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Author Details

Aris Baras
2006
87
40
PMIDPaper TitleJournal TitlePublished Year
36807635Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.Nature2023
37949852A large meta-analysis identifies genes associated with anterior uveitis.2023
37753809A Genetic Risk Variant for Multiple Sclerosis Severity is Associated with Brain Atrophy.Ann Neurol2023
37954898Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From Sepsis.Crit Care Explor2023
36639314Corrigendum to: "An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs" [J Hepatol 75 (2021) 572-581].J Hepatol2023
35263815Thrombotic risk determined by rare and common SERPINA1 variants in a population-based cohort study.Journal of Thrombosis and Haemostasis2022
35654975A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.Nat Genet2022
36038634Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.Nat Genet2022
35699965Loss-of-Function <i>FLNC</i> Variants Are Associated With Arrhythmogenic Cardiomyopathy Phenotypes When Identified Through Exome Sequencing of a General Clinical Population.Circ Genom Precis Med2022
35999217Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes.Nat Commun2022
35939579Germline Mutations in <i>CIDEB</i> and Protection against Liver Disease.N Engl J Med2022
36062972Calcium, Its Regulatory Hormones, and Their Causal Role on Blood Pressure: A Two-Sample Mendelian Randomization Study.Journal of Clinical Endocrinology and Metabolism2022
36381289Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle-aged and older adults: A population-based cohort study.Research and Practice in Thrombosis and Haemostasis2022
36450978Common and rare variant associations with clonal haematopoiesis phenotypes.Nature2022
35915156Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.Nat Med2022
35534559Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects.Nat Genet2022
34634447Clinical Implications of the Amyloidogenic V122I Transthyretin Variant in the General Population.J Card Fail2022
35219277Efficacy and Safety of Sarilumab in Hospitalized Patients With Coronavirus Disease 2019: A Randomized Clinical Trial.Clin Infect Dis2022
34970867Thrombomodulin (THBD) gene variants and thrombotic risk in a population-based cohort study.Journal of Thrombosis and Haemostasis2022
35149777UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab.Pharmacogenomics J2022
35021256Thrombotic Risk Determined by Protein C Receptor (PROCR) Variants among Middle-Aged and Older Adults: A Population-Based Cohort Study.Thrombosis and Haemostasis2022
35112923Classic Thrombophilias and Thrombotic Risk Among Middle-Aged and Older Adults: A Population-Based Cohort Study.Journal of the American Heart Association2022
35303419Mucus sialylation determines intestinal host-commensal homeostasis.Cell2022
34945778Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian Randomization.J Pers Med2021
34017140Computationally efficient whole-genome regression for quantitative and binary traits.Nat Genet2021
33909646Seroprevalence of anti-SARS-CoV-2 antibodies in a cohort of New York City metro blood donors using multiple SARS-CoV-2 serological assays: Implications for controlling the epidemic and "Reopening".PLoS One2021
33750777Disrupting upstream translation in mRNAs is associated with human disease.Nat Commun2021
33542107Heterozygosity for a Pathogenic Variant in <i>SLC12A3</i> That Causes Autosomal Recessive Gitelman Syndrome Is Associated with Lower Serum Potassium.J Am Soc Nephrol2021
34120448Causal Effect of Adiposity Measures on Blood Pressure Traits in 2 Urban Swedish Cohorts: A Mendelian Randomization Study.J Am Heart Assoc2021
34120153The genetic architecture of Plakophilin 2 cardiomyopathy.Genet Med2021
33692434Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease.Sci Rep2021
34115965Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.Am J Hum Genet2021
33619501Genome-wide analysis in 756,646 individuals provides first genetic evidence that <i>ACE2</i> expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease.medRxiv2021
34210852Sequencing of 640,000 exomes identifies <i>GPR75</i> variants associated with protection from obesity.Science2021
33655273A catalog of associations between rare coding variants and COVID-19 outcomes.medRxiv2021
33441424Kidney disease genetic risk variants alter lysosomal beta-mannosidase (<i>MANBA</i>) expression and disease severity.Sci Transl Med2021
34302758Safety and efficacy of itepekimab in patients with moderate-to-severe COPD: a genetic association study and randomised, double-blind, phase 2a trial.Lancet Respiratory Medicine,The2021
34184762Genome-wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals.Genet Epidemiol2021
33222547Clinical Evaluation of the Polygenetic Background of Blood Pressure in the Population-Based Setting.Hypertension2021
33432171Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations.Nat Med2021
34408292Correction to: The genetic architecture of Plakophilin 2 cardiomyopathy.Genet Med2021
34855475Genetic and functional evidence links a missense variant in <i>B4GALT1</i> to lower LDL and fibrinogen.Science2021
34727153ERAP1, ERAP2, and Two Copies of HLA-Aw19 Alleles Increase the Risk for Birdshot Chorioretinopathy in HLA-A29 Carriers.Invest Ophthalmol Vis Sci2021
34662886Exome sequencing and analysis of 454,787 UK Biobank participants.Nature2021
32498804Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease.J Am Coll Cardiol2020
32016367Understanding the use of observational and randomized data in cardiovascular medicine.Eur Heart J2020
31836692Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care Cohort.Diabetes2020
31707832Patients With High Genome-Wide Polygenic Risk Scores for Coronary Artery Disease May Receive Greater Clinical Benefit From Alirocumab Treatment in the ODYSSEY OUTCOMES Trial.Circulation2020
33096487Meta-analysis investigating the role of interleukin-6 mediated inflammation in type 2 diabetes.eBioMedicine2020
33087929Exome sequencing and characterization of 49,960 individuals in the UK Biobank.Nature2020
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