Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study.
about
Linkage analysis in the next-generation sequencing eraThe role of large pedigrees in an era of high-throughput sequencingMapping asthma-associated variants in admixed populationsGenetic contributors to otitis media: agnostic discovery approaches.Optimum designs for next-generation sequencing to discover rare variants for common complex disease.Association of ADIPOQ gene variants with body weight, type 2 diabetes and serum adiponectin concentrations: the Finnish Diabetes Prevention Study.Visualization of haplotype sharing patterns in pedigree samples.Enriching rare variants using family-specific linkage information.Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ.Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant.Genetic polymorphisms of the main transcription factors for adiponectin gene promoter in regulation of adiponectin levels: association analysis in three European cohorts.A comprehensive investigation of variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/R2), and their association with serum adiponectin, type 2 diabetes, insulin resistance and the metabolic syndrome.Review of the Diabetes Heart Study (DHS) family of studies: a comprehensively examined sample for genetic and epidemiological studies of type 2 diabetes and its complications.Genome-wide family-based linkage analysis of exome chip variants and cardiometabolic risk.Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels.Pleiotropic locus for emotion recognition and amygdala volume identified using univariate and bivariate linkage.Linkage analysis incorporating gene-age interactions identifies seven novel lipid loci: the Family Blood Pressure ProgramMolecular basis of obesity: current status and future prospectsPopulation-specific coding variant underlies genome-wide association with adiponectin level.Candidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study.A family-specific linkage analysis of blood lipid response to fenofibrate in the Genetics of Lipid Lowering Drug and Diet NetworkRare Variants in NOD1 Associated with Carotid Bifurcation Intima-Media Thickness in Dominican Republic Families.Family studies to find rare high risk variants in migraine.Association between ADIPOQ SNPs with plasma adiponectin and glucose homeostasis and adiposity phenotypes in the IRAS Family Study.Perspectives in Polycystic Ovary Syndrome: From Hair to EternityGenetic analysis of adiponectin variation and its association with type 2 diabetes in African Americans.Estimating the contributions of rare and common genetic variations and clinical measures to a model trait: adiponectin.PedWiz: a web-based tool for pedigree informatics.Fine mapping on chromosome 13q32-34 and brain expression analysis implicates MYO16 in schizophreniaThe next-generation sequencing revolution and its impact on genomics.Novel genomic techniques open new avenues in the analysis of monogenic disorders.Between candidate genes and whole genomes: time for alternative approaches in blood pressure genetics.Linkage analysis and the study of Mendelian disease in the era of whole exome and genome sequencing.Multiancestry Study of Gene-Lifestyle Interactions for Cardiovascular Traits in 610 475 Individuals From 124 Cohorts: Design and Rationale.Genetic Determination of Serum Levels of Diabetes-Associated AdipokinesExome sequencing reveals novel genetic loci influencing obesity-related traits in Hispanic children.Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study.Next generation sequencing in cardiovascular diseases.Adiponectin Isoform Patterns in Ethnic-Specific ADIPOQ Mutation Carriers: The IRAS Family Study.Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level.
P2860
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P2860
Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study.
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Molecular basis of a linkage p ...... gene in the IRAS Family Study.
@ast
Molecular basis of a linkage p ...... gene in the IRAS Family Study.
@en
Molecular basis of a linkage p ...... gene in the IRAS Family Study.
@nl
type
label
Molecular basis of a linkage p ...... gene in the IRAS Family Study.
@ast
Molecular basis of a linkage p ...... gene in the IRAS Family Study.
@en
Molecular basis of a linkage p ...... gene in the IRAS Family Study.
@nl
prefLabel
Molecular basis of a linkage p ...... gene in the IRAS Family Study.
@ast
Molecular basis of a linkage p ...... gene in the IRAS Family Study.
@en
Molecular basis of a linkage p ...... gene in the IRAS Family Study.
@nl
P2093
P2860
P356
P1476
Molecular basis of a linkage p ...... gene in the IRAS Family Study.
@en
P2093
Carl D Langefeld
Donald W Bowden
Gregory A Hawkins
Jill M Norris
Nicholette D Palmer
S Sandy An
Stephen M Haffner
W Mark Brown
Xiuqing Guo
Y-D Ida Chen
P2860
P304
P356
10.1093/HMG/DDQ327
P577
2010-08-05T00:00:00Z