952 related articles for article (PubMed ID: 31755958)
1. Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.
Blauwendraat C; Reed X; Krohn L; Heilbron K; Bandres-Ciga S; Tan M; Gibbs JR; Hernandez DG; Kumaran R; Langston R; Bonet-Ponce L; Alcalay RN; Hassin-Baer S; Greenbaum L; Iwaki H; Leonard HL; Grenn FP; Ruskey JA; Sabir M; Ahmed S; Makarious MB; Pihlstrøm L; Toft M; van Hilten JJ; Marinus J; Schulte C; Brockmann K; Sharma M; Siitonen A; Majamaa K; Eerola-Rautio J; Tienari PJ; ; Pantelyat A; Hillis AE; Dawson TM; Rosenthal LS; Albert MS; Resnick SM; Ferrucci L; Morris CM; Pletnikova O; Troncoso J; Grosset D; Lesage S; Corvol JC; Brice A; Noyce AJ; Masliah E; Wood N; Hardy J; Shulman LM; Jankovic J; Shulman JM; Heutink P; Gasser T; Cannon P; Scholz SW; Morris H; Cookson MR; Nalls MA; Gan-Or Z; Singleton AB
Brain; 2020 Jan; 143(1):234-248. PubMed ID: 31755958
[TBL] [Abstract][Full Text] [Related]
2. Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease.
Benitez BA; Davis AA; Jin SC; Ibanez L; Ortega-Cubero S; Pastor P; Choi J; Cooper B; Perlmutter JS; Cruchaga C
Mol Neurodegener; 2016 Apr; 11():29. PubMed ID: 27094865
[TBL] [Abstract][Full Text] [Related]
3. Glucocerebrosidase activity in Parkinson's disease with and without GBA mutations.
Alcalay RN; Levy OA; Waters CC; Fahn S; Ford B; Kuo SH; Mazzoni P; Pauciulo MW; Nichols WC; Gan-Or Z; Rouleau GA; Chung WK; Wolf P; Oliva P; Keutzer J; Marder K; Zhang X
Brain; 2015 Sep; 138(Pt 9):2648-58. PubMed ID: 26117366
[TBL] [Abstract][Full Text] [Related]
4. The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signal.
Berge-Seidl V; Pihlstrøm L; Maple-Grødem J; Forsgren L; Linder J; Larsen JP; Tysnes OB; Toft M
Neurosci Lett; 2017 Sep; 658():48-52. PubMed ID: 28830825
[TBL] [Abstract][Full Text] [Related]
5. Revisiting the non-Gaucher-GBA-E326K carrier state: Is it sufficient to increase Parkinson's disease risk?
Goldstein O; Gana-Weisz M; Cohen-Avinoam D; Shiner T; Thaler A; Cedarbaum JM; John S; Lalioti M; Gurevich T; Bar-Shira A; Mirelman A; Giladi N; Orr-Urtreger A
Mol Genet Metab; 2019 Dec; 128(4):470-475. PubMed ID: 31662221
[TBL] [Abstract][Full Text] [Related]
6. LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study.
Quadri M; Mandemakers W; Grochowska MM; Masius R; Geut H; Fabrizio E; Breedveld GJ; Kuipers D; Minneboo M; Vergouw LJM; Carreras Mascaro A; Yonova-Doing E; Simons E; Zhao T; Di Fonzo AB; Chang HC; Parchi P; Melis M; Correia Guedes L; Criscuolo C; Thomas A; Brouwer RWW; Heijsman D; Ingrassia AMT; Calandra Buonaura G; Rood JP; Capellari S; Rozemuller AJ; Sarchioto M; Fen Chien H; Vanacore N; Olgiati S; Wu-Chou YH; Yeh TH; Boon AJW; Hoogers SE; Ghazvini M; IJpma AS; van IJcken WFJ; Onofrj M; Barone P; Nicholl DJ; Puschmann A; De Mari M; Kievit AJ; Barbosa E; De Michele G; Majoor-Krakauer D; van Swieten JC; de Jong FJ; Ferreira JJ; Cossu G; Lu CS; Meco G; Cortelli P; van de Berg WDJ; Bonifati V;
Lancet Neurol; 2018 Jul; 17(7):597-608. PubMed ID: 29887161
[TBL] [Abstract][Full Text] [Related]
7. Augmentation of phenotype in a transgenic Parkinson mouse heterozygous for a Gaucher mutation.
Fishbein I; Kuo YM; Giasson BI; Nussbaum RL
Brain; 2014 Dec; 137(Pt 12):3235-47. PubMed ID: 25351739
[TBL] [Abstract][Full Text] [Related]
8. Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms.
