Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. - Wikidata - wikimedia - TriplyDB

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function.

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function.

http://www.wikidata.org/entity/Q36714212

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Genetic and epigenetic factors influencing chronic kidney disease Functional genomic annotation of genetic risk loci highlights inflammation and epithelial biology networks in CKD The potential of text mining in data integration and network biology for plant research: a case study on Arabidopsis Genome-wide association studies in pediatric chronic kidney disease.Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.Using previously genotyped controls in genome-wide association studies (GWAS): application to the Stroke Genetics Network (SiGN)The frequency of single nucleotide polymorphisms and their association with uric acid concentration based on data from genome-wide association studies in the Korean population.Incorporation of protein binding effects into likelihood ratio test for exome sequencing data.1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.DNA hypermethylation and DNA hypomethylation is present at different loci in chronic kidney disease Rare inherited kidney diseases: challenges, opportunities, and perspectives.Akt recruits Dab2 to albumin endocytosis in the proximal tubule.A genome-wide search for linkage of estimated glomerular filtration rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND).Akt Links Insulin Signaling to Albumin Endocytosis in Proximal Tubule Epithelial Cells.Serum urate gene associations with incident gout, measured in the Framingham Heart Study, are modified by renal disease and not by body mass index.Resistance to insulin and kidney disease in the cardiorenal metabolic syndrome; role for angiotensin II.Genes, Exomes, Genomes, Copy Number: What is Their Future in Pediatric Renal Disease.Common variants in Mendelian kidney disease genes and their association with renal function.Generalization of associations of kidney-related genetic loci to American Indians Advances in biotechnology and informatics to link variation in the genome to phenotypes in plants and animals Hypertension-attributed nephropathy: what's in a name?Albuminuria induces a proinflammatory and profibrotic response in cortical collecting ducts via the 24p3 receptor.Epigenetics of kidney disease.Endocytic receptor LRP2/megalin-of holoprosencephaly and renal Fanconi syndrome.Genetic-Variation-Driven Gene-Expression Changes Highlight Genes with Important Functions for Kidney Disease.Is High-Density Lipoprotein Cholesterol Causally Related to Kidney Function? Evidence From Genetic Epidemiological Studies Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study.Generalizability of genetic findings related to kidney function and albuminuria.The UMOD Locus: Insights into the Pathogenesis and Prognosis of Kidney Disease.Genome-wide association studies of albuminuria: towards genetic stratification in diabetes?Genetic variations in SLC3A2/CD98 gene as prognosis predictors in non-small cell lung cancer.

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P2860

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function.

http://www.wikidata.org/entity/Q36714212

description

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Human Molecular Genetics

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Integration of genome-wide ass ...... es related to kidney function.

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Aaron Isaacs

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Adrienne Tin

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Afshin Parsa

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Alan F Wright

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P2860

Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging

Prevalence of chronic kidney disease in population-based studies: systematic review

Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits

Identification of pleckstrin-homology-domain-containing proteins with novel phosphoinositide-binding specificities

Cloning of a new member of the TGF-beta family: a putative new activin beta C chain

The heterodimeric amino acid transporter 4F2hc/y+LAT2 mediates arginine efflux in exchange with glutamine

Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes

New loci associated with kidney function and chronic kidney disease

Hundreds of variants clustered in genomic loci and biological pathways affect human height

A second generation human haplotype map of over 3.1 million SNPs

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10.1093/HMG/DDS369

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24

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Tiit Nikopensius

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Murielle Bochud

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Fernando Rivadeneira

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genome-wide association study

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