Pirjo Isohanni

4.6k total citations
45 papers, 1.7k citations indexed

About

Pirjo Isohanni is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Pirjo Isohanni has authored 45 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 19 papers in Clinical Biochemistry and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Pirjo Isohanni's work include Mitochondrial Function and Pathology (25 papers), Metabolism and Genetic Disorders (19 papers) and ATP Synthase and ATPases Research (10 papers). Pirjo Isohanni is often cited by papers focused on Mitochondrial Function and Pathology (25 papers), Metabolism and Genetic Disorders (19 papers) and ATP Synthase and ATPases Research (10 papers). Pirjo Isohanni collaborates with scholars based in Finland, Sweden and Netherlands. Pirjo Isohanni's co-authors include Anu Suomalainen, Anders Paetau, Tuula Lönnqvist, Helena Pihko, Johanna Uusimaa, Henna Tyynismaa, Riitta Herva, Anna H. Hakonen, Liliya Euro and Nicole J. Lake and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Pirjo Isohanni

44 papers receiving 1.7k citations

Peers

Countries citing papers authored by Pirjo Isohanni

Since Specialization

Citations

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

Fields of papers citing papers by Pirjo Isohanni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pirjo Isohanni

This figure shows the co-authorship network connecting the top 25 collaborators of Pirjo Isohanni. A scholar is included among the top collaborators of Pirjo Isohanni 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 Pirjo Isohanni. Pirjo Isohanni 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	Without ENMG, detecting pediatric vincristine neuropathy is a challenge 2024 ·Clinical Neurophysiology Practice ·(unknown), Pirjo Isohanni, Jukka Kanerva, Tuula Lönnqvist, Leena Lauronen	0
2	Genetic etiology of progressive pediatric neurological disorders 2023 ·Pediatric Research ·(unknown), (unknown), (unknown), Virginia Brilhante, Tuula Lönnqvist, Pirjo Isohanni, Anu Suomalainen	5
3	Rare PMP22 variants in mild to severe neuropathy uncorrelated to plasma GDF15 or neurofilament light 2023 ·Neurogenetics ·(unknown), (unknown), (unknown), Nadine Huber, Sanna‐Kaisa Herukka, Annakaisa Haapasalo, Pirjo Isohanni, Henna Tyynismaa, Mari Auranen, Emil Ylikallio	3
4	Vegan diet in young children remodels metabolism and challenges the statuses of essential nutrients 2021 ·EMBO Molecular Medicine ·(unknown), Liisa Korkalo, Riitta Freese, Essi Skaffari, Pirjo Isohanni, Mikko Niemi, Jaakko Nevalainen, Helena Gylling, Nicola Zamboni, Maijaliisa Erkkola, Anu Suomalainen	65
5	Phenotypic spectrum and clinical course of single large-scale mitochondrial DNA deletion disease in the paediatric population: a multicentre study 2021 ·Journal of Medical Genetics ·(unknown), John Vissing, Elsebet Østergaard, Laurence A. Bindoff, I.F.M. de Coo, Martin Engvall, Omar Hikmat, Pirjo Isohanni, Gittan Kollberg, Christopher Lindberg, Kari Majamaa, K Naess, Johanna Uusimaa, M. Tulinius, Niklas Darín	11
6	The impact of gender, puberty, and pregnancy in patients with POLG disease 2020 ·Annals of Clinical and Translational Neurology ·Omar Hikmat, K Naess, Martin Engvall, Claus Klingenberg, Magnhild Rasmussen, Chantal Tallaksen, Christian Samsonsen, Eylert Brodtkorb, Elsebet Østergaard, I.F.M. de Coo, (unknown), Pirjo Isohanni, Johanna Uusimaa, Niklas Darín, Shamima Rahman, Laurence A. Bindoff	8
7	Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases 2020 ·Journal of Inherited Metabolic Disease ·Omar Hikmat, K Naess, Martin Engvall, Claus Klingenberg, Magnhild Rasmussen, Chantal Tallaksen, Eylert Brodtkorb, Elsebet Østergaard, I.F.M. de Coo, (unknown), Pirjo Isohanni, Johanna Uusimaa, Niklas Darín, Shamima Rahman, Laurence A. Bindoff	46
