Mika Martikainen
 M.D., Ph.D., Professor of Neurology


mikmar@utu.fi



Follow my tweets @mhmartikainen

ORCID identifierhttps://orcid.org/0000-0002-7604-8081

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Areas of expertise
Mitochondrial disease; movement disorders; neurogenetics; clinical neurology

Research community or research topic
My research team is part of the Turku Centre for Lifespan Research at the University of Turku.

Biography

Professor of neurology at the University of Oulu (since February 2023). Adjunct professor (docent) of neurology at the University of Turku since 2014. Associate Professor of neurology at University of Turku from September 2021 to January 2023. Post doc (Sigrid Jusélius Fellowship) at Wellcome Centre for Mitochondrial Research, Newcastle University, Newcastle-upon-Tyne, UK, in 2014-2015. Ph.D. (neurology) 2012. Medical specialist (neurology) 2009. M.D. 2002. Medical education and specialist training at the University of Turku, Finland. Erasmus Fellowship studies at the Trinity College, Dublin, Ireland, in 2001.



Research

Our research interests are focussed on the clinical, genetic, and epidemiological aspects of human mitochondrial disease. We are also involved in movement disorder neurology research, particularly in the context of inherited neurological disease (e.g. monogenic Parkinson's disease). Part of the MJFF Global Genetic Parkinson's Disease Study Group; part of DystoniaNet Europe. Collaboration with researchers at University of Helsinki (FIN), Newcastle University (UK), University of Groningen (NED), University of Lübeck (GER).



Teaching

Interest in Medical Education. Experience as a clinical teacher (neurology) since 2015. Special competence in Medical Education (Finnish Medical Association). Medical education studies at the University of Turku, Karolinska Institute (Sweden), ACGME (USA). National coordinator of postgraduate medical education development in Finland, 2018 - 2021.



Publications
  
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  • Clinical features and treatment of stroke-like episodes in mitochondrial disease: a cohort-based study  (2025)  
    • Journal of Neurology
     Mickelsson, Nora; Hirvonen, Jussi; Martikainen, Mika H.
    (
    A1 Refereed original research article in a scientific journal)


  • Incidence and prevalence of mtDNA-related adult mitochondrial disease in Southwest Finland, 2009-2022: an observational, population-based study  (2024)  
    • BMJ neurology open
     Martikainen Mika H., Majamaa Kari
    (
    A1 Refereed original research article in a scientific journal)


  • Novel SLC18A2 Variant in Infantile Dystonia-Parkinsonism Type 2  (2024)  
    • Case Reports in Neurological Medicine
     Kaasalainen Sakari, Arikka Harri, Martikainen Mika H., Kaasinen Valtteri
    (
    A1 Refereed original research article in a scientific journal)


  • Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort  (2023)  
    • Movement Disorders
     Vollstedt Eva-Juliane, Schaake Susen, Lohmann Katja, Padmanabhan Shalini, Brice Alexis, Lesage Suzanne, Tesson Christelle, Vidailhet Marie, Wurster Isabel, Hentati Faycel, Mirelman Anat, Giladi Nir, Marder Karen, Waters Cheryl, Fahn Stanley, Kasten Meike, Bruggemann Norbert, Borsche Max, Foroud Tatiana, Tolosa Eduardo, Garrido Alicia, Annesi Grazia, Gagliardi Monica, Bozi Maria, Stefanis Leonidas, Ferreira Joaquim J, Guedes Leonor Correia, Avenali Micol, Petrucci Simona, Clark Lorraine, Fedotova Ekaterina Y, Abramycheva Natalya Y, Alvarez Victoria, Menendez-Gonzalez Manuel, Maestre Silvia Jesús, Gómez-Garre Pilar, Mir Pablo, Belin Andrea Carmine, Ran Caroline, Lin Chin-Hsien, Kuo Ming-Che, Crosiers David, Wszolek Zbigniew K, Ross Owen A, Jankovic Joseph, Nishioka Kenya, Funayama Manabu, Clarimon Jordi, Williams-Gray Caroline H, Camacho Marta, Cornejo-Olivas Mario, Torres-Ramirez Luis, Wu Yih-Ru, Lee-Chen Guey-Jen, Morgadinho Ana, Pulkes Teeratorn, Termsarasab Pichet, Berg Daniela, Kuhlenbäumer G, Kuhn Andrea A, Borngraber Friederike, de Michele Giuseppe, De Rosa Anna, Zimprich Alexander, Puschmann Andreas, Mellick George D, Dorszewska Jolanta, Carr Jonathan, Ferese Rosangela, Gambardella Stefano, Chase Bruce, Markopoulou Katerina, Satake Wataru, Toda Tatsushi, Rossi Malco, Merello Marcelo, Lynch Timothy, Olszewska Diana A, Lim Shen-Yang, Ahmad-Annuar Azlina, Tan Ai Huey, Al-Mubarak Bashayer, Hanagasi Hasmet, Koziorowski Dariusz, Ertan Sibel, Genc Gencer, Aguiar Patricia De, Barkhuizen Melinda, Pimentel Marcia MG, Saunders-Pullman Rachel, van de Warrenburg Bart, Bressman Susan, Toft Mathias, Appel-Cresswell Silke, Lang Anthony E, Skorvanek Matej, Boon Agnita JW, Kruger Rejko, Sammler Esther M, Tumas Vitor, Zhang Bao-rong, Garraux Gaetan, Chung Sun Ju, Kim Yun Joong, Winkelmann Juliane, Sue Carolyn M, Tan Eng-King, Damasio Joana, Klivenyi Péter, Kostic VladimirS, Arkadir David, Martikainen Mika, Borges Vanderci, Hertz Jens Michael, Brighina Laura, Spitz Mariana, Suchowersky Oksana, Riess Olaf, Das Parimal, Mollenhauer Brit, Gatto Emilia M, Petersen Maria Skaalum, Hattori Nobutaka, Wu Ruey-Meei, Illarioshkin Sergey N, Valente Enza Maria, Aasly Jan O, Aasly Anna, Alcalay Roy N, Thaler Avner, Farrer Matthew J, Brockmann Kathrin, Corvol Jean-Christophe, Klein Christine; The MJFF Global Genetic Parkinson's Disease Study Group
    (
    A1 Refereed original research article in a scientific journal)


  • Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Project  (2023)  
    • PLoS ONE
     Vollstedt Eva-Juliane, Madoev Harutyun, Aasly Anna, Ahmad-Annuar Azlina, Al-Mubarak Bashayer, Alcalay Roy N., Alvarez Victoria, Amorin Ignacio, Annesi Grazia, Arkadir David, Bardien Soraya, Barker Roger A., Barkhuizen Melinda, Basak A. Nazli, Bonifati Vincenzo, Boon Agnita, Brighina Laura, Brockmann Kathrin, Belin Andrea Carmin, Carr Jonathan, Clarimon Jordi, Cornejo-Olivas Mario, Guedes Leonor Correia, Corvol Jean Christophe, Crosiers David, Damásio Joana, Das Parimal, de Carvalho Aguiar Patricia, De Rosa Anna, Dorszewska Jolanta, Ertan Sibel, Ferese Rosangela, Ferreira Joaquim, Gatto Emilia, Genç Gençer, Giladi Nir, Gómez-Garre Pilar, Hanagasi Hasmet, Hattori Nobutaka, Hentati Faycal, Hoffman-Zacharska Dorota, Illarioshkin Sergey N., Jankovic Joseph, Jesús Silvia, Kaasinen Valtteri, Kievit Anneke, Klivenyi Peter, Kostic Vladimir, Koziorowski Dariusz, Kühn Andrea A., Lang Anthony E., Lim Shen Yang, Lin Chin-Hsien, Lohmann Katja, Markovic Vladana, Martikainen Mika Henrik, Mellick George, Merello Marcelo, Milanowski Lukasz, Mir Pablo, Öztop-Çakmak Özgür., Pimentel Márcia Mattos Gonçalves, Pulkes Teeratorn, Puschmann Andreas, Rogaeva Ekaterina, Sammler Esther M., Petersen Maria Skaalum, Skorvanek Matej, Spitz Matej, Suchowersky Oksana, Tan Ai Huey, Termsarasab Pichet, Thaler Avner., Tumas Vitor., Valente Enza Maria, van de Warrenburg Bart, Williams-Gray Caroline H., Wu Ruey-Mei, Zhang Baorong, Zimprich Alexander, Solle Justin, Padmanabhan Shalini, Klein Christine
    (
    A1 Refereed original research article in a scientific journal)


  • Perheessä Parkinson: omaisen kuormitus sairauden eri vaiheissa  (2023)  
    • Gerontologia
     Martikainen Kirsti, Kinos Sirppa, Vahlberg Tero, Martikainen Mika H., Marttila Reijo
    (
    B1 Non-refereed article in a scientific journal)


  • CANVAS - tasapainovaikeuksien ja kroonisen yskän mahdollinen aiheuttaja  (2022)  
    • Duodecim
     Jokela Manu, Martikainen Mika H, Lund-Aho Tiina, Palmio Johanna, Airas Laura, Hietaharju Aki, Kaasinen Valtteri
    (
    D1 Article in a professional journal)


