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Author Details

Laura J Rasmussen-Torvik
Northwestern University, Center for Genetic Medicine
2003
150
42
PMIDPaper TitleJournal TitlePublished Year
36791419Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.Diabetes2023
37883979Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.Am J Hum Genet2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
36882149Missense Genetic Variation of ICAM1 and Incident Heart Failure.J Card Fail2023
36635319Secretory leukocyte protease inhibitor and risk of heart failure in the Multi-Ethnic Study of Atherosclerosis.Sci Rep2023
37259919Time of day for COVID vaccine administration linked to clinical effectiveness.J Clin Invest2023
37196047Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.PLoS One2023
36941441Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals.Nat Genet2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
36791419Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.Diabetes2023
37883979Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.Am J Hum Genet2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37196047Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.PLoS One2023
37259919Time of day for COVID vaccine administration linked to clinical effectiveness.J Clin Invest2023
36882149Missense Genetic Variation of ICAM1 and Incident Heart Failure.J Card Fail2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
36635319Secretory leukocyte protease inhibitor and risk of heart failure in the Multi-Ethnic Study of Atherosclerosis.Sci Rep2023
36941441Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals.Nat Genet2023
34369331Serologic Status and SARS-CoV-2 Infection over 6 Months of Follow Up in Healthcare Workers in Chicago: A Cohort Study.Infect Control Hosp Epidemiol2022
36376295Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure.Nat Commun2022
36169027Recognizing the importance of COVID-19 data wrangling.J Clin Invest2022
35765100Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.Genome Med2022
35701404Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.Nat Commun2022
36094046Changes in Sertraline Plasma Concentrations Across Pregnancy and Postpartum.Clin Pharmacol Ther2022
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
36254188Trajectories of Depressive and Anxiety Symptoms Across Pregnancy and Postpartum in Selective Serotonin Reuptake Inhibitor-Treated Women.Psychiatr Res Clin Pract2022
35339388Integrating clinical genetics in cardiology: Current practices and recommendations for education.Genet Med2022
35031113Validation of Heart Failure-Specific Risk Equations in 1.3 Million Israeli Adults and Usefulness of Combining Ambulatory and Hospitalization Data from a Large Integrated Health Care Organization.Am J Cardiol2022
35166069Genetic variation in sodium glucose co-transporter 1 and cardiac structure and function at middle age.ESC Heart Fail2022
34951656Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study.Diabetologia2022
34369331Serologic Status and SARS-CoV-2 Infection over 6 Months of Follow Up in Healthcare Workers in Chicago: A Cohort Study.Infect Control Hosp Epidemiol2022
35322684Practitioners' Confidence and Desires for Education in Cardiovascular and Sudden Cardiac Death Genetics.J Am Heart Assoc2022
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
35765100Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.Genome Med2022
35701404Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.Nat Commun2022
36169027Recognizing the importance of COVID-19 data wrangling.J Clin Invest2022
36094046Changes in Sertraline Plasma Concentrations Across Pregnancy and Postpartum.Clin Pharmacol Ther2022
36254188Trajectories of Depressive and Anxiety Symptoms Across Pregnancy and Postpartum in Selective Serotonin Reuptake Inhibitor-Treated Women.Psychiatr Res Clin Pract2022
36376295Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure.Nat Commun2022
34951656Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study.Diabetologia2022
35031113Validation of Heart Failure-Specific Risk Equations in 1.3 Million Israeli Adults and Usefulness of Combining Ambulatory and Hospitalization Data from a Large Integrated Health Care Organization.Am J Cardiol2022
35339388Integrating clinical genetics in cardiology: Current practices and recommendations for education.Genet Med2022
35322684Practitioners' Confidence and Desires for Education in Cardiovascular and Sudden Cardiac Death Genetics.J Am Heart Assoc2022
35166069Genetic variation in sodium glucose co-transporter 1 and cardiac structure and function at middle age.ESC Heart Fail2022
33439236Identification of Cardiac Fibrosis in Young Adults With a Homozygous Frameshift Variant in SERPINE1.JAMA Cardiol2021
37920232Facilitating Genetics Aware Clinical Decision Support: Putting the eMERGE Infrastructure into Practice.ACI open2021
34120723Functional evaluation of human ion channel variants using automated electrophysiology.Methods Enzymol2021
33535771Risk-Based Approach for the Prediction and Prevention of Heart Failure.Circ Heart Fail2021
33951936Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics Network.Circ Heart Fail2021
33558525Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
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Collaborators

James S Pankow
Co-authored papers 37
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Co-authored papers 24
Jennifer A Pacheco
University of Pennsylvania
Co-authored papers 23
Yii-Der Ida Chen
Co-authored papers 23
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Co-authored papers 22
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Co-authored papers 22
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Co-authored papers 22
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Jerome I Rotter
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Co-authored papers 21
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Baylor College of Medicine
Co-authored papers 21
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Kari E North
Co-authored papers 20
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Jose C Florez
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David R Crosslin
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Hasso Plattner Institute for Digital Health at Mount Sinai
Co-authored papers 16
Sharon L R Kardia
School of Public Health, University of Michigan ann arbor
Co-authored papers 16
Lawrence F Bielak
Co-authored papers 16
Ching-Ti Liu
Co-authored papers 16
Stephen S Rich
Co-authored papers 16
Patricia A Peyser
School of Public Health, University of Michigan ann arbor
Co-authored papers 16
Eric B Larson
University of Washington
Co-authored papers 15
Kent D Taylor
Co-authored papers 15
Release 1.2