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References   127




           Pena, S.D., Di Pietro, G., Fuchshuber-Moraes, M., Genro, J.P., Hutz, M.H., Kehdy Fde, S.,
              Suarez-Kurtz, G., 2011. The genomic ancestry of individuals from different geographical re-
              gions of Brazil is more uniform than expected. PLoS One 6 (2), e17063. doi: 10.1371/journal.
              pone.0017063.
           Peñas-lledó, E.M., Trejo, H.D., Dorado, P., Ortega, A., Jung, H., Alonso, E., Llerena, A., 2013.
              CYP2D6 ultrarapid metabolism and early dropout from fluoxetine or amitriptyline mono-
              therapy treatment in major depressive patients. Mol. Psychiatry 18 (1), 8–9. doi: 10.1038/
              mp.2012.91.
           Peralta-Leal, V., Leal-Ugarte, E., Meza-Espinoza, J.P., Gutierrez-Angulo, M., Hernandez-Benitez,
              C.T., Garcia-Rodriguez, A., Duran-Gonzalez, J., 2012. Association of serotonin transporter
              gene polymorphism 5-HTTLPR and depressive disorder in a Mexican population. Psychiatr.
              Genet. 22 (5), 265–266. doi: 10.1097/YPG.0b013e32834f3577.
           Perea, C.S., Nino, C.L., Lopez-Leon, S., Gutierrez, R., Ojeda, D., Arboleda, H., Forero, D.A., 2014.
              Study of a functional polymorphism in the PER3 gene and diurnal preference in a Colombian
              Sample. Open Neurol. J. 8, 7–10. doi: 10.2174/1874205x01408010007.
           Pereira, P.A., Bicalho, M.A., de Moraes, E.N., Malloy-Diniz, L., Bozzi, I.C., Nicolato, R., Romano-
              Silva, M.A., 2014. Genetic variant of AKT1 and AKTIP associated with late-onset depression
              in a Brazilian population. Int. J. Geriatr. Psychiatry 29 (4), 399–405. doi: 10.1002/gps.4018.
           Pereira, P.A., Romano-Silva, M.A., Bicalho, M.A., de Moraes, E.N., Malloy-Diniz, L., Pimenta, G.J.,
              Miranda, D.M., 2012. Catechol-O-methyltransferase genetic variant associated with the risk of
              Alzheimer’s disease in a Brazilian population. Dement Geriatr. Cogn. Disord. 34 (2), 90–95.
              doi: 10.1159/000341578.
           Pereira Pde, A., Romano-Silva, M.A., Bicalho, M.A., De Marco, L., Correa, H., de Campos, S.B.,
              de Miranda, D.M., 2011. Association between tryptophan hydroxylase-2 gene and late-onset
              depression. Am. J. Geriatr. Psychiatry 19 (9), 825–829. doi: 10.1097/JGP.0b013e31820eeb21.
           Polanczyk, G., Zeni, C., Genro, J.P., Guimaraes, A.P., Roman, T., Hutz, M.H., Rohde, L.A., 2007.
              Association of the adrenergic alpha2A receptor gene with methylphenidate improvement of
              inattentive symptoms in children and adolescents with attention-deficit/hyperactivity disor-
              der. Arch. Gen. Psychiatry 64 (2), 218–224. doi: 10.1001/archpsyc.64.2.218.
           Prestes, A.P., Marques, F.Z., Hutz, M.H., Bau, C.H., 2007. The GNB3 C825T polymorphism and
              depression among subjects with alcohol dependence. J. Neural Transm. (Vienna) 114 (4),
              469–472. doi: 10.1007/s00702-006-0550-2.
           Prince, M., Bryce, R., Albanese, E., Wimo, A., Ribeiro, W., Ferri, C.P., 2013. The global prevalence
              of dementia: a systematic review and metaanalysis. Alzheimers Dement 9 (1), 63–75.e62. doi:
              10.1016/j.jalz.2012.11.007.
           Pringsheim, T., Jette, N., Frolkis, A., Steeves, T.D., 2014. The prevalence of Parkinson’s disease: a sys-
              tematic review and meta-analysis. Mov Disord. 29 (13), 1583–1590. doi: 10.1002/mds.25945.
           Quinones, L.A., Lavanderos, M.A., Cayun, J.P., Garcia-Martin, E., Agundez, J.A., Caceres, D.D.,
              Lares-Assef, I., 2014. Perception of the usefulness of drug/gene pairs and barriers for pharma-
              cogenomics in Latin America. Curr. Drug Metab. 15 (2), 202–208.
           Reynolds, G.P., Fachim, H.A., 2016. Does DNA methylation influence the effects of psychiatric
              drugs? Epigenomics 8 (3), 309–312. doi: 10.2217/epi.15.116.
           Rocha, F.F., Alvarenga, N.B., Lage, N.V., Romano-Silva, M.A., Marco, L.A., Correa, H., 2011.
              Associations between polymorphic variants of the tryptophan hydroxylase 2 gene and obses-
              sive-compulsive disorder. Rev. Bras. Psiquiatr. 33 (2), 176–180.
           Rocha, F.F., Malloy-Diniz, L., Lage, N.V., Correa, H., 2010. Positive association between MET allele
              (BDNF Val66Met polymorphism) and obsessive-compulsive disorder. Rev. Bras. Psiquiatr. 32
              (3), 323–324.
           Rocha, F.F., Marco, L.A., Romano-Silva, M.A., Corrêa, H., 2009. Obsessive-compulsive disorder and
              5-HTTLPR. Rev. Bras. Psiquiatr. 31 (3), 287–288, PMID: 19784500.
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