Per Harald Jonson

1.8k total citations
31 papers, 779 citations indexed

About

Per Harald Jonson is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Per Harald Jonson has authored 31 papers receiving a total of 779 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 13 papers in Cardiology and Cardiovascular Medicine and 5 papers in Genetics. Recurrent topics in Per Harald Jonson's work include Muscle Physiology and Disorders (14 papers), Cardiomyopathy and Myosin Studies (13 papers) and RNA Research and Splicing (8 papers). Per Harald Jonson is often cited by papers focused on Muscle Physiology and Disorders (14 papers), Cardiomyopathy and Myosin Studies (13 papers) and RNA Research and Splicing (8 papers). Per Harald Jonson collaborates with scholars based in Finland, France and Italy. Per Harald Jonson's co-authors include Steffen B. Petersen, Maria Teresa Neves‐Petersen, Bjarne Udd, J. Sarparanta, Peter Hackman, Anna Vihola, Marco Savarese, Anni Evilä, H. Luque and Mark Screen and has published in prestigious journals such as PLoS ONE, Neurology and Biochemistry.

In The Last Decade

Per Harald Jonson

29 papers receiving 770 citations

Peers

Countries citing papers authored by Per Harald Jonson

Since Specialization

Citations

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

Fields of papers citing papers by Per Harald Jonson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Per Harald Jonson. 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 Per Harald Jonson. The network helps show where Per Harald Jonson may publish in the future.

Co-authorship network of co-authors of Per Harald Jonson

This figure shows the co-authorship network connecting the top 25 collaborators of Per Harald Jonson. A scholar is included among the top collaborators of Per Harald Jonson 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 Per Harald Jonson. Per Harald Jonson 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	OBSCN undergoes extensive alternative splicing during human cardiac and skeletal muscle development 2025 ·Skeletal Muscle ·Ali Oghabian, Per Harald Jonson, (unknown), Mridul Johari, (unknown), David Gómez‐Andrés, Francina Munell, Jessica Camacho, (unknown), Juha Sinisalo, Heli Tolppanen, (unknown), Peter Hackman, Marco Savarese, (unknown)	2
2	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
3	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
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	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
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	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	Abnormal Splicing of NEDD4 in Myotonic Dystrophy Type 2 2014 ·American Journal Of Pathology ·Mark Screen, Per Harald Jonson, Olayinka Raheem, Johanna Palmio, Reijo Laaksonen, Terho Lehtimäki, Mario Sirito, Ralf Krahe, Peter Hackman, Bjarne Udd	16
16	Gene Expression Profiling in Tibial Muscular Dystrophy Reveals Unfolded Protein Response and Altered Autophagy 2014 ·PLoS ONE ·Mark Screen, Olayinka Raheem, (unknown), Per Harald Jonson, Sanna Huovinen, Peter Hackman, Bjarne Udd	14
17	A critical view on conservative mutations 2001 ·Protein Engineering Design and Selection ·Per Harald Jonson, Steffen B. Petersen	30
18	Amino acid neighbours and detailed conformational analysis of cysteines in proteins 1999 ·Protein Engineering Design and Selection ·Maria Teresa Neves‐Petersen, Per Harald Jonson, Steffen B. Petersen	157
19	Protein engineering the surface of enzymes 1998 ·Journal of Biotechnology ·Steffen B. Petersen, Per Harald Jonson, Peter Fojan, Evamaria I. Petersen, Maria Teresa Neves‐Petersen, S.B. Hansen, (unknown), Edward Hough	49
20	The Origin of Trypsin: Evidence for Multiple Gene Duplications in Trypsins 1998 ·Journal of Molecular Evolution ·António M. Baptista, Per Harald Jonson, Edward Hough, Steffen B. Petersen	15

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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