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Genes to diseases (G2D) computational method to identify asthma candidate genesA computational framework to infer human disease-associated long noncoding RNAsLinking human diseases to animal models using ontology-based phenotype annotationCalling on a million minds for community annotation in WikiProteinsAnnotating the human genome with Disease OntologyHuman-specific histone methylation signatures at transcription start sites in prefrontal neuronsGenome-wide signatures of convergent evolution in echolocating mammalsPsyGeNET: a knowledge platform on psychiatric disorders and their genesThe role of complementary bipartite visual analytical representations in the analysis of SNPs: a case study in ancestral informative markersSystematic analysis, comparison, and integration of disease based human genetic association data and mouse genetic phenotypic informationMeta-analysis of haplotype-association studies: comparison of methods and empirical evaluation of the literatureToxicogenomic profiling of chemically exposed humans in risk assessmentA census of human soluble protein complexesA high-coverage genome sequence from an archaic Denisovan individualVnD: a structure-centric database of disease-related SNPs and drugsPATRIC: the comprehensive bacterial bioinformatics resource with a focus on human pathogenic speciesThe GenoChip: a new tool for genetic anthropologyA Large-scale genetic association study of esophageal adenocarcinoma riskMouse genetic and phenotypic resources for human geneticsUltraconserved cDNA segments in the human transcriptome exhibit resistance to folding and implicate function in translation and alternative splicingAfrican Americans with asthma: genetic insightsMultiple loci influence erythrocyte phenotypes in the CHARGE ConsortiumT1DBase, a community web-based resource for type 1 diabetes researchSpeeding disease gene discovery by sequence based candidate prioritizationImmunotoxicogenomics: gene expression and immunotoxicology in the age of genomicsWholePathwayScope: a comprehensive pathway-based analysis tool for high-throughput dataSystems biology approaches for discovering biomarkers for traumatic brain injuryNeurofunctional imaging of β-cell dynamicsA review of post-GWAS prioritization approachesEfficient and biologically relevant consensus strategy for Parkinson's disease gene prioritization.Exploring human disease using the Rat Genome DatabasePADB: published association databaseRMBase: a resource for decoding the landscape of RNA modifications from high-throughput sequencing dataGenome-wide prediction and functional characterization of the genetic basis of autism spectrum disorderMultiple genetic variants along candidate pathways influence plasma high-density lipoprotein cholesterol concentrationsDevelopment of a fingerprinting panel using medically relevant polymorphismsSystematic genetic analysis identifies Cis-eQTL target genes associated with glioblastoma patient survivalMeta-analysis of shared genetic architecture across ten pediatric autoimmune diseasesAssociating genes and protein complexes with disease via network propagationNetwork-based elucidation of human disease similarities reveals common functional modules enriched for pluripotent drug targets
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
The genetic association database
@ast
The genetic association database
@en
type
label
The genetic association database
@ast
The genetic association database
@en
prefLabel
The genetic association database
@ast
The genetic association database
@en
P2093
P2860
P3181
P356
P1433
P1476
The genetic association database
@en
P2093
Kathleen C Barnes
S Alex Wang
Tiffani J Bright
P2860
P2888
P304
P3181
P356
10.1038/NG0504-431
P407
P577
2004-05-01T00:00:00Z
P5875
P6179
1031425235