212 related articles for article (PubMed ID: 38173558)
1. Genetic landscape of Parkinson's disease and related diseases in Luxembourg.
Landoulsi Z; Pachchek S; Bobbili DR; Pavelka L; May P; Krüger R;
Front Aging Neurosci; 2023; 15():1282174. PubMed ID: 38173558
[TBL] [Abstract][Full Text] [Related]
2. Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease.
Zhu W; Huang X; Yoon E; Bandres-Ciga S; Blauwendraat C; Billingsley KJ; Cade JH; Wu BP; Williams VH; Schindler AB; Brooks J; Gibbs JR; Hernandez DG; Ehrlich D; Singleton AB; Narendra DP
Brain; 2022 Jun; 145(6):2077-2091. PubMed ID: 35640906
[TBL] [Abstract][Full Text] [Related]
3. Analysis of Heterozygous PRKN Variants and Copy-Number Variations in Parkinson's Disease.
Yu E; Rudakou U; Krohn L; Mufti K; Ruskey JA; Asayesh F; Estiar MA; Spiegelman D; Surface M; Fahn S; Waters CH; Greenbaum L; Espay AJ; Dauvilliers Y; Dupré N; Rouleau GA; Hassin-Baer S; Fon EA; Alcalay RN; Gan-Or Z
Mov Disord; 2021 Jan; 36(1):178-187. PubMed ID: 32970363
[TBL] [Abstract][Full Text] [Related]
4. Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study.
Tan MMX; Malek N; Lawton MA; Hubbard L; Pittman AM; Joseph T; Hehir J; Swallow DMA; Grosset KA; Marrinan SL; Bajaj N; Barker RA; Burn DJ; Bresner C; Foltynie T; Hardy J; Wood N; Ben-Shlomo Y; Grosset DG; Williams NM; Morris HR
Brain; 2019 Sep; 142(9):2828-2844. PubMed ID: 31324919
[TBL] [Abstract][Full Text] [Related]
5. Genetic study of early-onset Parkinson's disease in the Malaysian population.
Tay YW; Tan AH; Lim JL; Lohmann K; Ibrahim KA; Abdul Aziz Z; Chin YT; Mawardi AS; Lim TT; Looi I; Chia YK; Ooi JCE; Cheah WK; Dy Closas AMF; Lit LC; Hor JW; Toh TS; Muthusamy KA; Bauer P; Skrahin V; Rolfs A; Klein C; Ahmad-Annuar A; Lim SY
Parkinsonism Relat Disord; 2023 Jun; 111():105399. PubMed ID: 37209484
[TBL] [Abstract][Full Text] [Related]
6. Gene-based burden analysis of damaging private variants in PRKN, PARK7 and PINK1 in Parkinson's disease cohorts of European descent.
Hu J; Waters CH; Spiegelman D; Fon EA; Yu E; Asayesh F; Krohn L; Saini P; Alcalay RN; Hassin-Baer S; Gan-Or Z; Krainc D; Zhang B; Bustos BI; Lubbe SJ;
Neurobiol Aging; 2022 Nov; 119():136-138. PubMed ID: 36305379
[TBL] [Abstract][Full Text] [Related]
7. Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey.
Kessler C; Atasu B; Hanagasi H; Simón-Sánchez J; Hauser AK; Pak M; Bilgic B; Erginel-Unaltuna N; Gurvit H; Gasser T; Lohmann E
Parkinsonism Relat Disord; 2018 Mar; 48():34-39. PubMed ID: 29248340
[TBL] [Abstract][Full Text] [Related]
8. The genetic landscape of Parkinson's disease.
Lunati A; Lesage S; Brice A
Rev Neurol (Paris); 2018 Nov; 174(9):628-643. PubMed ID: 30245141
[TBL] [Abstract][Full Text] [Related]
9. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort.
Vollstedt EJ; Schaake S; Lohmann K; Padmanabhan S; Brice A; Lesage S; Tesson C; Vidailhet M; Wurster I; Hentati F; Mirelman A; Giladi N; Marder K; Waters C; Fahn S; Kasten M; Brüggemann N; Borsche M; Foroud T; Tolosa E; Garrido A; Annesi G; Gagliardi M; Bozi M; Stefanis L; Ferreira JJ; Correia Guedes L; Avenali M; Petrucci S; Clark L; Fedotova EY; Abramycheva NY; Alvarez V; Menéndez-González M; Jesús Maestre S; Gómez-Garre P; Mir P; Belin AC; Ran C; Lin CH; Kuo MC; Crosiers D; Wszolek ZK; Ross OA; Jankovic J; Nishioka K; Funayama M; Clarimon J; Williams-Gray CH; Camacho M; Cornejo-Olivas M; Torres-Ramirez L; Wu YR; Lee-Chen GJ; Morgadinho A; Pulkes T; Termsarasab P; Berg D; Kuhlenbäumer G; Kühn AA; Borngräber F; de Michele G; De Rosa A; Zimprich A; Puschmann A; Mellick GD; Dorszewska J; Carr J; Ferese R; Gambardella S; Chase B; Markopoulou K; Satake W; Toda T; Rossi M; Merello M; Lynch T; Olszewska DA; Lim SY; Ahmad-Annuar A; Tan AH; Al-Mubarak B; Hanagasi H; Koziorowski D; Ertan S; Genç G; de Carvalho Aguiar P; Barkhuizen M; Pimentel MMG; Saunders-Pullman R; van de Warrenburg B; Bressman S; Toft M; Appel-Cresswell S; Lang AE; Skorvanek M; Boon AJW; Krüger R; Sammler EM; Tumas V; Zhang BR; Garraux G; Chung SJ; Kim YJ; Winkelmann J; Sue CM; Tan EK; Damásio J; Klivényi P; Kostic VS; Arkadir D; Martikainen M; Borges V; Hertz JM; Brighina L; Spitz M; Suchowersky O; Riess O; Das P; Mollenhauer B; Gatto EM; Petersen MS; Hattori N; Wu RM; Illarioshkin SN; Valente EM; Aasly JO; Aasly A; Alcalay RN; Thaler A; Farrer MJ; Brockmann K; Corvol JC; Klein C;
Mov Disord; 2023 Feb; 38(2):286-303. PubMed ID: 36692014
[TBL] [Abstract][Full Text] [Related]
