Number of rare germline CNVs and TP53 mutation types

Por Silva, Amanda G, Achatz, Isabel Maria W, Krepischi, Ana CV, Pearson, Peter L, Rosenberg, Carla
Publicado em 2012

Mutational spectrum of WTX, WT1, CTNNB1, APC and PLCG2 genes in Wilms tumor defined by massive parallel resequencing

Por Barros, Bruna D, Torrezan, Giovana T, Ferreira, Elisa N, Maschietto, Mariana, Krepíschi, Ana CV, Carraro, Dirce M
Publicado em 2012

The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations

Por Silva, Amanda G, Krepischi, Ana CV, Pearson, Peter L, Hainaut, Pierre, Rosenberg, Carla, Achatz, Maria Isabel
Publicado em 2014

Breakpoint characterization of a novel large intragenic deletion of MUTYH detected in a MAP patient: Case report

Por Torrezan, Giovana T, da Silva, Felipe CC, Krepischi, Ana CV, Santos, Érika MM, de O Ferreira, Fábio, Rossi, Benedito M, Carraro, Dirce M
Publicado em 2011

LINE-1 hypermethylation in peripheral blood of cutaneous melanoma patients is associated with metastasis

Por De Araújo, Érica S.S., Kashiwabara, André Y., Achatz, Maria I.W., Moredo, Luciana F., De Sá, Bianca C.S., Duprat, João P., Rosenberg, Carla, Carraro, Dirce M., Krepischi, Ana C.V.
Publicado no Melanoma Res (2015)

Co-expression network of neural-differentiation genes shows specific pattern in schizophrenia

Por Maschietto, Mariana, Tahira, Ana C, Puga, Renato, Lima, Leandro, Mariani, Daniel, da Silveira Paulsen, Bruna, Belmonte-de-Abreu, Paulo, Vieira, Henrique, Krepischi, Ana CV, Carraro, Dirce M, Palha, Joana A, Rehen, Stevens, Brentani, Helena
Publicado no BMC Med Genomics (2015)

Germline DNA copy number variation in familial and early-onset breast cancer

Por Krepischi, Ana CV, Achatz, Maria Isabel W, Santos, Erika MM, Costa, Silvia S, Lisboa, Bianca CG, Brentani, Helena, Santos, Tiago M, Gonçalves, Amanda, Nóbrega, Amanda F, Pearson, Peter L, Vianna-Morgante, Angela M, Carraro, Dirce M, Brentani, Ricardo R, Rosenberg, Carla
Publicado em 2012

Does germ-line deletion of the PIP gene constitute a widespread risk for cancer?

Por Silva, Amanda G, Krepischi, Ana CV, Torrezan, Giovana T, Capelli, Leonardo P, Carraro, Dirce M, D'Angelo, Carla S, Koiffmann, Celia P, Zatz, Mayana, Naslavsky, Michel S, Masotti, Cibele, Otto, Paulo A, Achatz, Maria IW, Mills, Ryan E, Lee, Charles, Pearson, Peter L, Rosenberg, Carla
Publicado em 2014

Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes

Por Carvalho, Claudia M.B., Vasanth, Shivakumar, Shinawi, Marwan, Russell, Chad, Ramocki, Melissa B., Brown, Chester W., Graakjaer, Jesper, Skytte, Anne-Bine, Vianna-Morgante, Angela M., Krepischi, Ana C.V., Patel, Gayle S., Immken, LaDonna, Aleck, Kyrieckos, Lim, Cynthia, Cheung, Sau Wai, Rosenberg, Carla, Katsanis, Nicholas, Lupski, James R.
Publicado no Am J Hum Genet (2014)