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TKG
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Author Details
Full Name
Philip S Tsao
Affiliation
Stanford University School of Medicine.
ORCID
Career Start Year
2017
Papers
46
H Index
10
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36413508
E-cigarette exposure augments murine abdominal aortic aneurysm development: role of Chil1.
Cardiovasc Res
2023
35748351
Data Resource Profile: Self-reported data in the Million Veteran Program: survey development and insights from the first 850â¿¿736 participants.
Int J Epidemiol
2023
36413508
E-cigarette exposure augments murine abdominal aortic aneurysm development: role of Chil1.
Cardiovasc Res
2023
37600667
Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35.
Front Genet
2023
37798822
Genetic Inhibition of APOL1 Pore-Forming Function Prevents APOL1-Mediated Kidney Disease.
J Am Soc Nephrol
2023
37790568
Heterogeneous effects on type 2 diabetes and cardiovascular outcomes of genetic variants and traits associated with fasting insulin.
Res Sq
2023
38076879
Profiling the genome and proteome of metabolic dysfunction-associated steatotic liver disease identifies potential therapeutic targets.
medRxiv
2023
38074507
A missense variant in human perilipin 2 (<i>PLIN2</i> Ser251Pro) reduces hepatic steatosis in mice.
JHEP Rep
2023
37961706
CXCL12 regulates coronary artery dominance in diverse populations and links development to disease.
medRxiv
2023
37961335
<i>CYP2C19</i> Polymorphisms and Clinical Outcomes Following Percutaneous Coronary Intervention (PCI) in the Million Veterans Program.
medRxiv
2023
37609230
A Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization.
medRxiv
2023
37414900
A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease.
Nat Med
2023
37409455
Contemporary Polygenic Scores of Low-Density Lipoprotein Cholesterol and Coronary Artery Disease Predict Coronary Atherosclerosis in Adolescents and Young Adults.
Circ Genom Precis Med
2023
37284530
Overview of Efforts to Increase Women Enrollment in the Veterans Affairs Million Veteran Program.
Health Equity
2023
36827430
Pharmacogenetic allele variant frequencies: An analysis of the VA's Million Veteran Program (MVP) as a representation of the diversity in US population.
PLoS One
2023
37133828
Cardiovascular Disease Risk Assessment Using Traditional Risk Factors and Polygenic Risk Scores in the Million Veteran Program.
JAMA Cardiol
2023
37439367
Serum microRNA-501-3p is a potential diagnostic tool for detecting mild cognitive impairment: Ehime genome study.
J Neurochem
2023
37308786
Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program.
Nat Genet
2023
36540997
Predictive models for abdominal aortic aneurysms using polygenic scores and PheWAS-derived risk factors.
Pac Symp Biocomput
2023
37425708
Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program.
medRxiv
2023
37034679
Admixture Mapping of Peripheral Artery Disease in a Dominican Population Reveals a Novel Risk Locus on 2q35.
medRxiv
2023
37034649
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
medRxiv
2023
37961706
CXCL12 regulates coronary artery dominance in diverse populations and links development to disease.
medRxiv
2023
37961335
<i>CYP2C19</i> Polymorphisms and Clinical Outcomes Following Percutaneous Coronary Intervention (PCI) in the Million Veterans Program.
medRxiv
2023
38076879
Profiling the genome and proteome of metabolic dysfunction-associated steatotic liver disease identifies potential therapeutic targets.
medRxiv
2023
38074507
A missense variant in human perilipin 2 (<i>PLIN2</i> Ser251Pro) reduces hepatic steatosis in mice.
JHEP Rep
2023
37798822
Genetic Inhibition of APOL1 Pore-Forming Function Prevents APOL1-Mediated Kidney Disease.
J Am Soc Nephrol
2023
37790568
Heterogeneous effects on type 2 diabetes and cardiovascular outcomes of genetic variants and traits associated with fasting insulin.
Res Sq
2023
37609230
A Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization.
medRxiv
2023
37600667
Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35.
Front Genet
2023
35748351
Data Resource Profile: Self-reported data in the Million Veteran Program: survey development and insights from the first 850â¿¿736 participants.
Int J Epidemiol
2023
37425708
Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program.
medRxiv
2023
37414900
A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease.
Nat Med
2023
37284530
Overview of Efforts to Increase Women Enrollment in the Veterans Affairs Million Veteran Program.
Health Equity
2023
37409455
Contemporary Polygenic Scores of Low-Density Lipoprotein Cholesterol and Coronary Artery Disease Predict Coronary Atherosclerosis in Adolescents and Young Adults.
Circ Genom Precis Med
2023
37308786
Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program.
Nat Genet
2023
37439367
Serum microRNA-501-3p is a potential diagnostic tool for detecting mild cognitive impairment: Ehime genome study.
J Neurochem
2023
37133828
Cardiovascular Disease Risk Assessment Using Traditional Risk Factors and Polygenic Risk Scores in the Million Veteran Program.
JAMA Cardiol
2023
37034679
Admixture Mapping of Peripheral Artery Disease in a Dominican Population Reveals a Novel Risk Locus on 2q35.
medRxiv
2023
37034649
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
medRxiv
2023
36540997
Predictive models for abdominal aortic aneurysms using polygenic scores and PheWAS-derived risk factors.
Pac Symp Biocomput
2023
36827430
Pharmacogenetic allele variant frequencies: An analysis of the VA's Million Veteran Program (MVP) as a representation of the diversity in US population.
PLoS One
2023
35234888
Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study.
Hum Mol Genet
2022
36314129
Mild-to-Moderate Kidney Dysfunction and Cardiovascular Disease: Observational and Mendelian Randomization Analyses.
Circulation
2022
35771531
A <i>MUC5B</i> Gene Polymorphism, rs35705950-T, Confers Protective Effects Against COVID-19 Hospitalization but Not Severe Disease or Mortality.
Am J Respir Crit Care Med
2022
35653334
A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program.
PLoS Genet
2022
35759254
Association of Kidney Comorbidities and Acute Kidney Failure With Unfavorable Outcomes After COVID-19 in Individuals With the Sickle Cell Trait.
JAMA Intern Med
2022
35690068
Multiomic analysis reveals cell-type-specific molecular determinants of COVID-19 severity.
Cell Syst
2022
35482673
A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program.
PLoS Genet
2022
35861770
Race and Ethnicity Stratification for Polygenic Risk Score Analyses May Mask Disparities in Hispanics.
Circulation
2022
1 - 50 of 92
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