Relative impact of nucleotide and copy number variation on gene expression phenotypes - sprookjes - yvandenbroek - TriplyDB

Relative impact of nucleotide and copy number variation on gene expression phenotypes

Relative impact of nucleotide and copy number variation on gene expression phenotypes

http://www.wikidata.org/entity/Q29614883

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The DISC1 pathway modulates expression of neurodevelopmental, synaptogenic and sensory perception genes Discovery and validation of new potential biomarkers for early detection of colon cancer A preliminary study of copy number variation in Tibetans Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus Novel association strategy with copy number variation for identifying new risk Loci of human diseases A common and unstable copy number variant is associated with differences in Glo1 expression and anxiety-like behavior Isolated populations and complex disease gene identification Towards a comprehensive structural variation map of an individual human genome Mechanisms of change in gene copy number Systems medicine: the future of medical genomics and healthcare DELLY: structural variant discovery by integrated paired-end and split-read analysis A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease Copy number variation at 1q21.1 associated with neuroblastoma A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB A HaemAtlas: characterizing gene expression in differentiated human blood cells WGAViewer: software for genomic annotation of whole genome association studies The role of the CD58 locus in multiple sclerosis Paired-end mapping reveals extensive structural variation in the human genome Allele-specific gene expression patterns in primary leukemic cells reveal regulation of gene expression by CpG site methylation Structural variation of chromosomes in autism spectrum disorder Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk Diet and the evolution of human amylase gene copy number variation Revealing the architecture of gene regulation: the promise of eQTL studies Gene switching rate determines response to extrinsic perturbations in the self-activation transcriptional network motif Mechanisms underlying structural variant formation in genomic disorders Integration of genome scale data for identifying new players in colorectal cancer Integrating genetics and epigenetics in breast cancer: biological insights, experimental, computational methods and therapeutic potential Complexity of gene expression evolution after duplication: protein dosage rebalancing Association of the polymorphisms in the Fas/FasL promoter regions with cancer susceptibility: a systematic review and meta-analysis of 52 studies Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges Copy number variants and selective sweeps in natural populations of the house mouse (Mus musculus domesticus)Molecular Technologies in the Clinical Diagnostic Laboratory Clinical review: Genome-wide association studies of skeletal phenotypes: what we have learned and where we are headed Gene duplication as a mechanism of genomic adaptation to a changing environment Insights on the functional interactions between miRNAs and copy number variations in the aging brain The impact of human copy number variation on gene expression Linking the genetic architecture of cytosine modifications with human complex traits Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice Elusive copy number variation in the mouse genome Phenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse models

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Relative impact of nucleotide and copy number variation on gene expression phenotypes

http://www.wikidata.org/entity/Q29614883

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2007 nî lūn-bûn

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2007 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2007 թվականի փետրվարին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Relative impact of nucleotide and copy number variation on gene expression phenotypes

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Relative impact of nucleotide and copy number variation on gene expression phenotypes

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type

label

Relative impact of nucleotide and copy number variation on gene expression phenotypes

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Relative impact of nucleotide and copy number variation on gene expression phenotypes

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Relative impact of nucleotide and copy number variation on gene expression phenotypes

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Relative impact of nucleotide and copy number variation on gene expression phenotypes

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SCIENCE.1136678

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Relative impact of nucleotide and copy number variation on gene expression phenotypes

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Catherine E Ingle

http://www.w3.org/2001/XMLSchema#string

Charles Lee

http://www.w3.org/2001/XMLSchema#string

Christine P Bird

http://www.w3.org/2001/XMLSchema#string

Claude Beazley

http://www.w3.org/2001/XMLSchema#string

Emmanouil T Dermitzakis

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Matthew E Hurles

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Natalie Thorne

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Nigel Carter

http://www.w3.org/2001/XMLSchema#string

Simon Tavaré

http://www.w3.org/2001/XMLSchema#string

P2860

Genome-wide associations of gene expression variation in humans

Fine-scale structural variation of the human genome

Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes

Severe expressive-language delay related to duplication of the Williams-Beuren locus.

Global variation in copy number in the human genome

A haplotype map of the human genome

Multiple locus linkage analysis of genomewide expression in yeast.

Detection of large-scale variation in the human genome

Large-scale copy number polymorphism in the human genome

Genetics of gene expression surveyed in maize, mouse and man

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10.1126/SCIENCE.1136678

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5813

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315

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Chris Tyler-Smith

Barbara E. Stranger

Mark J. Dunning

Matthew S Forrest

Stephen W. Scherer

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2007-02-01T00:00:00Z

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6514955

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17289997

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genetic variation

regulation of gene expression

single-nucleotide polymorphism

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2665772

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