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

Peers

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

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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	Gene prioritisation for enhancing molecular diagnosis in rare skeletal muscle disease cohort 2025 ·Journal of Medical Genetics ·(unknown), (unknown), (unknown), Ivana Babič Božović, Annalaura Torella, Mridul Johari, Aleš Maver, Katarina Pelin, Filippo M. Santorelli, Vincenzo Nigro, Peter Hackman, (unknown), Bjarne Udd, Marco Savarese	1
3	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
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	Long‐term favorable prognosis in late onset dominant distal titinopathy: Tibial muscular dystrophy 2023 ·European Journal of Neurology ·(unknown), Marco Savarese, Niina Sandholm, Peter Hackman, Bjarne Udd	2
6	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
7	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
8	Mutation update for the ACTN2 gene 2022 ·Human Mutation ·(unknown), Montse Olivé, (unknown), (unknown), Cristina Domínguez‐González, Mridul Johari, Annalaura Torella, Johann Böhm, (unknown), Vincenzo Nigro, Peter Hackman, Jocelyn Laporte, Bjarne Udd, Marco Savarese	15
9	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
10	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
11	Is Gene-Size an Issue for the Diagnosis of Skeletal Muscle Disorders? 2020 ·Journal of Neuromuscular Diseases ·Marco Savarese, (unknown), Mridul Johari, Peter Hackman, Bjarne Udd	7
12	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
13	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
14	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
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	Mutation screening of SEMA3A and SEMA7A in patients with congenital hypogonadotropic hypogonadism 2014 ·Pediatric Research ·Johanna Känsäkoski, Rainer Fagerholm, Eeva‐Maria Laitinen, Kirsi Vaaralahti, Peter Hackman, Nelly Pitteloud, Taneli Raivio, Johanna Tommiska	57
17	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
18	Muscle magnetic resonance imaging shows distinct diagnostic patterns in Welander and tibial muscular dystrophy 2004 ·Acta Neurologica Scandinavica ·I. Mahjneh, Antti Lamminen, (unknown), Anders Paetau, Peter Hackman, O Korhola, Hannu Somer	17
19	Interaction between smoking and asbestos in human lung adenocarcinoma: role of K-ras mutations. 1993 ·Environmental Health Perspectives ·Harri Vainio, Kirsti Husgafvel‐Pursiainen, S. Anttila, Antti Karjalainen, Peter Hackman, Timo Partanen	14
20	Detection of ras gene mutations in human lung cancer: comparison of two screening assays based on the polymerase chain reaction. 1992 ·Environmental Health Perspectives ·Kirsti Husgafvel‐Pursiainen, Maaret Ridanpää, Peter Hackman, S. Anttila, Antti Karjalainen, Agneta Önfelt, A L Børresen, H Vainio	9

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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