These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
332 related articles for article (PubMed ID: 33423827)
41. C9ORF72 intermediate repeat expansion in patients affected by atypical parkinsonian syndromes or Parkinson's disease complicated by psychosis or dementia in a Sardinian population. Cannas A; Solla P; Borghero G; Floris GL; Chio A; Mascia MM; Modugno N; Muroni A; Orofino G; Di Stefano F; Calvo A; Moglia C; Restagno G; Meloni M; Farris R; Ciaccio D; Puddu R; Vacca MI; Melis R; Murru MR; Tranquilli S; Corongiu D; Rolesu M; Cuccu S; Marrosu MG; Marrosu F J Neurol; 2015 Nov; 262(11):2498-503. PubMed ID: 26275564 [TBL] [Abstract][Full Text] [Related]
42. Evaluation of common and rare variants of Alzheimer's disease-causal genes in Parkinson's disease. Zeng Q; Pan H; Zhao Y; Wang Y; Xu Q; Tan J; Yan X; Li J; Tang B; Guo J Parkinsonism Relat Disord; 2022 Apr; 97():8-14. PubMed ID: 35276586 [TBL] [Abstract][Full Text] [Related]
43. Genetic association study of synphilin-1 in idiopathic Parkinson's disease. Myhre R; Klungland H; Farrer MJ; Aasly JO BMC Med Genet; 2008 Mar; 9():19. PubMed ID: 18366718 [TBL] [Abstract][Full Text] [Related]
44. Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. Jansen IE; Ye H; Heetveld S; Lechler MC; Michels H; Seinstra RI; Lubbe SJ; Drouet V; Lesage S; Majounie E; Gibbs JR; Nalls MA; Ryten M; Botia JA; Vandrovcova J; Simon-Sanchez J; Castillo-Lizardo M; Rizzu P; Blauwendraat C; Chouhan AK; Li Y; Yogi P; Amin N; van Duijn CM; ; Morris HR; Brice A; Singleton AB; David DC; Nollen EA; Jain S; Shulman JM; Heutink P Genome Biol; 2017 Jan; 18(1):22. PubMed ID: 28137300 [TBL] [Abstract][Full Text] [Related]
46. Evaluating the role of ARSA in Chinese patients with Parkinson's disease. Pan HX; Wang YG; Zhao YW; Zeng Q; Wang Z; Fang ZH; Zhang Y; Zhou X; He RC; Xu Q; Sun QY; Tan JQ; Yan XX; Li JC; Tang BS; Guo JF Neurobiol Aging; 2022 Jan; 109():269-272. PubMed ID: 34531044 [TBL] [Abstract][Full Text] [Related]
47. DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study. Trinh J; Gustavsson EK; Vilariño-Güell C; Bortnick S; Latourelle J; McKenzie MB; Tu CS; Nosova E; Khinda J; Milnerwood A; Lesage S; Brice A; Tazir M; Aasly JO; Parkkinen L; Haytural H; Foroud T; Myers RH; Sassi SB; Hentati E; Nabli F; Farhat E; Amouri R; Hentati F; Farrer MJ Lancet Neurol; 2016 Nov; 15(12):1248-1256. PubMed ID: 27692902 [TBL] [Abstract][Full Text] [Related]
48. Common and rare variants in HFE are not associated with Parkinson's disease in Europeans. Saini P; Bandres-Ciga S; Alcantud JL; Ruz C; Postuma RB; Gan-Or Z; Neurobiol Aging; 2021 Nov; 107():174-177. PubMed ID: 34215448 [TBL] [Abstract][Full Text] [Related]
49. Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance. Lubbe SJ; Escott-Price V; Gibbs JR; Nalls MA; Bras J; Price TR; Nicolas A; Jansen IE; Mok KY; Pittman AM; Tomkins JE; Lewis PA; Noyce AJ; Lesage S; Sharma M; Schiff ER; Levine AP; Brice A; Gasser T; Hardy J; Heutink P; Wood NW; Singleton AB; Williams NM; Morris HR; Hum Mol Genet; 2016 Dec; 25(24):5483-5489. PubMed ID: 27798102 [TBL] [Abstract][Full Text] [Related]
50. Rare variant screening and burden analysis of PLXNA1 in Parkinson's disease. Li C; Lin J; Jiang Q; Shang H Eur J Neurol; 2022 Dec; 29(12):3737-3741. PubMed ID: 35852441 [TBL] [Abstract][Full Text] [Related]
51. Association of rs62063857 variant of the saitohin gene with Parkinson's disease. Sonmez E; Ozel MD; Islek EE; Sazci A; Idrisoglu HA Cell Mol Neurobiol; 2015 Jan; 35(1):115-21. PubMed ID: 25168738 [TBL] [Abstract][Full Text] [Related]
58. Genetic analysis of N6-methyladenosine modification genes in Parkinson's disease. Qin L; Min S; Shu L; Pan H; Zhong J; Guo J; Sun Q; Yan X; Chen C; Tang B; Xu Q Neurobiol Aging; 2020 Sep; 93():143.e9-143.e13. PubMed ID: 32371107 [TBL] [Abstract][Full Text] [Related]
59. Association Study of Zeng Q; Pan H; Zhao Y; Wang Y; Xu Q; Tan J; Yan X; Li J; Tang B; Guo J Front Neurosci; 2022; 16():846095. PubMed ID: 35464305 [TBL] [Abstract][Full Text] [Related]
60. Association of novel rare coding variants with juvenile idiopathic arthritis. Meng X; Hou X; Wang P; Glessner JT; Qu HQ; March ME; Zhang S; Qi X; Zhu C; Nguyen K; Gao X; Li X; Liu Y; Zhou W; Zhang S; Li J; Sun Y; Yang J; Sleiman PMA; Xia Q; Hakonarson H; Li J Ann Rheum Dis; 2021 May; 80(5):626-631. PubMed ID: 33408077 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]