Association of GWAS loci with PD in China

Association of GWAS loci with PD in China

10.1002/ajmg.b.31167

Saved in:

Bibliographic Details
Main Authors:	Chang, X.-L., Mao, X.-Y., Li, H.-H., Zhang, J.-H., Li, N.-N., Burgunder, J.-M., Peng, R., Tan, E.-K.
Other Authors:	DUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE
Format:	Article
Published:	2014
Subjects:	BST1 LRRK2 PARK16 Parkinson's disease SNCA SNP
Online Access:	http://scholarbank.nus.edu.sg/handle/10635/110493
Tags:	Add Tag No Tags, Be the first to tag this record!
Institution:	National University of Singapore

Similar Items

Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study
by: Wang L., et al.
Published: (2018)

Interaction between SNCA, LRRK2 and GAK increases susceptibility to Parkinson's disease in a Chinese population
by: Yu W.-J., et al.
Published: (2018)

PARK16 is associated with PD in the Malaysian population
by: Gopalai A.A., et al.
Published: (2018)

LRRK2 mutations are not frequent in Swiss patients with Parkinson's disease
by: Burgunder, J.-M., et al.
Published: (2011)

Functional parkin promoter polymorphism in Parkinson's disease: New data and meta-analysis
by: Chang, X.-L., et al.
Published: (2014)

SNCA rs356219 variant increases risk of sporadic Parkinson's disease in ethnic Chinese
by: Li, N.-N., et al.
Published: (2014)

Genetic analysis of LRRK2 A419V variant in ethnic Chinese
by: Li, N.-N., et al.
Published: (2014)

LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China
by: Zhang, Z., et al.
Published: (2015)

LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China
by: An, X.-K., et al.
Published: (2015)

Analysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians
by: Tan E.-K., et al.
Published: (2018)

GSK3β reduces risk of sporadic Parkinson's disease in ethnic Chinese
by: Zhao, D.-M., et al.
Published: (2014)

Pathogenicity of LRRK2 P755L variant in Parkinson's disease
by: Tan E.-K., et al.
Published: (2018)

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients
by: Tan E.K., et al.
Published: (2018)

MTHFR C677T variant reduces risk of sporadic Parkinson's disease in ethnic Chinese
by: Liao, Q., et al.
Published: (2016)

Multiple LRRK2 variants modulate risk of Parkinson disease: A Chinese multicenter study
by: Tan, E.-K., et al.
Published: (2014)

Analysis of LRRK2 G2019S and I2020T mutations in Parkinson's disease
by: Bialecka M., et al.
Published: (2018)

Targeting LRRK2 in Parkinson's disease: an update on recent developments
by: Chan S.L., et al.
Published: (2018)

IDENTIFICATION OF ALPHA-SYNUCLEIN DOMINANT MODIFIERS IN A DROSOPHILA MODEL OF NEURODEGENERATION
by: REN MENGDA
Published: (2020)

Genetic testing of LRRK2 in Parkinson's disease: Is there a clinical role?
by: Buhat D.M.L., et al.
Published: (2018)

Four-Year Longitudinal Study of Motor and Non-motor Symptoms in LRRK2-Related Parkinson's Disease
by: Deng, X, et al.
Published: (2024)

LRRK2 in Parkinson's disease: Genetic and clinical studies from patients
by: Kumari U., et al.
Published: (2018)

Genetic analysis of "leucine-rich repeat (LRR) and immunoglobulin (Ig) domain-containing, Nogo receptor-interacting protein-1 (LINGO1)" in two independent Chinese parkinson's disease populations
by: Wu, Y.-R., et al.
Published: (2014)

Patterns of linkage disequilibrium at PARK16 may explain variances in genetic association studies
by: Li H., et al.
Published: (2018)

Identification of targets from lrrk2 rescue phenotypes
by: Toh, Joanne, et al.
Published: (2022)

Non-mammalian animal models of Parkinson's disease for drug discovery
by: Lim, K.-L.
Published: (2014)

Genetic models of Parkinson disease
by: Lim, K.-L., et al.
Published: (2014)

Targeting leucine-rich repeat kinase 2 in Parkinson's disease
by: Chan S.L., et al.
Published: (2018)

LRRK2 variant associated with Alzheimer's disease
by: Zhao, Y., et al.
Published: (2014)

Case-control analysis of leucine-rich repeat kinase 2 protective variants in Alzheimer's disease
by: Ng A.S.L., et al.
Published: (2018)

A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease
by: Krüger R., et al.
Published: (2018)

Analysis of conductor loss in interdigital capacitor based measurement of dielectric constant of ferroelectric thin film
by: Wang, P., et al.
Published: (2014)

Effective algorithms for tag SNP selection
by: Liu, T.-F., et al.
Published: (2013)

The prevalence of restless legs syndrome in Thai patients with parkingson's disease and patients taking neuroleptic drugs
by: Priya Jagota
Published: (2012)

Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population
by: Pan, Hongxu, et al.
Published: (2024)

Study Of Barium Strontium Titanate Varactor At High Frequency
by: CHENG WEINING
Published: (2010)

MCCC1/LAMP3 reduces risk of sporadic Parkinson's disease in Han Chinese
by: Li, N.N., et al.
Published: (2014)

POTENTIALLY FUNCTIONAL SINGLE NUCLEOTIDE POLYMORPHISMS (PFSNPS) IN THE HUMAN GENOME AND THEIR POTENTIAL APPLICATIONS
by: WANG JINGBO
Published: (2013)

Realtime exonuclease-mediated allelic discrimination (READ): A simple homogeneous genotyping assay for SNPs at the ABC gene loci
by: Wang, Z., et al.
Published: (2011)

Validation of GWAS loci for atopic dermatitis in a Singapore chinese population
by: Andiappan, A.K., et al.
Published: (2014)

Essential tremor and the common LRRK2 G2385R variant
by: Tan E.-K., et al.
Published: (2018)