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Probing sporadic and familial Alzheimer’s disease using induced pluripotent stem cells MA Israel, SH Yuan, C Bardy, SM Reyna, Y Mu, C Herrera, MP Hefferan, ... Nature 482 (7384), 216-220, 2012 | 1418 | 2012 |
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Inhibition of hypoxia-inducible factor (HIF) hydroxylases by citric acid cycle intermediates: possible links between cell metabolism and stabilization of HIF P Koivunen, M Hirsilä, AM Remes, IE Hassinen, KI Kivirikko, J Myllyharju Journal of Biological Chemistry 282 (7), 4524-4532, 2007 | 640 | 2007 |
Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population K Majamaa, JS Moilanen, S Uimonen, AM Remes, PI Salmela, M Kärppä, ... The American Journal of Human Genetics 63 (2), 447-454, 1998 | 474 | 1998 |
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation JC Bis, X Jian, BW Kunkle, Y Chen, KL Hamilton-Nelson, WS Bush, ... Molecular psychiatry 25 (8), 1859-1875, 2020 | 235 | 2020 |
Differential diagnosis of neurodegenerative diseases using structural MRI data J Koikkalainen, H Rhodius-Meester, A Tolonen, F Barkhof, B Tijms, ... NeuroImage: Clinical 11, 435-449, 2016 | 178 | 2016 |
Dance and movement therapeutic methods in management of dementia: a randomized, controlled study L Hokkanen, L Rantala, AM Remes, B Härkönen, P Viramo, I Winblad Journal of the American Geriatrics Society 56 (4), 771-772, 2008 | 168 | 2008 |
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APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage A Rovelet-Lecrux, T Frebourg, H Tuominen, K Majamaa, D Campion, ... Journal of Neurology, Neurosurgery & Psychiatry 78 (10), 1158-1159, 2007 | 119 | 2007 |
Lifetime antipsychotic medication and cognitive performance in schizophrenia at age 43 years in a general population birth cohort AP Husa, J Moilanen, GK Murray, R Marttila, M Haapea, I Rannikko, ... Psychiatry research 247, 130-138, 2017 | 107 | 2017 |
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Homozygous W748S mutation in the POLG1 gene in patients with juvenile‐onset Alpers syndrome and status epilepticus J Uusimaa, R Hinttala, H Rantala, M Päivärinta, R Herva, M Röyttä, ... Epilepsia 49 (6), 1038-1045, 2008 | 97 | 2008 |
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Childhood encephalopathies and myopathies: a prospective study in a defined population to assess the frequency of mitochondrial disorders J Uusimaa, AM Remes, H Rantala, L Vainionpää, R Herva, K Vuopala, ... Pediatrics 105 (3), 598-603, 2000 | 93 | 2000 |
Adult‐onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNALeu(UUR) mutation AM Remes, K Majamaa, R Herva, IE Hassinen Neurology 43 (5), 1015-1015, 1993 | 89 | 1993 |
Ethical aspects of researching subjective experiences in early-stage dementia HM Pesonen, AM Remes, A Isola Nursing Ethics 18 (5), 651-661, 2011 | 88 | 2011 |
Genetic loci associated with Alzheimer’s disease and cerebrospinal fluid biomarkers in a Finnish case-control cohort LS Elias-Sonnenschein, S Helisalmi, T Natunen, A Hall, T Paajanen, ... PloS one 8 (4), e59676, 2013 | 85 | 2013 |
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A 3-year clinical follow-up of adult patients with 3243A> G in mitochondrial DNA KAM Majamaa-Voltti, S Winqvist, AM Remes, U Tolonen, J Pyhtinen, ... Neurology 66 (10), 1470-1475, 2006 | 82 | 2006 |