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

Year Number of Results
2004 1
2005 1
2006 1
2007 1
2008 3
2009 3
2011 1
2012 5
2013 2
2014 3
2015 2
2016 3
2017 2
2018 2
2019 3
2020 2
2021 5
2022 8
2023 9
2024 4

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53 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.
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.
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.
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.
Development and Validation of the Dystonia-Pain Classification System: A Multicenter Study.
Listik C, Listik E, de Paiva Santos Rolim F, Meneses Cury Portela DM, Perez Lloret S, de Alves Araújo NR, Carvalho PRA, Santos GC, Limongi JCP, Cardoso F, Mylius V, Brugger F, Fernandes AM, Reis Barbosa E, Jacobsen Teixeira M, Ferraz HB, Camargos ST; Pain in Dystonia Study Group; Cury RG, de Andrade DC. Listik C, et al. Among authors: camargos st. Mov Disord. 2023 Jul;38(7):1163-1174. doi: 10.1002/mds.29423. Epub 2023 May 20. Mov Disord. 2023. PMID: 37208983
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.
DYT-TUBB4A (DYT4 Dystonia): Clinical Anthology of 11 Cases and Systematized Review.
Bally JF, Kern DS, Fearon C, Camargos S, Pereira da Silva-Junior F, Barbosa ER, Ozelius LJ, de Carvalho Aguiar P, Lang AE. Bally JF, et al. Among authors: camargos s. Mov Disord Clin Pract. 2022 Apr 28;9(5):659-675. doi: 10.1002/mdc3.13452. eCollection 2022 Jul. Mov Disord Clin Pract. 2022. PMID: 35844288 Free PMC article. Review.
53 results