A.‐R. Moslemi

744 total citations
15 papers, 446 citations indexed

About

A.‐R. Moslemi is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, A.‐R. Moslemi has authored 15 papers receiving a total of 446 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 4 papers in Rheumatology. Recurrent topics in A.‐R. Moslemi's work include Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (7 papers) and ATP Synthase and ATPases Research (5 papers). A.‐R. Moslemi is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (7 papers) and ATP Synthase and ATPases Research (5 papers). A.‐R. Moslemi collaborates with scholars based in Sweden, United States and Iceland. A.‐R. Moslemi's co-authors include Anders Oldfors, Niklas Darín, E. Holme, M. Tulinius, Christopher Lindberg, Gittan Kollberg, Mattias Ohlsson, Lena Jonasson, Anna‐Karin Kroksmark and Marita Andersson Grönlund and has published in prestigious journals such as Neurology, British Journal of Ophthalmology and European Journal of Neurology.

In The Last Decade

A.‐R. Moslemi

15 papers receiving 441 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A.‐R. Moslemi Sweden	10	335	152	128	76	66	15	446
Yuta Ichinose Japan	10	112 0.3×	59 0.4×	20 0.2×	119 1.6×	24 0.4×	28	319
Mathilde Nizon France	13	239 0.7×	17 0.1×	70 0.5×	45 0.6×	22 0.3×	26	387
Katarzyna Tońska Poland	14	400 1.2×	22 0.1×	149 1.2×	46 0.6×	7 0.1×	40	502
G. C. Guazzi Italy	10	125 0.4×	15 0.1×	41 0.3×	52 0.7×	37 0.6×	26	273
Manu Jokela Finland	12	236 0.7×	37 0.2×	15 0.1×	83 1.1×	18 0.3×	35	356
K Barthel Germany	6	162 0.5×	273 1.8×	6 0.0×	52 0.7×	68 1.0×	6	363
S. Gambelli Italy	11	191 0.6×	24 0.2×	17 0.1×	88 1.2×	39 0.6×	20	347
Fong Ct United States	6	141 0.4×	17 0.1×	38 0.3×	23 0.3×	18 0.3×	186	296
M. Osborn United Kingdom	9	291 0.9×	44 0.3×	23 0.2×	81 1.1×	71 1.1×	13	495
Charalampos Karadimas Greece	14	473 1.4×	15 0.1×	245 1.9×	101 1.3×	55 0.8×	17	627

Countries citing papers authored by A.‐R. Moslemi

Since Specialization

Citations

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

Fields of papers citing papers by A.‐R. Moslemi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A.‐R. Moslemi

This figure shows the co-authorship network connecting the top 25 collaborators of A.‐R. Moslemi. A scholar is included among the top collaborators of A.‐R. 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 A.‐R. Moslemi. A.‐R. Moslemi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Darín, Niklas, et al.. (2017). Benign mitochondrial myopathy with exercise intolerance in a large multigeneration family due to a homoplasmic m.3250T>C mutation in MTTL1. European Journal of Neurology. 24(4). 587–593. 7 indexed citations

Roos, Sara, et al.. (2014). Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations. Neuromuscular Disorders. 24(8). 713–720. 6 indexed citations

Nilsson, Jonas, et al.. (2010). P4.46 Molecular pathogenesis of a new glycogenosis caused by a mutation in glycogenin-1. Neuromuscular Disorders. 20(9-10). 672–672. 1 indexed citations

Grönlund, Marita Andersson, A.‐R. Moslemi, Anders Oldfors, et al.. (2009). Ophthalmological findings in children and young adults with genetically verified mitochondrial disease. British Journal of Ophthalmology. 94(1). 121–127. 59 indexed citations

Lindberg, Christopher, A.‐R. Moslemi, & Anders Oldfors. (2007). MELAS syndrome in a patient with a point mutation in MTTS1. Acta Neurologica Scandinavica. 0(0). 2219978153–???. 11 indexed citations

Darín, Niklas, et al.. (2007). Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I. European Journal of Paediatric Neurology. 11(6). 353–357. 66 indexed citations

Larsson, Karolina, et al.. (2006). A Western blot and molecular genetic investigation of the estrogen receptor beta in giant cell arteritis.. PubMed. 24(2 Suppl 41). S17–9. 1 indexed citations

Oldfors, Anders, et al.. (2006). Mitochondrial abnormalities in inclusion-body myositis. Neurology. 66(1_suppl_1). S49–55. 95 indexed citations

Moslemi, A.‐R., et al.. (2005). Two New Mutations in theMTATP6Gene Associated with Leigh Syndrome. Neuropediatrics. 36(5). 314–318. 51 indexed citations

10.

Moslemi, A.‐R., Christopher Lindberg, Jens Toft, et al.. (2003). A novel mutation in the mitochondrial tRNAPhe gene associated with mitochondrial myopathy. Neuromuscular Disorders. 14(1). 46–50. 16 indexed citations

11.

Lindberg, Christopher, et al.. (2003). Inclusion Body Myositis: Clonal Expansions of Muscle‐Infiltrating T Cells Persist Over Time. Scandinavian Journal of Immunology. 58(2). 195–200. 50 indexed citations

12.

Tulinius, M., A.‐R. Moslemi, Niklas Darín, et al.. (2003). Leigh Syndrome with Cytochrome-c Oxidase Deficiency and a Single T Insertion nt 5537 in the Mitochondrial tRNA^TrpGene. Neuropediatrics. 34(2). 87–91. 27 indexed citations

13.

Moslemi, A.‐R., et al.. (2003). SURF1 gene mutations in three cases with Leigh syndrome and cytochrome c oxidase deficiency. Neurology. 61(7). 991–993. 27 indexed citations

14.

Moslemi, A.‐R., et al.. (2001). Estrogen receptor alpha in giant cell arteritis: a molecular genetic study.. PubMed. 19(3). 297–302. 4 indexed citations

15.

Fyhr, Ing‐Marie, A.‐R. Moslemi, A Tarkowski, Christopher Lindberg, & Anders Oldfors. (1996). Limited T‐Cell Receptor V Gene Usage in Inclusion Body Myositis. Scandinavian Journal of Immunology. 43(1). 109–114. 25 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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