True polyploid meiosis in the human male

por Pearson, Peter L., Madan, Kamlesh
Publicado 2018

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 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 2014

Germline DNA copy number variation in individuals with Argyrophilic grain disease reveals CTNS as a plausible candidate gene

por Villela, Darine, Kimura, Lilian, Schlesinger, David, Gonçalves, Amanda, Pearson, Peter L., Suemoto, Claudia K., Pasqualucci, Carlos, Krepischi, Ana Cristina, Grinberg, Lea T., Rosenberg, Carla
Publicado 2013

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 2012

Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil

por Krepischi, Ana C. V., Villela, Darine, da Costa, Silvia Souza, Mazzonetto, Patricia C., Schauren, Juliana, Migliavacca, Michele P., Milanezi, Fernanda, Santos, Juliana G., Guida, Gustavo, Guarischi-Sousa, Rodrigo, Campana, Gustavo, Kok, Fernando, Schlesinger, David, Kitajima, Joao Paulo, Campagnari, Francine, Bertola, Debora R., Vianna-Morgante, Angela M., Pearson, Peter L., Rosenberg, Carla
Publicado 2022