A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. - Wikidata - wikimedia - TriplyDB

A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.

A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.

http://www.wikidata.org/entity/Q35025798

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Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans SNPs associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease Genetic determinants of variability in glycated hemoglobin (HbA(1c)) in humans: review of recent progress and prospects for use in diabetes care Human metabolic individuality in biomedical and pharmaceutical research Genome-wide association study identifies a PSMD3 variant associated with neutropenia in interferon-based therapy for chronic hepatitis C Replication and characterisation of genetic variants in the fibrinogen gene cluster with plasma fibrinogen levels and haematological traits in the Third National Health and Nutrition Examination Survey TMEM14C is required for erythroid mitochondrial heme metabolism Snx3 regulates recycling of the transferrin receptor and iron assimilation TC1(C8orf4) regulates hematopoietic stem/progenitor cells and hematopoiesis Loci associated with adult stature also affect calf birth survival in cattle Global genetic architecture of an erythroid quantitative trait locus, HMIP-2 Sequencing of 2 subclinical atherosclerosis candidate regions in 3669 individuals: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study Evolutionary dynamics of co-segregating gene clusters associated with complex diseases Genome-wide association study of coronary artery disease in the Japanese Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot A genome-wide association study of a coronary artery disease risk variant A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.Genome-wide association study of smoking behaviours in patients with COPD Imputation-based meta-analysis of severe malaria in three African populations.A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease.Mapping and analysis of chromatin state dynamics in nine human cell types Systematic localization of common disease-associated variation in regulatory DNA 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.Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12.Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.Age- and sex-related variations in platelet count in Italy: a proposal of reference ranges based on 40987 subjects' data.Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.Hematological manifestations of celiac disease.Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a low-frequency noncoding RBM8A SNP: a new familial case.The genetics of platelet count and volume in humans.A post-genome-wide association study validating the association of the glycophorin C gene with serum hemoglobin level in pig Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.

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A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.

http://www.wikidata.org/entity/Q35025798

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2009 nî lūn-bûn

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2009 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2009 թվականի հոտեմբերին հրատարակված գիտական հոդված

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A map of recent positive selection in the human genome

Detecting recent positive selection in the human genome from haplotype structure

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

Hitchhiking under positive Darwinian selection

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Common variants near MC4R are associated with fat mass, weight and risk of obesity

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

Newly identified genetic risk variants for celiac disease related to the immune response

PLINK: a tool set for whole-genome association and population-based linkage analyses

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

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