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Author Details

Nicholas L Smith
University of Washington
1994
281
71
PMIDPaper TitleJournal TitlePublished Year
37918635Development and validation of a risk model for hospital-acquired venous thrombosis: the Medical Inpatients Thrombosis and Hemostasis study.J Thromb Haemost2024
37918635Development and validation of a risk model for hospital-acquired venous thrombosis: the Medical Inpatients Thrombosis and Hemostasis study.J Thromb Haemost2024
37968126Chronic respiratory symptoms following deployment-related occupational and environmental exposures among US veterans.Occup Environ Med2024
37968126Chronic respiratory symptoms following deployment-related occupational and environmental exposures among US veterans.Occup Environ Med2024
36031541Blood pressure and risk of venous thromboembolism: a cohort analysis of 5.5 million UK adults and Mendelian randomization studies.Cardiovasc Res2023
36031541Blood pressure and risk of venous thromboembolism: a cohort analysis of 5.5 million UK adults and Mendelian randomization studies.Cardiovasc Res2023
37286573Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism.Nat Commun2023
36716967DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood.J Thromb Haemost2023
37342252Development of a computable phenotype using electronic health records for venous thromboembolism in medical inpatients: the Medical Inpatient Thrombosis and Hemostasis study.Res Pract Thromb Haemost2023
37399490Polygenic risk of major depressive disorder as a risk factor for venous thromboembolism.Blood Adv2023
36960714Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.Circ Genom Precis Med2023
37398003Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.medRxiv2023
37075041High risk oral contraceptive hormones do not directly enhance endothelial cell procoagulant activity in vitro.PLoS One2023
37126548The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.Sci Adv2023
36696219The relative risk of bleeding after medical hospitalization: the medical inpatient thrombosis and hemorrhage study.J Thromb Haemost2023
36696182Novel genetic regulators of fibrinogen synthesis identified by an in vitro experimental platform.J Thromb Haemost2023
37046083Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.Nature2023
36791419Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.Diabetes2023
37286573Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism.Nat Commun2023
37046083Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.Nature2023
37342252Development of a computable phenotype using electronic health records for venous thromboembolism in medical inpatients: the Medical Inpatient Thrombosis and Hemostasis study.Res Pract Thromb Haemost2023
37075041High risk oral contraceptive hormones do not directly enhance endothelial cell procoagulant activity in vitro.PLoS One2023
37399490Polygenic risk of major depressive disorder as a risk factor for venous thromboembolism.Blood Adv2023
37398003Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.medRxiv2023
37126548The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.Sci Adv2023
36960714Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.Circ Genom Precis Med2023
36696219The relative risk of bleeding after medical hospitalization: the medical inpatient thrombosis and hemorrhage study.J Thromb Haemost2023
36696182Novel genetic regulators of fibrinogen synthesis identified by an in vitro experimental platform.J Thromb Haemost2023
36716967DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood.J Thromb Haemost2023
36791419Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.Diabetes2023
34664540Rare variant association study of veteran twin whole-genomes links severe depression with a nonsynonymous change in the neuronal gene <i>BHLHE22</i>.World J Biol Psychiatry2022
35910943Incident thrombus location and predicting risk of recurrent venous thromboembolism.Res Pract Thromb Haemost2022
36240095Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke.Neurology2022
35388009Publisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus.Nat Commun2022
35385311Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.Sci Adv2022
36285783Circulating Androgen Concentrations and Risk of Incident Heart Failure in Older Men: The Cardiovascular Health Study.J Am Heart Assoc2022
36154123Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.Circulation2022
35552711Whole-exome sequencing of 14â¿¿389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.Hum Mol Genet2022
35426248Venous thrombosis risk during and after medical and surgical hospitalizations: The medical inpatient thrombosis and hemostasis (MITH) study.J Thromb Haemost2022
35927319Rare genetic variants explain missing heritability in smoking.Nat Hum Behav2022
36477530Genetic diversity fuels gene discovery for tobacco and alcohol use.Nature2022
35264566Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus.Nat Commun2022
34664540Rare variant association study of veteran twin whole-genomes links severe depression with a nonsynonymous change in the neuronal gene <i>BHLHE22</i>.World J Biol Psychiatry2022
34553764Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.Hum Mol Genet2022
35285134Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations.J Thromb Haemost2022
35426248Venous thrombosis risk during and after medical and surgical hospitalizations: The medical inpatient thrombosis and hemostasis (MITH) study.J Thromb Haemost2022
35388009Publisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus.Nat Commun2022
35552711Whole-exome sequencing of 14â¿¿389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.Hum Mol Genet2022
35385311Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.Sci Adv2022
36477530Genetic diversity fuels gene discovery for tobacco and alcohol use.Nature2022
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Collaborators

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Co-authored papers 56
Joshua C Bis
Co-authored papers 54
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Co-authored papers 51
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Co-authored papers 51
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Co-authored papers 50
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Co-authored papers 45
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David S Siscovick
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Barbara McKnight
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Christopher J O'Donnell
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Daniel I Chasman
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Jennifer A Brody
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Charles Kooperberg
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Fernando Rivadeneira
University Medical Center Rotterdam
Co-authored papers 26
Frits R Rosendaal
Co-authored papers 26
Albert V Smith
University of Michigan School of Public Health ann arbor
Co-authored papers 25
Aaron R Folsom
Co-authored papers 25
Paul M Ridker
Co-authored papers 24
Release 1.2