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Page 1
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. doi: 10.1038/s41531-025-01245-z. Online ahead of print. NPJ Parkinsons Dis. 2026. PMID: 42009659 Free 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 Mar 11. doi: 10.1002/mds.70182. Online ahead of print. Mov Disord. 2026. PMID: 41808632
Association of LRRK2 p.A419V with Parkinson's Disease in East Asians and analysis of age at onset.
Lim KS, Periñan MT, Chew EGY, Lee PS, Akçimen F, Lim JL, Koretsky MJ, Funayama M, Yoshino H, Hattori N, Kaiyrzhanov R, Houlden H, Isayan M, Tay YW, Toh TS, Lit LC, Khairul Anuar AN, Ding HX, Screven L, Ibrahim NM, Lin CH, Kim HJ, Lee JY, Chung SJ, Foo JN, Tan EK, Lim SY, Tan AH, Bandres-Ciga S, Ahmad-Annuar A; Global Parkinson’s Genetics Program (GP2). Lim KS, et al. NPJ Parkinsons Dis. 2026 Feb 2;12(1):51. doi: 10.1038/s41531-026-01265-3. NPJ Parkinsons Dis. 2026. PMID: 41629305 Free PMC article.
Identification of common variants influencing risk of the three-repeat tauopathy Pick's disease: a genome wide association study.
Scotton WJ, Valentino RR, Martinez-Carrasco A, Real R, Macpherson HL, Tamvaka N, Mok K, Heckman MG, Kobylecki C, Escott-Price V, Rowe JB, Morris HR, Rademakers R, Roemer SF, Lashley T, Dickson DW, Rohrer JD, Hardy JA, Ross OA, Shoai M. Scotton WJ, et al. Among authors: martinez carrasco a. medRxiv [Preprint]. 2025 Dec 23:2025.12.21.25342758. doi: 10.64898/2025.12.21.25342758. medRxiv. 2025. PMID: 41480034 Free PMC article. Preprint.
Insights into ancestral diversity in Parkinson's disease risk: a comparative assessment of polygenic risk scores.
Saffie-Awad P, Grant SM, Makarious MB, Elsayed I, Sanyaolu AO, Crea PW, Schumacher Schuh AF, Levine KS, Vitale D, Koretsky MJ, Kim J, Peixoto Leal T, Periñán MT, Dey S, Noyce AJ, Reyes-Palomares A, Rodriguez-Losada N, Foo JN, Mohamed W, Heilbron K, Norcliffe-Kaufmann L; 23andMe Research Team; Rizig M, Okubadejo N, Nalls MA, Blauwendraat C, Singleton A, Leonard H; Global Parkinson’s Genetics Program (GP2); Mata IF, Bandres-Ciga S. Saffie-Awad P, et al. NPJ Parkinsons Dis. 2025 Jul 3;11(1):201. doi: 10.1038/s41531-025-00967-4. NPJ Parkinsons Dis. 2025. PMID: 40610451 Free PMC article.
Diagnostic and prognostic value of α-synuclein seed amplification assay kinetic measures in Parkinson's disease: a longitudinal cohort study.
Orrú CD, Vaughan DP, Vijiaratnam N, Real R, Martinez-Carrasco A, Fumi R, Jensen MT, Hodgson M, Girges C, Gil-Martinez AL, Stafford EJ, Wu L, Lerche S, Wurster I, Groveman BR, Hughson AG, Ansorge O, Quaegebeur A, Allinson KSJ, Warner TT, Jaunmuktane Z, Misbahuddin A, Leigh PN, Ghosh BCP, Bhatia KP, Church A, Kobylecki C, Hu MTM, Rowe JB, Parchi P, Brockmann K, Foltynie T, Morris HR, Caughey B, Jabbari E. Orrú CD, et al. Among authors: martinez carrasco a. Lancet Neurol. 2025 Jul;24(7):580-590. doi: 10.1016/S1474-4422(25)00157-7. Lancet Neurol. 2025. PMID: 40541208 Free article.
The balance evaluation systems test (BESTest), mini-BESTest and brief-BESTest as clinical tools to assess balance control across different populations: A reliability generalization meta-analysis.
Meseguer-Henarejos AB, López-García JJ, López-Pina JA, Martínez-González-Moro I, Martínez-Carrasco Á. Meseguer-Henarejos AB, et al. Among authors: martinez carrasco a. PLoS One. 2025 Apr 3;20(4):e0318302. doi: 10.1371/journal.pone.0318302. eCollection 2025. PLoS One. 2025. PMID: 40179067 Free PMC article.
The LRRK2 p.L1795F variant causes Parkinson's disease in the European population.
Lange LM, Levine K, Fox SH, Marras C, Ahmed N, Kuznetsov N, Vitale D, Iwaki H, Lohmann K, Marsili L, Espay AJ, Bauer P, Beetz C, Martin J, Factor SA, Higginbotham LA, Chen H, Leonard H, Nalls MA, Mencacci NE, Morris HR, Singleton AB, Klein C, Blauwendraat C, Fang ZH; Global Parkinson’s Genetics Program (GP2). Lange LM, et al. NPJ Parkinsons Dis. 2025 Mar 25;11(1):58. doi: 10.1038/s41531-025-00896-2. NPJ Parkinsons Dis. 2025. PMID: 40133296 Free PMC article.
37 results