  • Magnetic resonance imaging negative myelopathy in Leber’s hereditary optic neuropathy: a case report  (2022)  
    • BMC Neurology
     Martikainen Mika H., Suomela Miika, Majamaa Kari
    (
    A1 Refereed original research article in a scientific journal)


  • Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease  (2022)  
    • Annals of Neurology
     Jokela Manu, Karhu Jari, Nurminen Janne, Martikainen Mika H
    (
    B1 Non-refereed article in a scientific journal)


  • Validation of the Finnish Version of the Unified Dyskinesia Rating Scale  (2021)  
    • European Neurology
     Kaasinen Valtteri, Scheperjans Filip, Kärppä Mikko, Korpela Jaana, Brück Anna, Sipilä Jussi OT, Joutsa Juho, Järvelä Juha, Eerola-Rautio Johanna, Martikainen Mika H, Airaksinen Katja, Stebbins Glenn T, Martinez-Martin Pablo, Goetz Christopher G, Lin Jeffrey, Luo Sheng, Pekkonen Eeero
    (
    A1 Refereed original research article in a scientific journal)


  • Deep brain stimulation for monogenic Parkinson’s disease: a systematic review  (2020)  
    • Journal of Neurology
     Tomi Kuusimäki, Jaana Korpela, Eero Pekkonen, Mika H. Martikainen, Angelo Antonini, Valtteri Kaasinen
    (
    A2 Refereed review article in a scientific journal )


  • Mitochondrial DNA variation in sudden cardiac death: a population-based study  (2020)  
    • International Journal of Legal Medicine
     Kytövuori L., Junttila J., Huikuri H., Keinänen-Kiukaanniemi S., Majamaa K., Martikainen M.
    (
    A1 Refereed original research article in a scientific journal)


  • Consensus-based statements for the management of mitochondrial stroke-like episodes  (2019)  
    • Wellcome Open Research
     Ng Y.S., Bindoff L.A., Gorman G.S., Horvath R., Klopstock T., Mancuso M., Martikainen M.H., Mcfarland R., Nesbitt V., Pitceathly R.D.S., Schaefer A.M., Turnbull D.M.
    (
    A1 Refereed original research article in a scientific journal)


  • Erikoislääkärikoulutuksen koejakso - muutakin kuin hyväksytty tai hylätty  (2019)  
    • Lääkärilehti
     Mika H. Martikainen, Leila Niemi-Murola
    (
    D1 Article in a professional journal)


  • Erikoislääkärikoulutus uudistuu - missä mennään?  (2019)  
    • Lääkärilehti
     Mika H. Martikainen, Janne Liimatainen, Johanna Rellman, Mervi Ryytty, Terhi Savolainen, Leila Niemi-Murola
    (
    D1 Article in a professional journal)


  • Osaamisen arviointi erikoistuvan tukena  (2019)  
    • Duodecim
     Leila Niemi-Murola, Mika H. Martikainen
    (
    D1 Article in a professional journal)


  • Pathogenic Variants in MT-ATP6: A United Kingdom-Based Mitochondrial Disease Cohort Study  (2019)  
    • Annals of Neurology
     Yi Shiau Ng, Mika H. Martikainen, Gráinne S. Gorman, Alasdair Blain, Enrico Bugiardini, Apphia Bunting, Andrew M. Schaefer, Charlotte L. Alston, Emma L. Blakely, Sunil Sharma, Imelda Hughes, Albert Lim, Christian de Goede, Meriel McEntagart, Stefan Spinty, Iain Horrocks, Mark Roberts, Cathy E. Woodward, Patrick F. Chinnery, Rita Horvath, Victoria Nesbitt, Carl Fratter, Joanna Poulton, Michael G. Hanna, Robert D. S. Pitceathly, Robert W. Taylor, Doug M. Turnbull, Robert McFarland
    (
    A1 Refereed original research article in a scientific journal)


  • Särö-X-esimutaatio-oireyhtymä (FXTAS) - magneettikuvauksesta apua diagnosointiin  (2019)  
    • Duodecim
     Jokela M, Hietala M, Karhu J, Martikainen MH, Kaasinen V
    (
    D1 Article in a professional journal)


  • Deep brain stimulation for monogenic Parkinson’s disease: A systematic review  (2018)  
    • Movement Disorders
     Kuusimäki T, Korpela J, Pekkonen E, Martikainen M, Antonini A, Kaasinen V
    (
    Other publication)


  • Kun katse jähmettyy - muista mitokondriotaudin mahdollisuus  (2018)  
    • Duodecim
     Manu Jokela, Mika H. Martikainen, Janne Lähdesmäki, Harri Selin, Maria Gardberg, Matti K. Karvonen
    (
    D1 Article in a professional journal)



Last updated on 2023-12-07 at 12:41