Pekka Nokelainen

852 total citations
15 papers, 584 citations indexed

About

Pekka Nokelainen is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Pekka Nokelainen has authored 15 papers receiving a total of 584 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 4 papers in Genetics. Recurrent topics in Pekka Nokelainen's work include Mitochondrial Function and Pathology (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Muscle Physiology and Disorders (4 papers). Pekka Nokelainen is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Muscle Physiology and Disorders (4 papers). Pekka Nokelainen collaborates with scholars based in Finland, United Kingdom and United States. Pekka Nokelainen's co-authors include Merimaaria Espo, Ilkka Julkunen, Reija Alén, Tiina Wallden, Markku Partinen, Christer Hublin, Pekka Kaipainen, Miika Linna, Heli Sätilä and Ismo Ilveskoski and has published in prestigious journals such as Nature Genetics, PLoS ONE and Annals of Neurology.

In The Last Decade

Pekka Nokelainen

14 papers receiving 562 citations

Peers

Countries citing papers authored by Pekka Nokelainen

Since Specialization

Citations

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

Fields of papers citing papers by Pekka Nokelainen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pekka Nokelainen

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Methods for Detecting Abnormal Ventilation in Children - the Case Study of 13-Years old Pitt-Hopkins Girl 2023 ·Child Neurology Open ·Pekka Nokelainen, (unknown), Sari‐Leena Himanen, (unknown), M. Tenhunen	1
2	Finnish children who experienced narcolepsy after receiving the Pandemrix vaccine during the 2009–2010 H1N1 pandemic demonstrated high level of psychosocial problems 2021 ·Acta Paediatrica ·(unknown), Hannu Heiskala, Eeva T. Aronen, Outi Saarenpää‐Heikkilä, Päivi Olsén, Pekka Nokelainen, Turkka Kirjavainen	3
3	Atypical phenotypes in titinopathies explained by second titin mutations 2014 ·Annals of Neurology ·Anni Evilä, Anna Vihola, J. Sarparanta, Olayinka Raheem, Johanna Palmio, Satu Sandell, B. Eymard, Isabel Illa, Ricard Rojas‐García, Karolina Hankiewicz, Luís Negrão, Tuija Löppönen, Pekka Nokelainen, Mikko Kärppä, Sini Penttilä, Mark Screen, Tiina Suominen, Isabelle Richard, Peter Hackman, Bjarne Udd	63
4	P.3.11 Atypical phenotypes in titinopathies explained by second titin mutations and compound heterozygosity 2013 ·Neuromuscular Disorders ·Anni Evilä, Anna Vihola, J. Sarparanta, (unknown), Satu Sandell, B. Eymard, Isabel Illa, Ricard Rojas‐García, Karolina Hankiewicz, Luís Negrão, Tuija Löppönen, Pekka Nokelainen, Mikko Kärppä, (unknown), Mark Screen, Tiina Suominen, Isabelle Richard, Peter Hackman, B. Udd	2
5	Increased Incidence and Clinical Picture of Childhood Narcolepsy following the 2009 H1N1 Pandemic Vaccination Campaign in Finland 2012 ·PLoS ONE ·Markku Partinen, Outi Saarenpää‐Heikkilä, Ismo Ilveskoski, Christer Hublin, Miika Linna, Päivi Olsén, Pekka Nokelainen, Reija Alén, Tiina Wallden, Merimaaria Espo, Harri Rusanen, (unknown), Heli Sätilä, (unknown), Pekka Kaipainen, Ilkka Julkunen, Turkka Kirjavainen	286
6	Deep Serotonergic and Dopaminergic Structures in Fetal Alcoholic Syndrome: A Study with nor-β-CIT-Single-Photon Emission Computed Tomography and Magnetic Resonance Imaging Volumetry 2005 ·Biological Psychiatry ·Raili Riikonen, Pekka Nokelainen, (unknown), (unknown), Kirsti Kumpulainen, Mervi Könönen, (unknown), Jyrki T. Kuikka	60
7	Genetic effects on human cognition: lessons from the study of mental retardation syndromes 2002 ·Journal of Neurology Neurosurgery & Psychiatry ·Pekka Nokelainen	15
8	A Patient With 2 Different Repeat Expansion Mutations 2000 ·Archives of Neurology ·Pekka Nokelainen, Hannu Heiskala, Anna‐Elina Lehesjoki, Markus Kaski	5
9	Linkage Analyses in Tibial Muscular Dystrophy 1996 ·Human Heredity ·Pekka Nokelainen, (unknown), Hannu Somer, Leena Peltonen	1
10	Reply to “Meiotic drive and myotonic dystrophy” 1995 ·Nature Genetics ·Nessa Carey, Keith Johnson, Pekka Nokelainen, Leena Peltonen, (unknown), Vesa Juvonen, Maria Anvret, Ulla Grandell, Kokila Chotai, E. Graeme Robertson, Helen Middleton‐Price, Sue Malcolm	3
11	A microsatellite polymorphism in the von Willebrand factor gene: comparison of allele frequencies in different population samples and evaluation for forensic medicine 1994 ·Forensic Science International ·Antti Sajantila, (unknown), Matti Lukka, Ann‐Christine Syvänen, Pekka Nokelainen, Pertti Sistonen, Leena Peltonen, Bruce Budowle	26
12	The DM mutation; diagnostic applications in the Finnish population 1993 ·Clinical Genetics ·Pekka Nokelainen, Peggy Shelbourne, Duncan Shaw, J. David Brook, H G Harley, Keith Johnson, Hannu Somer, M L Savontaus, Leena Peltonen	3
13	Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophy 1992 ·Journal of the Neurological Sciences ·B. Udd, Juhani Rapola, Pekka Nokelainen, Eri Arikawa, Hannu Somer	29
14	Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations. 1992 ·Journal of Medical Genetics ·June Davies, Hidehisa Yamagata, Peggy Shelbourne, Jessica L. Buxton, Toshio Ogihara, Pekka Nokelainen, M. Nakagawa, R Williamson, Keith Johnson, T. Miki	79
15	Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population 1990 ·Human Genetics ·Pekka Nokelainen, (unknown), Robert Winqvist, (unknown), Hannu Somer, Jaakko Leisti, Keith Johnson, Marja‐Liisa Savontaus, Leena Peltonen	8

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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