Kari Majamaa

Parkinsonism, premature menopause, and mitochondrial DNA polymerase γ mutations: clinical and molecular genetic study

Petri Luoma, Atle Melberg, Juha O. Rinne et al. · The Lancet · 2004 · 540 citations

Neurodegenerative Diseases, Molecular Genetic Study, Genetic Disorder +12

Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population

Kari Majamaa, Jukka S. Moilanen, Seija Uimonen et al. · The American Journal of Human Genetics · 1998 · 383 citations · Full text

Strokelike Episodes, Lactic Acidosis, Mendelian Disorder +11

Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms

Cornelis Blauwendraat, Karl Heilbron, Costanza L. Vallerga et al. · Movement Disorders · 2019 · 365 citations · Full text

Phylogenetic Network for European mtDNA

Saara Finnilä, Mervi S. Lehtonen, Kari Majamaa · The American Journal of Human Genetics · 2001 · 356 citations · Full text

Phylogenetic Network, Phylogenetics, Molecular Ecology +7

Mitochondrial DNA and ACTN3 genotypes in Finnish elite endurance and sprint athletes

Anna‐Kaisa Niemi, Kari Majamaa · European Journal of Human Genetics · 2005 · 351 citations · Full text

Kinesiology, Mitochondrial Function, Skeletal Muscle +9