10. Pain in monogenic Parkinson's disease: a comprehensive review.
Alizadeh P; Terroba-Chambi C; Achen B; Bruno V
Front Neurol; 2023; 14():1248828. PubMed ID: 38020640
[TBL] [Abstract][Full Text] [Related]
11. Genome-Wide Polygenic Score Predicts Large Number of High Risk Individuals in Monogenic Undiagnosed Young Onset Parkinson's Disease Patients from India.
Kukkle PL; Geetha TS; Chaudhary R; Sathirapongsasuti JF; Goyal V; Kandadai RM; Kumar H; Borgohain R; Mukherjee A; Oliver M; Sunil M; Mootor MFE; Kapil S; Mandloi N; Wadia PM; Yadav R; Desai S; Kumar N; Biswas A; Pal PK; Muthane UB; Das SK; Sakthivel Murugan SM; Peterson AS; Stawiski EW; Seshagiri S; Gupta R; Ramprasad VL; Prai PRAOI
Adv Biol (Weinh); 2022 Nov; 6(11):e2101326. PubMed ID: 35810474
[TBL] [Abstract][Full Text] [Related]
12. Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease.
Torrealba-Acosta G; Yu E; Lobo-Prada T; Ruíz-Martínez J; Gorostidi-Pagola A; Gan-Or Z; Carazo-Céspedes K; Trempe JF; Mata IF; Fornaguera-Trías J
Front Neurol; 2021; 12():656342. PubMed ID: 34421783
[No Abstract] [Full Text] [Related]
13. 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]
14. Identification & characterization of leucine-rich repeat kinase 2 & parkin RBR E3 ubiquitin protein ligase variants in patients with Parkinson's disease.
Halder T; Verma SP; Raj J; Pandey S; Singh RK; Sharma V; Joshi D; Das P
Indian J Med Res; 2020 Nov; 152(5):498-507. PubMed ID: 33707392
[TBL] [Abstract][Full Text] [Related]
15. Novel and reported variants in Parkinson's disease genes confer high disease burden among Indians.
Kumar S; Yadav N; Pandey S; Muthane UB; Govindappa ST; Abbas MM; Behari M; Thelma BK
Parkinsonism Relat Disord; 2020 Sep; 78():46-52. PubMed ID: 32707456
[TBL] [Abstract][Full Text] [Related]
16. Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism.
Borsche M; König IR; Delcambre S; Petrucci S; Balck A; Brüggemann N; Zimprich A; Wasner K; Pereira SL; Avenali M; Deuschle C; Badanjak K; Ghelfi J; Gasser T; Kasten M; Rosenstiel P; Lohmann K; Brockmann K; Valente EM; Youle RJ; Grünewald A; Klein C
Brain; 2020 Oct; 143(10):3041-3051. PubMed ID: 33029617
[TBL] [Abstract][Full Text] [Related]
17. The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials.
Illés A; Csabán D; Grosz Z; Balicza P; Gézsi A; Molnár V; Bencsik R; Gál A; Klivényi P; Molnar MJ
Front Genet; 2019; 10():1061. PubMed ID: 31737044
[TBL] [Abstract][Full Text] [Related]
18. Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease.
Robak LA; Du R; Yuan B; Gu S; Alfradique-Dunham I; Kondapalli V; Hinojosa E; Stillwell A; Young E; Zhang C; Song X; Du H; Gambin T; Jhangiani SN; Coban Akdemir Z; Muzny DM; Tejomurtula A; Ross OA; Shaw C; Jankovic J; Bi W; Posey JE; Lupski JR; Shulman JM
Neurol Genet; 2020 Oct; 6(5):e498. PubMed ID: 32802956
[TBL] [Abstract][Full Text] [Related]
19. Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.
Camargos ST; Dornas LO; Momeni P; Lees A; Hardy J; Singleton A; Cardoso F
Mov Disord; 2009 Apr; 24(5):662-6. PubMed ID: 19205068
[TBL] [Abstract][Full Text] [Related]
20. The role of genetics in Parkinson's disease: a large cohort study in Chinese mainland population.
Zhao Y; Qin L; Pan H; Liu Z; Jiang L; He Y; Zeng Q; Zhou X; Zhou X; Zhou Y; Fang Z; Wang Z; Xiang Y; Yang H; Wang Y; Zhang K; Zhang R; He R; Zhou X; Zhou Z; Yang N; Liang D; Chen J; Zhang X; Zhou Y; Liu H; Deng P; Xu K; Xu K; Zhou C; Zhong J; Xu Q; Sun Q; Li B; Zhao G; Wang T; Chen L; Shang H; Liu W; Chan P; Xue Z; Wang Q; Guo L; Wang X; Xu C; Zhang Z; Chen T; Lei L; Zhang H; Wang C; Tan J; Yan X; Shen L; Jiang H; Zhang Z; Hu Z; Xia K; Yue Z; Li J; Guo J; Tang B
Brain; 2020 Jul; 143(7):2220-2234. PubMed ID: 32613234
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
