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Year Number of Results
2002 1
2003 2
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2005 2
2006 4
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2008 10
2009 6
2010 5
2011 6
2012 5
2013 7
2014 5
2015 7
2016 7
2017 5
2018 10
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2024 9
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129 results

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Page 1
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.
Nalls MA, Blauwendraat C, Vallerga CL, Heilbron K, Bandres-Ciga S, Chang D, Tan M, Kia DA, Noyce AJ, Xue A, Bras J, Young E, von Coelln R, Simón-Sánchez J, Schulte C, Sharma M, Krohn L, Pihlstrøm L, Siitonen A, Iwaki H, Leonard H, Faghri F, Gibbs JR, Hernandez DG, Scholz SW, Botia JA, Martinez M, Corvol JC, Lesage S, Jankovic J, Shulman LM, Sutherland M, Tienari P, Majamaa K, Toft M, Andreassen OA, Bangale T, Brice A, Yang J, Gan-Or Z, Gasser T, Heutink P, Shulman JM, Wood NW, Hinds DA, Hardy JA, Morris HR, Gratten J, Visscher PM, Graham RR, Singleton AB; 23andMe Research Team; System Genomics of Parkinson's Disease Consortium; International Parkinson's Disease Genomics Consortium. Nalls MA, et al. Lancet Neurol. 2019 Dec;18(12):1091-1102. doi: 10.1016/S1474-4422(19)30320-5. Lancet Neurol. 2019. PMID: 31701892 Free PMC article.
The genetic architecture of the human cerebral cortex.
Grasby KL, Jahanshad N, Painter JN, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Pizzagalli F, Ching CRK, McMahon MAB, Shatokhina N, Zsembik LCP, Thomopoulos SI, Zhu AH, Strike LT, Agartz I, Alhusaini S, Almeida MAA, Alnæs D, Amlien IK, Andersson M, Ard T, Armstrong NJ, Ashley-Koch A, Atkins JR, Bernard M, Brouwer RM, Buimer EEL, Bülow R, Bürger C, Cannon DM, Chakravarty M, Chen Q, Cheung JW, Couvy-Duchesne B, Dale AM, Dalvie S, de Araujo TK, de Zubicaray GI, de Zwarte SMC, den Braber A, Doan NT, Dohm K, Ehrlich S, Engelbrecht HR, Erk S, Fan CC, Fedko IO, Foley SF, Ford JM, Fukunaga M, Garrett ME, Ge T, Giddaluru S, Goldman AL, Green MJ, Groenewold NA, Grotegerd D, Gurholt TP, Gutman BA, Hansell NK, Harris MA, Harrison MB, Haswell CC, Hauser M, Herms S, Heslenfeld DJ, Ho NF, Hoehn D, Hoffmann P, Holleran L, Hoogman M, Hottenga JJ, Ikeda M, Janowitz D, Jansen IE, Jia T, Jockwitz C, Kanai R, Karama S, Kasperaviciute D, Kaufmann T, Kelly S, Kikuchi M, Klein M, Knapp M, Knodt AR, Krämer B, Lam M, Lancaster TM, Lee PH, Lett TA, Lewis LB, Lopes-Cendes I, Luciano M, Macciardi F, Marquand AF, Mathias SR, Melzer TR, Milaneschi Y, Mirza-Schreiber N, Moreira JCV, Mühleisen TW, Müller-Myhso… See abstract for full author list ➔ Grasby KL, et al. Among authors: dalrymple alford jc. Science. 2020 Mar 20;367(6484):eaay6690. doi: 10.1126/science.aay6690. Science. 2020. PMID: 32193296 Free PMC article.
Acquired Stuttering in Parkinson's Disease.
Gooch EA, Horne KL, Melzer TR, McAuliffe MJ, MacAskill M, Dalrymple-Alford JC, Anderson TJ, Theys C. Gooch EA, et al. Among authors: dalrymple alford jc. Mov Disord Clin Pract. 2023 May 8;10(6):956-966. doi: 10.1002/mdc3.13758. eCollection 2023 Jun. Mov Disord Clin Pract. 2023. PMID: 37332649 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.
