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Page 1
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease.
Keller MF, Saad M, Bras J, Bettella F, Nicolaou N, Simón-Sánchez J, Mittag F, Büchel F, Sharma M, Gibbs JR, Schulte C, Moskvina V, Durr A, Holmans P, Kilarski LL, Guerreiro R, Hernandez DG, Brice A, Ylikotila P, Stefánsson H, Majamaa K, Morris HR, Williams N, Gasser T, Heutink P, Wood NW, Hardy J, Martinez M, Singleton AB, Nalls MA; International Parkinson's Disease Genomics Consortium (IPDGC); Wellcome Trust Case Control Consortium 2 (WTCCC2). Keller MF, et al. Among authors: ylikotila p. Hum Mol Genet. 2012 Nov 15;21(22):4996-5009. doi: 10.1093/hmg/dds335. Epub 2012 Aug 13. Hum Mol Genet. 2012. PMID: 22892372 Free PMC article.
Genome wide assessment of young onset Parkinson's disease from Finland.
Hernandez DG, Nalls MA, Ylikotila P, Keller M, Hardy JA, Majamaa K, Singleton AB. Hernandez DG, et al. Among authors: ylikotila p. PLoS One. 2012;7(7):e41859. doi: 10.1371/journal.pone.0041859. Epub 2012 Jul 24. PLoS One. 2012. PMID: 22911860 Free PMC article.
Genetic risk factors in Finnish patients with Parkinson's disease.
Ylönen S, Siitonen A, Nalls MA, Ylikotila P, Autere J, Eerola-Rautio J, Gibbs R, Hiltunen M, Tienari PJ, Soininen H, Singleton AB, Majamaa K. Ylönen S, et al. Among authors: ylikotila p. Parkinsonism Relat Disord. 2017 Dec;45:39-43. doi: 10.1016/j.parkreldis.2017.09.021. Epub 2017 Sep 29. Parkinsonism Relat Disord. 2017. PMID: 29029963 Free PMC article.
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.
Nalls MA, Blauwendraat C, Vallerga CL, Heilbron K, Bandres-Ciga S, Chang D, Tan M, Kia DA, Noyce AJ, Xue A, Bras J, Young E, von Coelln R, Simón-Sánchez J, Schulte C, Sharma M, Krohn L, Pihlstrøm L, Siitonen A, Iwaki H, Leonard H, Faghri F, Gibbs JR, Hernandez DG, Scholz SW, Botia JA, Martinez M, Corvol JC, Lesage S, Jankovic J, Shulman LM, Sutherland M, Tienari P, Majamaa K, Toft M, Andreassen OA, Bangale T, Brice A, Yang J, Gan-Or Z, Gasser T, Heutink P, Shulman JM, Wood NW, Hinds DA, Hardy JA, Morris HR, Gratten J, Visscher PM, Graham RR, Singleton AB; 23andMe Research Team; System Genomics of Parkinson's Disease Consortium; International Parkinson's Disease Genomics Consortium. Nalls MA, et al. Lancet Neurol. 2019 Dec;18(12):1091-1102. doi: 10.1016/S1474-4422(19)30320-5. Lancet Neurol. 2019. PMID: 31701892 Free PMC article.
Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson's disease.
Leonard H, Blauwendraat C, Krohn L, Faghri F, Iwaki H, Ferguson G, Day-Williams AG, Stone DJ, Singleton AB, Nalls MA, Gan-Or Z; International Parkinson's Disease Genomic Consortium (IPDGC). Leonard H, et al. J Med Genet. 2020 May;57(5):331-338. doi: 10.1136/jmedgenet-2019-106283. Epub 2019 Nov 29. J Med Genet. 2020. PMID: 31784483 Free PMC article.
Epidemiology of early-onset Parkinson's disease in Finland.
Ylikotila P, Tiirikka T, Moilanen JS, Kääriäinen H, Marttila R, Majamaa K. Ylikotila P, et al. Parkinsonism Relat Disord. 2015 Aug;21(8):938-42. doi: 10.1016/j.parkreldis.2015.06.003. Epub 2015 Jun 4. Parkinsonism Relat Disord. 2015. PMID: 26071818
Obesity and the Risk of Cryptogenic Ischemic Stroke in Young Adults.
Jaakonmäki N, Zedde M, Sarkanen T, Martinez-Majander N, Tuohinen S, Sinisalo J, Ryödi E, Autere J, Hedman M, Junttola U, Huhtakangas JK, Grimaldi T, Pascarella R, Nordanstig A, Bech-Hanssen O, Holbe C, Busch R, Fromm A, Ylikotila P, Turgut EE, Amorim I, Ryliskiene K, Tulkki L, Pascasio LA, Licenik R, Ferdinand P, Tsivgoulis G, Jatužis D, Kõrv L, Kõrv J, Pezzini A, Fonseca AC, Yesilot N, Roine RO, Waje-Andreassen U, von Sarnowski B, Redfors P, Huhtakangas J, Numminen H, Jäkälä P, Putaala J; SECRETO Study Group. Jaakonmäki N, et al. Among authors: ylikotila p. J Stroke Cerebrovasc Dis. 2022 May;31(5):106380. doi: 10.1016/j.jstrokecerebrovasdis.2022.106380. Epub 2022 Feb 19. J Stroke Cerebrovasc Dis. 2022. PMID: 35193029 Free article.
39 results