Human genetic variation and its contribution to complex traits
about
The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factorsHeritability and demographic analyses in the large isolated population of Val Borbera suggest advantages in mapping complex traits genesEnrichment of sequencing targets from the human genome by solution hybridizationHuman genetics and genomics a decade after the release of the draft sequence of the human genomeFast identification and removal of sequence contamination from genomic and metagenomic datasetsSex-dependent association of common variants of microcephaly genes with brain structureGenotyping sleep disorders patientsBreast cancer in the personal genomics eraExtrachromosomal microDNAs and chromosomal microdeletions in normal tissuesGenetic susceptibility to lung cancer and co-morbiditiesGerm line variation in nucleotide excision repair genes and lung cancer risk in smokersTargeted capture and massively parallel sequencing of 12 human exomesBivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family StudyA weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levelsIdentifying druggable disease-modifying gene productsMolecular Genetic of Atopic dermatitis: An UpdateMicroRNAs in Nonalcoholic Fatty Liver DiseaseGenetic predisposition to acute kidney injury--a systematic reviewPolyallelic structural variants can provide accurate, highly informative genetic markers focused on diagnosis and therapeutic targets: Accuracy vs. PrecisionAn introductory review of parallel independent component analysis (p-ICA) and a guide to applying p-ICA to genetic data and imaging phenotypes to identify disease-associated biological pathways and systems in common complex disordersStatistical analysis for genome-wide association studyPairomics, the omics way to mate choiceToward developmental models of psychiatric disorders in zebrafishPerioperative genomicsObesity: interactions of genome and nutrients intakeChild development and molecular genetics: 14 years laterNuclear receptor coregulators: modulators of pathology and therapeutic targetsThe Human Genome Project, and recent advances in personalized genomicsSystematic meta-analyses and field synopsis of genetic association studies in colorectal cancerDental phenomics: advancing genotype to phenotype correlations in craniofacial researchConserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary SignalingGenetic vulnerability and susceptibility to substance dependence.Rapid phenotyping of knockout mice to identify genetic determinants of bone strengthImpact of DNA mismatch repair system alterations on human fertility and related treatmentsStrategies for Imputing and Analyzing Rare Variants in Association StudiesAyurnutrigenomics: Ayurveda-inspired personalized nutrition from inception to evidenceMapping asthma-associated variants in admixed populationsApplication of large-scale sequencing to marker discovery in plantsCancer evolution and individual susceptibilityEvidence for the role of EPHX2 gene variants in anorexia nervosa
P2860
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P2860
Human genetic variation and its contribution to complex traits
description
2009 nî lūn-bûn
@nan
2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Human genetic variation and its contribution to complex traits
@ast
Human genetic variation and its contribution to complex traits
@en
type
label
Human genetic variation and its contribution to complex traits
@ast
Human genetic variation and its contribution to complex traits
@en
prefLabel
Human genetic variation and its contribution to complex traits
@ast
Human genetic variation and its contribution to complex traits
@en
P3181
P356
P1476
Human genetic variation and its contribution to complex traits
@en
P2093
Nicholas J Schork
Sarah S Murray
P2888
P304
P3181
P356
10.1038/NRG2554
P407
P577
2009-04-01T00:00:00Z
P5875
P6179
1011407465