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Genome-wide association analysis identifies multiple loci related to resting heart rateGenetic variants in novel pathways influence blood pressure and cardiovascular disease riskMeta-analyses of genome-wide association studies identify multiple loci associated with pulmonary functionSingle nucleotide polymorphisms associated with coronary heart disease predict incident ischemic stroke in the atherosclerosis risk in communities studyA comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery diseaseLarge-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repairGenome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary functionMeta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsRare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African AmericansRare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFDirectional dominance on stature and cognition in diverse human populationsLow-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibilitySequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyGene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP ConsortiaAssociation of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyTargeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing StudyWhole-genome sequence-based analysis of high-density lipoprotein cholesterolGenome-wide association study of cardiac structure and systolic function in African Americans: the Candidate Gene Association Resource (CARe) studySingle-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference.Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study.Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.Integrative pathway genomics of lung function and airflow obstruction.Genome-wide association analysis identifies six new loci associated with forced vital capacityAssociation of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacksCommon and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstructionGenome-wide association and large-scale follow up identifies 16 new loci influencing lung function.Association of exome sequences with plasma C-reactive protein levels in >9000 participants.Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.Duffy antigen receptor for chemokines (Darc) polymorphism regulates circulating concentrations of monocyte chemoattractant protein-1 and other inflammatory mediators.The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program.Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe HypercholesterolemiaDiabetes genes and prostate cancer in the Atherosclerosis Risk in Communities study.Association of NOS3 Glu298Asp SNP with hypertension and possible effect modification of dietary fat intake in the ARIC study.Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism.Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function.
P50
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P50
description
hulumtuese
@sq
onderzoeker
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researcher
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հետազոտող
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name
Alanna Morrison
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Alanna Morrison
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Alanna Morrison
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Alanna Morrison
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Alanna Morrison
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type
label
Alanna Morrison
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Alanna Morrison
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Alanna Morrison
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Alanna Morrison
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Alanna Morrison
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Alanna C Morrison
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Morrison AC
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prefLabel
Alanna Morrison
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Alanna Morrison
@en
Alanna Morrison
@es
Alanna Morrison
@nl
Alanna Morrison
@sl
P106
P1153
7402258577
P21
P31
P496
0000-0001-6381-4296