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


mikmar@utu.fi



Follow my tweets @mhmartikainen

https://orcid.org/0000-0002-7604-8081

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Mitochondrial disease; movement disorders; neurogenetics; clinical neurology


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


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.




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).




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.



  
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  •   (2025)  
    • Journal of Neurology
     Mickelsson, Nora; Hirvonen, Jussi; Martikainen, Mika H.


  •   (2024)  
    • BMJ neurology open
     Martikainen Mika H., Majamaa Kari


  • Novel SLC18A2 Variant in Infantile Dystonia-Parkinsonism Type 2  (2024)  
    • Case Reports in Neurological Medicine
     Kaasalainen Sakari, Arikka Harri, Martikainen Mika H., Kaasinen Valtteri


  • 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


  •   (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


  • Perheessä Parkinson: omaisen kuormitus sairauden eri vaiheissa  (2023)  
    • Gerontologia
     Martikainen Kirsti, Kinos Sirppa, Vahlberg Tero, Martikainen Mika H., Marttila Reijo


  • 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


  •   (2022)  
    • BMC NeurologyLääkärilehti
     Martikainen Mika H., Suomela Miika, Majamaa Kari


  •   (2022)  
    • Annals of NeurologyDuodecim
     Jokela Manu, Karhu Jari, Nurminen Janne, Martikainen Mika H


  • Validation of the Finnish Version of the Unified Dyskinesia Rating Scale  (2021)  
    • European NeurologyAnnals of 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


  • Deep brain stimulation for monogenic Parkinson’s disease: a systematic review2020
    • Journal of NeurologyDuodecim
     Tomi Kuusimäki, Jaana Korpela, Eero Pekkonen, Mika H. Martikainen, Angelo Antonini, Valtteri Kaasinen


  • Mitochondrial DNA variation in sudden cardiac death: a population-based study  (2020)  
    • International Journal of Legal MedicineMovement Disorders
     Kytövuori L., Junttila J., Huikuri H., Keinänen-Kiukaanniemi S., Majamaa K., Martikainen M.


  • 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.


  • Erikoislääkärikoulutuksen koejakso - muutakin kuin hyväksytty tai hylätty  (2019)  
    • Lääkärilehti
     Mika H. Martikainen, Leila Niemi-Murola


  • Erikoislääkärikoulutus uudistuu - missä mennään?  (2019)  
       Mika H. Martikainen, Janne Liimatainen, Johanna Rellman, Mervi Ryytty, Terhi Savolainen, Leila Niemi-Murola


    • Osaamisen arviointi erikoistuvan tukena  (2019)  
         Leila Niemi-Murola, Mika H. Martikainen


      • Pathogenic Variants in MT-ATP6: A United Kingdom-Based Mitochondrial Disease Cohort Study  (2019)  
           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


        • Särö-X-esimutaatio-oireyhtymä (FXTAS) - magneettikuvauksesta apua diagnosointiin  (2019)  
             Jokela M, Hietala M, Karhu J, Martikainen MH, Kaasinen V


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


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



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