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- 2019
- PublishedKConFab Investigators, Brandao, R. D., Mensaert, K., Lopez-Perolio, I., Tserpelis, D., Xenakis, M., ... Blok, M. J. (2019). Targeted RNA-seq successfully identifies normal and pathogenic splicing events in breast/ovarian cancer susceptibility and Lynch syndrome genes. International Journal of Cancer, 145(2), 401-414. https://doi.org/10.1002/ijc.32114
- PublishedCouvreur, T. L. P., Helmstetter, A. J., Koenen, E. J. M., Bethune, K., Dias Brandão, R., Little, S. A., ... Erkens, R. (2019). Phylogenomics of the major tropical plant family Annonaceae using targeted enrichment of nuclear genes. Frontiers in Plant Science, 9, [1941]. https://doi.org/10.3389/fpls.2018.01941
- 2018
- PublishedFrench COVAR group collaborators, Caputo, S. M., Leone, M., Damiola, F., Ehlen, A., Carreira, A., ... Rouleau, E. (2018). Full in-frame exon 3 skipping of BRCA2 confers high risk of breast and/or ovarian cancer. OncoTarget, 9(25), 17334-17348. https://doi.org/10.18632/oncotarget.24671
- PublishedAltara, R., Zouein, F. A., Brandao, R. D., Bajestani, S. N., Cataliotti, A., & Booz, G. W. (2018). In Silico Analysis of Differential Gene Expression in Three Common Rat Models of Diastolic Dysfunction. Frontiers in cardiovascular medicine, 5, [11]. https://doi.org/10.3389/fcvm.2018.00011
- 2017
- PublishedHoekstra, P. H., Wieringa, J. J., Smets, E., Brandão, R. D., Lopes, J. D. C., Erkens, R. H. J., & Chatrou, L. W. (2017). Correlated evolutionary rates across genomic compartments in Annonaceae. Molecular Phylogenetics and Evolution, 114, 63-72. https://doi.org/10.1016/j.ympev.2017.05.026
- PublishedKamps, R., Brandao, R. D., van den Bosch, B. J., Paulussen, A. D. C., Xanthoulea, S., Blok, M. J., & Romano, A. (2017). Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification. International Journal of Molecular Sciences, 18(2), [308]. https://doi.org/10.3390/ijms18020308
- 2016
- PublishedFackenthal, J. D., Yoshimatsu, T., Zhang, B., de Garibay, G. R., Colombo, M., De Vecchi, G., ... de la Hoya, M. (2016). Naturally occurring BRCA2 alternative mRNA splicing events in clinically relevant samples. Journal of Medical Genetics, 53(8), 548-558. https://doi.org/10.1136/jmedgenet-2015-103570
- 2012
- PublishedENIGMA Consortsium, Dias Brandão, R., Blok, R. M. J., & Gomez Garcia, E. (2012). BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk. Journal of Medical Genetics, 49(8), 525-532. https://doi.org/10.1136/jmedgenet-2012-101037
- PublishedENIGMA, Dias Brandão, R., Gomez Garcia, E., & Blok, R. M. J. (2012). ENIGMA-Evidence-Based Network for the Interpretation of Germline Mutant Alleles: An International Initiative to Evaluate Risk and Clinical Significance Associated with Sequence Variation in BRCA1 and BRCA2 Genes. Human Mutation, 33(1), 2-7. https://doi.org/10.1002/humu.21628
- 2011
- PublishedBrandao, R. D., van Roozendaal, K., Tserpelis, D., Garcia, E. G., & Blok, M. J. (2011). Characterisation of unclassified variants in the BRCA1/2 genes with a putative effect on splicing. Breast Cancer Research and Treatment, 129(3), 971-982. https://doi.org/10.1007/s10549-011-1599-7