Profil

CODONI Veronica

University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB) > Bioinformatics Core

ORCID
0000-0002-0604-5504
Main Referenced Co-authors
Civelek, Mete (5)
Björkegren, Johan L. M. (4)
Lusis, Aldons J. (4)
Trégouët, David-Alexandre (4)
Johnson, Andrew D. (3)
Main Referenced Keywords
Humans (8); Male (5); Genome-Wide Association Study (4); Animals (3); Gene Regulatory Networks (3);
Main Referenced Disciplines
Genetics & genetic processes (7)
Hematology (1)

Publications (total 9)

The most cited

905 citations (WOS)

Malik, R., Chauhan, G., Traylor, M., Sargurupremraj, M., Okada, Y., Mishra, A., Rutten-Jacobs, L., Giese, A.-K., van der Laan, S. W., Gretarsdottir, S., Anderson, C. D., Chong, M., Adams, H. H. H., Ago, T., Almgren, P., Amouyel, P., Ay, H., Bartz, T. M., Benavente, O. R., ... Dichgans, M. (2018). Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nature Genetics, 50 (4), 524-537. doi:10.1038/s41588-018-0058-3 https://hdl.handle.net/10993/53224

Crawford, K., Xian, J., Helbig, K. L., Galer, P. D., Parthasarathy, S., Lewis-Smith, D., Kaufman, M. C., Fitch, E., Ganesan, S., O'Brien, M., Codoni, V., Ellis, C. A., Conway, L. J., Taylor, D., Krause, R., & Helbig, I. (2021). Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders. Genetics in medicine : official journal of the American College of Medical Genetics, 23 (7), 1263-1272. doi:10.1038/s41436-021-01120-1
Peer reviewed

Malik, R., Chauhan, G., Traylor, M., Sargurupremraj, M., Okada, Y., Mishra, A., Rutten-Jacobs, L., Giese, A.-K., van der Laan, S. W., Gretarsdottir, S., Anderson, C. D., Chong, M., Adams, H. H. H., Ago, T., Almgren, P., Amouyel, P., Ay, H., Bartz, T. M., Benavente, O. R., ... Dichgans, M. (2019). Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nature Genetics, 51 (7), 1192-1193. doi:10.1038/s41588-019-0449-0
Peer Reviewed verified by ORBi

Tiacci, E., Venanzi, A., Ascani, S., Marra, A., Cardinali, V., Martino, G., Codoni, V., Schiavoni, G., Martelli, M. P., & Falini, B. (2018). High-Risk Clonal Hematopoiesis as the Origin of AITL and NPM1-Mutated AML. The New England journal of medicine, 379 (10), 981-984. doi:10.1056/NEJMc1806413
Peer reviewed

Malik, R., Chauhan, G., Traylor, M., Sargurupremraj, M., Okada, Y., Mishra, A., Rutten-Jacobs, L., Giese, A.-K., van der Laan, S. W., Gretarsdottir, S., Anderson, C. D., Chong, M., Adams, H. H. H., Ago, T., Almgren, P., Amouyel, P., Ay, H., Bartz, T. M., Benavente, O. R., ... Dichgans, M. (2018). Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nature Genetics, 50 (4), 524-537. doi:10.1038/s41588-018-0058-3
Peer Reviewed verified by ORBi

Shu, L., Chan, K. H. K., Zhang, G., Huan, T., Kurt, Z., Zhao, Y., Codoni, V., Trégouët, D.-A., Yang, J., Wilson, J. G., Luo, X., Levy, D., Lusis, A. J., Liu, S., & Yang, X. (2017). Shared genetic regulatory networks for cardiovascular disease and type 2 diabetes in multiple populations of diverse ethnicities in the United States. PLoS Genetics, 13 (9), 1007040. doi:10.1371/journal.pgen.1007040
Peer Reviewed verified by ORBi

Touat-Hamici, Z., Weidmann, H., Blum, Y., Proust, C., Durand, H., Iannacci, F., Codoni, V., Gaignard, P., Thérond, P., Civelek, M., Karabina, S. A., Lusis, A. J., Cambien, F., & Ninio, E. (2016). Role of lipid phosphate phosphatase 3 in human aortic endothelial cell function. Cardiovascular Research, 112 (3), 702-713. doi:10.1093/cvr/cvw217
Peer Reviewed verified by ORBi

Codoni, V., Blum, Y., Civelek, M., Proust, C., Franzén, O., Björkegren, J. L. M., Le Goff, W., Cambien, F., Lusis, A. J., & Trégouët, D.-A. (2016). Preservation Analysis of Macrophage Gene Coexpression Between Human and Mouse Identifies PARK2 as a Genetically Controlled Master Regulator of Oxidative Phosphorylation in Humans. G3 (Bethesda, Md.), 6 (10), 3361-3371. doi:10.1534/g3.116.033894
Peer reviewed

Marchand, A., Atassi, F., Mougenot, N., Clergue, M., Codoni, V., Berthuin, J., Proust, C., Trégouët, D.-A., Hulot, J.-S., & Lompré, A.-M. (2016). miR-322 regulates insulin signaling pathway and protects against metabolic syndrome-induced cardiac dysfunction in mice. Biochimica et biophysica acta, 1862 (4), 611-621. doi:10.1016/j.bbadis.2016.01.010
Peer reviewed

Brænne, I., Civelek, M., Vilne, B., Di Narzo, A., Johnson, A. D., Zhao, Y., Reiz, B., Codoni, V., Webb, T. R., Foroughi Asl, H., Hamby, S. E., Zeng, L., Trégouët, D.-A., Hao, K., Topol, E. J., Schadt, E. E., Yang, X., Samani, N. J., Björkegren, J. L. M., ... Lusis, A. J. (2015). Prediction of Causal Candidate Genes in Coronary Artery Disease Loci. Arteriosclerosis, Thrombosis and Vascular Biology, 35 (10), 2207-17. doi:10.1161/ATVBAHA.115.306108
Peer Reviewed verified by ORBi

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