Alanna C Morrison


Ontology type: schema:Person     


Person Info

NAME

Alanna C

SURNAME

Morrison

Publications in SciGraph latest 50 shown

  • 2019-12 Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity in NATURE COMMUNICATIONS
  • 2018-12 GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes in NATURE COMMUNICATIONS
  • 2018-12 Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function in NATURE COMMUNICATIONS
  • 2018-12 Author Correction: GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk in NATURE COMMUNICATIONS
  • 2018-12 Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-12 Reply to ‘Misestimation of heritability and prediction accuracy of male-pattern baldness’ in NATURE COMMUNICATIONS
  • 2018-10 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-01 Genetic variants in microRNA genes and targets associated with cardiovascular disease risk factors in the African-American population in HUMAN GENETICS
  • 2017-12 Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism in SCIENTIFIC REPORTS
  • 2017-12 Hypertension Susceptibility Loci are Associated with Anthracycline-related Cardiotoxicity in Long-term Childhood Cancer Survivors in SCIENTIFIC REPORTS
  • 2017-12 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-12 Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos in LIPIDS IN HEALTH AND DISEASE
  • 2017-12 GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk in NATURE COMMUNICATIONS
  • 2017-11 Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology in NATURE GENETICS
  • 2017-03 Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk in NATURE GENETICS
  • 2016-12 Whole genome sequence analysis of serum amino acid levels in GENOME BIOLOGY
  • 2016-10 Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci in NATURE GENETICS
  • 2016-10 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals in NATURE GENETICS
  • 2016-09 Association of the IGF1 gene with fasting insulin levels in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-05 Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans in MOLECULAR PSYCHIATRY
  • 2016-01-21 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function in NATURE COMMUNICATIONS
  • 2015-12 Rare coding variants and X-linked loci associated with age at menarche in NATURE COMMUNICATIONS
  • 2015-12 Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children in NATURE COMMUNICATIONS
  • 2015-12 Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C in NPJ AGING AND MECHANISMS OF DISEASE
  • 2015-12 Secondary findings and carrier test frequencies in a large multiethnic sample in GENOME MEDICINE
  • 2015-12 Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility in NATURE COMMUNICATIONS
  • 2015-11 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair in NATURE GENETICS
  • 2015-10 A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease in NATURE GENETICS
  • 2015-07-01 Directional dominance on stature and cognition in diverse human populations in NATURE
  • 2015-06 Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease in NATURE GENETICS
  • 2014-07 Genome-wide association analysis identifies six new loci associated with forced vital capacity in NATURE GENETICS
  • 2013-08 Whole-genome sequence-based analysis of high-density lipoprotein cholesterol in NATURE GENETICS
  • 2013-06 Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders in NATURE GENETICS
  • 2011-11 Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function in NATURE GENETICS
  • 2011-10 Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk in NATURE
  • 2011-10 Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure in NATURE GENETICS
  • 2010-02 Association of NOS3 Glu298Asp SNP with hypertension and possible effect modification of dietary fat intake in the ARIC study in HYPERTENSION RESEARCH
  • 2010-01 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function in NATURE GENETICS
  • 2009-06 Genome-wide association study of blood pressure and hypertension in NATURE GENETICS
  • 2008-12 Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2007-10 Five common gene variants identify elevated genetic risk for coronary heart disease in GENETICS IN MEDICINE
  • 2007-06 Gene–environment interaction and the GNB3 gene in the Atherosclerosis Risk in Communities Study in INTERNATIONAL JOURNAL OF OBESITY
  • 2006-04 The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1999-10-06 β3-Adrenergic receptor Trp64Arg polymorphism does not predict incident CHD or carotid intima-media thickness in a community-based sample of whites: the ARIC study in HUMAN GENETICS
  • 1999-10 β3-Adrenergic receptor Trp64Arg polymorphism does not predict incident CHD or carotid intima-media thickness in a community-based sample of whites: the ARIC study in HUMAN GENETICS
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