Author details

Full Name

Carolina Roselli

Affiliation

ORCID

Career Start Year

2013

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37502935	The Cardiovascular Impact and Genetics of Pericardial Adiposity.	medRxiv	2023
35980763	A polygenic risk score predicts atrial fibrillation in cardiovascular disease.	Eur Heart J	2023
37814896	Cardiovascular Disease Knowledge Portal: A Community Resource for Cardiovascular Disease Research.	Circ Genom Precis Med	2023
37081215	Genetics of myocardial interstitial fibrosis in the human heart and association with disease.	Nat Genet	2023
36576811	Predictive Utility of a Coronary Artery Disease Polygenic Risk Score in Primary Prevention.	JAMA Cardiol	2023
37264683	Association of genetic risk and outcomes in patients with atrial fibrillation: interactions with early rhythm control in the EAST-AFNET4 trial.	Cardiovasc Res	2023
36610736	The precuneus as a central node in declarative memory retrieval.		2023
35245370	Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse.	Eur Heart J	2022
36050321	Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.	Nat Commun	2022
35594314	Resting heart rate and incident atrial fibrillation: A stratified Mendelian randomization in the AFGen consortium.	PLoS One	2022
34480422	The genomics of heart failure: design and rationale of the HERMES consortium.	ESC Heart Fail	2021
34319147	Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.	Circ Genom Precis Med	2021
33185476	Clinical Application of a Novel Genetic Risk Score for Ischemic Stroke in Patients With Cardiometabolic Disease.	Circulation	2021
33434447	Genetic Risk Score to Identify Risk of Venous Thromboembolism in Patients With Cardiometabolic Disease.	Circ Genom Precis Med	2021
32716721	Genetics of Atrial Fibrillation in 2020: GWAS, Genome Sequencing, Polygenic Risk, and Beyond.	Circ Res	2020
31691645	Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results From a National Biobank.	Circ Res	2020
32403949	Transcriptional and Cellular Diversity of the Human Heart.	Circulation	2020
32223429	The Effect of PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Inhibition on the Risk of Venous Thromboembolism.	Circulation	2020
31707849	Predicting Benefit From Evolocumab Therapy in Patients With Atherosclerotic Disease Using a Genetic Risk Score: Results From the FOURIER Trial.	Circulation	2020
31919934	Genetic risk and atrial fibrillation in patients with heart failure.	Eur J Heart Fail	2020
32439900	Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.	Nat Commun	2020
33155827	Epigenetic Analyses of Human Left Atrial Tissue Identifies Gene Networks Underlying Atrial Fibrillation.	Circ Genom Precis Med	2020
31211625	Genetic Link Between Arterial Stiffness and Atrial Fibrillation.	Circ Genom Precis Med	2019
30586733	Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction.	Circulation	2019
29531354	Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.	Nat Genet	2018
29892015	Multi-ethnic genome-wide association study for atrial fibrillation.	Nat Genet	2018
30104762	Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.	Nat Genet	2018
30535219	Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation.	JAMA	2018
27793994	Genetic Risk Prediction of Atrial Fibrillation.	Circulation	2017
28379579	Discovery of novel heart rate-associated loci using the Exome Chip.	Hum Mol Genet	2017
28416818	Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.	Nat Genet	2017
28753427	A Genetic Variant Associated with Five Vascular Diseases Is a Distal Regulator of Endothelin-1 Gene Expression.	Cell	2017
28747752	Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.	Nat Genet	2017
29237688	Heritability of Atrial Fibrillation.	Circ Cardiovasc Genet	2017
27589061	Whole Exome Sequencing in Atrial Fibrillation.	PLoS Genet	2016
23750895	Sleep timing is more important than sleep length or quality for medical school performance.	Chronobiol Int	2013