Mika Martikainen
M.D., Ph.D., Professor of Neurology
mikmar@utu.fi Follow my tweets @mhmartikainen ORCID identifier: https://orcid.org/0000-0002-7604-8081 |
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.
- Decreased male reproductive success in association with mitochondrial dysfunction (2017)
- European Journal of Human Genetics
(A1 Refereed original research article in a scientific journal) - SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population (2017)
- Neurobiology of Aging
(A1 Refereed original research article in a scientific journal) - The m.7510T > C mutation: Hearing impairment and a complex neurologic phenotype (2017)
- Brain and Behavior
(A1 Refereed original research article in a scientific journal) - A novel mutation m.8561C > G in MT-ATP6/8 causing a mitochondrial syndrome with ataxia, peripheral neuropathy, diabetes mellitus, and hypergonadotropic hypogonadism (2016)
- Journal of Neurology
(A1 Refereed original research article in a scientific journal) - Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease (2016)
- JAMA Neurology
(A1 Refereed original research article in a scientific journal) - Spectrum of Movement Disorders in Mitochondrial Disorders Reply (2016)
- JAMA Neurology
(B1 Non-refereed article in a scientific journal) - Association of mitochondrial DNA haplogroups and vascular complications of diabetes mellitus: A population-based study (2015)
- Diabetes and Vascular Disease Research
(A1 Refereed original research article in a scientific journal) - Clinical and imaging findings in Parkinson's disease associated with the A53E SNCA mutation (2015)
- Neurology-Genetics
(A1 Refereed original research article in a scientific journal) - Creutzfeldt-Jakobin taudin ilmiasu ja ilmaantuvuus Suomessa vuosina 1997-2013 (2015)
- Duodecim
(A1 Refereed original research article in a scientific journal) - Constant high adrenal FDG uptake in PET/CT associated with mitochondrial disease. (2014)
- Journal of Inherited Metabolic Disease
(A1 Refereed original research article in a scientific journal) - Novel mitofusin 2 splice-site mutation causes Charcot-Marie-Tooth disease type 2 with prominent sensory dysfunction (2014)
- Neuromuscular Disorders
(A1 Refereed original research article in a scientific journal) - Progressive external ophthalmoplegia in Southwestern Finland: a clinical and genetic study (2012)
- Neuroepidemiology
(A1 Refereed original research article in a scientific journal)