Mohammad Miryounesi
Impact in
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- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
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- Metabolism and Genetic Disorders
Papers in
- Genetics 24
- Genetics and Neurodevelopmental Disorders 9
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 5
- Co-authors
- Soudeh Ghafouri‐Fard (28 shared papers)Mohammad Hossein Modarressi (8 shared papers)Majid Fardaei (11 shared papers)Fatemeh Mansouri (2 shared papers)Vahid Reza Yassaee (13 shared papers)Parvin Mehdipour (1 shared paper)Reza Shirkoohi (2 shared papers)Shadab Salehpour (13 shared papers)
- Journals
- Neurological Sciences (5 papers)BMC Medical Genomics (3 papers)Scientific Reports (3 papers)Neuromuscular Disorders (2 papers)Biochemical Genetics (2 papers)
- Partner nations
- IranCanadaUnited Kingdom
In The Last Decade
Mohammad Miryounesi
57 papers receiving 320 citations
Peers
Comparison fields: 5 of 59
- Cancer Research 57
- Clinical Biochemistry 21
- Genetics 69
- Molecular Biology 160
- Genetics 22
Countries citing papers authored by Mohammad Miryounesi
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
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-authors
The 25 scholars most cited alongside Mohammad Miryounesi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 72 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 49 | |
| 2 | Co-culture of Mouse Embryonic Stem Cells with Sertoli Cells Promote in vitro Generation of Germ Cells. | 2013 | 18 |
| 3 | 2022 | 17 | |
| 4 | Evaluation of in vitro spermatogenesis system effectiveness to study genes behavior: monitoring the expression of the testis specific 10 (Tsga10) gene as a model. | 2014 | 15 |
| 5 | The Spectrum of β -thalassemia Mutations in Isfahan Province of Iran | 2008 | 14 |
| 6 | 2019 | 13 | |
| 7 | 2018 | 13 | |
| 8 | 2014 | 11 | |
| 9 | Homozygosity for a Robertsonian Translocation (13q;14q) in a Phenotypically Normal 44, XX Female with a History of Recurrent Abortion and a Normal Pregnancy Outcome. | 2016 | 9 |
| 10 | 2019 | 9 | |
| 11 | 2016 | 8 | |
| 12 | 2019 | 8 | |
| 13 | 2013 | 8 | |
| 14 | Association of a Novel Nonsense Mutation in KIAA1279 with Goldberg-Shprintzen Syndrome. | 2017 | 7 |
| 15 | 2017 | 7 | |
| 16 | 2019 | 6 | |
| 17 | 2022 | 6 | |
| 18 | 2018 | 6 | |
| 19 | Limb Girdle Muscular Dystrophy Type 2E Due to a Novel Large Deletion in SGCB Gene. | 2017 | 6 |
| 20 | Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a Mutation in TRIOBP Gene. | 2015 | 6 |
About Mohammad Miryounesi
Mohammad Miryounesi is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Physiology and Cell Biology, having authored 72 papers that have together received 322 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Metabolism and Genetic Disorders (9 papers), Genomics and Rare Diseases (8 papers), Lysosomal Storage Disorders Research (5 papers), Genomic variations and chromosomal abnormalities (5 papers), MicroRNA in disease regulation (5 papers), Cellular transport and secretion (4 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). The work is most often cited by research in Cancer Research (57 citations), Clinical Biochemistry (21 citations), Genetics (69 citations), Molecular Biology (160 citations) and Genetics (22 citations). Mohammad Miryounesi has collaborated with scholars based in Iran, Canada and United Kingdom. Frequent co-authors include Soudeh Ghafouri‐Fard, Mohammad Hossein Modarressi, Majid Fardaei, Fatemeh Mansouri, Vahid Reza Yassaee, Parvin Mehdipour, Reza Shirkoohi, Shadab Salehpour, Forouzandeh Fereidooni and Karim Nayernia. Their work appears in journals such as Neurological Sciences, BMC Medical Genomics, Scientific Reports, Neuromuscular Disorders and Biochemical Genetics.
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.