Detalhe da pesquisa
1.
Evolutionary toggling of the MAPT 17q21.31 inversion region.
Nat Genet
; 40(9): 1076-83, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19165922
2.
Eukaryotic translation initiation factor 4-γ, 1 gene mutations are rare in Parkinson's disease among Taiwanese.
J Formos Med Assoc
; 115(9): 728-33, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26490695
3.
Genotype, haplotype and copy-number variation in worldwide human populations.
Nature
; 451(7181): 998-1003, 2008 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-18288195
4.
Association of AXIN1 With Parkinson's Disease in a Taiwanese Population.
J Mov Disord
; 15(1): 33-37, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34781631
5.
The correlation of small fiber neuropathy with pain intensity and age in patients with Fabry's disease: A cross sectional study within a large Taiwanese family.
Biomed J
; 45(2): 406-413, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35595648
6.
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
Hum Mol Genet
; 18(8): 1524-32, 2009 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19193627
7.
Polymorphisms of Interleukin-6 and Interleukin-8 Are Not Associated with Parkinson's Disease in Taiwan.
Brain Sci
; 11(6)2021 Jun 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34207646
8.
Fibroblast Growth Factor 20 Gene Polymorphism in Parkinson's Disease in Asian Population: A Meta-Analysis.
Genes (Basel)
; 12(5)2021 04 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33947140
9.
Role of LRP10 in Parkinson's disease in a Taiwanese cohort.
Parkinsonism Relat Disord
; 89: 79-83, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34246039
10.
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans.
PLoS Genet
; 3(6): e108, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17590087
11.
Association of genetic variants within HLA-DR region with Parkinson's disease in Taiwan.
Neurobiol Aging
; 87: 140.e13-140.e18, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31818508
12.
Association of RIT2 and RAB7L1 with Parkinson's disease: a case-control study in a Taiwanese cohort and a meta-analysis in Asian populations.
Neurobiol Aging
; 87: 140.e5-140.e11, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31818509
13.
SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications.
Hum Genet
; 125(4): 437-44, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19229559
14.
PPP2R2B CAG repeat length in the Han Chinese in Taiwan: Association analyses in neurological and psychiatric disorders and potential functional implications.
Am J Med Genet B Neuropsychiatr Genet
; 150B(1): 124-9, 2009 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18484086
15.
Polymorphisms of ACMSD-TMEM163, MCCC1, and BCKDK-STX1B Are Not Associated with Parkinson's Disease in Taiwan.
Parkinsons Dis
; 2019: 3489638, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30719275
16.
Amyloid PET pattern with dementia and amyloid angiopathy in Taiwan familial AD with D678H APP mutation.
J Neurol Sci
; 398: 107-116, 2019 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30703749
17.
CCM1 and CCM2 variants in patients with cerebral cavernous malformation in an ethnically Chinese population in Taiwan.
Sci Rep
; 9(1): 12387, 2019 08 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31455779
18.
Genomewide SNP assay reveals mutations underlying Parkinson disease.
Hum Mutat
; 29(2): 315-22, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17994548
19.
Structural genomic variation in ischemic stroke.
Neurogenetics
; 9(2): 101-8, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18288507
20.
DLG2, but not TMEM229B, GPNMB, and ITGA8 polymorphism, is associated with Parkinson's disease in a Taiwanese population.
Neurobiol Aging
; 64: 158.e1-158.e6, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29290481