Global network and local vulnerabilities underlie brain atrophy across Parkinson's disease stages.
Vo A, Tremblay C, Rahayel S, Al-Bachari S, Berendse HW, Bright JK, Cendes F, d'Angremont E, Dalrymple-Alford JC, Debove I, Dirkx MF, Druzgal J, Garraux G, Helmich RC, Hu MT, Jahanshad N, Johansson ME, Klein JC, Laansma MA, McMillan CT, Melzer TR, Misic B, Mosley P, Owens-Walton C, Parkes LM, Pellicano C, Piras F, Poston KL, Rango M, Rummel C, Schwingenschuh P, Suette M, Thompson PM, Tosun D, Tsai CC, van Balkom TD, van den Heuvel OA, van der Werf YD, van Heese EM, Vriend C, Wang JJ, Wiest R, Yasuda CL, Dagher A. Vo A, et al. Among authors: dalrymple alford jc. Brain. 2026 Jul 7;149(7):2380-2394. doi: 10.1093/brain/awaf432. Brain. 2026. PMID: 41237265 Free PMC article.
The New Zealand Parkinson's progression programme.
MacAskill MR, Pitcher TL, Melzer TR, Myall DJ, Horne KL, Shoorangiz R, Almuqbel MM, Livingston L, Grenfell S, Pascoe MJ, Marshall ET, Marsh S, Perry SE, Meissner WG, Theys C, Le Heron CJ, Keenan RJ, Dalrymple-Alford JC, Anderson TJ. MacAskill MR, et al. Among authors: dalrymple alford jc. J R Soc N Z. 2022 Aug 14;53(4):466-488. doi: 10.1080/03036758.2022.2111448. eCollection 2023. J R Soc N Z. 2022. PMID: 39439968 Free PMC article.
Attention/Working Memory and Executive Function in Parkinson's Disease: Review, Critique, and Recommendations.
Biundo R, Bezdicek O, Cammisuli DM, Cholerton B, Dalrymple-Alford JC, Edelstyn N, Fiorenzato E, Holker E, Martinez-Horta S, Martini A, Santangelo G, Segura B, Siri C, Tröster A, Mestre TA, Ferro ÁS, Hyczy de Siqueira Tosin M, Skorvanek M, Weintraub D, Geurtsen GJ; members of the MDS Clinical Outcome Assessment Scientific Evaluation Committee. Biundo R, et al. Among authors: dalrymple alford jc. Mov Disord. 2025 Sep;40(9):1791-1804. doi: 10.1002/mds.30293. Epub 2025 Jul 18. Mov Disord. 2025. PMID: 40678921 Free PMC article. Review.
Neuroimaging-based data-driven subtypes of spatiotemporal atrophy due to Parkinson's disease.
Shawa Z, Shand C, Taylor B, Berendse HW, Vriend C, van Balkom TD, van den Heuvel OA, van der Werf YD, Wang JJ, Tsai CC, Druzgal J, Newman BT, Melzer TR, Pitcher TL, Dalrymple-Alford JC, Anderson TJ, Garraux G, Rango M, Schwingenschuh P, Suette M, Parkes LM, Al-Bachari S, Klein J, Hu MTM, McMillan CT, Piras F, Vecchio D, Pellicano C, Zhang C, Poston KL, Ghasemi E, Cendes F, Yasuda CL, Tosun D, Mosley P, Thompson PM, Jahanshad N, Owens-Walton C, d'Angremont E, van Heese EM, Laansma MA, Altmann A; ENIGMA Parkinson’s Disease Working Group; Weil RS, Oxtoby NP. Shawa Z, et al. Among authors: dalrymple alford jc. Brain Commun. 2025 Apr 16;7(2):fcaf146. doi: 10.1093/braincomms/fcaf146. eCollection 2025. Brain Commun. 2025. PMID: 40303603 Free PMC 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.
129 results