Detalhe da pesquisa
1.
Genetic landscape of human mitochondrial genome using whole-genome sequencing.
Hum Mol Genet
; 31(11): 1747-1761, 2022 06 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34897451
2.
GGC expansions in NOTCH2NLC contribute to Parkinson disease and dopaminergic neuron degeneration.
Eur J Neurol
; 31(2): e16145, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37975799
3.
Association of rare PPARGC1A variants with Parkinson's disease risk.
J Hum Genet
; 67(12): 687-690, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-35996014
4.
The Chinese Parkinson's Disease Registry (CPDR): Study Design and Baseline Patient Characteristics.
Mov Disord
; 37(7): 1335-1345, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35503029
5.
The role of genetics in Parkinson's disease: a large cohort study in Chinese mainland population.
Brain
; 143(7): 2220-2234, 2020 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32613234
6.
Association of HIF1A and Parkinson's disease in a Han Chinese population demonstrated by molecular inversion probe analysis.
Neurol Sci
; 40(9): 1927-1931, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31025220
7.
UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Brain
; 144(6): e54, 2021 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33779694
8.
PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Brain
; 144(3): e25, 2021 04 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33793763
9.
ATP10B variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Acta Neuropathol
; 141(5): 805-806, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33599816
10.
Genetic analysis of transcription factors in dopaminergic neuronal development in Parkinson's disease.
Chin Med J (Engl)
; 137(4): 450-456, 2024 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37341647
11.
Comprehensive variant analysis of phospholipase A2 superfamily genes in large Chinese Parkinson' s disease cohorts.
Mech Ageing Dev
; 219: 111940, 2024 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38750970
12.
Screen-printed highly stretchable and stable flexible electrodes with a negative Poisson's ratio structure for supercapacitors.
Nanoscale
; 15(3): 1260-1272, 2023 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36541665
13.
Evaluating the association between DNM1L variants and Parkinson's disease in the Chinese population.
Front Neurol
; 14: 1133449, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36908591
14.
Characteristics of fatigue in Parkinson's disease: A longitudinal cohort study.
Front Aging Neurosci
; 15: 1133705, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36967819
15.
Genetic analysis of dystonia-related genes in Parkinson's disease.
Front Aging Neurosci
; 15: 1207114, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37304079
16.
Evaluating the Genetic Role of Circadian Clock Genes in Parkinson's Disease.
Mol Neurobiol
; 60(5): 2729-2736, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36717479
17.
Evaluation of the role of FMR1 CGG repeat allele in Parkinson's disease from the Chinese population.
Front Aging Neurosci
; 15: 1234027, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37583466
18.
Mutational spectrum and clinical features of GBA1 variants in a Chinese cohort with Parkinson's disease.
NPJ Parkinsons Dis
; 9(1): 129, 2023 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37658046
19.
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population.
NPJ Parkinsons Dis
; 9(1): 22, 2023 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36759515
20.
Association between NOTCH3 gene and Parkinson's disease based on whole-exome sequencing.
Front Aging Neurosci
; 14: 995330, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36570541