Ali‐Reza Moslemi

1.8k total citations
40 papers, 1.2k citations indexed

About

Ali‐Reza Moslemi is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Ali‐Reza Moslemi has authored 40 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 17 papers in Clinical Biochemistry and 7 papers in Genetics. Recurrent topics in Ali‐Reza Moslemi's work include Mitochondrial Function and Pathology (21 papers), Metabolism and Genetic Disorders (17 papers) and ATP Synthase and ATPases Research (13 papers). Ali‐Reza Moslemi is often cited by papers focused on Mitochondrial Function and Pathology (21 papers), Metabolism and Genetic Disorders (17 papers) and ATP Synthase and ATPases Research (13 papers). Ali‐Reza Moslemi collaborates with scholars based in Sweden, Iran and Palestinian Territory. Ali‐Reza Moslemi's co-authors include Anders Oldfors, Elisabeth Holme, Niklas Darín, M. Tulinius, Christopher Lindberg, Atle Melberg, Ing‐Marie Fyhr, Gittan Kollberg, Homa Tajsharghi and Johanna Nilsson and has published in prestigious journals such as New England Journal of Medicine, PLoS ONE and Brain.

In The Last Decade

Ali‐Reza Moslemi

40 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ali‐Reza Moslemi Sweden 20 956 546 192 162 154 40 1.2k
Gittan Kollberg Sweden 19 750 0.8× 343 0.6× 105 0.5× 142 0.9× 108 0.7× 33 1.1k
Ali Dursun Türkiye 17 434 0.5× 438 0.8× 88 0.5× 165 1.0× 38 0.2× 97 995
Lock Hock Ngu Malaysia 18 503 0.5× 299 0.5× 90 0.5× 113 0.7× 30 0.2× 59 899
Elżbieta Ciara Poland 17 647 0.7× 218 0.4× 72 0.4× 95 0.6× 27 0.2× 88 1.1k
Dorota Piekutowska‐Abramczuk Poland 17 773 0.8× 353 0.6× 54 0.3× 33 0.2× 24 0.2× 59 1.0k
Adekunle M. Adesina United States 10 633 0.7× 192 0.4× 54 0.3× 22 0.1× 34 0.2× 12 808
Susana Teijeira Spain 16 305 0.3× 48 0.1× 71 0.4× 322 2.0× 120 0.8× 38 689
Tomàs Pinós Spain 17 347 0.4× 67 0.1× 40 0.2× 348 2.1× 114 0.7× 58 810
F. A. Beemer Netherlands 12 232 0.2× 106 0.2× 101 0.5× 248 1.5× 31 0.2× 21 714
Sandesh C.S. Nagamani United States 17 544 0.6× 106 0.2× 200 1.0× 164 1.0× 16 0.1× 43 1.2k

Countries citing papers authored by Ali‐Reza Moslemi

Since Specialization
Citations

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

Fields of papers citing papers by Ali‐Reza Moslemi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ali‐Reza Moslemi. 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 Ali‐Reza Moslemi. The network helps show where Ali‐Reza Moslemi may publish in the future.

