Mari Auranen

4.2k total citations
59 papers, 2.2k citations indexed

About

Mari Auranen is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Mari Auranen has authored 59 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 18 papers in Genetics and 17 papers in Cellular and Molecular Neuroscience. Recurrent topics in Mari Auranen's work include Mitochondrial Function and Pathology (12 papers), Hereditary Neurological Disorders (12 papers) and Muscle Physiology and Disorders (10 papers). Mari Auranen is often cited by papers focused on Mitochondrial Function and Pathology (12 papers), Hereditary Neurological Disorders (12 papers) and Muscle Physiology and Disorders (10 papers). Mari Auranen collaborates with scholars based in Finland, United States and United Kingdom. Mari Auranen's co-authors include Irma Järvelä, Anu Suomalainen, Raija Vanhala, Vidya Velagapudi, Leena Peltonen, Henna Tyynismaa, Emil Ylikallio, Nahid Khan, Eija Pirinen and Elli Kempas and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Cell Metabolism.

In The Last Decade

Mari Auranen

58 papers receiving 2.1k citations

Peers

Mari Auranen

GENET

CMN

PHYSI

Darius Ebrahimi‐Fakhari United States

Daniel P. Seeburg United States

Gamze Tanrιöver Türkiye

Jaan‐Olle Andressoo Finland

Patrı́cia Maciel Portugal

Liviu Aron United States

Anne‐Laurence Boutillier France

Timothy W. Yu United States

Zygmunt Galdzicki United States

Katja Lohmann Germany

Darius Ebrahimi‐Fakhari United States

Mari Auranen

999 ×0.8

493 ×0.9

GENET

241 ×0.7

779 ×2.3

CMN

747 ×2.2

PHYSI

Citations per year, relative to Mari Auranen Mari Auranen (= 1×) peers Darius Ebrahimi‐Fakhari

Countries citing papers authored by Mari Auranen

Since Specialization

Citations

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

Fields of papers citing papers by Mari Auranen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mari Auranen

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

All Works

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20 of 20 papers shown

Wallgren‐Pettersson, Carina, Manu Jokela, Vilma‐Lotta Lehtokari, et al.. (2023). Variants in tropomyosins TPM2 and TPM3 causing muscle hypertonia. Neuromuscular Disorders. 35. 29–32. 2 indexed citations

Seppänen, Hanna, et al.. (2023). Lactate and ammonia measurements during cardiopulmonary exercise testing and its recovery phase—Consideration of age and sex in its interpretation. Clinical Physiology and Functional Imaging. 43(4). 278–290. 2 indexed citations

Auranen, Mari, Jouni Kvist, Henrik Zetterberg, et al.. (2022). Serum Creatine, Not Neurofilament Light, Is Elevated in CHCHD10-Linked Spinal Muscular Atrophy. Frontiers in Neurology. 13. 793937–793937. 7 indexed citations

Kortelainen, Mika, Anders Paetau, Pentti J. Tienari, et al.. (2021). Effectiveness of clinical exome sequencing in adult patients with difficult‐to‐diagnose neurological disorders. Acta Neurologica Scandinavica. 145(1). 63–72. 22 indexed citations

Kaukonen, Jyrki, et al.. (2021). IMPDH2: a new gene associated with dominant juvenile-onset dystonia-tremor disorder. European Journal of Human Genetics. 29(12). 1833–1837. 16 indexed citations

Forsström, Saara, Christopher B. Jackson, Christopher J. Carroll, et al.. (2019). Fibroblast Growth Factor 21 Drives Dynamics of Local and Systemic Stress Responses in Mitochondrial Myopathy with mtDNA Deletions. Cell Metabolism. 30(6). 1040–1054.e7. 175 indexed citations

Kämppi, Antti, et al.. (2018). Focal atrophy of the unilateral masticatory muscles caused by pure trigeminal motor neuropathy: case report. Clinical Case Reports. 6(5). 939–943. 10 indexed citations

Auranen, Mari, Anders Paetau, Päivi Piirilä, et al.. (2017). Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy. Neuromuscular Disorders. 27(6). 581–584. 22 indexed citations

Auranen, Mari, Jussi Toppila, Saranya Suriyanarayanan, et al.. (2017). Clinical and metabolic consequences of L-serine supplementation in hereditary sensory and autonomic neuropathy type 1C. Molecular Case Studies. 3(6). a002212–a002212. 23 indexed citations

10.

Kelly, John J., Jessica L. Esseltine, Qing Shao, et al.. (2016). Specific functional pathologies of Cx43 mutations associated with oculodentodigital dysplasia. Molecular Biology of the Cell. 27(14). 2172–2185. 20 indexed citations

11.

Piirilä, Päivi, Minna E. Similä, Johanna Palmio, et al.. (2016). Unique Exercise Lactate Profile in Muscle Phosphofructokinase Deficiency (Tarui Disease); Difference Compared with McArdle Disease. Frontiers in Neurology. 7. 82–82. 9 indexed citations

12.

Ylikallio, Emil, Doyoun Kim, Pirjo Isohanni, et al.. (2015). Dominant transmission of de novo KIF1A motor domain variant underlying pure spastic paraplegia. European Journal of Human Genetics. 23(10). 1427–1430. 36 indexed citations

13.

Palmio, Johanna, Per Harald Jonson, Anni Evilä, et al.. (2015). Novel mutations in DNAJB6 gene cause a very severe early-onset limb-girdle muscular dystrophy 1D disease. Neuromuscular Disorders. 25(11). 835–842. 28 indexed citations

14.

Suriyanarayanan, Saranya, Mari Auranen, Jussi Toppila, et al.. (2015). The Variant p.(Arg183Trp) in SPTLC2 Causes Late-Onset Hereditary Sensory Neuropathy. NeuroMolecular Medicine. 18(1). 81–90. 19 indexed citations

15.

Palmio, Johanna, Mari Auranen, Sari Kiuru‐Enari, et al.. (2014). Screening for late-onset Pompe disease in Finland. Neuromuscular Disorders. 24(11). 982–985. 22 indexed citations

16.

Peippo, Maarit, K. O. J. Simola, Leena Valanne, et al.. (2006). Pitt–Hopkins syndrome in two patients and further definition of the phenotype. Clinical Dysmorphology. 15(2). 47–54. 43 indexed citations

17.

Ylisaukko‐oja, Tero, Karola Rehnström, Mari Auranen, et al.. (2005). Analysis of four neuroligin genes as candidates for autism. European Journal of Human Genetics. 13(12). 1285–1292. 114 indexed citations

18.

Hackman, Peter, Vesa Juvonen, J. Sarparanta, et al.. (2004). Enrichment of the R77C α‐sarcoglycan gene mutation in finnish LGMD2D patients. Muscle & Nerve. 31(2). 199–204. 21 indexed citations

19.

Auranen, Mari, Teppo Varilo, Reija Alén, et al.. (2003). Evidence for allelic association on chromosome 3q25–27 in families with autism spectrum disorders originating from a subisolate of Finland. Molecular Psychiatry. 8(10). 879–884. 29 indexed citations

20.

Auranen, Mari, Sirpa Ala‐Mello, Joni A. Turunen, & Irma Järvelä. (2001). Further evidence for linkage of autosomal-dominant medullary cystic kidney disease on chromosome 1q21. Kidney International. 60(4). 1225–1232. 22 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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