Blauwendraat C; Heilbron K; Vallerga CL; Bandres-Ciga S; von Coelln R; Pihlstrøm L; Simón-Sánchez J; Schulte C; Sharma M; Krohn L; Siitonen A; Iwaki H; Leonard H; Noyce AJ; Tan M; Gibbs JR; Hernandez DG; Scholz SW; Jankovic J; Shulman LM; Lesage S; Corvol JC; Brice A; van Hilten JJ; Marinus J; ; Eerola-Rautio J; Tienari P; Majamaa K; Toft M; Grosset DG; Gasser T; Heutink P; Shulman JM; Wood N; Hardy J; Morris HR; Hinds DA; Gratten J; Visscher PM; Gan-Or Z; Nalls MA; Singleton AB;
Mov Disord; 2019 Jun; 34(6):866-875. PubMed ID: 30957308
[TBL] [Abstract][Full Text] [Related]
9. Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture.
Chia R; Sabir MS; Bandres-Ciga S; Saez-Atienzar S; Reynolds RH; Gustavsson E; Walton RL; Ahmed S; Viollet C; Ding J; Makarious MB; Diez-Fairen M; Portley MK; Shah Z; Abramzon Y; Hernandez DG; Blauwendraat C; Stone DJ; Eicher J; Parkkinen L; Ansorge O; Clark L; Honig LS; Marder K; Lemstra A; St George-Hyslop P; Londos E; Morgan K; Lashley T; Warner TT; Jaunmuktane Z; Galasko D; Santana I; Tienari PJ; Myllykangas L; Oinas M; Cairns NJ; Morris JC; Halliday GM; Van Deerlin VM; Trojanowski JQ; Grassano M; Calvo A; Mora G; Canosa A; Floris G; Bohannan RC; Brett F; Gan-Or Z; Geiger JT; Moore A; May P; Krüger R; Goldstein DS; Lopez G; Tayebi N; Sidransky E; ; Norcliffe-Kaufmann L; Palma JA; Kaufmann H; Shakkottai VG; Perkins M; Newell KL; Gasser T; Schulte C; Landi F; Salvi E; Cusi D; Masliah E; Kim RC; Caraway CA; Monuki ES; Brunetti M; Dawson TM; Rosenthal LS; Albert MS; Pletnikova O; Troncoso JC; Flanagan ME; Mao Q; Bigio EH; Rodríguez-Rodríguez E; Infante J; Lage C; González-Aramburu I; Sanchez-Juan P; Ghetti B; Keith J; Black SE; Masellis M; Rogaeva E; Duyckaerts C; Brice A; Lesage S; Xiromerisiou G; Barrett MJ; Tilley BS; Gentleman S; Logroscino G; Serrano GE; Beach TG; McKeith IG; Thomas AJ; Attems J; Morris CM; Palmer L; Love S; Troakes C; Al-Sarraj S; Hodges AK; Aarsland D; Klein G; Kaiser SM; Woltjer R; Pastor P; Bekris LM; Leverenz JB; Besser LM; Kuzma A; Renton AE; Goate A; Bennett DA; Scherzer CR; Morris HR; Ferrari R; Albani D; Pickering-Brown S; Faber K; Kukull WA; Morenas-Rodriguez E; Lleó A; Fortea J; Alcolea D; Clarimon J; Nalls MA; Ferrucci L; Resnick SM; Tanaka T; Foroud TM; Graff-Radford NR; Wszolek ZK; Ferman T; Boeve BF; Hardy JA; Topol EJ; Torkamani A; Singleton AB; Ryten M; Dickson DW; Chiò A; Ross OA; Gibbs JR; Dalgard CL; Traynor BJ; Scholz SW
Nat Genet; 2021 Mar; 53(3):294-303. PubMed ID: 33589841
[TBL] [Abstract][Full Text] [Related]
10. Mutations in the glucocerebrosidase gene are common in patients with Parkinson's disease from Eastern Canada.
Han F; Grimes DA; Li F; Wang T; Yu Z; Song N; Wu S; Racacho L; Bulman DE
Int J Neurosci; 2016; 126(5):415-21. PubMed ID: 26000814
[TBL] [Abstract][Full Text] [Related]
11. Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease.
Neumann J; Bras J; Deas E; O'Sullivan SS; Parkkinen L; Lachmann RH; Li A; Holton J; Guerreiro R; Paudel R; Segarane B; Singleton A; Lees A; Hardy J; Houlden H; Revesz T; Wood NW
Brain; 2009 Jul; 132(Pt 7):1783-94. PubMed ID: 19286695
[TBL] [Abstract][Full Text] [Related]
12. Glucocerebrosidase gene variants are accumulated in idiopathic REM sleep behavior disorder.
Gámez-Valero A; Iranzo A; Serradell M; Vilas D; Santamaria J; Gaig C; Álvarez R; Ariza A; Tolosa E; Beyer K
Parkinsonism Relat Disord; 2018 May; 50():94-98. PubMed ID: 29487000
[TBL] [Abstract][Full Text] [Related]
13. Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson's disease and increase susceptibility to dementia in a Flanders-Belgian cohort.
Crosiers D; Verstraeten A; Wauters E; Engelborghs S; Peeters K; Mattheijssens M; De Deyn PP; Theuns J; Van Broeckhoven C; Cras P
Neurosci Lett; 2016 Aug; 629():160-164. PubMed ID: 27397011
[TBL] [Abstract][Full Text] [Related]
14. Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease.
Robak LA; Jansen IE; van Rooij J; Uitterlinden AG; Kraaij R; Jankovic J; ; Heutink P; Shulman JM
Brain; 2017 Dec; 140(12):3191-3203. PubMed ID: 29140481
[TBL] [Abstract][Full Text] [Related]
15. Characterization of Brain Lysosomal Activities in GBA-Related and Sporadic Parkinson's Disease and Dementia with Lewy Bodies.
Moors TE; Paciotti S; Ingrassia A; Quadri M; Breedveld G; Tasegian A; Chiasserini D; Eusebi P; Duran-Pacheco G; Kremer T; Calabresi P; Bonifati V; Parnetti L; Beccari T; van de Berg WDJ
Mol Neurobiol; 2019 Feb; 56(2):1344-1355. PubMed ID: 29948939
[TBL] [Abstract][Full Text] [Related]
16. Effect of GBA gene variants on clinical characteristics of dementia with Lewy bodies: a review and meta-analyses.
Liu L; Li J; Quan W; Qin Y; Zhang Q; Pei X; Su H; Xu J; Chen J
Neurol Sci; 2022 Jun; 43(6):3541-3550. PubMed ID: 35332438
[TBL] [Abstract][Full Text] [Related]
17. Association of glucocerebrosidase polymorphisms and mutations with dementia in incident Parkinson's disease.
Lunde KA; Chung J; Dalen I; Pedersen KF; Linder J; Domellöf ME; Elgh E; Macleod AD; Tzoulis C; Larsen JP; Tysnes OB; Forsgren L; Counsell CE; Alves G; Maple-Grødem J
Alzheimers Dement; 2018 Oct; 14(10):1293-1301. PubMed ID: 29792872
[TBL] [Abstract][Full Text] [Related]
18. Survival and dementia in GBA-associated Parkinson's disease: The mutation matters.
Cilia R; Tunesi S; Marotta G; Cereda E; Siri C; Tesei S; Zecchinelli AL; Canesi M; Mariani CB; Meucci N; Sacilotto G; Zini M; Barichella M; Magnani C; Duga S; Asselta R; Soldà G; Seresini A; Seia M; Pezzoli G; Goldwurm S
Ann Neurol; 2016 Nov; 80(5):662-673. PubMed ID: 27632223
[TBL] [Abstract][Full Text] [Related]
19. GBA Mutations Are Associated With Earlier Onset and Male Sex in Dementia With Lewy Bodies.
Gámez-Valero A; Prada-Dacasa P; Santos C; Adame-Castillo C; Campdelacreu J; Reñé R; Gascón-Bayarri J; Ispierto L; Álvarez R; Ariza A; Beyer K
Mov Disord; 2016 Jul; 31(7):1066-70. PubMed ID: 27027900
[TBL] [Abstract][Full Text] [Related]
20. Glucocerebrosidase mutations confer a greater risk of dementia during Parkinson's disease course.
Setó-Salvia N; Pagonabarraga J; Houlden H; Pascual-Sedano B; Dols-Icardo O; Tucci A; Paisán-Ruiz C; Campolongo A; Antón-Aguirre S; Martín I; Muñoz L; Bufill E; Vilageliu L; Grinberg D; Cozar M; Blesa R; Lleó A; Hardy J; Kulisevsky J; Clarimón J
Mov Disord; 2012 Mar; 27(3):393-9. PubMed ID: 22173904
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
