Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease
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Summary
An inversion polymorphism of approximately 900kb on chromosome 17q21, which includes the microtubule‐associated protein tau (MAPT) gene defines two haplotype clades, H1 and H2, which are observed to have a marginally significant excess among patients with Parkinson's disease.
- Type
- article
- Published
- 2007-08-01
- Cited by
- 167
- References
- 46
- Access
- Open access
- OpenAlex
- https://openalex.org/W1983643492
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:7659581
Keywords
Haplotype, Single-nucleotide polymorphism, Odds ratio, Biology, SNP
References
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- Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
- N-acetyltransferase 2 (NAT2) gene polymorphisms in Parkinson's disease
- The Saitohin 'Q7R' polymorphism and tau haplotype in multi-ethnic Alzheimer disease and Parkinson's disease cohorts.
- Mutation in the tau gene in familial multiple system tauopathy with presenile dementia.
- The Tau Gene Haplotype H1 Confers a Susceptibility to Parkinson’s Disease
- Significant association between the tau gene A0/A0 genotype and Parkinson's disease
- Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium.
- Strong association between Saitohin gene polymorphism and tau haplotype in the Polish population.
- Case‐control study of the extended tau gene haplotype in Parkinson's disease
- Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies
- The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases
- Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype
- Linkage disequilibrium and association of MAPT H1 in Parkinson disease.
- Tau gene and Parkinson’s disease: a case–control study and meta-analysis
- Association of the Tau haplotype with Parkinson's disease in the Greek population
- Association of Tau Haplotype-Tagging Polymorphisms with Parkinson’s Disease in Diverse Ethnic Parkinson’s Disease Cohorts
- Tau haplotypes regulate transcription and are associated with Parkinson's disease
- Initiation and Synergistic Fibrillization of Tau and Alpha-Synuclein
- The tau locus is not significantly associated with pathologically confirmed sporadic Parkinson's disease.
Cited by
- Cognitive and Pathological Influences of Tau Pathology in Lewy Body Disorders
- De la stimulation cérébrale profonde à l’étude physiopathologique de certaines formes génétiques de la Maladie de Parkinson
- Identifying PD-causing genes and genetic susceptibility factors: current approaches and future prospects.
- LRRK2 genetics and expression in the Parkinsonian brain
- ASYN and tau interaction : new drug target for neurodegenerative diseases
- Strategies and statistical methods for linkage disequilibrium-based mapping of complex traits
- Cognitive Impairment and Dementia in Patients with Parkinson Disease
- The genetic architecture of Parkinson's disease : emphasis on genetic susceptibility
- Whole Exome Analysis of Early Onset Alzheimer's Disease
- LRRK2 Mutations and Risk Variants in Japanese Patients with Parkinson’s Disease
- Phenotypic Heterogeneity of the GRN Asp22fs Mutation in a Large Italian Kindred
- The Neurobiological Basis of Cognitive Impairment in Parkinson'S Disease
- Copy number variation analysis of the 17q21.31 region and its role in neurodegenerative diseases
- Functions of GDNF/Ret signaling in models of autosomal recessive Parkinson’s disease
- Tau as a biomarker of neurodegenerative diseases.
- Association of the MAPT locus with Parkinson’s disease
- Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease
- Genomewide association study for susceptibility genes contributing to familial Parkinson disease
- Haplotypes and gene expression implicate the MAPT region for Parkinson disease
- A robust and efficient statistical method for genetic association studies using case and control samples from multiple cohorts
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