Mari Auranen

4.2k citations

59 papers · 2.2k indexed · h-index 23

Molecular Biology top 5%
Genetics top 5%
Cognitive Neuroscience top 5%
Cellular and Molecular Neuroscience top 5%
Physiology top 10%

Co-authors: Irma Järvelä Anu Suomalainen Raija Vanhala Vidya Velagapudi Leena Peltonen Henna Tyynismaa Emil Ylikallio Nahid Khan
Topics: Mitochondrial Function and Pathology (12 papers)Hereditary Neurological Disorders (12 papers)Muscle Physiology and Disorders (10 papers)
Cited by: Geriatrics and Gerontology Clinical Biochemistry Physiology
Journals: SHILAP Revista de lepidopterologíaNeurology Cell Metabolism
Partner nations: Finland United States United Kingdom

In The Last Decade

Mari Auranen

58 papers receiving 2.1k citations

Peers

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

#	Work	Indexed citations
1	Variants in tropomyosins TPM2 and TPM3 causing muscle hypertonia 2023 ·Neuromuscular Disorders ·Carina Wallgren‐Pettersson,Manu Jokela,Vilma‐Lotta Lehtokari,Henna Tyynismaa,(unknown),Emil Ylikallio,Olli Tynninen,Katarina Pelin,Mari Auranen	2
2	Lactate and ammonia measurements during cardiopulmonary exercise testing and its recovery phase—Consideration of age and sex in its interpretation 2023 ·Clinical Physiology and Functional Imaging ·(unknown),Hanna Seppänen,(unknown),Vesa‐Petteri Kouri,Mari Auranen,Ritva Luukkonen,Päivi Piirilä	2
3	Serum Creatine, Not Neurofilament Light, Is Elevated in CHCHD10-Linked Spinal Muscular Atrophy 2022 ·Frontiers in Neurology ·(unknown),(unknown),(unknown),Mari Auranen,Jouni Kvist,Henrik Zetterberg,(unknown),Marko Lehtonen,Anna Maija Saukkonen,Manu Jokela,Emil Ylikallio,Henna Tyynismaa	7
4	Effectiveness of clinical exome sequencing in adult patients with difficult‐to‐diagnose neurological disorders 2021 ·Acta Neurologica Scandinavica ·(unknown),(unknown),(unknown),Mika Kortelainen,(unknown),Anders Paetau,Pentti J. Tienari,Emil Ylikallio,Mari Auranen,Henna Tyynismaa	22
5	IMPDH2: a new gene associated with dominant juvenile-onset dystonia-tremor disorder 2021 ·European Journal of Human Genetics ·(unknown),(unknown),Jyrki Kaukonen,(unknown),Mari Auranen,(unknown),Vidya Velagapudi,Anu Suomalainen	16
6	Fibroblast Growth Factor 21 Drives Dynamics of Local and Systemic Stress Responses in Mitochondrial Myopathy with mtDNA Deletions 2019 ·Cell Metabolism ·Saara Forsström,Christopher B. Jackson,Christopher J. Carroll,Mervi Kuronen,Eija Pirinen,(unknown),(unknown),Mari Auranen,(unknown),Nahid Khan,Anne Roivainen,Päivi Marjamäki,Heidi Liljenbäck,Liya Wang,Brendan J. Battersby,Uwe Richter,Vidya Velagapudi,Joni Nikkanen,Liliya Euro,Anu Suomalainen	175
7	Focal atrophy of the unilateral masticatory muscles caused by pure trigeminal motor neuropathy: case report 2018 ·Clinical Case Reports ·Antti Kämppi,(unknown),Pentti Kemppainen,Mari Kanerva,Jussi Toppila,Mari Auranen	10
8	Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy 2017 ·Neuromuscular Disorders ·Mari Auranen,Anders Paetau,Päivi Piirilä,(unknown),Tapani Salmi,Antti Lamminen,Mervi Löfberg,Signe Mosegaard,Rikke Katrine Jentoft Olsen,Tiina Tyni	22
9	Clinical and metabolic consequences of L-serine supplementation in hereditary sensory and autonomic neuropathy type 1C 2017 ·Molecular Case Studies ·Mari Auranen,Jussi Toppila,Saranya Suriyanarayanan,Museer A. Lone,Anders Paetau,Henna Tyynismaa,Thorsten Hornemann,Emil Ylikallio	23
10	Specific functional pathologies of Cx43 mutations associated with oculodentodigital dysplasia 2016 ·Molecular Biology of the Cell ·John J. Kelly,Jessica L. Esseltine,Qing Shao,Ethylin Wang Jabs,Jacinda B. Sampson,Mari Auranen,Donglin Bai,Dale W. Laird	20
