Bjarne Udd

10.7k total citations
158 papers, 5.2k citations indexed

About

Bjarne Udd is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Bjarne Udd has authored 158 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 122 papers in Molecular Biology, 81 papers in Cardiology and Cardiovascular Medicine and 42 papers in Cellular and Molecular Neuroscience. Recurrent topics in Bjarne Udd's work include Muscle Physiology and Disorders (91 papers), Cardiomyopathy and Myosin Studies (77 papers) and Genetic Neurodegenerative Diseases (38 papers). Bjarne Udd is often cited by papers focused on Muscle Physiology and Disorders (91 papers), Cardiomyopathy and Myosin Studies (77 papers) and Genetic Neurodegenerative Diseases (38 papers). Bjarne Udd collaborates with scholars based in Finland, France and United States. Bjarne Udd's co-authors include Peter Hackman, Anna Vihola, J. Sarparanta, Isabelle Richard, Johanna Palmio, Marco Savarese, Sini Penttilä, Ralf Krahe, Hannu Somer and Per Harald Jonson and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and PLoS ONE.

In The Last Decade

Bjarne Udd

152 papers receiving 5.1k citations

Peers

Countries citing papers authored by Bjarne Udd

Since Specialization

Citations

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

Fields of papers citing papers by Bjarne Udd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bjarne Udd

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

All Works

Sort: Min cites: Since: Top N: Style:

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	Different Lower Limb Muscle MRI Patterns in Autosomal Dominant Titinopathies 2025 ·European Journal of Neurology ·David Gómez‐Andrés, (unknown), Jordi Díaz‐Manera, Katrin Õunap, (unknown), (unknown), Marco Savarese, Francina Munell, Bjarne Udd	0
3	Protein‐extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregation 2024 ·Annals of Clinical and Translational Neurology ·(unknown), Kevin J. Felice, Per Harald Jonson, J. Sarparanta, (unknown), Inès Harzallah, Renaud Touraine, Lynn Pais, Christina Austin‐Tse, Vijay Ganesh, (unknown), Heidi L. Rehm, Michael K. Hehir, S. H. Subramony, Qian Wu, Bjarne Udd, Marco Savarese	1
4	Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions 2024 ·Communications Biology ·Huahua Zhong, (unknown), Mridul Johari, Shintaro Katayama, Ali Oghabian, Per Harald Jonson, Peter Hackman, Marco Savarese, Bjarne Udd	2
5	CACNA1S Variant Associated With a Myalgic Myopathy Phenotype 2023 ·Neurology ·(unknown), Johanna Palmio, Manu Jokela, Päivi Hartikainen, Anna Vihola, Tuomas Rauramaa, Bjarne Udd	6
6	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
7	Adult‐onset dominant muscular dystrophy in Greek families caused by Annexin A11 2022 ·Annals of Clinical and Translational Neurology ·Mridul Johari, George K. Papadimas, Constantinos Papadopoulos, Sophia Xirou, (unknown), (unknown), (unknown), Marco Savarese, Peter Hackman, Bjarne Udd	12
8	Use of animal models to understand titin physiology and pathology 2022 ·Journal of Cellular and Molecular Medicine ·(unknown), (unknown), Marco Savarese, Bjarne Udd	9
9	Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New Results 2020 ·International Journal of Molecular Sciences ·J. Sarparanta, Per Harald Jonson, (unknown), Bjarne Udd	48
10	1st ENMC European meeting: The EURO-NMD pathology working group Recommended Standards for Muscle Pathology Amsterdam, The Netherlands, 7 December 2018 2019 ·Neuromuscular Disorders ·Bjarne Udd, Werner Stenzel, Anders Oldfors, Montse Olivé, Norma B. Romero, Martin Lammens, Benno Küsters, C. Sewry, Hans‐Hilmar Goebel, Teresinha Evangelista	34
11	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
12	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
13	The complexity of titin splicing pattern in human adult skeletal muscles 2018 ·Skeletal Muscle ·Marco Savarese, Per Harald Jonson, Sanna Huovinen, Lars Paulín, Petri Auvinen, Bjarne Udd, Peter Hackman	46
14	Novel valosin-containing protein mutations associated with multisystem proteinopathy 2018 ·Neuromuscular Disorders ·(unknown), (unknown), Hiroshi Yoshioka, Anita Lakatos, (unknown), Marjorie R. Grafe, Johanna Palmio, (unknown), Yadollah Harati, M. Omizo, Bjarne Udd, Virginia Kimonis	13
15	Association study reveals novel risk loci for sporadic inclusion body myositis 2017 ·European Journal of Neurology ·Mridul Johari, Meharji Arumilli, Johanna Palmio, Marco Savarese, Giorgio Tasca, Massimiliano Mirabella, Niina Sandholm, Hannes Lohi, Peter Hackman, Bjarne Udd	9
16	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
17	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
18	Lihastautien diagnostiikka tarkentuu: potilaita Suomessa yli 10000 2007 ·Bjarne Udd	1
19	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
20	Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia 2000 ·European Journal of Human Genetics ·(unknown), Bjarne Udd, Vesa Juvonen, Peter M. Andersen, (unknown), (unknown), P. Sistonen, (unknown), Lisbeth Tranebjærg, Carina Wallgren‐Pettersson, (unknown)	18

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.

Explore authors with similar magnitude of impact