C. Roselli

Large-Scale Proteomic Profiling of Incident Heart Failure and Its Subtypes in Older Adults.
20260 citationsauthor #196
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions
20251 citationsauthor #328
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
202518 citationsauthor #13
Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals
20250 citationsauthor #349
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
202516 citationsauthor #18
Predicting Atrial Fibrillation After Stroke by Combining Polygenic Risk Scores and Clinical Features
20250 citationsauthor #12
Machine Learning-Based Plasma Protein Risk Score Improves Atrial Fibrillation Prediction Over Clinical and Genomic Models.
20255 citationsauthor #6
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies
20258 citationsauthor #333
The impact of common and rare genetic variants on bradyarrhythmia development
202510 citationsauthor #36
Contributions of Common, Rare, and Somatic Genetic Variants to Incidence of Atrial Fibrillation.
20253 citationsauthor #9
Cardiovascular Significance and Genetics of Epicardial and Pericardial Adiposity.
202431 citationsauthor #5
Rare coding variant analysis for human diseases across biobanks and ancestries
202433 citationsauthor #12
Large-scale single-nuclei profiling identifies role for ATRNL1 in atrial fibrillation
20248 citationsauthor #3
Integrating Clinical, Genetic, and Electrocardiogram-Based Artificial Intelligence to Estimate Risk of Incident Atrial Fibrillation
20243 citationsauthor #5
Common and Rare Variant Contributions to Bradyarrhythmias from Multi-Ancestry Meta-Analyses
20230 citationsauthor #35
Abstract 14750: Performance of a Polygenic Risk Score for Coronary Artery Disease Across the Spectrum of ASCVD: An Analysis of 60k Patients From 6 TIMI Randomized Trials
20230 citationsauthor #4
Clonal haematopoiesis and risk of chronic liver disease
2023151 citationsauthor #339
GENETICALLY MEDIATED VASCULAR ENDOTHELIAL CELL DYSFUNCTION AND ITS DEPENDENCE ON SERUM LDL CHOLESTEROL LEVELS FOR THE DEVELOPMENT OF CORONARY ARTERY ATHEROSCLEROSIS: GENETIC INSIGHTS FROM THE UKBB AND FOURIER TRIAL
20230 citationsauthor #4
Author Correction: Clonal haematopoiesis and risk of chronic liver disease
20231 citationsauthor #339
Cardiovascular Disease Knowledge Portal: A Community Resource for Cardiovascular Disease Research.
202313 citationsauthor #2
Abstract 14346: The Cardiovascular Disease Associations and Genetic Determinants of Pericardial Adipose Tissue
20230 citationsauthor #5
Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma
202310 citationsauthor #323
A comprehensive analysis of 30 Biomarkers and their association with cardiovascular outcomes and mortality in the UK Biobank
20230 citationsauthor #7
Association of genetic risk and outcomes in patients with atrial fibrillation: interactions with early rhythm control in the EAST-AFNET4 trial
202311 citationsauthor #3
The precuneus as a central node in declarative memory retrieval.
202320 citationsauthor #5
Abstract 15339: CAD Polygenic Risk Score and Incident Complex Coronary Revascularization in Adults With Atherosclerosis
20230 citationsauthor #4
Genetic insights into resting heart rate and its role in cardiovascular disease
202324 citationsauthor #42
The Cardiovascular Impact and Genetics of Pericardial Adiposity
20233 citationsauthor #5
Abstract 16950: The Genetic Basis of Atrial Fibrillation in a Large-Scale Multi-Ancestry Sample
20230 citationsauthor #2
Mapping the aetiological foundations of the heart failure spectrum using human genetics
20235 citationsauthor #13
Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank
2022133 citationsauthor #9
Abstract 12228: Development of a Novel Polygenic Risk Score to Predict Risk of Aortic Stenosis Events
20221 citationsauthor #4
Abstract 12593: Type 2 Diabetes Mellitus Polygenic Score Predicts New Onset Diabetes in Patients With Established Atherosclerotic Cardiovascular Disease: A FOURIER Sub-Study
20220 citationsauthor #6
A polygenic risk score predicts atrial fibrillation in cardiovascular disease.
202260 citationsauthor #5
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals
202239 citationsauthor #327
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
2022244 citationsauthor #323
Resting heart rate and incident atrial fibrillation: A stratified Mendelian randomization in the AFGen consortium
202213 citationsauthor #3
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse.
202210 citationsauthor #1
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
202245 citationsauthor #31
Predictive Utility of a Coronary Artery Disease Polygenic Risk Score in Primary Prevention.
202296 citationsauthor #7
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
202244 citationsauthor #326
Variant-specific inflation factors for assessing population stratification at the phenotypic variance level
202116 citationsauthor #322
Abstract 9110: Use of a Genetic Risk Score to Predict Atrial Fibrillation in Patients With Cardiovascular Disease
20210 citationsauthor #5
Genetic analyses of the QT interval and its components in over 250K individuals identifies new loci and pathways affecting ventricular depolarization and repolarization
20211 citationsauthor #31
Genetic Risk Score to Identify Risk of Venous Thromboembolism in Patients with Cardiometabolic Disease.
