Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time. - Wikidata - awgldk - TriplyDB

Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time.

Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time.

http://www.wikidata.org/entity/Q33772986

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Genetics of venous thrombosis: insights from a new genome wide association study Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans.Coagulation factor XII protease domain crystal structure.Alcohol consumption and lifetime change in cognitive ability: a gene × environment interaction study Associations between APOE and low-density lipoprotein cholesterol genotypes and cognitive and physical capability: the HALCyon programme.A multi-cohort study of polymorphisms in the GH/IGF axis and physical capability: the HALCyon programme.Cohort profile: the Lothian Birth Cohorts of 1921 and 1936.Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ.Associations between a polymorphism in the pleiotropic GCKR and Age-related phenotypes: the HALCyon programme.Absence of association of a single-nucleotide polymorphism in the TERT-CLPTM1L locus with age-related phenotypes in a large multicohort study: the HALCyon programme.Genetic predictors of fibrin D-dimer levels in healthy adults.Genes from a translational analysis support a multifactorial nature of white matter hyperintensities.Alzheimer's disease genes are associated with measures of cognitive ageing in the lothian birth cohorts of 1921 and 1936 ACTN3 genotype, athletic status, and life course physical capability: meta-analysis of the published literature and findings from nine studies.A genetic association study of activated partial thromboplastin time in European Americans and African Americans: the ARIC Study Evolutionary conserved longevity genes and human cognitive abilities in elderly cohorts.Human complex trait genetics: lifting the lid of the genomics toolbox - from pathways to prediction.Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease The Central Role of KNG1 Gene as a Genetic Determinant of Coagulation Pathway-Related Traits: Exploring Metaphenotypes.Dissecting the genetic determinants of hemostasis and thrombosis Genetic markers of bone and joint health and physical capability in older adults: the HALCyon programme.A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array.Genetic variants influencing biomarkers of nutrition are not associated with cognitive capability in middle-aged and older adults Coagulation factor XII genetic variation, ex vivo thrombin generation, and stroke risk in the elderly: results from the Cardiovascular Health Study.Genome-wide association studies identify genetic loci for low von Willebrand factor levels Identification of ITGA2B and ITGB3 Single-Nucleotide Polymorphisms and Their Influences on the Platelet Function Lessons from genome-wide association studies in venous thrombosis.Current knowledge on the genetics of incident venous thrombosis.Next generation sequencing to dissect the genetic architecture of KNG1 and F11 loci using factor XI levels as an intermediate phenotype of thrombosis.A rare variant association test in family-based designs and non-normal quantitative traits.The pharmacoepigenomics informatics pipeline defines a pathway of novel and known warfarin pharmacogenomics variants.MTHFR polymorphisms and cognitive ageing in the ninth decade: the Lothian Birth Cohort 1921.The role of ECE1 variants in cognitive ability in old age and Alzheimer's disease risk.Proteomic and lipidomic analyses of paraoxonase defined high density lipoprotein particles: Association of paraoxonase with the anti-coagulant, protein S.The Influence of Dyslexia Candidate Genes on Reading Skill in Old Age What is currently known about the genetics of venous thromboembolism at the dawn of next generation sequencing technologies Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project

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P2860

Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time.

http://www.wikidata.org/entity/Q33772986

description

2010 nî lūn-bûn

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2010 թուականի Մարտին հրատարակուած գիտական յօդուած

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2010 թվականի մարտին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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American Journal of Human Genetics

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Common variants of large effec ...... d partial thromboplastin time.

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Albert Tenesa

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David C Liewald

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Gail Davies

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John M Starr

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Sarah E Harris

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P2860

The Lothian Birth Cohort 1936: a study to examine influences on cognitive ageing from age 11 to age 70 and beyond

WGAViewer: software for genomic annotation of whole genome association studies

STRING 8--a global view on proteins and their functional interactions in 630 organisms

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

Histidine-rich glycoprotein: A novel adaptor protein in plasma that modulates the immune, vascular and coagulation systems

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

Human non-synonymous SNPs: server and survey

Deletion of murine kininogen gene 1 (mKng1) causes loss of plasma kininogen and delays thrombosis

Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels.

Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia.

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