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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: majamaa k. 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: majamaa k. PLoS One. 2012;7(7):e41859. doi: 10.1371/journal.pone.0041859. Epub 2012 Jul 24. PLoS One. 2012. PMID: 22911860 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. Among authors: majamaa k. Lancet Neurol. 2019 Dec;18(12):1091-1102. doi: 10.1016/S1474-4422(19)30320-5. Lancet Neurol. 2019. PMID: 31701892 Free PMC article.
Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease.
Blauwendraat C, Iwaki H, Makarious MB, Bandres-Ciga S, Leonard HL, Grenn FP, Lake J, Krohn L, Tan M, Kim JJ, Gibbs JR, Hernandez DG, Ruskey JA, Pihlstrøm L, Toft M, van Hilten JJ, Marinus J, Schulte C, Brockmann K, Sharma M, Siitonen A, Majamaa K, Eerola-Rautio J, Tienari PJ, Grosset DG, Lesage S, Corvol JC, Brice A, Wood N, Hardy J, Gan-Or Z, Heutink P, Gasser T, Morris HR, Noyce AJ, Nalls MA, Singleton AB; International Parkinson's Disease Genomics Consortium (IPDGC). Blauwendraat C, et al. Among authors: majamaa k. Ann Neurol. 2021 Jul;90(1):35-42. doi: 10.1002/ana.26090. Epub 2021 May 24. Ann Neurol. 2021. PMID: 33901317 Free PMC article.
Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset.
Billingsley KJ, Barbosa IA, Bandrés-Ciga S, Quinn JP, Bubb VJ, Deshpande C, Botia JA, Reynolds RH, Zhang D, Simpson MA, Blauwendraat C, Gan-Or Z, Gibbs JR, Nalls MA, Singleton A; International Parkinson’s Disease Genomics Consortium (IPDGC); Ryten M, Koks S. Billingsley KJ, et al. NPJ Parkinsons Dis. 2019 May 22;5:8. doi: 10.1038/s41531-019-0080-x. eCollection 2019. NPJ Parkinsons Dis. 2019. PMID: 31123700 Free PMC article.
Associating mitochondrial DNA variation with complex traits.
Elson JL, Majamaa K, Howell N, Chinnery PF. Elson JL, et al. Among authors: majamaa k. Am J Hum Genet. 2007 Feb;80(2):378-82; author reply 382-3. doi: 10.1086/511652. Am J Hum Genet. 2007. PMID: 17304709 Free PMC article. No abstract available.
Treatment for mitochondrial disorders.
Pfeffer G, Majamaa K, Turnbull DM, Thorburn D, Chinnery PF. Pfeffer G, et al. Among authors: majamaa k. Cochrane Database Syst Rev. 2012 Apr 18;2012(4):CD004426. doi: 10.1002/14651858.CD004426.pub3. Cochrane Database Syst Rev. 2012. PMID: 22513923 Free PMC article. Review.
Treatment for mitochondrial disorders.
Chinnery P, Majamaa K, Turnbull D, Thorburn D. Chinnery P, et al. Among authors: majamaa k. Cochrane Database Syst Rev. 2006 Jan 25;(1):CD004426. doi: 10.1002/14651858.CD004426.pub2. Cochrane Database Syst Rev. 2006. PMID: 16437486 Updated. Review.
[Use of CSF biomarkers in the diagnostics of memory diseases].
Remes A, Leikola M, Majamaa K, Nikkanen M, Ruokonen LI, Rusanen M, Tapiola T, Ylikotila P, Vallittu AM, Pirttilä T. Remes A, et al. Among authors: majamaa k. Duodecim. 2009;125(20):2215-22. Duodecim. 2009. PMID: 19998760 Finnish.
The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event.
Behar DM, Metspalu E, Kivisild T, Achilli A, Hadid Y, Tzur S, Pereira L, Amorim A, Quintana-Murci L, Majamaa K, Herrnstadt C, Howell N, Balanovsky O, Kutuev I, Pshenichnov A, Gurwitz D, Bonne-Tamir B, Torroni A, Villems R, Skorecki K. Behar DM, et al. Among authors: majamaa k. Am J Hum Genet. 2006 Mar;78(3):487-97. doi: 10.1086/500307. Epub 2006 Jan 11. Am J Hum Genet. 2006. PMID: 16404693 Free PMC article.
219 results