Page 134 - Genomic Medicine in Emerging Economies
P. 134

References   123




           Gregório, S.P., Mury, F.B., Ojopi, E.B., Sallet, P.C., Moreno, D.H., Yacubian, J., Dias-Neto, E., 2005.
              Nogo CAA 3’UTR Insertion polymorphism is not associated with Schizophrenia nor with
              bipolar disorder. Schizophr. Res. 75 (1), 5–9. doi: 10.1016/j.schres.2004.11.010.
           Guerra, M., Ferri, C.P., Sosa, A.L., Salas, A., Gaona, C., Gonzales, V., Prince, M., 2009. Late-life
              depression in Peru, Mexico and Venezuela: the 10/66 population-based study. Br. J. Psychiatry
              195 (6), 510–515. doi: 10.1192/bjp.bp.109.064055.
           Guimaraes, A.P., Schmitz, M., Polanczyk, G.V., Zeni, C., Genro, J., Roman, T., Hutz, M.H., 2009a.
              Further evidence for the association between attention deficit/hyperactivity disorder and the
              serotonin receptor 1B gene. J. Neural Transm. (Vienna) 116 (12), 1675–1680. doi: 10.1007/
              s00702-009-0305-y.
           Guimaraes, A.P., Zeni, C., Polanczyk, G., Genro, J.P., Roman, T., Rohde, L.A., Hutz, M.H., 2009b.
              MAOA is associated with methylphenidate improvement of oppositional symptoms in boys
              with attention deficit hyperactivity disorder. Int. J. Neuropsychopharmacol. 12 (5), 709–714.
              doi: 10.1017/s1461145709000212.
           Guimaraes, A.P., Zeni, C., Polanczyk, G.V., Genro, J.P., Roman, T., Rohde, L.A., Hutz, M.H., 2007.
              Serotonin genes and attention deficit/hyperactivity disorder in a Brazilian sample: preferential
              transmission of the HTR2A 452His allele to affected boys. Am. J Med. Genet. B Neuropsychi-
              atr. Genet. 144B (1), 69–73. doi: 10.1002/ajmg.b.30400.
           Guio-Vega, G.P., Forero, D.A., 2017. Functional genomics of candidate genes derived from
              genome-wide association studies for five common neurological diseases. Int. J. Neurosci. 127
              (2), 118–123. doi: 10.3109/00207454.2016.1149172.
           Hernandez, H.G., Mahecha, M.F., Mejia, A., Arboleda, H., Forero, D.A., 2014. Global long
              interspersed nuclear element 1 DNA methylation in a Colombian sample of patients with
              late-onset Alzheimer’s disease. Am. J. Alzheimers Dis. Other Demen. 29 (1), 50–53. doi:
              10.1177/1533317513505132.
           Hernandez, S., Camarena, B., Gonzalez, L., Caballero, A., Flores, G., Aguilar, A., 2016. A family-
              based association study of the HTR1B gene in eating disorders. Rev. Bras. Psiquiatr 38 (3),
              239–242. doi: 10.1590/1516-4446-2016-1936.
           Hounie, A.G., Cappi, C., Cordeiro, Q., Sampaio, A.S., Moraes, I., Rosario, M.C., Miguel, E.C., 2008.
              TNF-alpha polymorphisms are associated with obsessive-compulsive disorder. Neurosci. Lett.
              442 (2), 86–90. doi: 10.1016/j.neulet.2008.07.022.
           Isordia-Salas, I., Barinagarrementeria-Aldatz, F., Leanos-Miranda, A., Borrayo-Sanchez, G.,
              Vela-Ojeda, J., Garcia-Chavez, J., Majluf-Cruz, A., 2010. The C677T polymorphism of the meth-
              ylenetetrahydrofolate reductase gene is associated with idiopathic ischemic stroke in the young
              Mexican-Mestizo population. Cerebrovasc. Dis. 29 (5), 454–459. doi: 10.1159/000289349.
           Jimenez-Castro, L., Raventos-Vorst, H., Escamilla, M., 2011. Substance use disorder and schizo-
              phrenia: prevalence and sociodemographic characteristics in the Latin American population.
              Actas Esp Psiquiatr. 39 (2), 123–130.
           Junqueira, R., Cordeiro, Q., Meira-Lima, I., Gattaz, W.F., Vallada, H., 2004. Allelic association
              analysis of phospholipase A2 genes with schizophrenia. Psychiatr. Genet. 14 (3), 157–160.
           Karam, S.M., Barros, A.J., Matijasevich, A., Dos Santos, I.S., Anselmi, L., Barros, F., Black, M.M.,
              2016. Intellectual disability in a birth cohort: prevalence, etiology, and determinants at the age
              of 4 years. Public Health Genomics 19 (5), 290–297. doi: 10.1159/000448912.
           Kisely, S., Alichniewicz, K.K., Black, E.B., Siskind, D., Spurling, G., Toombs, M., 2017. The preva-
              lence of depression and anxiety disorders in indigenous people of the Americas: a systematic
              review and meta-analysis. J. Psychiatr. Res. 84, 137–152. doi: 10.1016/j.jpsychires.2016.09.032.
           Kohlrausch,  F.B.,  Gama,  C.S.,  Lobato,  M.I.,  Belmonte-de-Abreu,  P.,  Callegari-Jacques,  S.M.,
              Gesteira, A., Hutz, M.H., 2008a. Naturalistic pharmacogenetic study of treatment resis-
              tance to typical neuroleptics in European-Brazilian schizophrenics. Pharmacogenet. Genomics
              18 (7), 599–609. doi: 10.1097/FPC.0b013e328301a763.
   129   130   131   132   133   134   135   136   137   138   139