Author details

Full Name

Alanna C Morrison

Affiliation

ORCID

Career Start Year

1999

Papers

255

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36723951	Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart Disease.	JAMA Cardiol	2023
36194249	Proteomic analysis of diabetes genetic risk scores identifies complement C2 and neuropilin-2 as predictors of type 2 diabetes: the Atherosclerosis Risk in Communities (ARIC) Study.	Diabetologia	2023
36444934	Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.	Hum Mol Genet	2023
37857625	Author Correction: Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations.	Nat Commun	2023
38028628	Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.	Front Genet	2023
37749248	Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.	Nat Genet	2023
37662265	WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.	medRxiv	2023
38014529	Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis.	Circ Genom Precis Med	2023
37986948	Genome-Wide Interaction Analysis with DASH Diet Score Identified Novel Loci for Systolic Blood Pressure.	medRxiv	2023
37802043	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.	Am J Hum Genet	2023
37891690	Multi-tissue epigenetic analysis identifies distinct associations underlying insulin resistance and Alzheimer's disease at CPT1A locus.	Clin Epigenetics	2023
37886448	A new Approach to Identify Gene-Environment Interactions and Reveal New Biological Insight in Complex traits.	Res Sq	2023
37961350	A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.	bioRxiv	2023
36716967	DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood.	J Thromb Haemost	2023
36960714	Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.	Circ Genom Precis Med	2023
37398003	Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.	medRxiv	2023
37268629	Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups.	Nat Commun	2023
37327218	Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study.	PLoS One	2023
37066281	StocSum: stochastic summary statistics for whole genome sequencing studies.	bioRxiv	2023
36696182	Novel genetic regulators of fibrinogen synthesis identified by an in vitro experimental platform.	J Thromb Haemost	2023
37253714	Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations.	Nat Commun	2023
36791419	Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.	Diabetes	2023
37425772	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.	medRxiv	2023
37038335	Genetic susceptibility to cognitive decline following craniospinal irradiation for pediatric central nervous system tumors.	Neuro Oncol	2023
36918541	Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.	Nat Commun	2023
37546893	Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus.	medRxiv	2023
35285134	Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations.	J Thromb Haemost	2022
36180445	Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.	Nat Commun	2022
36042188	Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.	Nat Commun	2022
35766891	Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data.	Hum Mol Genet	2022
35652341	Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.	Hypertension	2022
35389749	Monogenic and Polygenic Contributions to QTc Prolongation in the Population.	Circulation	2022
35385699	Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.	Am J Hum Genet	2022
35385311	Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.	Sci Adv	2022
36220816	Whole genome sequence analysis of blood lipid levels in >66,000 individuals.	Nat Commun	2022
35552711	Whole-exome sequencing of 14â¿¿389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.	Hum Mol Genet	2022
35995843	Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populations.	Commun Biol	2022
35619825	Trends and Correlates of Breakthrough Infections With SARS-CoV-2.	Front Public Health	2022
35729114	A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood.	Nat Commun	2022
36195771	Case growth analysis to inform local response to COVID-19 epidemic in a diverse U.S community.	Sci Rep	2022
36050321	Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.	Nat Commun	2022
36513073	Correlations between complex human phenotypes vary by genetic background, gender, and environment.	Cell Rep Med	2022
36481753	Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program.	Nat Commun	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
36544485	Multi-omics insights into the biological mechanisms underlying statistical gene-by-lifestyle interactions with smoking and alcohol consumption.	Front Genet	2022
34743536	Clonal Hematopoiesis Is Associated With Higher Risk of Stroke.	Stroke	2022
34779012	A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.	Genet Epidemiol	2022
34553764	Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.	Hum Mol Genet	2022
35094551	American Heart Association's Life's Simple 7: Lifestyle Recommendations, Polygenic Risk, and Lifetime Risk of Coronary Heart Disease.	Circulation	2022
35085396	Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts.	Diabetes Care	2022