Mohammad Miryounesi

643 total citations
70 papers, 337 citations indexed

About

Mohammad Miryounesi is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Mohammad Miryounesi has authored 70 papers receiving a total of 337 indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 30 papers in Genetics and 9 papers in Clinical Biochemistry. Recurrent topics in Mohammad Miryounesi's work include Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (11 papers) and Metabolism and Genetic Disorders (9 papers). Mohammad Miryounesi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (11 papers) and Metabolism and Genetic Disorders (9 papers). Mohammad Miryounesi collaborates with scholars based in Iran, Canada and United Kingdom. Mohammad Miryounesi's co-authors include Soudeh Ghafouri‐Fard, Mohammad Hossein Modarressi, Fatemeh Mansouri, Majid Fardaei, Mehdi Dianatpour, Vahid Reza Yassaee, Reza Shirkoohi, Forouzandeh Fereidooni, Shadab Salehpour and Parvin Mehdipour and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Clinica Chimica Acta.

In The Last Decade

Mohammad Miryounesi

57 papers receiving 335 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 Miryounesi Iran 10 191 83 63 28 28 70 337
Yousheng Yan China 10 181 0.9× 68 0.8× 60 1.0× 23 0.8× 29 1.0× 46 322
Silvina Gutiérrez Argentina 14 202 1.1× 112 1.3× 64 1.0× 41 1.5× 28 1.0× 44 471
Lilia Romdhane Tunisia 12 150 0.8× 189 2.3× 40 0.6× 37 1.3× 39 1.4× 29 394
Adriano Torres Antonucci Italy 13 242 1.3× 78 0.9× 54 0.9× 42 1.5× 25 0.9× 41 452
Paola Cuccarolo Italy 12 239 1.3× 40 0.5× 56 0.9× 28 1.0× 42 1.5× 19 433
Khalid Al‐Thihli Oman 13 219 1.1× 116 1.4× 21 0.3× 22 0.8× 21 0.8× 50 456
Gergely Talabér Hungary 13 197 1.0× 68 0.8× 37 0.6× 15 0.5× 87 3.1× 17 586
Leena Paul United States 10 276 1.4× 28 0.3× 79 1.3× 27 1.0× 19 0.7× 15 466
Angela Liou United States 9 296 1.5× 96 1.2× 98 1.6× 12 0.4× 46 1.6× 13 723
Ivan Carcamo‐Orive United States 11 244 1.3× 85 1.0× 51 0.8× 41 1.5× 67 2.4× 14 432

Countries citing papers authored by Mohammad Miryounesi

Since Specialization
Citations

This map shows the geographic impact of Mohammad Miryounesi'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 Miryounesi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mohammad Miryounesi more than expected).

Fields of papers citing papers by Mohammad Miryounesi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mohammad Miryounesi. 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 Miryounesi. The network helps show where Mohammad Miryounesi may publish in the future.

