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Year Number of Results
2009 1
2015 1
2017 1
2020 3
2021 2
2022 2
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2024 8
2025 4
2026 7

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30 results

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Page 1
Global Perspectives on Returning Genetic Research Results in Parkinson Disease.
Tan AH, Saffie-Awad P, Schumacher Schuh AF, Lim SY, Madoev H, Ahmad-Annuar A, Solle J, Wegel CE, Doquenia ML, Dey S, Perinan MT, Makarious MB, Fiske B, Morris HR, Noyce AJ, Alcalay RN, Kumar KR, Klein C; Global Parkinson's Genetic Program (GP2). Tan AH, et al. Neurol Genet. 2024 Dec 5;10(6):e200213. doi: 10.1212/NXG.0000000000200213. eCollection 2024 Dec. Neurol Genet. 2024. PMID: 39807215 Free PMC article.
Exploring MAPT-containing H1 and H2 haplotypes in Parkinson's disease across diverse populations.
Reyes-Pérez P, Hor JW, Toh TS, Sanyaolu AO, Pantazis CB, Leal TP, Yeboah S, Bandres-Ciga S, Morris HR, Makarious MB, Senkevich K; Latin American Research Consortium on the Genetics of Parkinson’s Disease (LARGE-PD); Global Parkinson’s Genetics Program (GP2); Leonard H, Atterling Brolin K. Reyes-Pérez P, et al. NPJ Parkinsons Dis. 2026 Jun 24;12(1):187. doi: 10.1038/s41531-026-01394-9. NPJ Parkinsons Dis. 2026. PMID: 42342696 Free PMC article.
Parkinson's families project: a UK-wide study of early onset and familial Parkinson's disease.
Towns C, Fang ZH, Tan MMX, Jasaityte S, Schmaderer TM, Stafford EJ, Pollard M, Tilney R, Hodgson M, Wu L, Labrum R, Hehir J, Polke J, Lange LM, Schapira AHV, Bhatia KP; Parkinson’s Families Project (PFP) Study Group; Global Parkinson’s Genetics Program (GP2); Singleton AB, Blauwendraat C, Klein C, Houlden H, Wood NW, Jarman PR, Morris HR, Real R. Towns C, et al. NPJ Parkinsons Dis. 2024 Oct 17;10(1):188. doi: 10.1038/s41531-024-00778-z. NPJ Parkinsons Dis. 2024. PMID: 39420034 Free PMC article.
Genome-wide association study of copy number variations in Parkinson's disease.
Landoulsi Z, Sreelatha AAK, Kuznetsov N, Schulte C, Bobbili DR, Montanucci L, Leu C, Niestroj LM, Hassanin E, Domenighetti C, Sugier PE, Radivojkov-Blagojevic M, Lichtner P, Portugal B, Edsall C, Krüger J, Hernandez DG, Blauwendraat C, Mellick GD, Zimprich A, Pirker W, Tan M, Rogaeva E, Lang A, Koks S, Taba P, Lesage S, Brice A, Corvol JC, Chartier-Harlin MC, Mutez E, Brockmann K, Deutschländer AB, Hadjigeorgiou GM, Dardiotis E, Stefanis L, Simitsi AM, Valente EM, Petrucci S, Straniero L, Zecchinelli A, Pezzoli G, Brighina L, Ferrarese C, Annesi G, Quattrone A, Gagliardi M, Burbulla LF, Matsuo H, Nakayama A, Hattori N, Nishioka K, Chung SJ, Kim YJ, Pavelka L, Kolber P, van de Warrenburg BP, Bloem BR, Singleton AB, Vitale D, Toft M, Pihlstrom L, Guedes LC, Ferreira JJ, Bardien S, Carr J, Tolosa E, Ezquerra M, Pastor P, Wirdefeldt K, Pedersen NL, Ran C, Belin AC, Puschmann A, Clarke CE, Morrison KE, Krainc D, Farrer MJ, Lal D; Global Parkinson Genetics Program (GP2); Elbaz A, Gasser T, Krüger R, Sharma M, May P; Comprehensive Unbiased Risk Factor Assessment for Genetics and Environment in Parkinson’s Disease (COURAGE-PD) consortium. Landoulsi Z, et al. NPJ Parkinsons Dis. 2026 Apr 20;12(1):160. doi: 10.1038/s41531-025-01245-z. NPJ Parkinsons Dis. 2026. PMID: 42009659 Free PMC article.
Genome-Wide Assessment Reveals Ancestral Differences in Homozygosity Patterns Potentially Linked to Parkinson's Disease Etiology.
Step K, Hernández CF, Khani M, Eltaraifee E, Hernández-Medrano AJ, Kung PJ, Ostrožovičová M, Zirra A, Pérez-Palma E, Mencacci NE, Keller Sarmiento IJ, Morris HR, Mata IF, Acosta-Uribe J, Fang ZH, Bandres-Ciga S; Global Parkinson's Genetics Program (GP2). Step K, et al. Mov Disord. 2026 May;41(5):1128-1140. doi: 10.1002/mds.70182. Epub 2026 Mar 11. Mov Disord. 2026. PMID: 41808632 Free PMC article.
Defining the underlying pathology of corticobasal syndrome using clinical features and biomarkers.
Vaughan DP, Jensen MT, Real R, Fumi RG, Wu L, Lux D, Hodgson M, Jones PS, Holland N, Scotton WJ, Serrano-Assensio O, Quattrone A, Heslegrave AJ, Veleva E, Swann O, Zetterberg H, Lynch T, Mir P, Stamelou M, Seppi K, Vandenberghe R, Warner TT, Lees A, Bhatia KP, Church A, Kobylecki C, Leigh PN, Hu MT, Taba P, Matsalu T, Pavese N, Ghosh BCP, Picillo M, Wallin J, Svenningson P, Sánchez-Gómez A, Fernández M, Cámara A, Planellas L, Compta Y; PROSPECT consortium, MD-GAP; Quaegebeur A, Jaunmuktane Z, Revesz T, Jabbari E, Rohrer JD, Rowe JB, Morris HR. Vaughan DP, et al. Brain. 2026 Aug 6:awag257. doi: 10.1093/brain/awag257. Online ahead of print. Brain. 2026. PMID: 42557872 Free article.
Malignant transformation of sacrococcygeal teratoma versus presacral teratoma in Currarino syndrome: Results of 'The SCT-study'.
van Heurn LJ, Derikx JPM, Hall NJ, AbouZeid AA, de Campos Vieira Abib S, Chirdan LB, Fumino S, Kim SC, Muensterer O, Olivos M, StPeter SD, Twisk J, Vinit N, Yang T, Zani A, Ernst van Heurn LW; SCT-study consortium. van Heurn LJ, et al. J Pediatr Surg. 2026 Jun;61(6):162848. doi: 10.1016/j.jpedsurg.2025.162848. Epub 2026 Mar 30. J Pediatr Surg. 2026. PMID: 42250912 Free article.
Pathology and Genetics in a Global Cohort of Parkinsonian Disorders.
Wu LY, du Toit T, Georgiades T, Stafford EJ, Levine K, Fang ZH, Jasaityte S, Martinez AG, Cullinane P, De Pablo-Fernandez E, Blauwendraat C, Singleton AB, Scholz SW, Traynor BJ, Wood N, Hardy J, Chinnery P, Houlden H, Cain R, Troakes C, Chelban V, Serrano GE, Gveric D, McLean C, Love S, King A, Robinson AC, Roncaroli F, Shepherd C, Halliday G, Parkkinen L, Morris CM, Smith C, Beach TG, Gentleman S, Warner TT, Lashley T, Jaunmuktane Z, Real R, Morris HR; Global Parkinson’s Genetic Program (GP2). Wu LY, et al. JAMA Neurol. 2026 Aug 1;83(8):798-807. doi: 10.1001/jamaneurol.2026.1634. JAMA Neurol. 2026. PMID: 42258190 Free PMC article.
30 results