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Researcher

Dias Brandão, R.

Researcher

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  1. 2019
  2. Published
    Couvreur, 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, [1941]. DOI: 10.3389/fpls.2018.01941
  3. 2018
  4. Published
    Altara, 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. DOI: 10.3389/fcvm.2018.00011
  5. 2017
  6. Published
    Hoekstra, 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. DOI: 10.1016/j.ympev.2017.05.026
  7. Published
    Kamps, 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]. DOI: 10.3390/ijms18020308
  8. 2016
  9. Published
    Fackenthal, 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. DOI: 10.1136/jmedgenet-2015-103570
  10. 2012
  11. Published
    ENIGMA 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. DOI: 10.1136/jmedgenet-2012-101037
  12. Published
    ENIGMA, 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. DOI: 10.1002/humu.21628
  13. 2011
  14. Published
    Brandao, 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. DOI: 10.1007/s10549-011-1599-7

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