Co-authorship network of co-authors of Ali‐Reza Moslemi

This figure shows the co-authorship network connecting the top 25 collaborators of Ali‐Reza Moslemi. A scholar is included among the top collaborators of Ali‐Reza Moslemi 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 Ali‐Reza Moslemi. Ali‐Reza Moslemi 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.
Darín, Niklas, Triinu Siibak, Bradley Peter, et al.. (2021). Functional analysis of a novel POLγA mutation associated with a severe perinatal mitochondrial encephalomyopathy. Neuromuscular Disorders. 31(4). 348–358. 1 indexed citations
2.
Kariminejad, Ariana, Emmanuelle Szenker‐Ravi, Homa Tajsharghi, et al.. (2019). Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia. The American Journal of Human Genetics. 105(6). 1294–1301. 16 indexed citations
3.
Kariminejad, Ariana, et al.. (2016). Lethal multiple pterygium syndrome, the extreme end of the RYR1 spectrum. BMC Musculoskeletal Disorders. 17(1). 109–109. 14 indexed citations
4.
5.
Nilsson, Johanna, Adnan Halim, Erik Larsson, et al.. (2013). LC–MS/MS characterization of combined glycogenin-1 and glycogenin-2 enzymatic activities reveals their self-glucosylation preferences. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1844(2). 398–405. 13 indexed citations
6.
Moslemi, Ali‐Reza, et al.. (2013). Phenotypes of Myopathy-Related Beta-Tropomyosin Mutants in Human and Mouse Tissue Cultures. PLoS ONE. 8(9). e72396–e72396. 5 indexed citations
7.
Roos, Sara, Niklas Darín, Gittan Kollberg, et al.. (2012). A novel mitochondrial tRNA Arg mutation resulting in an anticodon swap in a patient with mitochondrial encephalomyopathy. European Journal of Human Genetics. 21(5). 571–573. 8 indexed citations
8.
Nilsson, Johanna, Adnan Halim, Ali‐Reza Moslemi, et al.. (2011). Molecular pathogenesis of a new glycogenosis caused by a glycogenin-1 mutation. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(4). 493–499. 12 indexed citations
9.
Hedberg, Carola, Christopher Lindberg, G Mathé, Ali‐Reza Moslemi, & Anders Oldfors. (2011). Myopathy in a woman and her daughter associated with a novel splice site MTM1 mutation. Neuromuscular Disorders. 22(3). 244–251. 13 indexed citations
10.
Kollberg, Gittan, Niklas Darín, Ali‐Reza Moslemi, et al.. (2009). A novel homozygous RRM2B missense mutation in association with severe mtDNA depletion. Neuromuscular Disorders. 19(2). 147–150. 52 indexed citations
11.
Melberg, Atle, et al.. (2008). A patient with two mitochondrial DNA mutations causing PEO and LHON. European Journal of Medical Genetics. 52(1). 47–48. 4 indexed citations
12.
Mayr, Johannes A., Ali‐Reza Moslemi, Wolfgang Muss, et al.. (2006). A novel sporadic mutation G14739A of the mitochondrial tRNAGlu in a girl with exercise intolerance. Neuromuscular Disorders. 16(12). 874–877. 11 indexed citations
13.
Kollberg, Gittan, Monica Jansson, Åsa Pérez-Bercoff, et al.. (2005). Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutations. European Journal of Human Genetics. 13(4). 463–469. 28 indexed citations
14.
Darín, Niklas, Anders Oldfors, Ali‐Reza Moslemi, Elisabeth Holme, & M. Tulinius. (2001). The incidence of mitochondrial encephalomyopathies in childhood: Clinical features and morphological, biochemical, and DNA abnormalities. Annals of Neurology. 49(3). 377–383. 9 indexed citations
15.
Houshmand, Massoud, Christopher Lindberg, Ali‐Reza Moslemi, Anders Oldfors, & Elisabeth Holme. (1999). A novel heteroplasmic point mutation in the mitochondrial tRNALys gene in a sporadic case of mitochondrial encephalomyopathy: De novo mutation and no transmission to the offspring. Human Mutation. 13(3). 203–209. 22 indexed citations
16.
Fyhr, Ing‐Marie, Ali‐Reza Moslemi, Christopher Lindberg, & Anders Oldfors. (1998). T cell receptor β-chain repertoire in inclusion body myositis. Journal of Neuroimmunology. 91(1-2). 129–134. 25 indexed citations
17.
Moslemi, Ali‐Reza, M. Tulinius, Elisabeth Holme, & Anders Oldfors. (1998). Threshold expression of the tRNALys A8344G mutation in single muscle fibres. Neuromuscular Disorders. 8(5). 345–349. 38 indexed citations
18.
Moslemi, Ali‐Reza, Christopher Lindberg, & Anders Oldfors. (1997). Analysis of multiple mitochondrial DNA deletions in inclusion body myositis. Human Mutation. 10(5). 381–386. 51 indexed citations
19.
Fyhr, Ing‐Marie, et al.. (1997). Oligoclonal expansion of muscle infiltrating T cells in inclusion body myositis. Journal of Neuroimmunology. 79(2). 185–189. 37 indexed citations
20.
Moslemi, Ali‐Reza, Anders Oldfors, Atle Melberg, & Elisabeth Holme. (1996). Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia. Annals of Neurology. 40(5). 707–713. 75 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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