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Carolina Roselli
Carolina Roselli
Broad Institute of MIT and Harvard, University of Groningen
Verified email at broadinstitute.org
Title
Cited by
Cited by
Year
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations
AV Khera, M Chaffin, KG Aragam, ME Haas, C Roselli, SH Choi, ...
Nature genetics 50 (9), 1219, 2018
24742018
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
R Malik, G Chauhan, M Traylor, M Sargurupremraj, Y Okada, A Mishra, ...
Nature genetics 50 (4), 524, 2018
11962018
Multi-ethnic genome-wide association study for atrial fibrillation
C Roselli, MD Chaffin, LC Weng, S Aeschbacher, G Ahlberg, CM Albert, ...
Nature genetics 50 (9), 1225, 2018
5942018
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
S Shah, A Henry, C Roselli, H Lin, G Sveinbjörnsson, G Fatemifar, ...
Nature Communications 11 (1), 1-12, 2020
5132020
A genetic variant associated with five vascular diseases is a distal regulator of endothelin-1 gene expression
RM Gupta, J Hadaya, A Trehan, SM Zekavat, C Roselli, D Klarin, ...
Cell 170 (3), 522-533. e15, 2017
3982017
Transcriptional and cellular diversity of the human heart
NR Tucker, M Chaffin, SJ Fleming, AW Hall, VA Parsons, KC Bedi Jr, ...
Circulation 142 (5), 466-482, 2020
3482020
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
IE Christophersen, M Rienstra, C Roselli, X Yin, B Geelhoed, J Barnard, ...
Nature genetics 49 (6), 946, 2017
3122017
Whole-genome sequencing to characterize monogenic and polygenic contributions in patients hospitalized with early-onset myocardial infarction
AV Khera, M Chaffin, SM Zekavat, RL Collins, C Roselli, P Natarajan, ...
Circulation 139 (13), 1593-1602, 2019
2362019
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
KG Aragam, T Jiang, A Goel, S Kanoni, BN Wolford, DS Atri, EM Weeks, ...
Nature Genetics, 1-13, 2022
1892022
Predicting benefit from evolocumab therapy in patients with atherosclerotic disease using a genetic risk score: results from the FOURIER trial
NA Marston, FK Kamanu, F Nordio, Y Gurmu, C Roselli, PS Sever, ...
Circulation 141 (8), 616-623, 2020
1572020
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation
SH Choi, LC Weng, C Roselli, H Lin, CM Haggerty, MB Shoemaker, ...
Jama 320 (22), 2354-2364, 2018
1502018
Genetics of atrial fibrillation in 2020: GWAS, genome sequencing, polygenic risk, and beyond
C Roselli, M Rienstra, PT Ellinor
Circulation Research 127 (1), 21-33, 2020
1362020
Deep learning enables genetic analysis of the human thoracic aorta
JP Pirruccello, MD Chaffin, EL Chou, SJ Fleming, H Lin, M Nekoui, ...
Nature Genetics, 1-12, 2021
1112021
Sleep timing is more important than sleep length or quality for medical school performance
L Genzel, K Ahrberg, C Roselli, S Niedermaier, A Steiger, M Dresler, ...
Chronobiology international 30 (6), 766-771, 2013
1112013
Genetic Risk Prediction of Atrial Fibrillation
SA Lubitz, X Yin, HJ Lin, M Kolek, JG Smith, S Trompet, M Rienstra, ...
Circulation 135 (14), 1311-1320, 2017
1032017
Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results From a National Biobank
SH Choi, SJ Jurgens, LC Weng, JP Pirruccello, C Roselli, M Chaffin, ...
Circulation Research 126 (2), 200-209, 2020
842020
Heritability of Atrial Fibrillation
LC Weng, SH Choi, D Klarin, JG Smith, PR Loh, M Chaffin, C Roselli, ...
Circulation: Genomic and Precision Medicine 10 (6), e001838, 2017
802017
Assessment of the relationship between genetic determinants of thyroid function and atrial fibrillation: a mendelian randomization study
C Ellervik, C Roselli, IE Christophersen, A Alonso, M Pietzner, CM Sitlani, ...
JAMA cardiology 4 (2), 144-152, 2019
782019
Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank
SJ Jurgens, SH Choi, VN Morrill, M Chaffin, JP Pirruccello, JL Halford, ...
Nature Genetics, 1-11, 2022
762022
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
I Ntalla, LC Weng, JH Cartwright, AW Hall, G Sveinbjornsson, NR Tucker, ...
Nature communications 11 (1), 1-12, 2020
712020
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