Peter Hackman

7.1k total citations
96 papers, 3.6k citations indexed

About

Peter Hackman is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Peter Hackman has authored 96 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Molecular Biology, 48 papers in Cardiology and Cardiovascular Medicine and 21 papers in Genetics. Recurrent topics in Peter Hackman's work include Muscle Physiology and Disorders (49 papers), Cardiomyopathy and Myosin Studies (48 papers) and Neurogenetic and Muscular Disorders Research (21 papers). Peter Hackman is often cited by papers focused on Muscle Physiology and Disorders (49 papers), Cardiomyopathy and Myosin Studies (48 papers) and Neurogenetic and Muscular Disorders Research (21 papers). Peter Hackman collaborates with scholars based in Finland, France and United States. Peter Hackman's co-authors include Bjarne Udd, Anna Vihola, J. Sarparanta, Bjarne Udd, Sylvie Marchand, Isabelle Richard, Anni Evilä, Marco Savarese, Isabelle Richard and Henna Haravuori and has published in prestigious journals such as Science, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Peter Hackman

92 papers receiving 3.5k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Peter Hackman 2.8k 1.5k 674 592 527 96 3.6k
Bjarne Udd 3.8k 1.4× 2.1k 1.3× 1.2k 1.8× 977 1.7× 831 1.6× 158 5.2k
Dennis Dooijes 3.2k 1.2× 2.1k 1.4× 598 0.9× 438 0.7× 304 0.6× 110 5.7k
Duygu Selcen 2.3k 0.8× 979 0.6× 765 1.1× 382 0.6× 1.1k 2.1× 87 3.8k
Satomi Mitsuhashi 1.8k 0.7× 333 0.2× 375 0.6× 299 0.5× 299 0.6× 99 2.4k
Bernd Wollnik 2.8k 1.0× 532 0.3× 306 0.5× 186 0.3× 304 0.6× 138 4.3k
Louise R. Rodino‐Klapac 3.8k 1.4× 853 0.6× 489 0.7× 741 1.3× 307 0.6× 102 4.5k
Rita Barresi 2.8k 1.0× 506 0.3× 623 0.9× 424 0.7× 519 1.0× 52 3.5k
Andreas Roos 1.3k 0.5× 195 0.1× 501 0.7× 250 0.4× 492 0.9× 134 2.1k
Eduard Gallardo 2.2k 0.8× 363 0.2× 1.1k 1.7× 407 0.7× 435 0.8× 133 4.6k
Nathalie Bourg 2.7k 1.0× 548 0.4× 943 1.4× 235 0.4× 1.2k 2.3× 34 3.1k

Countries citing papers authored by Peter Hackman

Since Specialization
Citations

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

Fields of papers citing papers by Peter Hackman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Hackman

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

All Works

20 of 20 papers shown
1.
Jokela, Manu, Sanna Huovinen, Cornelia Kornblum, et al.. (2025). Characterization of novel CASQ1 variants in two families with unusual phenotypic features. Journal of Neurology. 272(12). 789–789.
2.
Božović, Ivana Babič, Annalaura Torella, Mridul Johari, et al.. (2025). Gene prioritisation for enhancing molecular diagnosis in rare skeletal muscle disease cohort. Journal of Medical Genetics. 62(5). 350–357. 1 indexed citations
3.
Oghabian, Ali, Per Harald Jonson, Mridul Johari, et al.. (2025). OBSCN undergoes extensive alternative splicing during human cardiac and skeletal muscle development. Skeletal Muscle. 15(1). 5–5. 2 indexed citations
4.
Zhong, Huahua, Mridul Johari, Shintaro Katayama, et al.. (2024). Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions. Communications Biology. 7(1). 438–438. 2 indexed citations
5.
Savarese, Marco, et al.. (2023). Long‐term favorable prognosis in late onset dominant distal titinopathy: Tibial muscular dystrophy. European Journal of Neurology. 30(4). 1080–1088. 2 indexed citations
6.
Sarparanta, J., Per Harald Jonson, Jens Reimann, et al.. (2023). Extension of the DNAJB2a isoform in a dominant neuromyopathy family. Human Molecular Genetics. 32(21). 3029–3039. 4 indexed citations
7.
Olivé, Montse, Cristina Domínguez‐González, Mridul Johari, et al.. (2022). Mutation update for the ACTN2 gene. Human Mutation. 43(12). 1745–1756. 15 indexed citations
8.
Johari, Mridul, Anna Vihola, Johanna Palmio, et al.. (2022). Comprehensive transcriptomic analysis shows disturbed calcium homeostasis and deregulation of T lymphocyte apoptosis in inclusion body myositis. Journal of Neurology. 269(8). 4161–4173. 14 indexed citations
9.
Johari, Mridul, George K. Papadimas, Constantinos Papadopoulos, et al.. (2022). Adult‐onset dominant muscular dystrophy in Greek families caused by Annexin A11. Annals of Clinical and Translational Neurology. 9(10). 1660–1667. 12 indexed citations
10.
Savarese, Marco, Anna Vihola, Manu Jokela, et al.. (2021). Out-of-Frame Mutations in ACTN2 Last Exon Cause a Dominant Distal Myopathy With Facial Weakness. Neurology Genetics. 7(5). e619–e619. 7 indexed citations
11.
Savarese, Marco, et al.. (2020). Is Gene-Size an Issue for the Diagnosis of Skeletal Muscle Disorders?. Journal of Neuromuscular Diseases. 7(3). 203–216. 7 indexed citations
12.
Savarese, Marco, Johanna Palmio, Juan José Poza, et al.. (2019). Actininopathy: A new muscular dystrophy caused by ACTN2 dominant mutations. Annals of Neurology. 85(6). 899–906. 26 indexed citations
13.
Palmio, Johanna, Per Harald Jonson, Michio Inoue, et al.. (2019). Mutations in the J domain of DNAJB6 cause dominant distal myopathy. Neuromuscular Disorders. 30(1). 38–46. 22 indexed citations
14.
Savarese, Marco, Per Harald Jonson, Sanna Huovinen, et al.. (2018). The complexity of titin splicing pattern in human adult skeletal muscles. Skeletal Muscle. 8(1). 11–11. 46 indexed citations
15.
Johari, Mridul, Meharji Arumilli, Johanna Palmio, et al.. (2017). Association study reveals novel risk loci for sporadic inclusion body myositis. European Journal of Neurology. 24(4). 572–577. 9 indexed citations
16.
Palmio, Johanna, Tiina Suominen, Anni Evilä, et al.. (2012). Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5. Neurology. 78(12). 897–903. 82 indexed citations
17.
Lange, Stephan, Fengqing Xiang, Anna Vihola, et al.. (2005). The Kinase Domain of Titin Controls Muscle Gene Expression and Protein Turnover. Science. 308(5728). 1599–1603. 454 indexed citations
18.
Mahjneh, I., Antti Lamminen, Anders Paetau, et al.. (2004). Muscle magnetic resonance imaging shows distinct diagnostic patterns in Welander and tibial muscular dystrophy. Acta Neurologica Scandinavica. 110(2). 87–93. 17 indexed citations
19.
Vainio, Harri, Kirsti Husgafvel‐Pursiainen, S. Anttila, et al.. (1993). Interaction between smoking and asbestos in human lung adenocarcinoma: role of K-ras mutations.. Environmental Health Perspectives. 101(suppl 3). 189–192. 14 indexed citations
20.
Husgafvel‐Pursiainen, Kirsti, Maaret Ridanpää, Peter Hackman, et al.. (1992). Detection of ras gene mutations in human lung cancer: comparison of two screening assays based on the polymerase chain reaction.. Environmental Health Perspectives. 98. 183–185. 9 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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