193 related articles for article (PubMed ID: 37304079)
1. Genetic analysis of dystonia-related genes in Parkinson's disease.
Wang Y; Zhao Y; Pan H; Zeng Q; Zhou X; Xiang Y; Zhou Z; Xu Q; Sun Q; Tan J; Yan X; Li J; Guo J; Tang B; Yu Q; Liu Z
Front Aging Neurosci; 2023; 15():1207114. PubMed ID: 37304079
[TBL] [Abstract][Full Text] [Related]
2. Study of the collagen type VI alpha 3 (COL6A3) gene in Parkinson's disease.
Jin CY; Zheng R; Lin ZH; Xue NJ; Chen Y; Gao T; Yan YQ; Fang Y; Yan YP; Yin XZ; Tian J; Pu JL; Zhang BR
BMC Neurol; 2021 May; 21(1):187. PubMed ID: 33964895
[TBL] [Abstract][Full Text] [Related]
3. Evaluating the Genetic Role of Circadian Clock Genes in Parkinson's Disease.
Xiang Y; Huang J; Wang Y; Huang X; Zeng Q; Li L; Zhao Y; Pan H; Xu Q; Liu Z; Sun Q; Wang J; Tan J; Shen L; Jiang H; Yan X; Li J; Tang B; Guo J
Mol Neurobiol; 2023 May; 60(5):2729-2736. PubMed ID: 36717479
[TBL] [Abstract][Full Text] [Related]
4. Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up.
Zech M; Boesch S; Jochim A; Weber S; Meindl T; Schormair B; Wieland T; Lunetta C; Sansone V; Messner M; Mueller J; Ceballos-Baumann A; Strom TM; Colombo R; Poewe W; Haslinger B; Winkelmann J
Mov Disord; 2017 Apr; 32(4):549-559. PubMed ID: 27666935
[TBL] [Abstract][Full Text] [Related]
5. The Association Between Lysosomal Storage Disorder Genes and Parkinson's Disease: A Large Cohort Study in Chinese Mainland Population.
Zhao YW; Pan HX; Liu Z; Wang Y; Zeng Q; Fang ZH; Luo TF; Xu K; Wang Z; Zhou X; He R; Li B; Zhao G; Xu Q; Sun QY; Yan XX; Tan JQ; Li JC; Guo JF; Tang BS
Front Aging Neurosci; 2021; 13():749109. PubMed ID: 34867278
[No Abstract] [Full Text] [Related]
6. Genetic Analysis of Six Transmembrane Protein Family Genes in Parkinson's Disease in a Large Chinese Cohort.
Zhao Y; Zhang K; Pan H; Wang Y; Zhou X; Xiang Y; Xu Q; Sun Q; Tan J; Yan X; Li J; Guo J; Tang B; Liu Z
Front Aging Neurosci; 2022; 14():889057. PubMed ID: 35860667
[TBL] [Abstract][Full Text] [Related]
7. GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study.
Pan HX; Zhao YW; Mei JP; Fang ZH; Wang Y; Zhou X; Zhou YJ; Zhang R; Zhang KL; Jiang L; Zeng Q; He Y; Wang Z; Liu ZH; Xu Q; Sun QY; Yang Y; Hu YC; Chen YS; Du J; Lei LF; Zhang HN; Wang CY; Yan XX; Shen L; Jiang H; Tan JQ; Li JC; Tang BS; Guo JF
Transl Neurodegener; 2020 Aug; 9(1):31. PubMed ID: 32746945
[TBL] [Abstract][Full Text] [Related]
8. Genetic analysis of transcription factors in dopaminergic neuronal development in Parkinson's disease.
Zhao Y; Qin L; Pan H; Song T; Wang Y; Zhou X; Xiang Y; Li J; Liu Z; Sun Q; Guo J; Yan X; Tang B; Xu Q
Chin Med J (Engl); 2024 Feb; 137(4):450-456. PubMed ID: 37341647
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Large-Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia Genes.