20217 citationsauthor #6
A framework for detecting noncoding rare variant associations of large-scale whole-genome sequencing studies
202186 citationsauthor #328
The genomics of heart failure: design and rationale of the HERMES consortium
202119 citationsauthor #114
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
2021489 citationsauthor #12
Genetic analysis of right heart structure and function in 40,000 people
202187 citationsauthor #9
Abstract 9393: A Genetic Risk Score to Predict Peripheral Artery Disease and Acute Limb Ischemia in Patients With Cardiometabolic Disease
20210 citationsauthor #5
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program
20211 citationsauthor #270
Genetics of myocardial interstitial fibrosis in the human heart and association with disease
202167 citationsauthor #13
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes
20210 citationsauthor #318
Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes
202111 citationsauthor #28
Genetic risk and atrial fibrillation in patients with heart failure
202025 citationsauthor #3
Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium
202025 citationsauthor #369
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
20200 citationsauthor #267
Rare Genetic Variation Underlying Human Diseases and Traits: Results from 200,000 Individuals in the UK Biobank
202013 citationsauthor #9
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale
2020225 citationsauthor #313
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
2020275 citationsauthor #3
Deep learning enables genetic analysis of the human thoracic aorta
2020165 citationsauthor #17
Monogenic and Polygenic Contributions to Atrial Fibrillation Risk
202089 citationsauthor #5
PERFORMANCE OF A NOVEL GENETIC RISK SCORE TO IDENTIFY RISK OF VENOUS THROMBOEMBOLISM IN PATIENTS WITH CARDIOMETABOLIC DISEASE
20200 citationsauthor #6
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
2020170 citationsauthor #318
The Effect of PCSK9 Inhibition on the Risk of Venous Thromboembolism.
202058 citationsauthor #9
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
20200 citationsauthor #9
Clinical Application of a Novel Genetic Risk Score for Ischemic Stroke in Patients with Cardiometabolic Disease.
202038 citationsauthor #6
Genetics of Atrial Fibrillation in 2020
2020141 citationsauthor #1
Epigenetic Analyses of Human Left Atrial Tissue Identifies Gene Networks Underlying Atrial Fibrillation
202014 citationsauthor #3
Transcriptional and Cellular Diversity of the Human Heart
2020409 citationsauthor #11
Genetic Susceptibility for Atrial Fibrillation in Patients Undergoing Atrial Fibrillation Ablation
202040 citationsauthor #3
Genome-Wide Association Study of Over One Million Participants Identifies 49 Novel Loci Associated With Coronary Artery Disease
20191 citationsauthor #10
Assessment of the Relationship Between Genetic Determinants of Thyroid Function and Atrial Fibrillation: A Mendelian Randomization Study
201985 citationsauthor #2
Detailed Regulatory Interaction Map of the Human Heart Facilitates Gene Discovery for Cardiovascular Disease
201910 citationsauthor #6
Genome sequencing unveils a regulatory landscape of platelet reactivity
201939 citationsauthor #319
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (vol 50, pg 524, 2018)
201937 citationsauthor #137
Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children with asthma.
20196 citationsauthor #270
Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure
20196 citationsauthor #3
Genetic risk prediction of atrial fibrillation in a contemporary heart failure cohort
20190 citationsauthor #3
Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
20198 citationsauthor #137
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
201991 citationsauthor #9
Genetic Link Between Arterial Stiffness and Atrial Fibrillation.
201913 citationsauthor #2
Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction
2019226 citationsauthor #5
Antisense regulation of atrial natriuretic peptide expression.
201917 citationsauthor #4
Predicting Benefit From Evolocumab Therapy in Patients With Atherosclerotic Disease Using a Genetic Risk Score
2019146 citationsauthor #5
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation
2018180 citationsauthor #3
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
2018110 citationsauthor #137
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
20186 citationsauthor #267
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
201892 citationsauthor #267
4346The genetic risk and interactions in atrial fibrillation, evidence from 335,070 uk biobank participants
20180 citationsauthor #3
Multi-ethnic genome-wide association study for atrial fibrillation
2018667 citationsauthor #1
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
20181,354 citationsauthor #137
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations
20182,531 citationsauthor #5
Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes
201840 citationsauthor #16
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
2018148 citationsauthor #246
An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels.
201811 citationsauthor #254
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
20181 citationsauthor #267
Genetic Risk Prediction of Atrial Fibrillation
201792 citationsauthor #36
Abstract P100: Heritability of Atrial Fibrillation
20170 citationsauthor #6
Heritability of Atrial Fibrillation
201782 citationsauthor #8

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