11	Unique Exercise Lactate Profile in Muscle Phosphofructokinase Deficiency (Tarui Disease); Difference Compared with McArdle Disease 2016 ·Frontiers in Neurology ·Päivi Piirilä,Minna E. Similä,Johanna Palmio,Tomi Wuorimaa,Emil Ylikallio,Satu Sandell,(unknown),Lasse Uotila,Henna Tyynismaa,Bjarne Udd,Mari Auranen	9
12	Dominant transmission of de novo KIF1A motor domain variant underlying pure spastic paraplegia 2015 ·European Journal of Human Genetics ·Emil Ylikallio,Doyoun Kim,Pirjo Isohanni,Mari Auranen,Eunjoon Kim,Tuula Lönnqvist,Henna Tyynismaa	36
13	Novel mutations in DNAJB6 gene cause a very severe early-onset limb-girdle muscular dystrophy 1D disease 2015 ·Neuromuscular Disorders ·Johanna Palmio,Per Harald Jonson,Anni Evilä,Mari Auranen,Volker Straub,Kate Bushby,Anna Sárközy,Sari Kiuru‐Enari,Satu Sandell,Helena Pihko,Peter Hackman,Bjarne Udd	28
14	The Variant p.(Arg183Trp) in SPTLC2 Causes Late-Onset Hereditary Sensory Neuropathy 2015 ·NeuroMolecular Medicine ·Saranya Suriyanarayanan,Mari Auranen,Jussi Toppila,Anders Paetau,(unknown),Eino Palin,Wei Yu,(unknown),Beate Schlotter‐Weigel,(unknown),Angela Abicht,Bernd Rautenstrauß,Henna Tyynismaa,Maggie C. Walter,Thorsten Hornemann,Emil Ylikallio	19
15	Screening for late-onset Pompe disease in Finland 2014 ·Neuromuscular Disorders ·Johanna Palmio,Mari Auranen,Sari Kiuru‐Enari,Mervi Löfberg,Olaf A. Bodamer,Bjarne Udd	22
16	Pitt–Hopkins syndrome in two patients and further definition of the phenotype 2006 ·Clinical Dysmorphology ·Maarit Peippo,K. O. J. Simola,Leena Valanne,(unknown),Marketta Kähkönen,Mari Auranen,Jaakko Ignatius	43
17	Analysis of four neuroligin genes as candidates for autism 2005 ·European Journal of Human Genetics ·Tero Ylisaukko‐oja,Karola Rehnström,Mari Auranen,Raija Vanhala,Reija Alén,Elli Kempas,Pekka Ellonen,Joni A. Turunen,Ismo Makkonen,Raili Riikonen,Taina Nieminen‐von Wendt,Lennart von Wendt,Leena Peltonen,Irma Järvelä	114
18	Enrichment of the R77C α‐sarcoglycan gene mutation in finnish LGMD2D patients 2004 ·Muscle & Nerve ·Peter Hackman,Vesa Juvonen,J. Sarparanta,Maila Penttinen,T Äärimaa,(unknown),Mari Auranen,Helena Pihko,Reija Alén,(unknown),Tuula Lönnqvist,Hannu Kalimo,Bjarne Udd	21
19	Evidence for allelic association on chromosome 3q25–27 in families with autism spectrum disorders originating from a subisolate of Finland 2003 ·Molecular Psychiatry ·Mari Auranen,Teppo Varilo,Reija Alén,Raija Vanhala,Kristin L. Ayers,Elli Kempas,Tero Ylisaukko‐oja,Leena Peltonen,Irma Järvelä	29
20	Further evidence for linkage of autosomal-dominant medullary cystic kidney disease on chromosome 1q21 2001 ·Kidney International ·Mari Auranen,Sirpa Ala‐Mello,Joni A. Turunen,Irma Järvelä	22

About Mari Auranen

Mari Auranen is a scholar working on Clinical Biochemistry, Cellular and Molecular Neuroscience and Cell Biology, having authored 59 papers that have together received 2.2k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (12 papers), Hereditary Neurological Disorders (12 papers) and Muscle Physiology and Disorders (10 papers). The work is most often cited by research in Geriatrics and Gerontology (185 citations), Clinical Biochemistry (253 citations) and Physiology (106 citations). Mari Auranen has collaborated with scholars based in Finland, United States and United Kingdom. Frequent co-authors include Irma Järvelä, Anu Suomalainen, Raija Vanhala, Vidya Velagapudi, Leena Peltonen, Henna Tyynismaa, Emil Ylikallio, Nahid Khan, Eija Pirinen and Elli Kempas. Their work appears in journals such as SHILAP Revista de lepidopterología, Neurology and Cell Metabolism.

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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