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

Year Number of Results
2013 5
2014 10
2015 9
2016 14
2017 11
2018 10
2019 8
2020 6
2021 6
2022 1
2023 6
2024 3

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76 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.
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study.
Rizig M, Bandres-Ciga S, Makarious MB, Ojo OO, Crea PW, Abiodun OV, Levine KS, Abubakar SA, Achoru CO, Vitale D, Adeniji OA, Agabi OP, Koretsky MJ, Agulanna U, Hall DA, Akinyemi RO, Xie T, Ali MW, Shamim EA, Ani-Osheku I, Padmanaban M, Arigbodi OM, Standaert DG, Bello AH, Dean MN, Erameh CO, Elsayed I, Farombi TH, Okunoye O, Fawale MB, Billingsley KJ, Imarhiagbe FA, Jerez PA, Iwuozo EU, Baker B, Komolafe MA, Malik L, Nwani PO, Daida K, Nwazor EO, Miano-Burkhardt A, Nyandaiti YW, Fang ZH, Obiabo YO, Kluss JH, Odeniyi OA, Hernandez DG, Odiase FE, Tayebi N, Ojini FI, Sidranksy E, Onwuegbuzie GA, D'Souza AM, Osaigbovo GO, Berhe B, Osemwegie N, Reed X, Oshinaike OO, Leonard HL, Otubogun FM, Alvarado CX, Oyakhire SI, Ozomma SI, Samuel SC, Taiwo FT, Wahab KW, Zubair YA, Iwaki H, Kim JJ, Morris HR, Hardy J, Nalls MA, Heilbron K, Norcliffe-Kaufmann L; Nigeria Parkinson Disease Research Network; International Parkinson's Disease Genomics Consortium Africa; Black and African American Connections to Parkinson's Disease Study Group; 23andMe Research Team; Blauwendraat C, Houlden H, Singleton A, Okubadejo NU; Global Parkinson's Genetics Program. Rizig M, et al. Lancet Neurol. 2023 Nov;22(11):1015-1025. doi: 10.1016/S1474-4422(23)00283-1. Epub 2023 Aug 23. Lancet Neurol. 2023. PMID: 37633302
Gait in Parkinson's Disease.
Martinez-Ramirez D, Rodriguez-Violante M, Ramirez-Zamora A. Martinez-Ramirez D, et al. Parkinsons Dis. 2019 Oct 20;2019:1962123. doi: 10.1155/2019/1962123. eCollection 2019. Parkinsons Dis. 2019. PMID: 31772732 Free PMC article. No abstract available.
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.
Commentary: Juvenile Dystonia-Parkinsonism due to DNAJC6 Mutation.
Barsottini O, Garza-Brambila D, Esparza-Hernández CN, Ramirez-Zenteno J, Martinez-Ramirez D, Fasano A. Barsottini O, et al. Among authors: martinez ramirez d. Mov Disord Clin Pract. 2021 Sep 3;8(Suppl 1):S29-S31. doi: 10.1002/mdc3.13305. eCollection 2021 Aug. Mov Disord Clin Pract. 2021. PMID: 34514043 Free PMC article. No abstract available.
Review of Hereditary and Acquired Rare Choreas.
Martinez-Ramirez D, Walker RH, Rodríguez-Violante M, Gatto EM; Rare Movement Disorders Study Group of International Parkinson’s Disease. Martinez-Ramirez D, et al. Tremor Other Hyperkinet Mov (N Y). 2020 Aug 6;10:24. doi: 10.5334/tohm.548. Tremor Other Hyperkinet Mov (N Y). 2020. PMID: 32832197 Free PMC article. Review.
Editorial: Managing Parkinson's Disease With a Multidisciplinary Perspective.
Fereshtehnejad SM, Rodríguez-Violante M, Martinez-Ramirez D, Ramirez-Zamora A. Fereshtehnejad SM, et al. Among authors: martinez ramirez d. Front Neurol. 2021 Nov 26;12:799017. doi: 10.3389/fneur.2021.799017. eCollection 2021. Front Neurol. 2021. PMID: 34899588 Free PMC article. No abstract available.
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.
Comment on: "Cancer in Parkinson's disease".
Nozile WR, Nozile-Firth K, Martinez-Ramirez D, Longo MI. Nozile WR, et al. Among authors: martinez ramirez d. Parkinsonism Relat Disord. 2018 Aug;53:115. doi: 10.1016/j.parkreldis.2018.05.004. Epub 2018 May 16. Parkinsonism Relat Disord. 2018. PMID: 29784562 No abstract available.
76 results