Co-authorship network of co-authors of Mohammad Miryounesi

This figure shows the co-authorship network connecting the top 25 collaborators of Mohammad Miryounesi. A scholar is included among the top collaborators of Mohammad Miryounesi 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 Miryounesi. Mohammad Miryounesi 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.
2.
Sadeghi, Hossein, et al.. (2024). Expanding genetic and clinical aspects of Schwartz-Jampel syndrome: A report of two cases with literature review. Molecular Genetics and Metabolism Reports. 40. 101125–101125.
3.
4.
Miryounesi, Mohammad, et al.. (2024). An overview of genetic mutations in Aicardi-Goutières syndrome in Iranian population. Neurological Sciences. 46(2). 999–1007. 1 indexed citations
5.
Salehpour, Shadab, et al.. (2024). Broadening the Phenotype and Genotype Spectrum of Glycogen Storage Disease by Unraveling Novel Variants in an Iranian Patient Cohort. Biochemical Genetics. 63(2). 1752–1779. 1 indexed citations
6.
Sadeghi, Hossein, Shadab Salehpour, Seyed Hassan Tonekaboni, et al.. (2023). Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infection. Neurological Sciences. 44(12). 4491–4498. 3 indexed citations
7.
Miryounesi, Mohammad, et al.. (2022). The role of excitatory amino acid transporter 2 (EAAT2) in epilepsy and other neurological disorders. Metabolic Brain Disease. 38(1). 1–16. 14 indexed citations
8.
Salehpour, Shadab, Mohammad‐Reza Ghasemi, Hossein Sadeghi, et al.. (2022). Identification of a novel de novo mutation in the CTNNB1 gene in an Iranian patient with intellectual disability. Neurological Sciences. 43(4). 2859–2863. 6 indexed citations
9.
10.
Salehpour, Shadab, et al.. (2019). Mutations in the VPS13B Gene in Iranian Patients with Different Phenotypes of Cohen Syndrome. Journal of Molecular Neuroscience. 70(1). 21–25. 9 indexed citations
11.
Miryounesi, Mohammad, et al.. (2019). ELMO Domain Containing 1 (ELMOD1) Gene Mutation Is Associated with Mental Retardation and Autism Spectrum Disorder. Journal of Molecular Neuroscience. 69(2). 312–315. 6 indexed citations
12.
Ghafouri‐Fard, Soudeh, Majid Fardaei, Kaoru Tabei, Mehdi Dianatpour, & Mohammad Miryounesi. (2018). A CDH3 Mutation is Segregated in an Iranian Family with Congenital Hypotrichosis and Juvenile Macular Dystrophy. SHILAP Revista de lepidopterología. 1 indexed citations
13.
Ghafouri‐Fard, Soudeh, et al.. (2018). Whole exome sequencing unraveled the mystery of neurodevelopmental disorders in three Iranian families. Gene Reports. 13. 141–145. 1 indexed citations
14.
Ghafouri‐Fard, Soudeh, et al.. (2018). A new mutation in steroidogenic acute regulatory protein (StAR) is segregated in an Iranian family. Meta Gene. 16. 196–198. 1 indexed citations
15.
Miryounesi, Mohammad, Kaoru Tabei, Mehdi Dianatpour, Majid Fardaei, & Soudeh Ghafouri‐Fard. (2018). Report of three cases with hereditary spastic paraplegia and investigation of the mutations. Meta Gene. 16. 105–107. 1 indexed citations
16.
Miryounesi, Mohammad, Majid Fardaei, Kaoru Tabei, & Soudeh Ghafouri‐Fard. (2017). Autosomal recessive polycystic kidney disorder due to two novel compound heterozygote mutations in PKHD1 gene: case report. SHILAP Revista de lepidopterología.
17.
Ghafouri‐Fard, Soudeh, Mehdi Dianatpour, Kaoru Tabei, & Mohammad Miryounesi. (2017). Mental retardation due to chromosomal translocation in an Iranian consanguineous family: report of three cases. SHILAP Revista de lepidopterología.
18.
Ghafouri‐Fard, Soudeh, Shadab Salehpour, Vahid Reza Yassaee, & Mohammad Miryounesi. (2016). A New Nonsense Mutation in CDKL5 Gene in a Male Patient with Early Onset Refractory Epilepsy: a Case Report. SHILAP Revista de lepidopterología. 1 indexed citations
19.
Miryounesi, Mohammad, Karim Nayernia, Maryam Beigom Mobasheri, et al.. (2014). Evaluation of in vitro spermatogenesis system effectiveness to study genes behavior: monitoring the expression of the testis specific 10 (Tsga10) gene as a model.. PubMed. 17(10). 692–7. 15 indexed citations
20.
Heidari, Maryam, et al.. (2008). The Spectrum of β -thalassemia Mutations in Isfahan Province of Iran. SHILAP Revista de lepidopterología. 37(2). 106–111. 14 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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