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	Elevated cerebrospinal fluid protein in POLG‐related epilepsy: Diagnostic and prognostic implications 2018 ·Epilepsia ·Omar Hikmat, K Naess, Martin Engvall, Claus Klingenberg, Magnhild Rasmussen, Chantal Tallaksen, Eylert Brodtkorb, Torunn Fiskerstrand, Pirjo Isohanni, Johanna Uusimaa, Niklas Darín, Shamima Rahman, Laurence A. Bindoff	6
10	Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome 2017 ·Human Molecular Genetics ·(unknown), Christopher J. Carroll, Uwe Richter, Liliya Euro, (unknown), Anders Paetau, Pirjo Isohanni, Anu Suomalainen	41
11	A complex genomic locus drives mt DNA replicase POLG expression to its disease‐related nervous system regions 2017 ·EMBO Molecular Medicine ·Joni Nikkanen, (unknown), Diego Balboa, Maarja Haugas, Juha Partanen, Anders Paetau, Pirjo Isohanni, Virginia Brilhante, Anu Suomalainen	6
12	ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia 2017 ·Human Molecular Genetics ·Helen Cooper, Yang Yang, Emil Ylikallio, Rafil Khairullin, (unknown), (unknown), Liliya Euro, Eino Palin, Alexander Wolf, Ras Trokovic, Pirjo Isohanni, Seppo Kaakkola, Mari Auranen, Tuula Lönnqvist, Sjoerd Wanrooij, Henna Tyynismaa	53
13	Modified Atkins diet induces subacute selective ragged‐red‐fiber lysis in mitochondrial myopathy patients 2016 ·EMBO Molecular Medicine ·Sofia Ahola, Mari Auranen, Pirjo Isohanni, (unknown), (unknown), Jana Buzková, Vidya Velagapudi, Nina Lundbom, Antti Hakkarainen, (unknown), Päivi Piirilä, Kirsi H. Pietiläinen, Anu Suomalainen	50
14	Leigh Syndrome 2015 ·Journal of Neuropathology & Experimental Neurology ·Nicole J. Lake, Matthew Bird, Pirjo Isohanni, Anders Paetau	107
15	Dominant transmission of de novo KIF1A motor domain variant underlying pure spastic paraplegia 2015 ·European Journal of Human Genetics ·Emil Ylikallio, Doyoun Kim, Pirjo Isohanni, Mari Auranen, Eunjoon Kim, Tuula Lönnqvist, Henna Tyynismaa	36
16	A multicenter study on Leigh syndrome: disease course and predictors of survival 2014 ·Orphanet Journal of Rare Diseases ·Kalliopi Sofou, I.F.M. de Coo, Pirjo Isohanni, Elsebet Østergaard, K Naess, Linda De Meırleır, Charalampos Tzoulis, Johanna Uusimaa, (unknown), Tuula Lönnqvist, Helena Pihko, Katariina Mankinen, Laurence A. Bindoff, M. Tulinius, Niklas Darín	161
17	Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy 2012 ·Human Molecular Genetics ·(unknown), Srujana S. Yadavalli, Liliya Euro, Pirjo Isohanni, Alexandra Götz, Christopher J. Carroll, Leena Valanne, Fowzan S. Alkuraya, Johanna Uusimaa, Anders Paetau, (unknown), Helena Pihko, Michael Ibba, Henna Tyynismaa, Anu Suomalainen	123
18	DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis 2009 ·Journal of Medical Genetics ·Pirjo Isohanni, Tarja Linnankivi, Jana Buzková, Tuula Lönnqvist, Helena Pihko, Leena Valanne, Pentti J. Tienari, Irina Elovaara, Tuula Pirttilä, Mauri Reunanen, Keijo Koivisto, Sanna Marjavaara, Anu Suomalainen	48
19	Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome 2008 ·Brain ·Alexandra Götz, Pirjo Isohanni, Helena Pihko, Anders Paetau, Riitta Herva, Outi Saarenpää‐Heikkilä, Leena Valanne, Sanna Marjavaara, Anu Suomalainen	61
20	Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion 2007 ·Brain ·Anna H. Hakonen, Pirjo Isohanni, Anders Paetau, Riitta Herva, Anu Suomalainen, Tuula Lönnqvist	145

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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