Phenopedia and Genopedia: disease-centered and gene-centered views of the evolving knowledge of human genetic associations - Wikidata - awgldk - TriplyDB

Phenopedia and Genopedia: disease-centered and gene-centered views of the evolving knowledge of human genetic associations

Phenopedia and Genopedia: disease-centered and gene-centered views of the evolving knowledge of human genetic associations

http://www.wikidata.org/entity/Q33551828

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Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region Multiple common variants for celiac disease influencing immune gene expression CADgene: a comprehensive database for coronary artery disease genes Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci Genetics and outcomes after traumatic brain injury (TBI): what do we know about pediatric TBI?Systematic meta-analyses and field synopsis of genetic association studies in colorectal cancer Optimization of cell lines as tumour models by integrating multi-omics data.Cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes Finding novel molecular connections between developmental processes and disease.Gene regulatory network reveals oxidative stress as the underlying molecular mechanism of type 2 diabetes and hypertension.Network analysis of the genomic basis of the placebo effect.Extending pathways and processes using molecular interaction networks to analyse cancer genome data Type 2 diabetes genetic association database manually curated for the study design and odds ratio.Integrative analysis of the transcriptome profiles observed in type 1, type 2 and gestational diabetes mellitus reveals the role of inflammation Gene expression in the rodent brain is associated with its regional connectivity.DOSim: an R package for similarity between diseases based on Disease Ontology.The differential disease regulome The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes Construction and analysis of the protein-protein interaction networks for schizophrenia, bipolar disorder, and major depression Predicting disease associations via biological network analysis.EnrichNet: network-based gene set enrichment analysis.Addiction and reward-related genes show altered expression in the postpartum nucleus accumbens.Heterogeneity of the phenotypic definition of coronary artery disease and its impact on genetic association studies.Genome-wide linkage and positional candidate gene study of blood pressure response to dietary potassium intervention: the genetic epidemiology network of salt sensitivity study.Functional analysis of microRNA and transcription factor synergistic regulatory network based on identifying regulatory motifs in non-small cell lung cancer Development of a versatile enrichment analysis tool reveals associations between the maternal brain and mental health disorders, including autism The genetics of POAG in black South Africans: a candidate gene association study.Understanding Epistatic Interactions between Genes Targeted by Non-coding Regulatory Elements in Complex Diseases.Cancer GAMAdb: database of cancer genetic associations from meta-analyses and genome-wide association studies.ICan: an integrated co-alteration network to identify ovarian cancer-related genes Identifying a polymorphic 'switch' that influences miRNAs' regulation of a myasthenia gravis risk pathway.Amyloid precursor protein interaction network in human testis: sentinel proteins for male reproduction.GWAS Integrator: a bioinformatics tool to explore human genetic associations reported in published genome-wide association studies.Linkage and association analysis of obesity traits reveals novel loci and interactions with dietary n-3 fatty acids in an Alaska Native (Yup'ik) population.CardioGenBase: A Literature Based Multi-Omics Database for Major Cardiovascular Diseases Genomic structure and expression of the human serotonin 2A receptor gene (HTR2A) locus: identification of novel HTR2A and antisense (HTR2A-AS1) exons.Comorbid Analysis of Genes Associated with Autism Spectrum Disorders Reveals Differential Evolutionary Constraints No Association of BDNF, COMT, MAOA, SLC6A3, and SLC6A4 Genes and Depressive Symptoms in a Sample of Healthy Colombian Subjects.Crohn disease risk prediction-Best practices and pitfalls with exome data.The genetics of alcohol dependence: advancing towards systems-based approaches.

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Phenopedia and Genopedia: disease-centered and gene-centered views of the evolving knowledge of human genetic associations

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Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases

KEGG: kyoto encyclopedia of genes and genomes

The human disease network

Pathway mapping tools for analysis of high content data.

GAPscreener: an automatic tool for screening human genetic association literature in PubMed using the support vector machine technique

Tracking the epidemiology of human genes in the literature: the HuGE Published Literature database.

An open source infrastructure for managing knowledge and finding potential collaborators in a domain-specific subset of PubMed, with an example from human genome epidemiology

SNP genotyping: technologies and biomedical applications.

Assessment of cumulative evidence on genetic associations: interim guidelines.

The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention?

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