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Carolina Roselli

Name	Carolina Roselli
Place	Cambridge (Wirkungsort) Großbritannien
Gender	weiblich
Related	Massachusetts Institute of Technology Medizinische Informatik (Thema)
Further information	Phd candidate at University of Groningen and Senior Computational Associate at Broad Institute of MIT and Harvard
Record type	Person
GND-Identifier	1209144786
Record ID	1209144786
Involved in show all Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes The impact of common and rare genetic variants on bradyarrhythmia development Rare coding variant analysis for human diseases across biobanks and ancestries Genetic insights into resting heart rate and its role in cardiovascular disease Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations Multi-ethnic genome-wide association study for atrial fibrillation Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

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Carolina Roselli

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes

The impact of common and rare genetic variants on bradyarrhythmia development

Rare coding variant analysis for human diseases across biobanks and ancestries

Genetic insights into resting heart rate and its role in cardiovascular disease

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations

Multi-ethnic genome-wide association study for atrial fibrillation

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes