Roselli, Carolina
Broad Institute · University Medical Center Groningen · University of Groningen
10 papers on CoChatORCID 0000-0001-5267-6756
Most cited papers
- Verified
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations
Khera, A. V., Chaffin, M., Aragam, K. G., Haas, M. E., Roselli, C., Choi, S. H., Natarajan, P., Lander, E. S., Lubitz, S. A., Ellinor, P. T., et al. (2018) · Nature Genetics
Genetic Associations and EpidemiologyGenetic and phenotypic traits in livestock
Cited by 2,953
- Verified
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Taliun, D., Harris, D. N., Kessler, M. D., Carlson, J., Szpiech, Z. A., Torres, R., Taliun, S. A. G., Corvelo, A., Gogarten, S. M., Kang, H. M., et al. (2021) · Nature
Genetic Associations and EpidemiologyGenomics and Rare Diseases
Cited by 2,213
- Verified
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Bick, A. G., Weinstock, J. S., Nandakumar, S. K., Fulco, C. P., Bao, E. L., Zekavat, S. M., Szeto, M. D., Liao, X., Leventhal, M. J., Nasser, J., et al. (2020) · Nature
Acute Myeloid Leukemia ResearchGenetic Associations and Epidemiology
Cited by 733
- Verified
Transcriptional and Cellular Diversity of the Human Heart
Tucker, N. R., Chaffin, M., Fleming, S. J., Hall, A. W., Parsons, V. A., Bedi, K. C., Akkad, A.-D., Herndon, C. N., Arduini, A., Papangeli, I., et al. (2020) · Circulation
Single-cell and spatial transcriptomicsCongenital heart defects research
Cited by 554
- Verified
A Genetic Variant Associated with Five Vascular Diseases Is a Distal Regulator of Endothelin-1 Gene Expression
Gupta, R. M., Hadaya, J., Trehan, A., Zekavat, S. M., Roselli, C., Klarin, D., Emdin, C. A., Hilvering, C. R. E., Bianchi, V., Mueller, C., et al. (2017) · Cell
Genetic Associations and EpidemiologyCerebrovascular and genetic disorders
Cited by 450
- Verified
Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction
Khera, A. V., Chaffin, M., Zekavat, S. M., Collins, R. L., Roselli, C., Natarajan, P., Lichtman, J. H., D’Onofrio, G., Mattera, J., Dreyer, R., et al. (2019) · Circulation
Lipoproteins and Cardiovascular HealthGenetic Associations and Epidemiology
Cited by 315
- Verified
Deep learning enables genetic analysis of the human thoracic aorta
Pirruccello, J. P., Chaffin, M. D., Chou, E. L., Fleming, S. J., Lin, H., Nekoui, M., Khurshid, S., Friedman, S. F., Bick, A. G., Arduini, A., et al. (2022) · Nature Genetics
Genetic Associations and EpidemiologyAortic Disease and Treatment Approaches
Cited by 210
- Verified
Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease
Katz, D. H., Tahir, U. A., Bick, A. G., Pampana, A., Ngo, D., Benson, M. D., Yu, Z., Robbins, J. M., Chen, Z.-Z., Cruz, D. E., et al. (2022) · Circulation
Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals
Cited by 92
- Verified
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Young, W. J., Lahrouchi, N., Isaacs, A., Duong, T., Foco, L., Ahmed, F., Brody, J. A., Salman, R., Noordam, R., Benjamins, J.-W., et al. (2022) · Nature Communications
Cardiac electrophysiology and arrhythmiasGenetic Associations and Epidemiology
Cited by 49
- Verified
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program
Cade, B. E., Lee, J., Sofer, T., Wang, H., Zhang, M., Chen, H., Gharib, S. A., Gottlieb, D. J., Guo, X., Lane, J. M., et al. (2021) · Genome Medicine
Obstructive Sleep Apnea ResearchGenetic Associations and Epidemiology
Cited by 33
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