Twenty-year cytogenetic and molecular follow-up of a patient with ring chromosome 15: a case report

por Guilherme, Roberta S, Meloni, Vera de FA, Takeno, Sylvia S, Pellegrino, Renata, Brunoni, Decio, Kulikowski, Leslie D, Melaragno, Maria I
Publicado 2012

Mechanisms of ring chromosome formation, ring instability and clinical consequences

por Guilherme, Roberta S, Ayres Meloni, Vera F, Kim, Chong A, Pellegrino, Renata, Takeno, Sylvia S, Spinner, Nancy B, Conlin, Laura K, Christofolini, Denise M, Kulikowski, Leslie D, Melaragno, Maria I
Publicado 2011

Marfan syndrome with a complex chromosomal rearrangement including deletion of the FBN1 gene

por Colovati, Mileny ES, da Silva, Luciana RJ, Takeno, Sylvia S, Mancini, Tatiane I, N Dutra, Ana R, Guilherme, Roberta S, de Mello, Cláudia B, Melaragno, Maria I, A Perez, Ana B
Publicado 2012

Catechol-O-methyltransferase (COMT) polymorphisms modulate working memory in individuals with schizophrenia and healthy controls

por Matsuzaka, Camila T., Christofolini, Denise, Ota, Vanessa K., Gadelha, Ary, Berberian, Arthur A., Noto, Cristiano, Mazzotti, Diego R., Spindola, Leticia M., Moretti, Patricia N., Smith, Marilia A.C., Melaragno, Maria I., Belangero, Sintia I.
Publicado 2017

PRODH Polymorphisms, Cortical Volumes and Thickness in Schizophrenia

por Ota, Vanessa K., Bellucco, Fernanda T., Gadelha, Ary, Santoro, Marcos L., Noto, Cristiano, Christofolini, Denise M., Assunção, Idaiane B., Yamada, Karen M., Ribeiro-dos-Santos, Ândrea K., Santos, Sidney, Mari, Jair J., Smith, Marília A. C., Melaragno, Maria I., Bressan, Rodrigo A., Sato, João R., Jackowski, Andrea P., Belangero, Sintia I.
Publicado 2014