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132 results

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Page 1
DRD1 rs4532 polymorphism: a potential pharmacogenomic marker for treatment response to antipsychotic drugs.
Ota VK, Spíndola LN, Gadelha A, dos Santos Filho AF, Santoro ML, Christofolini DM, Bellucco FT, Ribeiro-dos-Santos ÂK, Santos S, Mari Jde J, Melaragno MI, Bressan RA, Smith Mde A, Belangero SI. Ota VK, et al. Among authors: melaragno mi. Schizophr Res. 2012 Dec;142(1-3):206-8. doi: 10.1016/j.schres.2012.08.003. Epub 2012 Oct 1. Schizophr Res. 2012. PMID: 23036699
Deletion 22q11.2: report of a complex meiotic mechanism of origin.
Nogueira SI, Hacker AM, Bellucco FT, Kulikowski LD, Christofolini DM, Cernach MC, Melaragno MI, Emanuel BS. Nogueira SI, et al. Among authors: melaragno mi. Am J Med Genet A. 2007 Aug 1;143A(15):1778-81. doi: 10.1002/ajmg.a.31834. Am J Med Genet A. 2007. PMID: 17603802 Free PMC article.
Atypical 22q11.2 deletion in a patient with DGS/VCFS spectrum.
Nogueira SI, Hacker AM, Bellucco FT, Christofolini DM, Kulikowski LD, Cernach MC, Emanuel BS, Melaragno MI. Nogueira SI, et al. Among authors: melaragno mi. Eur J Med Genet. 2008 May-Jun;51(3):226-30. doi: 10.1016/j.ejmg.2008.02.001. Epub 2008 Feb 8. Eur J Med Genet. 2008. PMID: 18342595 Free PMC article.
Pure duplication 1q41-qter: further delineation of trisomy 1q syndromes.
Kulikowski LD, Bellucco FT, Nogueira SI, Christofolini DM, Smith Mde A, de Mello CB, Brunoni D, Melaragno MI. Kulikowski LD, et al. Among authors: melaragno mi. Am J Med Genet A. 2008 Oct 15;146A(20):2663-7. doi: 10.1002/ajmg.a.32510. Am J Med Genet A. 2008. PMID: 18798309
Evaluation of clinical checklists for fragile X syndrome screening in Brazilian intellectually disabled males: proposal for a new screening tool.
Christofolini DM, Abbud EM, Lipay MV, Costa SS, Vianna-Morgante AM, Bellucco FT, Nogueira SI, Kulikowski LD, Brunoni D, Juliano Y, Ramos MA, Melaragno MI. Christofolini DM, et al. Among authors: melaragno mi. J Intellect Disabil. 2009 Sep;13(3):239-48. doi: 10.1177/1744629509348429. J Intellect Disabil. 2009. PMID: 19786505
A rare case of trisomy 15pter-q21.2 due to a de novo marker chromosome.
Pacanaro AN, Christofolini DM, Kulikowski LD, Belangero SI, da Silva Bellucco FT, Varela MC, Koiffmann CP, Yoshimoto M, Squire JA, Schiavon AV, Heck B, Melaragno MI. Pacanaro AN, et al. Among authors: melaragno mi. Am J Med Genet A. 2010 Mar;152A(3):753-8. doi: 10.1002/ajmg.a.33308. Am J Med Genet A. 2010. PMID: 20186782
The UFD1L rs5992403 polymorphism is associated with age at onset of schizophrenia.
Ota VK, Belangero SI, Gadelha A, Bellucco FT, Christofolini DM, Mancini TI, Ribeiro-dos-Santos AK, Santos SE, Mari Jde J, Bressan RA, Melaragno MI, Smith Mde A. Ota VK, et al. Among authors: melaragno mi. J Psychiatr Res. 2010 Nov;44(15):1113-5. doi: 10.1016/j.jpsychires.2010.04.008. Epub 2010 May 14. J Psychiatr Res. 2010. PMID: 20471029 No abstract available.
132 results