Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed wi

Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed wi

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http://www.wikidata.org/entity/Q33998500

Q33998500

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Association between genetic variations in prostaglandin E2 receptor subtype EP3 gene (Ptger3) and asthma in the Korean population Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects Genome-wide association studies for common diseases and complex traits Japan PGx Data Science Consortium Database: SNPs and HLA genotype data from 2994 Japanese healthy individuals for pharmacogenomics studies.An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets.Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analyses Test of association between haplotypes and phenotypes in case-control studies: examination of validity of the application of an algorithm for samples from cohort or clinical trials to case-control samples using simulated and real data.Evaluation of sample size effect on the identification of haplotype blocks.STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement.Genetic variations of PIP4K2A confer vulnerability to poor antipsychotic response in severely ill schizophrenia patients.Anti-citrullinated peptide antibody-negative RA is a genetically distinct subset: a definitive study using only bone-erosive ACPA-negative rheumatoid arthritis ACPA-negative RA consists of two genetically distinct subsets based on RF positivity in Japanese Linkage disequilibrium patterns vary substantially among populations.Estimating proportions of explained variance: a comparison of whole genome subsets.A Comprehensive In Silico Analysis on the Structural and Functional Impact of SNPs in the Congenital Heart Defects Associated with NKX2-5 Gene-A Molecular Dynamic Simulation Approach.Recent advances in the identification of genes for human hypertension.Japanese single nucleotide polymorphism database for 267 possible drug-related genes.STrengthening the REporting of Genetic Association studies (STREGA)--an extension of the STROBE statement.Dopaminergic gene polymorphisms and cognitive function in a north Indian schizophrenia cohort.Genome-wide strategies for discovering genetic influences on cognition and cognitive disorders: methodological considerations.Haplotype analysis of the ARMS2/HTRA1 region in Japanese patients with typical neovascular age-related macular degeneration or polypoidal choroidal vasculopathy.Association test algorithm between a qualitative phenotype and a haplotype or haplotype set using simultaneous estimation of haplotype frequencies, diplotype configurations and diplotype-based penetrances.Positive association of the serotonin 5-HT7 receptor gene with schizophrenia in a Japanese population.Dopamine transporter polymorphisms and risperidone response in Chinese schizophrenia patients: an association study.Haplotype analysis of ESR2 in Japanese patients with spermatogenic failure.Relationship between nicotine dependence and the endophenotype-related trait of cognitive function but not acoustic startle reponses in Japanese patients with schizophrenia.Haplotype analysis of the estrogen receptor 1 gene in male genital and reproductive abnormalities.Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE statement A single-nucleotide polymorphism tagging set for human drug metabolism and transport

P2860

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P2860

Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed wi

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http://www.wikidata.org/entity/Q33998500

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2004 nî lūn-bûn

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2004 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2004 թվականի հունիսին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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