Page 130 - Genomic Medicine in Emerging Economies
P. 130

References   119




           Castilhos, R.M., Augustin, M.C., Santos, J.A., Perandones, C., Saraiva-Pereira, M.L., Jardim, L.B.,
              2016. Rede Neurogenetica Genetic aspects of Huntington’s disease in Latin America. A system-
              atic review. Clin. Genet. 89 (3), 295–303. doi: 10.1111/cge.12641.
           Castro, T., Mateus, H.E., Fonseca, D.J., Forero, D., Restrepo, C.M., Talero, C., Laissue, P., 2013.
              Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyper-
              activity disorder. Neurol. Sci. 34 (12), 2219–2222. doi: 10.1007/s10072-013-1569-4.
           Cespedes-Garro, C., Naranjo, M.E., Ramirez, R., Serrano, V., Farinas, H., Barrantes, R., 2015. Phar-
              macogenomics Ribef Pharmacogenetics in Central American healthy volunteers: interethnic
              variability. Drug Metab. Pers. Ther. 30 (1), 19–31. doi: 10.1515/dmdi-2014-0025.
           Cia, A.H., Rojas, R.C., Adad, M.A., 2010. Current clinical advances and future perspectives in the
              psychiatry/mental health field of Latin America. Int. Rev. Psychiatry 22 (4), 340–346. doi:
              10.3109/09540261.2010.501167.
           Contini, V., Bertuzzi, G.P., Polina, E.R., Hunemeier, T., Hendler, E.M., Hutz, M.H., Bau, C.H., 2012.
              A haplotype analysis is consistent with the role of functional HTR1B variants in alcohol de-
              pendence. Drug Alcohol Depend. 122 (1–2), 100–104. doi: 10.1016/j.drugalcdep.2011.09.020.
           Contini, V., Marques, F.Z., Garcia, C.E., Hutz, M.H., Bau, C.H., 2006. MAOA-uVNTR polymor-
              phism in a Brazilian sample: further support for the association with impulsive behaviors and
              alcohol dependence. Am. J. Med. Genet. B Neuropsychiatr. Genet. 141B (3), 305–308. doi:
              10.1002/ajmg.b.30290.
           Contini, V., Victor, M.M., Cerqueira, C.C., Polina, E.R., Grevet, E.H., Salgado, C.A., Bau, C.H., 2011.
              Adrenergic alpha2A receptor gene is not associated with methylphenidate response in adults with
              ADHD. Eur. Arch. Psychiatry Clin. Neurosci. 261 (3), 205–211. doi: 10.1007/s00406-010-0172-4.
           Contini, V., Victor, M.M., Marques, F.Z., Bertuzzi, G.P., Salgado, C.A., Silva, K.L., Bau, C.H., 2010.
              Response to methylphenidate is not influenced by DAT1 polymorphisms in a sample of Bra-
              zilian adult patients with ADHD. J. Neural Transm. (Vienna) 117 (2), 269–276. doi: 10.1007/
              s00702-009-0362-2.
           Cordeiro, Q., Silva, R.T., Vallada, H., 2012. Association study between the rs165599 catechol-O-
              methyltransferase genetic polymorphism and schizophrenia in a Brazilian sample. Arq Neu-
              ropsiquiatr. 70 (12), 913–916.
           Cordeiro, Q., Siqueira-Roberto, J., Vallada, H., 2010. Association between the SLC6A3 A1343G
              polymorphism and schizophrenia. Arq Neuropsiquiatr. 68 (5), 716–719.
           Cordeiro, Q., Siqueira-Roberto, J., Zung, S., Vallada, H., 2009a. Association between the DRD2-
              141C insertion/deletion polymorphism and schizophrenia. Arq Neuropsiquiatr. 67 (2A),
              191–194.
           Cordeiro, Q., Souza, B.R., Correa, H., Guindalini, C., Hutz, M.H., Vallada, H., Romano-Silva,
              M.A., 2009b. A review of psychiatric genetics research in the Brazilian population. Rev. Bras.
              Psiquiatr. 31 (2), 154–162.
           Cordeiro, Q., Talkowski, M.E., Chowdari, K.V., Wood, J., Nimgaonkar, V., Vallada, H., 2005. Asso-
              ciation and linkage analysis of RGS4 polymorphisms with schizophrenia and bipolar disorder
              in Brazil. Genes Brain Behav. 4 (1), 45–50. doi: 10.1111/j.1601-183x.2004.00096.x.
           Cordeiro, Q., Talkowski, M., Wood, J., Ikenaga, E., Vallada, H., 2004. Lack of association between
              VNTR polymorphism of dopamine transporter gene (SLC6A3) and schizophrenia in a Brazil-
              ian sample. Arq Neuropsiquiatr. 62 (4), 973–976, /S0004-282x2004000600008.
           Corregiari, F.M., Bernik, M., Cordeiro, Q., Vallada, H., 2012. Endophenotypes and serotonergic
              polymorphisms associated with treatment response in obsessive-compulsive disorder. Clinics
              (Sao Paulo) 67 (4), 335–340.
           Costa Dde, S., Rosa, D.V., Barros, A.G., Romano-Silva, M.A., Malloy-Diniz, L.F., Mattos, P., de
              Miranda, D.M., 2015. Telomere length is highly inherited and associated with hyperactivity-
              impulsivity in children with attention deficit/hyperactivity disorder. Front. Mol. Neurosci. 8
              (28)doi: 10.3389/fnmol.2015.00028.
   125   126   127   128   129   130   131   132   133   134   135