Abreu-Silva RS, Rincon D, Horimoto AR, Sguillar AP, Ricardo LA, Kimura L, Batissoco AC, Auricchio MT, Otto PA, Mingroni-Netto R C. The search of a genetic basis for noise-induced hearing loss (NIHL). Annals of Human Biology; 38(2):210-8, 2011

Angeli CB, Kimura L, Auricchio MTBM, Vicente JP, Mattevi VS, Zembrzuski VM, Hutz MH, Pereira AC, Pereira TV, Mingroni-Netto RC. Multilocus analyses of seven candidate genes suggest interacting pathways for obesity-related traits in Brazilian populations. Obesity 19: 1244-1251, 2011

Araújo LV, Malkowski S, Braghetto KR, Passos-Bueno MR, Zatz M, Pu C, Ferreira JE. A rigorous approach to facilitate and guarantee the correctness of the genetic testing management in human genome information systems. BMC Genomics. 2011 Dec 22;12 Suppl 4:S13. doi: 10.1186/1471-2164-12-S4-S13. Epub 2011 Dec 22.

Bertola D, Aguena M, Yamamoto G, Ae Kim C, Passos-Bueno MR. Obesity in pycnodysostosis due to UPD1: possible effect of an imprinted gene on chromosome 1. Am J Med Genet A. 2011 Jun; 155A(6):1483-6. 

Boing AF, Antunes JLF, de Carvalho MB, de Gois Filho JF, Kowalski LP, Michaluart P, Gencapo, Okamoto OK, Eluf-Neto J, Boffetta P, Wunsch-Filho V. How much do smoking and alcohol consumption explain socioeconomic inequalities in head and neck cancer risk? Journal of Epidemiology and Community Health, v. 65, p. 709-714, 2011.

Bonaldi A; Mazzeu JF; Costa SS; Honjo RS; Bertola DR; Albano LMJ; Furquim IM; Kim CA; Vianna-Morgante AM. Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver-Russell syndrome. Am J Med Genet A. 2011 Oct;155A (10):2479-83

Brito LA, Cruz LA, Rocha KM, Barbara LK, Silva CB, Bueno DF, Aguena M, Bertola DR, Franco D, Costa AM, Alonso N, Otto PA, Passos-Bueno MR. Genetic contributions for non-syndromic cleft lip with or without cleft palate (NS CL/P) in different regions of Brazil and implications for association studies.  Am J Med Genet A. 2011 Jul; 155(7):1581-7.

Amorim S, Otto Helse C, Santos S, Macedo-Souza LI, Zatz M, Kok F. Nerve conduction studies in spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome. Department of Neurology, University of São Paulo School of Medicine, São Paulo, Brazil. Célula 1Célula 2Célula 3Célula 4