Mika Martikainen
M.D., Ph.D., Professor of Neurology
mikmar@utu.fi Follow my tweets @mhmartikainen ORCID-tunniste: https://orcid.org/0000-0002-7604-8081 |
Mitokondriotaudit; liikehäiriösairaudet; perinnölliset neurologiset sairaudet; kliininen neurologia
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 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population (2017)
- Neurobiology of Aging
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - The m.7510T > C mutation: Hearing impairment and a complex neurologic phenotype (2017)
- Brain and Behavior
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - 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 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease (2016)
- JAMA Neurology
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Spectrum of Movement Disorders in Mitochondrial Disorders Reply (2016)
- JAMA Neurology
(B1 Vertaisarvioimaton kirjoitus tieteellisessä lehdessä ) - Association of mitochondrial DNA haplogroups and vascular complications of diabetes mellitus: A population-based study (2015)
- Diabetes and Vascular Disease Research
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Clinical and imaging findings in Parkinson's disease associated with the A53E SNCA mutation (2015)
- Neurology-Genetics
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Creutzfeldt-Jakobin taudin ilmiasu ja ilmaantuvuus Suomessa vuosina 1997-2013 (2015)
- Duodecim
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Constant high adrenal FDG uptake in PET/CT associated with mitochondrial disease. (2014)
- Journal of Inherited Metabolic Disease
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Novel mitofusin 2 splice-site mutation causes Charcot-Marie-Tooth disease type 2 with prominent sensory dysfunction (2014)
- Neuromuscular Disorders
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä ) - Progressive external ophthalmoplegia in Southwestern Finland: a clinical and genetic study (2012)
- Neuroepidemiology
(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )