Association between GRN rs5848 Polymorphism and Parkinson′s Disease in Taiwanese Population
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Title
Association between GRN rs5848 Polymorphism and Parkinson′s Disease in Taiwanese Population
Authors
Keywords
Parkinson disease, Alleles, Variant genotypes, Human genetics, Molecular genetics, Genetic polymorphism, Genotyping, Population genetics
Journal
PLoS One
Volume 8, Issue 1, Pages e54448
Publisher
Public Library of Science (PLoS)
Online
2013-01-17
DOI
10.1371/journal.pone.0054448
References
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Note: Only part of the references are listed.- Genome-Wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population
- (2011) Xinmin Liu et al. BMC Medical Genetics
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- (2011) Taye H. Hamza et al. PLoS Genetics
- Genome-Wide Association Study Confirms SNPs inSNCAand theMAPTRegion as Common Risk Factors for Parkinson Disease
- (2010) Todd L. Edwards et al. ANNALS OF HUMAN GENETICS
- Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population
- (2010) M. Saad et al. HUMAN MOLECULAR GENETICS
- Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
- (2010) et al. HUMAN MOLECULAR GENETICS
- rs5848 polymorphism and serum progranulin level
- (2010) Ging-Yuek R. Hsiung et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
- (2010) Taye H Hamza et al. NATURE GENETICS
- Analysis of GWAS-linked loci in Parkinson disease reaffirms PARK16 as a susceptibility locus
- (2010) E.- K. Tan et al. NEUROLOGY
- Evidence for Gender-Specific Transcriptional Profiles of Nigral Dopamine Neurons in Parkinson Disease
- (2010) Filip Simunovic et al. PLoS One
- Serum biomarker for progranulin-associated frontotemporal lobar degeneration
- (2009) Kristel Sleegers et al. ANNALS OF NEUROLOGY
- Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members
- (2009) N. Finch et al. BRAIN
- GRN3′UTR+78 C>T is not associated with risk for Parkinson’s disease
- (2009) B. Jasinska-Myga et al. EUROPEAN JOURNAL OF NEUROLOGY
- Independent influences of sex steroids of systemic and central origin in a rat model of Parkinson's disease: A contribution to sex-specific neuroprotection by estrogens
- (2009) Glenda E. Gillies et al. HORMONES AND BEHAVIOR
- Roles of Progranulin in Sexual Differentiation of the Developing Brain and Adult Neurogenesis
- (2009) Masatoshi SUZUKI et al. JOURNAL OF REPRODUCTION AND DEVELOPMENT
- Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
- (2009) Wataru Satake et al. NATURE GENETICS
- Genome-wide association study reveals genetic risk underlying Parkinson's disease
- (2009) Javier Simón-Sánchez et al. NATURE GENETICS
- Different Prevalence Rates of Parkinson’s Disease in Urban and Rural Areas: A Population-Based Study in Taiwan
- (2009) Chih Chuan Chen et al. NEUROEPIDEMIOLOGY
- Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
- (2008) Owen A. Ross et al. ANNALS OF NEUROLOGY
- Genomewide association study for susceptibility genes contributing to familial Parkinson disease
- (2008) Nathan Pankratz et al. HUMAN GENETICS
- Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
- (2008) Rosa Rademakers et al. HUMAN MOLECULAR GENETICS
- Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival
- (2008) Philip Van Damme et al. JOURNAL OF CELL BIOLOGY
- Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration
- (2008) R. Ghidoni et al. NEUROLOGY
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