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 · 383 citations · Full text

Strokelike Episodes, Lactic Acidosis, Mendelian Disorder +11

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 · 156 citations · Full text

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

Genetics, Renal Pathology, Pathology +18

Atypical phenotypes in titinopathies explained by second titin mutations

Anni Evilä, Anna Vihola, J. Sarparanta et al. · Annals of Neurology · 2014 · 91 citations

Hereditary myopathy with early respiratory failure: occurrence in various populations

Johanna Palmio, Anni Evilä, Françoise Chapon et al. · Journal of Neurology Neurosurgery & Psychiatry · 2013 · 85 citations · Full text