Mikko Kärppä

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 · 385 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

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

Mikko Kärppä, Jane Yardley, Kate Pinner et al. · SLEEP · 2020 · 165 citations · Full text

Medicine, Pharmacology, Pharmacotherapy +17

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy

John F. O’Toole, Yangjian Liu, Erica E. Davis et al. · Journal of Clinical Investigation · 2010 · 118 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Atypical phenotypes in titinopathies explained by second titin mutations

Anni Evilä, Anna Vihola, J. Sarparanta et al. · Annals of Neurology · 2014 · 94 citations

Life Sciences, Genetics, Molecular Genetics +16

Long-term effectiveness and safety of lemborexant in adults with insomnia disorder: results from a phase 3 randomized clinical trial

Jane Yardley, Mikko Kärppä, Yuichi Inoue et al. · Sleep Medicine · 2021 · 87 citations · Full text

Medicine, Pharmacology, Pharmacotherapy +17