Anna Vihola

4.8k total citations
51 papers, 2.5k citations indexed

About

Anna Vihola is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Anna Vihola has authored 51 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 34 papers in Cardiology and Cardiovascular Medicine and 11 papers in Cell Biology. Recurrent topics in Anna Vihola's work include Muscle Physiology and Disorders (39 papers), Cardiomyopathy and Myosin Studies (33 papers) and RNA Research and Splicing (9 papers). Anna Vihola is often cited by papers focused on Muscle Physiology and Disorders (39 papers), Cardiomyopathy and Myosin Studies (33 papers) and RNA Research and Splicing (9 papers). Anna Vihola collaborates with scholars based in Finland, France and United States. Anna Vihola's co-authors include Peter Hackman, Bjarne Udd, J. Sarparanta, Bjarne Udd, Isabelle Richard, Sylvie Marchand, Isabelle Richard, Henna Haravuori, Stephan Lange and Mathias Gautel and has published in prestigious journals such as Science, Journal of Biological Chemistry and Brain.

In The Last Decade

Anna Vihola

48 papers receiving 2.5k citations

Peers

Countries citing papers authored by Anna Vihola

Since Specialization

Citations

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

Fields of papers citing papers by Anna Vihola

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Vihola

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Vihola. A scholar is included among the top collaborators of Anna Vihola 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 Anna Vihola. Anna Vihola 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	Characterization of novel CASQ1 variants in two families with unusual phenotypic features 2025 ·Journal of Neurology ·(unknown), Manu Jokela, (unknown), Sanna Huovinen, Cornelia Kornblum, Jens Reimann, Mridul Johari, Anna Vihola, J. Sarparanta, Bjarne Udd, Peter Hackman, Vilma‐Lotta Lehtokari, Katarina Pelin	0
2	A Titin Truncating Variant Causing a Dominant Myopathy With Cardiac Involvement in a Large Family 2024 ·Neurology Genetics ·Kristl G. Claeys, Marco Savarese, Per Harald Jonson, (unknown), Ana Töpf, Anna Vihola, Volker Straub, Bjarne Udd	0
3	CACNA1S Variant Associated With a Myalgic Myopathy Phenotype 2023 ·Neurology ·(unknown), Johanna Palmio, Manu Jokela, Päivi Hartikainen, Anna Vihola, Tuomas Rauramaa, Bjarne Udd	6
4	Extension of the DNAJB2a isoform in a dominant neuromyopathy family 2023 ·Human Molecular Genetics ·J. Sarparanta, Per Harald Jonson, Jens Reimann, Anna Vihola, H. Luque, Sini Penttilä, Mridul Johari, Marco Savarese, Peter Hackman, Cornelia Kornblum, Bjarne Udd	4
5	Comprehensive transcriptomic analysis shows disturbed calcium homeostasis and deregulation of T lymphocyte apoptosis in inclusion body myositis 2022 ·Journal of Neurology ·Mridul Johari, Anna Vihola, Johanna Palmio, Manu Jokela, Per Harald Jonson, J. Sarparanta, Sanna Huovinen, Marco Savarese, Peter Hackman, Bjarne Udd	14
6	Out-of-Frame Mutations in ACTN2 Last Exon Cause a Dominant Distal Myopathy With Facial Weakness 2021 ·Neurology Genetics ·Marco Savarese, Anna Vihola, Manu Jokela, Sanna Huovinen, Simonetta Gerevini, Annalaura Torella, Mridul Johari, Marina Scarlato, Per Harald Jonson, (unknown), Peter Hackman, Mathias Gautel, Vincenzo Nigro, Stefano C. Previtali, Bjarne Udd	7
7	Congenital asymmetric distal myopathy with hemifacial weakness caused by a heterozygous large de novo mosaic deletion in nebulin 2021 ·Neuromuscular Disorders ·(unknown), Vilma‐Lotta Lehtokari, (unknown), Anna Vihola, Maria Gardberg, Peter Hackman, Katarina Pelin, Manu Jokela, K. Kiiski, Bjarne Udd, Carina Wallgren‐Pettersson	6
8	An unusual ryanodine receptor 1 (RYR1) phenotype 2019 ·Neurology ·Manu Jokela, Giorgio Tasca, Anna Vihola, Eugenio Mercuri, Per Harald Jonson, Sara Lehtinen, (unknown), Marika Pane, Maria Alice Donati, Mridul Johari, Marco Savarese, Sanna Huovinen, Pirjo Isohanni, Johanna Palmio, Päivi Hartikainen, Bjarne Udd	12
9	Actininopathy: A new muscular dystrophy caused by ACTN2 dominant mutations 2019 ·Annals of Neurology ·Marco Savarese, Johanna Palmio, Juan José Poza, Jan Weinberg, Montse Olivé, Ana María Cobo, Anna Vihola, Per Harald Jonson, J. Sarparanta, F. García-Bragado, Jon Andoni Urtizberea, Peter Hackman, Bjarne Udd	26
10	Mutations in the J domain of DNAJB6 cause dominant distal myopathy 2019 ·Neuromuscular Disorders ·Johanna Palmio, Per Harald Jonson, Michio Inoue, J. Sarparanta, Rocío Bengoechea, Marco Savarese, Anna Vihola, Manu Jokela, Masanori Nakagawa, S. Noguchi, Montse Olivé, (unknown), Emı́lia Kerty, Peter Hackman, Conrad C. Weihl, Ichizo Nishino, Bjarne Udd	22
11	Differential Isoform Expression and Selective Muscle Involvement in Muscular Dystrophies 2015 ·American Journal Of Pathology ·Sanna Huovinen, Sini Penttilä, Panu Somervuo, (unknown), Petri Auvinen, Anna Vihola, (unknown), Katarina Pelin, Olayinka Raheem, Juha Salenius, Tiina Suominen, Peter Hackman, Bjarne Udd	10
12	CAPN3-mediated processing of C-terminal titin replaced by pathological cleavage in titinopathy 2015 ·Human Molecular Genetics ·Karine Charton, J. Sarparanta, Anna Vihola, (unknown), Per Harald Jonson, Laurence Suel, H. Luque, (unknown), Isabelle Richard, Bjarne Udd	36
13	The Phenotype of Dysferlin-Deficient Mice Is Not Rescued by Adeno-Associated Virus–Mediated Transfer of Anoctamin 5 2013 ·PubMed ·(unknown), (unknown), (unknown), Anna Vihola, Sylvie Marchand, Carinne Roudaut, (unknown), (unknown), Isabelle Richard, Karine Charton	14
14	Altered expression and splicing of Ca²⁺ metabolism genes in myotonic dystrophies DM1 and DM2 2012 ·Neuropathology and Applied Neurobiology ·Anna Vihola, Mario Sirito, Linda L. Bachinski, (unknown), Mark Screen, (unknown), Ralf Krahe, Bjarne Udd	22
15	Removal of the calpain 3 protease reverses the myopathology in a mouse model for titinopathies 2010 ·Human Molecular Genetics ·Karine Charton, Nathalie Danièle, Anna Vihola, Carinne Roudaut, Evelyne Gicquel, (unknown), Anne Couturier‐Tarrade, J. Sarparanta, Bjarne Udd, Isabelle Richard	30
16	Mutant (CCTG)n Expansion Causes Abnormal Expression of Zinc Finger Protein 9 (ZNF9) in Myotonic Dystrophy Type 2 2010 ·American Journal Of Pathology ·Olayinka Raheem, Shodimu-Emmanuel Olufemi, Linda L. Bachinski, Anna Vihola, Mario Sirito, (unknown), Hannu Haapasalo, Yiping Li, Bjarne Udd, Ralf Krahe	61
17	G.P.14.14 Differences in aberrant expression and splicing of genes involved in Ca2+ metabolism between myotonic dystrophy type 2 (DM2) and type 1 (DM1) 2007 ·Neuromuscular Disorders ·Anna Vihola, Mario Sirito, Linda L. Bachinski, Shodimu Emmanuel Olufemi, (unknown), Tiina Suominen, Bjarne Udd, Ralf Krahe	1
18	The Kinase Domain of Titin Controls Muscle Gene Expression and Protein Turnover 2005 ·Science ·Stephan Lange, Fengqing Xiang, (unknown), Anna Vihola, Peter Hackman, Elena Rostkova, Jakob Kristensen, Birgit Brandmeier, (unknown), Birgitta Hedberg, Lars Gunnarsson, Simon M. Hughes, Sylvie Marchand, Thomas Sejersen, Isabelle Richard, Lars Edström, Elisabeth Ehler, Bjarne Udd, Mathias Gautel	454
19	New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2) 2004 ·Neuromuscular Disorders ·Riitta Sallinen, Anna Vihola, Linda L. Bachinski, Kirsi Huoponen, Hannu Haapasalo, Peter Hackman, Shaozeng Zhang, Mario Sirito, Hannu Kalimo, G. Meola, Nina Horelli‐Kuitunen, Maija Wessman, Ralf Krahe, Bjarne Udd	37
20	The role of titin in muscular disorders 2003 ·Annals of Medicine ·(unknown), Anna Vihola, (unknown)	28

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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