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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1998 1
2000 1
2002 1
2004 1
2005 1
2006 1
2007 1
2008 3
2009 3
2010 1
2011 2
2012 6
2013 3
2014 3
2015 2
2016 3
2017 2
2018 2
2019 3
2020 2
2021 5
2022 8
2023 10
2024 4

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59 results

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Page 1
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease.
Kim JJ, Vitale D, Otani DV, Lian MM, Heilbron K; 23andMe Research Team; Iwaki H, Lake J, Solsberg CW, Leonard H, Makarious MB, Tan EK, Singleton AB, Bandres-Ciga S, Noyce AJ; Global Parkinson’s Genetics Program (GP2); Blauwendraat C, Nalls MA, Foo JN, Mata I. Kim JJ, et al. Nat Genet. 2024 Jan;56(1):27-36. doi: 10.1038/s41588-023-01584-8. Epub 2023 Dec 28. Nat Genet. 2024. PMID: 38155330 Free PMC article.
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).
Towns C, Richer M, Jasaityte S, Stafford EJ, Joubert J, Antar T, Martinez-Carrasco A, Makarious MB, Casey B, Vitale D, Levine K, Leonard H, Pantazis CB, Screven LA, Hernandez DG, Wegel CE, Solle J, Nalls MA, Blauwendraat C, Singleton AB, Tan MMX, Iwaki H, Morris HR; Global Parkinson’s Genetics Program (GP2). Towns C, et al. NPJ Parkinsons Dis. 2023 Sep 12;9(1):131. doi: 10.1038/s41531-023-00533-w. NPJ Parkinsons Dis. 2023. PMID: 37699923 Free PMC article.
Selective visuoconstructional impairment following mild COVID-19 with inflammatory and neuroimaging correlation findings.
de Paula JJ, Paiva RERP, Souza-Silva NG, Rosa DV, Duran FLS, Coimbra RS, Costa DS, Dutenhefner PR, Oliveira HSD, Camargos ST, Vasconcelos HMM, de Oliveira Carvalho N, da Silva JB, Silveira MB, Malamut C, Oliveira DM, Molinari LC, de Oliveira DB, Januário JN, Silva LC, De Marco LA, Queiroz DMM, Meira W, Busatto G, Miranda DM, Romano-Silva MA. de Paula JJ, et al. Among authors: camargos st. Mol Psychiatry. 2023 Feb;28(2):553-563. doi: 10.1038/s41380-022-01632-5. Epub 2022 Jun 14. Mol Psychiatry. 2023. PMID: 35701598 Free PMC article.
Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).
Lange LM, Avenali M, Ellis M, Illarionova A, Keller Sarmiento IJ, Tan AH, Madoev H, Galandra C, Junker J, Roopnarain K, Solle J, Wegel C, Fang ZH, Heutink P, Kumar KR, Lim SY, Valente EM, Nalls M, Blauwendraat C, Singleton A, Mencacci N, Lohmann K, Klein C; Global Parkinson’s Genetic Program (GP2). Lange LM, et al. NPJ Parkinsons Dis. 2023 Sep 13;9(1):133. doi: 10.1038/s41531-023-00560-7. NPJ Parkinsons Dis. 2023. PMID: 37704671 Free PMC article. No abstract available.
Characterisation of ataxia in Sjogren's syndrome.
Jaques CS, de Moraes MPM, Silva EAR, Coimbra-Neto AR, Martinez ARM, Camargos ST, Cardoso F, França MC, Nucci A, Pedroso JL, Barsottini OGP. Jaques CS, et al. Among authors: camargos st. J Neurol Neurosurg Psychiatry. 2020 Apr;91(4):446-448. doi: 10.1136/jnnp-2019-322373. Epub 2020 Feb 3. J Neurol Neurosurg Psychiatry. 2020. PMID: 32015088 No abstract available.
GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians.
Ojo OO, Bandres-Ciga S, Makarious MB, Crea PW, Hernandez DG, Houlden H, Rizig M, Singleton AB, Noyce AJ, Nalls MA, Blauwendraat C, Okubadejo NU; Nigeria Parkinson's Disease Research Network and the Global Parkinson's Genetics Program (GP2). Ojo OO, et al. Mov Disord. 2024 Apr;39(4):728-733. doi: 10.1002/mds.29753. Epub 2024 Feb 23. Mov Disord. 2024. PMID: 38390630
Genotype-Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review.
Lange LM, Junker J, Loens S, Baumann H, Olschewski L, Schaake S, Madoev H, Petkovic S, Kuhnke N, Kasten M, Westenberger A, Domingo A, Marras C, König IR, Camargos S, Ozelius LJ, Klein C, Lohmann K. Lange LM, et al. Among authors: camargos s. Mov Disord. 2021 May;36(5):1086-1103. doi: 10.1002/mds.28485. Epub 2021 Jan 27. Mov Disord. 2021. PMID: 33502045 Review.
Handicap as a Measure of Perceived-Health Status in Parkinson's Disease.
Silva DP, Coelho M, Soares T, Vale TC, Correia Guedes L, Maciel ROH, Antunes AP, Camargos ST, Valadas A, Godinho C, Maia DP, Pita Lobo P, Maia RD, Teodoro T, Rieder CR, Velon AG, Tumas V, Barbosa ER, Teive HAG, Ferraz HB, Rosas MJ, Calado A, Lampreia T, Simões R, Vila-Chã N, Costa MM, Rodrigues AM, Caniça V, Cardoso F, Ferreira JJ; MDS‐UPDRS Portuguese Validation Study Group. Silva DP, et al. Among authors: camargos st. Mov Disord Clin Pract. 2023 Jul 7;10(8):1172-1180. doi: 10.1002/mdc3.13826. eCollection 2023 Aug. Mov Disord Clin Pract. 2023. PMID: 37635780
59 results