Mikko Kärppä
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, Sleep and related disorders, Genetic Neurodegenerative Diseases, ATP Synthase and ATPases Research
Most-Cited Works
- → Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population(1998)384 cited
- → Long-term efficacy and tolerability of lemborexant compared with placebo in adults with insomnia disorder: results from the phase 3 randomized clinical trial SUNRISE 2(2020)158 cited
- → Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy(2010)118 cited
- → Atypical phenotypes in titinopathies explained by second titin mutations(2014)93 cited
- → Hereditary myopathy with early respiratory failure: occurrence in various populations(2013)85 cited
- → Long-term effectiveness and safety of lemborexant in adults with insomnia disorder: results from a phase 3 randomized clinical trial(2021)83 cited
- → The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct(1997)73 cited
- → A 3-year clinical follow-up of adult patients with 3243A>G in mitochondrial DNA(2006)67 cited
- → Peripheral neuropathy in patients with the 3243A>G mutation in mitochondrial DNA(2003)56 cited
- → Prevalence of large-scale mitochondrial DNA deletions in an adult Finnish population(2005)51 cited