Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population.
about
Customisation of the exome data analysis pipeline using a combinatorial approachPolymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophreniaTrace amine-associated receptors and their ligandsMutation and evolutionary analyses identify NR2E1-candidate-regulatory mutations in humans with severe cortical malformationsCharacterization of population-based variation and putative functional elements for the multiple-cancer susceptibility loci at 5p15.33Evolutionary genomics of epidemic visceral leishmaniasis in the Indian subcontinentBAYSIC: a Bayesian method for combining sets of genome variants with improved specificity and sensitivity.A framework for variation discovery and genotyping using next-generation DNA sequencing dataEffects of natural selection on interpopulation divergence at polymorphic sites in human protein-coding LociGenetic diversity and function in the human cytosolic sulfotransferases.Dendritic trafficking of BDNF mRNA is mediated by translin and blocked by the G196A (Val66Met) mutation.Effective filtering strategies to improve data quality from population-based whole exome sequencing studies.Pharmacogenomics of neuropsychiatric disorders: analysis of genetic variability in 162 identified neuroreceptors using 1000 Genomes Project data.Establishment of a pipeline to analyse non-synonymous SNPs in Bos taurusA novel statistical method to estimate the effective SNP size in vertebrate genomes and categorized genomic regions.Accurate detection and genotyping of SNPs utilizing population sequencing dataCatalog of microRNA seed polymorphisms in vertebratesInference and analysis of haplotypes from combined genotyping studies deposited in dbSNPA simple method for analyzing exome sequencing data shows distinct levels of nonsynonymous variation for human immune and nervous system genes.Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.Evaluation of an integrated clinical workflow for targeted next-generation sequencing of low-quality tumor DNA using a 51-gene enrichment panel.Evidence for abundant slightly deleterious polymorphisms in bacterial populationsLooking for Darwin in all the wrong places: the misguided quest for positive selection at the nucleotide sequence level.Performance comparison of four exome capture systems for deep sequencing.Comparative Genome of GK and Wistar Rats Reveals Genetic Basis of Type 2 Diabetes.Assessment of the latest NGS enrichment capture methods in clinical context.Complete Sequence and Analysis of Coconut Palm (Cocos nucifera) Mitochondrial GenomeGenome-wide SNP typing reveals signatures of population history.Targeted sequencing of both DNA strands barcoded and captured individually by RNA probes to identify genome-wide ultra-rare mutations.MiST: a new approach to variant detection in deep sequencing datasets.Near neutrality: leading edge of the neutral theory of molecular evolution.AntCaller: an accurate variant caller incorporating ancient DNA damage.Analyses of porcine public SNPs in coding-gene regions by re-sequencing and phenotypic association studies.Analysis of the CTAGE5 P521A variation with the risk of familial idiopathic basal ganglia calcification in an Iranian population.High-throughput and parallel SNP discovery in selected candidate genes in Eucalyptus camaldulensis using Illumina NGS platform.A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci.Systematic investigation of genetic variability in 111 human genes-implications for studying variable drug response.Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics
P2860
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P2860
Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population.
description
2003 nî lūn-bûn
@nan
2003 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Single nucleotide variation an ...... le of the European population.
@ast
Single nucleotide variation an ...... le of the European population.
@en
type
label
Single nucleotide variation an ...... le of the European population.
@ast
Single nucleotide variation an ...... le of the European population.
@en
prefLabel
Single nucleotide variation an ...... le of the European population.
@ast
Single nucleotide variation an ...... le of the European population.
@en
P2093
P2860
P50
P356
P1433
P1476
Single nucleotide variation an ...... le of the European population.
@en
P2093
Jan Freudenberg
Nadine Kluck
Yun Freudenberg-Hua
P2860
P304
P356
10.1101/GR.1299703
P407
P577
2003-10-01T00:00:00Z