Laura J. Rasmussen‐Torvik

Northwestern University — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

59h-index18.4kcitations293works12.72yr avg
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Research Topics

Genetic Associations and Epidemiology(107), Genomics and Rare Diseases(28), Genetic Mapping and Diversity in Plants and Animals(25), Nutrition, Genetics, and Disease(22), Cardiovascular Function and Risk Factors(19)

Publications244 total

Rationale and Design of the HeartShare/AMP-HF Deep Phenotyping Study to Improve Understanding of Heart Failure With Preserved Ejection Fraction
JACC Heart Failure·2025· 1 citedOpen Access
Genetic and Genomic Testing in Cardiovascular Disease: A Policy Statement From the American Heart Association
Circulation·2025Open Access
Abstract 4361649: Polysocial Risk Scores and Genetic Risk Factors Are Independently and Additively Associated with Cardiometabolic Diseases Across Self-Identified Race/Ethnicity Groups
Circulation·2025
Abstract 4346455: The ICAM1 p.K56M HFpEF Risk Variant and Measures of Adiposity
Circulation·2025
A combined genomic arrhythmia propensity score delineates cumulative risk
Cell Reports Medicine·2025Open Access
Optimizing Cascade Testing to Advance Health Equity in Cardiac Amyloidosis
JAMA Cardiology·2025
Genome‐wide meta‐analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans
UNC Libraries·2025Open Access
Covering medical care costs for participants in the eMERGE Network: Challenges for equity and implementation
Genetics in Medicine·2025· 1 cited
Whole Genome Sequencing Analysis of Severe, Early-onset Chronic Obstructive Pulmonary Disease
American Journal of Respiratory and Critical Care Medicine·2025
Abstract P3084: Yield of Various Recruitment Approaches for an Observational Cohort of Patients with Heart Failure with Preserved Ejection Fraction: A Single Center Experience from HeartShare
Circulation·2025
Genome-wide meta-analysis identifies novel risk loci for uterine fibroids within and across multiple ancestry groups
Nature Communications·2025· 5 citedOpen Access
Mapping the use of cardiovascular genetic services in pediatric clinical care: challenges and opportunities for improvement
Frontiers in Genetics·2025· 1 citedOpen Access
Corrigendum: An Online Tool for Correcting Performance Measures of Electronic Phenotyping Algorithms for Verification Bias
ACI Open·2025Open Access
Serum Metabolomic Profiling of Incident Type 2 Diabetes Mellitus in the Multi-ethnic Study of Atherosclerosis and Rotterdam Study
The Journal of Clinical Endocrinology & Metabolism·2024· 2 citedOpen Access
Abstract 4143464: Comparison of The Burden of Cardiovascular-Kidney-Metabolic Syndrome Components in Heart Failure with Preserved Ejection Fraction clinical trials and Heart Failure in the General United States Population
Circulation·2024
The importance of diverse multiomics datasets and analyses
Journal of Clinical Investigation·2024Open Access
Whole Genome Sequence Analysis of Pulmonary Function and COPD in 44,287 Multi-ancestry Participants
2024Open Access
From Calculation to Communication: Using Risk Score Calculators to Inform Clinical Decision Making and Facilitate Patient Engagement
Medical Decision Making·2024· 4 cited
Proteomic Profile of the ICAM1 p.K56M HFpEF Risk Variant
JACC Basic to Translational Science·2024· 3 citedOpen Access
Fetal behavior and gestational serotonin reuptake inhibitor exposure: relationships between behavior, drug dosage, plasma drug level, and a measure of drug bioeffect
Neuropsychopharmacology·2024· 1 citedOpen Access
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Frequent Co-authors

Ching‐Ti Liu(18), Jennifer A. Pacheco(12), Xiuqing Guo(11), Gail P. Jarvik(11), David R. Crosslin(11), Marylyn D. Ritchie(11), Iftikhar J. Kullo(11), Omri Gottesman(10), Myriam Fornage(10), Lawrence F. Bielak(9), James S. Pankow(9), Erwin P. Böttinger(9), Dan M. Roden(9), Yingchang Lu(9), Joshua C. Denny(9), Suzette J. Bielinski(9), Jerome I. Rotter(9), Man Li(8), Ping An(8), Rex L. Chisholm(8)