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Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies.
Dou J, Bakulski K, Guo K, Hur J, Zhao L, Saez-Atienzar S, Stark A, Chia R, García-Redondo A, Rojas-Garcia R, Vázquez Costa JF, Fernandez Santiago R, Bandres-Ciga S, Gómez-Garre P, Periñán MT, Mir P, Pérez-Tur J, Cardona F, Menendez-Gonzalez M, Riancho J, Borrego-Hernández D, Galán-Dávila L, Infante Ceberio J, Pastor P, Paradas C, Dols-Icardo O, Traynor BJ, Feldman EL, Goutman SA; Spanish Neurological Consortium. Dou J, et al. Neurol Genet. 2023 May 31;9(4):e200079. doi: 10.1212/NXG.0000000000200079. eCollection 2023 Aug. Neurol Genet. 2023. PMID: 37293291 Free PMC article.
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms.
Blauwendraat C, Heilbron K, Vallerga CL, Bandres-Ciga S, von Coelln R, Pihlstrøm L, Simón-Sánchez J, Schulte C, Sharma M, Krohn L, Siitonen A, Iwaki H, Leonard H, Noyce AJ, Tan M, Gibbs JR, Hernandez DG, Scholz SW, Jankovic J, Shulman LM, Lesage S, Corvol JC, Brice A, van Hilten JJ, Marinus J; 23andMe Research Team; Eerola-Rautio J, Tienari P, Majamaa K, Toft M, Grosset DG, Gasser T, Heutink P, Shulman JM, Wood N, Hardy J, Morris HR, Hinds DA, Gratten J, Visscher PM, Gan-Or Z, Nalls MA, Singleton AB; International Parkinson's Disease Genomics Consortium (IPDGC). Blauwendraat C, et al. Mov Disord. 2019 Jun;34(6):866-875. doi: 10.1002/mds.27659. Epub 2019 Apr 7. Mov Disord. 2019. PMID: 30957308 Free PMC article.
Comprehensive assessment of PINK1 variants in Parkinson's disease.
Krohn L, Grenn FP, Makarious MB, Kim JJ, Bandres-Ciga S, Roosen DA, Gan-Or Z, Nalls MA, Singleton AB, Blauwendraat C; International Parkinson's Disease Genomics Consortium (IPDGC). Krohn L, et al. Neurobiol Aging. 2020 Jul;91:168.e1-168.e5. doi: 10.1016/j.neurobiolaging.2020.03.003. Epub 2020 Mar 10. Neurobiol Aging. 2020. PMID: 32249012 Free PMC article.
The Parkinson's Disease DNA Variant Browser.
Kim JJ, Makarious MB, Bandres-Ciga S, Gibbs JR, Ding J, Hernandez DG, Brooks J, Grenn FP, Iwaki H, Singleton AB, Nalls MA, Blauwendraat C; International Parkinson's Disease Genomics Consortium (IPDGC). Kim JJ, et al. Mov Disord. 2021 May;36(5):1250-1258. doi: 10.1002/mds.28488. Epub 2021 Jan 26. Mov Disord. 2021. PMID: 33497488 Free PMC article.
Lack of evidence for association of UQCRC1 with Parkinson's disease in Europeans.
Senkevich K, Bandres-Ciga S, Gan-Or Z, Krohn L; International Parkinson's Disease Genomics Consortium (IPDGC). Senkevich K, et al. Neurobiol Aging. 2021 May;101:297.e1-297.e4. doi: 10.1016/j.neurobiolaging.2020.10.030. Epub 2020 Nov 2. Neurobiol Aging. 2021. PMID: 33248804 Free PMC article.
Replication assessment of NUS1 variants in Parkinson's disease.
Bustos BI, Bandres-Ciga S, Gibbs JR, Krainc D, Mencacci NE, Gan-Or Z, Lubbe SJ; International Parkinson's Disease Genomics Consortium (IPDGC). Bustos BI, et al. Neurobiol Aging. 2021 May;101:300.e1-300.e3. doi: 10.1016/j.neurobiolaging.2020.11.007. Epub 2020 Nov 13. Neurobiol Aging. 2021. PMID: 33309333 Free PMC article.
MIDN locus structural variants and Parkinson's Disease risk.
Billingsley KJ, Bandres-Ciga S, Ding J, Hernandez D, Gibbs JR, Blauwendraat C; International Parkinson’s Disease Genomics Consortium (IPDGC). Billingsley KJ, et al. Ann Clin Transl Neurol. 2020 Apr;7(4):602-603. doi: 10.1002/acn3.51012. Epub 2020 Mar 24. Ann Clin Transl Neurol. 2020. PMID: 32212230 Free PMC article. No abstract available.
136 results