Mohammad Amin Tabatabaiefar

1.2k total citations
98 papers, 906 citations indexed

About

Mohammad Amin Tabatabaiefar is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Mohammad Amin Tabatabaiefar has authored 98 papers receiving a total of 906 indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 20 papers in Genetics and 19 papers in Sensory Systems. Recurrent topics in Mohammad Amin Tabatabaiefar's work include Hearing, Cochlea, Tinnitus, Genetics (19 papers), RNA regulation and disease (10 papers) and Vestibular and auditory disorders (10 papers). Mohammad Amin Tabatabaiefar is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (19 papers), RNA regulation and disease (10 papers) and Vestibular and auditory disorders (10 papers). Mohammad Amin Tabatabaiefar collaborates with scholars based in Iran, United States and France. Mohammad Amin Tabatabaiefar's co-authors include Morteza Hashemzadeh Chaleshtori, Laleh Shariati, Saeed Shoja, Soodabeh Rostami, Mohammad Reza Noori–Daloii, Effat Farrokhi, Ahmad Farajzadeh Sheikh, Abbas Jolodar, Zahra Hejazi and Mohammad Hossein Modarressi and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Mohammad Amin Tabatabaiefar

88 papers receiving 883 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Mohammad Amin Tabatabaiefar Iran 17 494 164 157 103 95 98 906
Anil V. Nair United States 18 658 1.3× 42 0.3× 156 1.0× 100 1.0× 15 0.2× 31 1.2k
Ziyi Liu China 12 270 0.5× 51 0.3× 93 0.6× 61 0.6× 22 0.2× 40 727
Annabel N. Smith United Kingdom 18 1.0k 2.1× 43 0.3× 27 0.2× 386 3.7× 29 0.3× 25 1.8k
Kyle Caution United States 20 673 1.4× 59 0.4× 23 0.1× 23 0.2× 49 0.5× 26 1.2k
Xuefeng Li China 16 471 1.0× 14 0.1× 36 0.2× 39 0.4× 33 0.3× 38 914
Dong He China 25 947 1.9× 13 0.1× 18 0.1× 26 0.3× 27 0.3× 68 1.8k
Yoon Young Go South Korea 15 226 0.5× 20 0.1× 27 0.2× 24 0.2× 36 0.4× 27 574
Sarah E. Ernst United States 19 451 0.9× 33 0.2× 13 0.1× 116 1.1× 10 0.1× 34 1.3k
Pan Zhu China 19 538 1.1× 44 0.3× 7 0.0× 30 0.3× 28 0.3× 40 1.1k
Christina Caputo United States 11 332 0.7× 17 0.1× 53 0.3× 39 0.4× 6 0.1× 13 738

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

20 of 20 papers shown
1.
Adelian, Samaneh, et al.. (2025). A novel NBN germline mutation as the likely inherited etiology of various cancer types in an Iranian family. Egyptian Journal of Medical Human Genetics. 26(1).
2.
Biglari, Sajjad, et al.. (2024). A Novel Homozygote Pathogenic Variant in the DIAPH1 Gene Associated With Seizures, Cortical Blindness, and Microcephaly Syndrome (SCBMS): Report of a Family and Literature Review. Molecular Genetics & Genomic Medicine. 12(11). e70031–e70031. 1 indexed citations
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Biglari, Sajjad, Mohammad Amin Tabatabaiefar, Roya Sherkat, et al.. (2023). Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review. Genetics in Medicine. 26(2). 101028–101028. 1 indexed citations
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Moakhar, Roozbeh Siavash, Mahsa Jalali, Alireza Sanati, et al.. (2022). A Versatile Biomimic Nanotemplating Fluidic Assay for Multiplex Quantitative Monitoring of Viral Respiratory Infections and Immune Responses in Saliva and Blood. Advanced Science. 9(33). e2204246–e2204246. 40 indexed citations
9.
Tabatabaiefar, Mohammad Amin, et al.. (2021). 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). 973–981. 4 indexed citations
10.
Sehhati, Mohammadreza, et al.. (2021). Genetic variant effect prediction by supervised nonnegative matrix tri-factorization. Molecular Omics. 17(5). 740–751. 2 indexed citations
11.
Abtahi, Hamidreza, et al.. (2020). A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. BMC Medical Genetics. 21(1). 127–127. 5 indexed citations
12.
Kheirollahi, Majid, et al.. (2020). New Variants in the CDH1 Gene in Iranian Families with Hereditary Diffuse Gastric Cancer. SHILAP Revista de lepidopterología. 11(4). 493–501. 1 indexed citations
13.
Tabatabaiefar, Mohammad Amin, et al.. (2019). Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome. Endocrine. 66(2). 185–191. 3 indexed citations
14.
Darbouy, Mojtaba, et al.. (2018). Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation. Journal of Cellular Biochemistry. 120(3). 3367–3372. 6 indexed citations
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Tabatabaiefar, Mohammad Amin, et al.. (2014). Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent. SHILAP Revista de lepidopterología. 1 indexed citations
17.
Noruzinia, Mehrdad, Mohammad Amin Tabatabaiefar, Masoud Soleimani, et al.. (2014). The Role of Epigenetics in the Induction of Fetal Hemoglobin: A Combination Therapy Approach. SHILAP Revista de lepidopterología. 4 indexed citations
18.
Tabatabaiefar, Mohammad Amin, et al.. (2011). Large-Scale Screening of Mitochondrial DNA Mutations Among Iranian Patients with Prelingual Nonsyndromic Hearing Impairment. Genetic Testing and Molecular Biomarkers. 16(4). 271–278. 9 indexed citations
19.
Alizadeh, Fatemeh, et al.. (2011). Association of P1635 and P1655 polymorphisms in dysbindin (DTNBP1) gene with schizophrenia. Acta Neuropsychiatrica. 24(3). 155–159. 3 indexed citations
20.
Zamani, Mahdi, et al.. (2005). CORRELATION BETWEEN THE CD4 GENE POLYMORPHISM WITH TYPE 1 DIABETES MELLITUS IN THE IRANIAN POPULATION. Iranian Journal of Diabetes and Metabolism. 4(4). 1–9. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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