Missing heritability of common diseases and treatments outside the protein-coding exome. - Wikidata - thesis-toulmin - TriplyDB

Missing heritability of common diseases and treatments outside the protein-coding exome.

Missing heritability of common diseases and treatments outside the protein-coding exome.

http://www.wikidata.org/entity/Q34212558

about

The epigenome, 4D nucleome and next-generation neuropsychiatric pharmacogenomics Application of Zebrafish Models in Inflammatory Bowel Disease Conditional entropy in variation-adjusted windows detects selection signatures associated with expression quantitative trait loci (eQTLs).Analyzing allele specific RNA expression using mixture models.Allele-Selective Transcriptome Recruitment to Polysomes Primed for Translation: Protein-Coding and Noncoding RNAs, and RNA Isoforms.Genetic Variation Determines PPARγ Function and Anti-diabetic Drug Response In Vivo.RNA sequencing of transcriptomes in human brain regions: protein-coding and non-coding RNAs, isoforms and alleles Verification of the Chromosome Region 9q21 Association with Pelvic Organ Prolapse Using RegulomeDB Annotations Non-linear interactions between candidate genes of myocardial infarction revealed in mRNA expression profiles.Uncovering drug-responsive regulatory elements.A review of genome-wide association studies for multiple sclerosis: classical and hypothesis-driven approaches.Resolving the etiology of atopic disorders by using genetic analysis of racial ancestry.Human genetics special issue on computational molecular medicine Predicting brain structure in population-based samples with biologically informed genetic scores for schizophrenia.Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16-20 October 2015.The genetics of alcohol dependence: Twin and SNP-based heritability, and genome-wide association study based on AUDIT scores.Discovery of functional non-coding conserved regions in the α-synuclein gene locus.Adiposity amplifies the genetic risk of fatty liver disease conferred by multiple loci.Assessing the Heritability of Complex Traits in Humans: Methodological Challenges and Opportunities.Next generation sequencing applications for cardiovascular disease.Rare Variants of the Serotonin Transporter Are Associated With Psychiatric Comorbidity in Irritable Bowel Syndrome.Whole Transcriptome Profiling: An RNA-Seq Primer and Implications for Pharmacogenomics Research.IBD. Fishing for missing heritability in IBD.Pharmacogenomics of Hypertension and Preeclampsia: Focus on Gene-Gene Interactions.AmpliSeq transcriptome analysis of human alveolar and monocyte-derived macrophages over time in response to Mycobacterium tuberculosis infection.

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P2860

Missing heritability of common diseases and treatments outside the protein-coding exome.

http://www.wikidata.org/entity/Q34212558

description

2014 nî lūn-bûn

@nan

2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի օգոստոսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

@zh-hk

2014年論文

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2014年論文

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2014年论文

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name

Missing heritability of common diseases and treatments outside the protein-coding exome.

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Missing heritability of common diseases and treatments outside the protein-coding exome.

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Missing heritability of common diseases and treatments outside the protein-coding exome.

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type

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Missing heritability of common diseases and treatments outside the protein-coding exome.

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Missing heritability of common diseases and treatments outside the protein-coding exome.

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Missing heritability of common diseases and treatments outside the protein-coding exome.

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prefLabel

Missing heritability of common diseases and treatments outside the protein-coding exome.

@ast

Missing heritability of common diseases and treatments outside the protein-coding exome.

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Missing heritability of common diseases and treatments outside the protein-coding exome.

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Missing heritability of common diseases and treatments outside the protein-coding exome.

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Grzegorz A Rempala

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

Katherine Hartmann

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

Maciej Pietrzak

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

Michał Seweryn

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Samuel K Handelman

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P2860

Pervasive transcription of the human genome produces thousands of previously unidentified long intergenic noncoding RNAs

Integrative annotation of variants from 1092 humans: application to cancer genomics

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

An integrated encyclopedia of DNA elements in the human genome

Finding the missing heritability of complex diseases

A periodic pattern of mRNA secondary structure created by the genetic code

DrugBank 4.0: shedding new light on drug metabolism

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

Mutational robustness can facilitate adaptation

A ceRNA hypothesis: the Rosetta Stone of a hidden RNA language?

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