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Bettencourt, C., & Lima, M. (2013). "Mimicking" capacity of spinocerebellar ataxia type 3: The details matter. Journal of the Neurological Sciences.
Bettencourt, C., Raposo, M., Kazachkova, N., Cymbron, T., et al. (2011). The APOE ε 2 allele increases the risk of earlier age at onset in Machado-Joseph disease. Archives of Neurology, 68(12), 1580 - 1583.
Bettencourt, B. F., Pinheiro, J. P., & Brüges-Armas, J. (2016). Killer-cell immunoglobulin-like receptors genotyping of 127 individuals from Terceira Island, Azores, Portugal. Human Immunology, 77(12), 1113.
Bettencourt, A., Pereira, C., Carvalho, L., Carvalho, C., et al. (2008). New insights of HLA class I association to Behçet's disease in Portuguese patients. Tissue Antigens, 72(4), 379 - 382.
Bettencourt, C., Raposo, M., Kazachkova, N., Santos, C., et al. (2012). Sequence analysis of 5′ regulatory regions of the Machado-Joseph disease gene (ATXN3). Cerebellum, 11(4), 1045 - 1050.
Bettencourt, C., Raposo, M., Ros, R., Montiel, R., et al. (2013). Transcript Diversity of Machado-Joseph Disease Gene (ATXN3) Is Not Directly Determined by SNPs in Exonic or Flanking Intronic Regions. Journal of Molecular Neuroscience, 49(3), 539 - 543.
Bettencourt, C., Santos, C., Coutinho, P., Rizzu, P., et al. (2011). Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): A two-case report. BMC Neurology, 11.
Bettencourt, C., Quintáns, B., Ros, R., Ampuero, I., et al. (2012). Revisiting genotype-phenotype overlap in neurogenetics: Triplet-repeat expansions mimicking spastic paraplegias. Human Mutation, 33(9), 1315 - 1323.
Bettencourt, C., Santos, C., Montiel, R., do Carmo Costa, M., et al. (2010). Increased transcript diversity: Novel splicing variants of Machado-Joseph Disease gene (ATXN3). Neurogenetics, 11(2), 193 - 202.
Bettencourt, C., Santos, C., Montiel, R., Kay, T., et al. (2010). The (CAG)n tract of Machado-Joseph Disease gene (ATXN3): A comparison between DNA and mRNA in patients and controls. European Journal of Human Genetics, 18(5), 621 - 623.
Bettencourt, C., Fialho, R. N., Santos, C., Montiel, R., et al. (2008). Segregation distortion of wild-type alleles at the Machado-Joseph disease locus: A study in normal families from the Azores islands (Portugal). Journal of Human Genetics, 53(4), 333 - 339.
Bettencourt, B. F., Rocha, F. L., Alves, H., Amorim, R., et al. (2013). Protective effect of an ERAP1 haplotype in ankylosing spondylitis: Investigating non-MHC genes in HLA-B27-positive individuals. Rheumatology (United Kingdom), 52(12), 2168 - 2176.
Bettencourt, C., & Lima, M. (2011). Machado-Joseph disease: From first descriptions to new perspectives. Orphanet Journal of Rare Diseases, 6(1).
Bettencourt, C., Raposo, M., Ros, R., Montiel, R., et al. (2012). Transcript Diversity of Machado-Joseph Disease Gene (ATXN3) Is Not Directly Determined by SNPs in Exonic or Flanking Intronic Regions. Journal of Molecular Neuroscience.
Bettencourt, B. F., Santos, M. R., Pereira, J., Amaro, B., et al. (2016). HLA-A, -B, -C, -DQA1, -DQB1, -DRB1, -E, -F and -G genotyping of 130 individuals from Terceira Island, Azores, Portugal. Human Immunology, 77(6), 445 - 446.
Bessa, J., Tena, J. J., De La Calle-Mustienes, E., Fernández-Miñán, A., et al. (2009). Zebrafish Enhancer Detection (ZED) vector: A new tool to facilitate transgenesis and the functional analysis of cis-regulatory regions in zebrafish. Developmental Dynamics, 238(9), 2409 - 2417.
Bessa, C., Teixeira, C. A. F., Mangas, M., Dias, A., et al. (2006). Two novel CLN5 mutations in a Portuguese patient with vLINCL: Insights into molecular mechanisms of CLN5 deficiency. Molecular Genetics and Metabolism, 89(3), 245 - 253.
Bessa, J., Carmona, L., & Casares, F. (2009). Zinc-finger paralogues tsh and tio are functionally equivalent during imaginal development in Drosophila and maintain their expression levels through auto- and cross-negative feedback loops. Developmental Dynamics, 238(1), 19 - 28.
Bessa, C., Pereira, C., Leão, M., Maciel, C., et al. (2013). Using yeast to uncover the regulation of protein kinase Cδ by ceramide. FEMS Yeast Research, 13(7), 700 - 705.
Bessa, J., Tavares, M. J., Santos, J., Kikuta, H., et al. (2008). meis1 regulates cyclin D1 and c-myc expression, and controls the proliferation of the multipotent cells in the early developing zebrafish eye. Development, 135(5), 799 - 803.
Bessa, J., & Casares, F. (2005). Restricted teashirt expression confers eye-specific responsiveness to Dpp and Wg signals during eye specification in Drosophila. Development, 132(22), 5011 - 5020.
Berce, V., Kozmus, C. E. P., & Potočnik, U. (2012). Association among ORMDL3 gene expression, 17q21 polymorphism and response to treatment with inhaled corticosteroids in children with asthma. Pharmacogenomics Journal.
Berce, V., Kozmus, C. E. P., & Potočnik, U. (2016). CTLA4 expression in childhood asthma and the effect of treatment with inhaled corticosteroid and Leukotriene receptor antagonist. Annual Research and Review in Biology, 10(2).
Bento, V. F., Cruz, V. T., Ribeiro, D. D., Branco, C., & Coutinho, P. (2013). The potential of motion quantification systems in the automatic evaluation of motor function after stroke. International Journal of Stroke, 8(6), - .
Benninger, Y., Thurnherr, T., Pereira, J. A., Krause, S., et al. (2007). Essential and distinct roles for cdc42 and rac1 in the regulation of Schwann cell biology during peripheral nervous system development. Journal of Cell Biology, 177(6), 1051 - 1061.

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