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51. Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

52. Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants.

53. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.

54. Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels

55. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.

56. Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

57. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.

58. DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood

61. Gene-lifestyle interactions in the genomics of human complex traits

62. Antithrombin, PC (Protein C), and PS (Protein S): Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels

63. Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program

64. New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders

65. Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

66. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data

67. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies

68. Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels

69. Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease

70. Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels

71. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

72. Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

74. Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes

75. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

76. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

77. The power of genetic diversity in genome-wide association studies of lipids

78. Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function.

79. Common Coding Variants in SCN10A Are Associated With the Nav1.8 Late Current and Cardiac Conduction

80. Gene-by-Psychosocial Factor Interactions Influence Diastolic Blood Pressure in European and African Ancestry Populations: Meta-Analysis of Four Cohort Studies

81. DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation

82. The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeup

83. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

84. Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

85. Association of Clonal Hematopoiesis With Incident Heart Failure

86. Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology

87. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.

88. Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function

89. Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study

90. Genome-Wide Interaction Analysis with DASH Diet Score Identified Novel Loci for Systolic Blood Pressure

91. A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatment

93. A Mendelian randomization of γ′ and total fibrinogen levels in relation to venous thromboembolism and ischemic stroke

94. Lifestyle Risk Score: handling missingness of individual lifestyle components in meta-analysis of gene-by-lifestyle interactions

96. A polygenic risk score of atrial fibrillation improves prediction of lifetime risk for heart failure

97. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

98. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

99. Association of the IGF1 gene with fasting insulin levels

100. An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene‐Lifestyle Interactions Working Group

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