Thomsen M; Marth K; Loens S; Everding J; Junker J; Borngräber F; Ott F; Jesús S; Gelderblom M; Odorfer T; Kuhlenbäumer G; Kim HJ; Schaeffer E; Becktepe J; Kasten M; Brüggemann N; Pfister R; Kollewe K; Krauss JK; Lohmann E; Hinrichs F; Berg D; Jeon B; Busch H; Altenmüller E; Mir P; Kamm C; Volkmann J; Zittel S; Ferbert A; Zeuner KE; Rolfs A; Bauer P; Kühn AA; Bäumer T; Klein C; Lohmann K
Mov Disord; 2024 Mar; 39(3):526-538. PubMed ID: 38214203
[TBL] [Abstract][Full Text] [Related]
11. Rare Variants Analysis of Lysosomal Related Genes in Early-Onset and Familial Parkinson's Disease in a Chinese Cohort.
Chen YP; Gu XJ; Song W; Hou YB; Ou RW; Zhang LY; Liu KC; Su WM; Cao B; Wei QQ; Zhao B; Wu Y; Shang HF
J Parkinsons Dis; 2021; 11(4):1845-1855. PubMed ID: 34250953
[TBL] [Abstract][Full Text] [Related]
12. Genetic Analysis of HSP40/DNAJ Family Genes in Parkinson's Disease: a Large Case-Control Study.
Zhang K; Pan H; Zhao Y; Wang Y; Zeng Q; Zhou X; He R; Zhou X; Xiang Y; Zhou Z; Li Y; Xu Q; Sun Q; Tan J; Yan X; Li J; Guo J; Tang B; Liu Z
Mol Neurobiol; 2022 Sep; 59(9):5443-5451. PubMed ID: 35715682
[TBL] [Abstract][Full Text] [Related]
13. Rare variant analysis of essential tremor-associated genes in early-onset Parkinson's disease.
Liang D; Zhao Y; Pan H; Zhou X; He R; Zhou X; Yang J; Wang Y; Zhou X; Zhou Z; Xu Q; Yan X; Li J; Guo J; Tang B; Sun Q
Ann Clin Transl Neurol; 2021 Jan; 8(1):119-125. PubMed ID: 33185019
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations.
Rudakou U; Yu E; Krohn L; Ruskey JA; Asayesh F; Dauvilliers Y; Spiegelman D; Greenbaum L; Fahn S; Waters CH; Dupré N; Rouleau GA; Hassin-Baer S; Fon EA; Alcalay RN; Gan-Or Z
Brain; 2021 Mar; 144(2):462-472. PubMed ID: 33349842
[TBL] [Abstract][Full Text] [Related]
16. Genetic Analysis of Prosaposin, the Lysosomal Storage Disorder Gene in Parkinson's Disease.
Chen YP; Gu XJ; Ou RW; Zhang LY; Hou YB; Liu KC; Cao B; Wei QQ; Song W; Zhao B; Wu Y; Cheng JQ; Shang HF
Mol Neurobiol; 2021 Apr; 58(4):1583-1592. PubMed ID: 33219486
[TBL] [Abstract][Full Text] [Related]
17. Systematically analyzing rare variants of autosomal-dominant genes for sporadic Parkinson's disease in a Chinese cohort.
Yang N; Zhao Y; Liu Z; Zhang R; He Y; Zhou Y; Xu Q; Sun Q; Yan X; Guo J; Tang B
Neurobiol Aging; 2019 Apr; 76():215.e1-215.e7. PubMed ID: 30598256
[TBL] [Abstract][Full Text] [Related]
18. Association of rare PPARGC1A variants with Parkinson's disease risk.
Li LZ; Zhao YW; Pan HX; Xiang YQ; Wang YG; Xu Q; Yan XX; Tan JQ; Li JC; Tang BS; Guo JF
J Hum Genet; 2022 Dec; 67(12):687-690. PubMed ID: 35996014
[TBL] [Abstract][Full Text] [Related]
19. Role of ANO3 mutations in dystonia: A large-scale mutational screening study.
Olschewski L; Jesús S; Kim HJ; Tunc S; Löns S; Junker J; Zeuner KE; Kühn AA; Kuhlenbäumer G; Schäffer E; Berg D; Kasten M; Ferbert A; Altenmüller E; Brüggemann N; Bauer P; Rolfs A; Jeon B; Bäumer T; Mir P; Klein C; Lohmann K
Parkinsonism Relat Disord; 2019 May; 62():196-200. PubMed ID: 30712998
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]