about
Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseasesToward modernizing the systematic review pipeline in genetics: efficient updating via data miningGene-environment interactions in cancer epidemiology: a National Cancer Institute Think Tank reportA kinesin-1 binding motif in vaccinia virus that is widespread throughout the human genomemESAdb: microRNA expression and sequence analysis databaseThe PhenX Toolkit: get the most from your measuresThe UCSC Genome Browser Database: update 2009Forward Individualized Medicine from Personal Genomes to InteractomesDrosophila and Caenorhabditis elegans as Discovery Platforms for Genes Involved in Human Alcohol Use DisorderThe Human Genome Project, and recent advances in personalized genomicsA public resource facilitating clinical use of genomesGenetic vulnerability and susceptibility to substance dependence.Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorderGenetic variants and the risk of gestational diabetes mellitus: a systematic reviewTilting at quixotic trait loci (QTL): an evolutionary perspective on genetic causationNetwork Analysis of Human Genes Influencing Susceptibility to Mycobacterial InfectionsNetwork signatures link hepatic effects of anti-diabetic interventions with systemic disease parametersMK4MDD: a multi-level knowledge base and analysis platform for major depressive disorderAssessing and managing risk when sharing aggregate genetic variant dataTrends in population-based studies of human genetics in infectious diseasesCollaboratively charting the gene-to-phenotype network of human congenital heart defectsBeyond accuracy: creating interoperable and scalable text-mining web servicesHuman genomics and preparedness for infectious threats.Association of Forced Vital Capacity with the Developmental Gene NCOR2.RAvariome: a genetic risk variants database for rheumatoid arthritis based on assessment of reproducibility between or within human populations.PriVar: a toolkit for prioritizing SNVs and indels from next-generation sequencing data.PUMA: a unified framework for penalized multiple regression analysis of GWAS dataInsights into TREM2 biology by network analysis of human brain gene expression data.Discovering transnosological molecular basis of human brain diseases using biclustering analysis of integrated gene expression data.MNS16A tandem repeats minisatellite of human telomerase gene and cancer risk: a meta-analysis.GAPscreener: an automatic tool for screening human genetic association literature in PubMed using the support vector machine techniqueGene Prospector: an evidence gateway for evaluating potential susceptibility genes and interacting risk factors for human diseasesThe need for genetic variant naming standards in published abstracts of human genetic association studiesDetecting purely epistatic multi-locus interactions by an omnibus permutation test on ensembles of two-locus analyses.Synopsis and data synthesis of genetic association studies in hypertension for the adrenergic receptor family genes: the CUMAGAS-HYPERT database.Phenopedia and Genopedia: disease-centered and gene-centered views of the evolving knowledge of human genetic associationsThe COPD genetic association compendium: a comprehensive online database of COPD genetic associationsA whole genome SNP genotyping by DNA microarray and candidate gene association study for kidney stone diseaseDietary iron, iron homeostatic gene polymorphisms and the risk of advanced colorectal adenoma and cancer.MicroRNA-integrated and network-embedded gene selection with diffusion distance
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
A navigator for human genome epidemiology.
@en
A navigator for human genome epidemiology.
@nl
type
label
A navigator for human genome epidemiology.
@en
A navigator for human genome epidemiology.
@nl
prefLabel
A navigator for human genome epidemiology.
@en
A navigator for human genome epidemiology.
@nl
P356
P1433
P1476
A navigator for human genome epidemiology.
@en
P2093
Ajay Yesupriya
P2888
P304
P356
10.1038/NG0208-124
P407
P577
2008-02-01T00:00:00Z
P5875
P6179
1002893574