Talita Ferreira Aguiar (Talita F M Aguiar, Ana C V Krepischi)

Publication Activity (10 Years)

Years Active: 2023-2023
Publications (10 Years): 6

Top Topics

Gestational Age

Magnetic Resonance

Multiple Myeloma

Top Venues

Science advances

Annals of human genetics

Pediatric blood & cancer

This page only lists publications with an associated author ORCID identifier.

Publications

Shunya Mashiko, Ronzon R Shihab, Sarah B See, Luca G Z Schahadat, Talita Ferreira Aguiar, Poulomi Roy, Fabrice Porcheray, Emmanuel Zorn
Broad responses to chemical adducts shape the natural antibody repertoire in early infancy. Science advances 9 (19) (2023)
Shunya Mashiko, Ronzon R Shihab, Sarah B See, Luca G Z Schahadat, Talita Ferreira Aguiar, Poulomi Roy, Fabrice Porcheray, Emmanuel Zorn
Broad responses to chemical adducts shape the natural antibody repertoire in early infancy. Science advances 9 (19) (2023)
Shunya Mashiko, Ronzon R Shihab, Sarah B See, Luca G Z Schahadat, Talita Ferreira Aguiar, Poulomi Roy, Fabrice Porcheray, Emmanuel Zorn
Broad responses to chemical adducts shape the natural antibody repertoire in early infancy. Science advances 9 (19) (2023)
Gustavo Dib Dangoni, Anne Caroline Barbosa Teixeira, Talita Ferreira Aguiar, Sofia Mizuho Miura Sugayama, Vicente Odone Filho, Débora Romeo Bertola, Ana Cristina Victorino Krepischi
A rare case of hepatoblastoma in a syndromic child with a de novo germline JAG1 mutation. Pediatric blood & cancer (2023)
Shunya Mashiko, Ronzon R Shihab, Sarah B See, Luca G Z Schahadat, Talita Ferreira Aguiar, Poulomi Roy, Fabrice Porcheray, Emmanuel Zorn
Broad responses to chemical adducts shape the natural antibody repertoire in early infancy. Science advances 9 (19) (2023)
Patricia C Mazzonetto, Darine Villela, Silvia Souza da Costa, Talita Ferreira Aguiar, Fernanda Milanezi, Michele P Migliavacca, Paulo M Pierry, Adriano Bonaldi, Luiz Gustavo D Almeida, Camila Alves De Souza, José Eduardo Kroll, Marcelo G Paula, Rodrigo Guarischi-Sousa, Cristovam Scapulatempo-Neto, Carla Rosenberg
Low-pass whole genome sequencing is a reliable and cost-effective approach for copy number variant analysis in the clinical setting. Annals of human genetics (2023)