patients with Prelingual Nonsyndromic Hearing Impairment 2011 ·Genetic Testing and Molecular Biomarkers ·(unknown),Mohammad Amin Tabatabaiefar,(unknown),Effat Farrokhi,Mohammad Taghi Akbari,Morteza Hashemzadeh Chaleshtori	9
19	Association of P1635 and P1655 polymorphisms in dysbindin (DTNBP1) gene with schizophrenia 2011 ·Acta Neuropsychiatrica ·Fatemeh Alizadeh,Mohammad Amin Tabatabaiefar,M. Reza Ghadiri,Mir Saeed Yekaninejad,(unknown),Mohammad Reza Noori–Daloii	3
20	CORRELATION BETWEEN THE CD4 GENE POLYMORPHISM WITH TYPE 1 DIABETES MELLITUS IN THE IRANIAN POPULATION 2005 ·Iranian Journal of Diabetes and Metabolism ·Mahdi Zamani,Mohammad Amin Tabatabaiefar,(unknown),(unknown),(unknown),Bagher Larijani	1

About Mohammad Amin Tabatabaiefar

Mohammad Amin Tabatabaiefar is a scholar working on Sensory Systems, Applied Microbiology and Biotechnology and Neurology, having authored 98 papers that have together received 906 indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (19 papers), RNA regulation and disease (10 papers) and Vestibular and auditory disorders (10 papers). The work is most often cited by research in Sensory Systems (164 citations), Molecular Medicine (157 citations) and Applied Microbiology and Biotechnology (56 citations). Mohammad Amin Tabatabaiefar has collaborated with scholars based in Iran, United States and France. Frequent co-authors include Morteza Hashemzadeh Chaleshtori, Laleh Shariati, Soodabeh Rostami, Saeed Shoja, Mohammad Reza Noori–Daloii, Effat Farrokhi, Ahmad Farajzadeh Sheikh, Abbas Jolodar, Zahra Hejazi and Mohammad Hossein Modarressi. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

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