Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes. - Wikidata - awgldk - TriplyDB

Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes.

Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes.

http://www.wikidata.org/entity/Q47677207

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Genetics of Insulin Resistance and the Metabolic Syndrome Insights into metabolic disease from studying genetics in isolated populations: stories from Greece to Greenland Recent progress in genetic and epigenetic research on type 2 diabetes 60 YEARS OF POMC: From POMC and α-MSH to PAM, molecular oxygen, copper, and vitamin C New insights from monogenic diabetes for "common" type 2 diabetes Rare-variant association analysis: study designs and statistical tests Strategies for Imputing and Analyzing Rare Variants in Association Studies Insights from exome sequencing for endocrine disorders Pharmacogenomics in diabetes mellitus: insights into drug action and drug discovery Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data The genetic architecture of type 2 diabetes Rare and low-frequency coding variants alter human adult height Human genetics as a model for target validation: finding new therapies for diabetes.Genetics of Type 2 Diabetes: the Power of Isolated Populations.Islet biology, the CDKN2A/B locus and type 2 diabetes risk.Early eukaryotic origins for cilia-associated bioactive peptide-amidating activity.Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis.Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.The impact of rare and low-frequency genetic variants in common disease Prediction of gene expression with cis-SNPs using mixed models and regularization methods Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes.Identification of a novel gene for diabetic traits in rats, mice, and humans.Repurposing cAMP-modulating medications to promote β-cell replication.Variants associated with type 2 diabetes identified by the transethnic meta-analysis study: assessment in American Indians and evidence for a new signal in LPP.The pancreatic β cell: recent insights from human genetics.Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.Using genetically isolated populations to understand the genomic basis of disease.Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes.Rare variant association studies: considerations, challenges and opportunities.Genetics of type 2 diabetes-pitfalls and possibilities.Association of genetic variants with hypertension in a longitudinal population-based genetic epidemiological study.Communication is the key. : Part 2 : Direct to consumer genetics in our future daily life ?Can genomics help usher schizophrenia into the age of RDoC and DSM-6?New basal cell carcinoma susceptibility loci.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.Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population.Association between SLC30A8 rs13266634 Polymorphism and Type 2 Diabetes Risk: A Meta-Analysis.A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease.The contribution of protein intrinsic disorder to understand the role of genetic variants uncovered by autism spectrum disorders exome studies.

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Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes.

http://www.wikidata.org/entity/Q47677207

description

2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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2014年學術文章

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2014年學術文章

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name

Identification of low-frequenc ...... duced risk of type 2 diabetes.

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Identification of low-frequenc ...... duced risk of type 2 diabetes.

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type

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Identification of low-frequenc ...... duced risk of type 2 diabetes.

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Identification of low-frequenc ...... duced risk of type 2 diabetes.

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Identification of low-frequenc ...... duced risk of type 2 diabetes.

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Identification of low-frequenc ...... duced risk of type 2 diabetes.

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Nature Genetics

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Identification of low-frequenc ...... duced risk of type 2 diabetes.

@en

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Agnar Helgason

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Annelli Sandbæk

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Asgeir Sigurdsson

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Astradur B Hreidarsson

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Cramer Christensen

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Gisli Masson

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Gunnar Sigurdsson

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Hannes Helgason

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Hrefna Johannsdottir

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Marie N Harder

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P2860

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Genetics of gene expression and its effect on disease

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

A variant in CDKAL1 influences insulin response and risk of type 2 diabetes

NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

Cyclins D2 and D1 are essential for postnatal pancreatic beta-cell growth

Probing the production of amidated peptides following genetic and dietary copper manipulations.

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion.

Detection of sharing by descent, long-range phasing and haplotype imputation.

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294-298

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scholarly article

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10.1038/NG.2882

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3

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46

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Gudmar Thorleifsson

Unnur Þorsteinsdóttir

Valgerdur Steinthorsdottir

Oluf Borbye Pedersen

Rafn Benediktsson

Daniel F Gudbjartsson

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2014-01-26T00:00:00Z

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259918718

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24464100

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P921

type-2 diabetes