Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits - Wikidata - awgldk - TriplyDB

Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits

Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits

http://www.wikidata.org/entity/Q28239018

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Inherited platelet disorders: toward DNA-based diagnosis Next-generation gene discovery for variants of large impact on lipid traits Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits.The genetics of platelet count and volume in humans.Dysplasia of Granulocytes in a Patient with HPV Disease, Recurrent Infections, and B Lymphopenia: A Novel Variant of WHIM Syndrome?Examining rare and low-frequency genetic variants previously associated with lone or familial forms of atrial fibrillation in an electronic medical record system: a cautionary note.Rare variant association studies: considerations, challenges and opportunities.The second transferrin receptor regulates red blood cell production in mice.A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis Low-frequency coding variants at 6p21.33 and 20q11.21 are associated with lung cancer risk in Chinese populations Whole-exome Sequence Analysis Implicates Rare Il17REL Variants in Familial and Sporadic Inflammatory Bowel Disease.Replication and Characterization of Association between ABO SNPs and Red Blood Cell Traits by Meta-Analysis in Europeans.Low-frequency germline variants across 6p22.2-6p21.33 are associated with non-obstructive azoospermia in Han Chinese men.Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.Trans-ethnic follow-up of breast cancer GWAS hits using the preferential linkage disequilibrium approach.Rare and low-frequency variants in human common diseases and other complex traits.SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.Exome Variant Analysis of Chronic Periodontitis in 2 Large Cohort Studies.Prioritizing individual genetic variants after kernel machine testing using variable selection.Rare coding variants pinpoint genes that control human hematological traits.The effect of phenotypic outliers and non-normality on rare-variant association testing.Cardiac Function Improvement and Bone Marrow Response -: Outcome Analysis of the Randomized PERFECT Phase III Clinical Trial of Intramyocardial CD133+ Application After Myocardial Infarction.Chromosome 18q deletion syndrome with autoimmune diabetes mellitus: putative genomic loci for autoimmunity and immunodeficiency.FARVATX: Family-Based Rare Variant Association Test for X-Linked Genes.Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data.A robust and powerful two-step testing procedure for local ancestry adjusted allelic association analysis in admixed populations.TEX15: A DNA repair gene associated with prostate cancer risk in Han Chinese.Congenital neutropenia in the era of genomics: classification, diagnosis, and natural history.TUBB1 variants and human platelet traits.Recurrent somatic JAK-STAT pathway variants within a RUNX1-mutated pedigree.Low-frequency nonsynonymous variants in FKBPL and ARPC1B genes are associated with breast cancer risk in Chinese women.Application of whole-exome sequencing to unravel the molecular basis of undiagnosed syndromic congenital neutropenia with intellectual disability.Hematopoietic deletion of transferrin receptor 2 in mice leads to a block in erythroid differentiation during iron-deficient anemia.Childhood Trauma, Perceived Stress, and Hair Cortisol in Adults With and Without Cardiovascular Disease.

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Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits

http://www.wikidata.org/entity/Q28239018

description

2014 nî lūn-bûn

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2014 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հունիսին 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

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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

Rare and low-frequency coding ...... ated with hematological traits

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Rare and low-frequency coding ...... ated with hematological traits

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Rare and low-frequency coding ...... ated with hematological traits

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type

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Rare and low-frequency coding ...... ated with hematological traits

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Rare and low-frequency coding ...... ated with hematological traits

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Rare and low-frequency coding ...... ated with hematological traits

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Rare and low-frequency coding ...... ated with hematological traits

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Rare and low-frequency coding ...... ated with hematological traits

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Rare and low-frequency coding ...... ated with hematological traits

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Nature Genetics

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Rare and low-frequency coding ...... ated with hematological traits

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Alexander P Reiner

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Chris Carlson

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Frank Schmidt

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George A Diaz

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Guillaume Lettre

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Jean-Claude Tardif

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Jeff Haessler

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Ken Sin Lo

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Li Hsu

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Nathalie Chami

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P2860

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans

Fast-evolving noncoding sequences in the human genome

An integrated map of genetic variation from 1,092 human genomes

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

Genome-wide detection and characterization of positive selection in human populations

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

The human genome browser at UCSC

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10.1038/NG.2962

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6

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46

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Andrew Jackson O'Shaughnessy

Alexander Teumer

Charles Kooperberg

Marie-Pierre Dubé

Louis-Philippe Lemieux Perreault

Andreas Greinacher

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2014-06-01T00:00:00Z

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261955921

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24777453

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