Maria Rita Passos-Bueno

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 8

Top Topics

Autism Spectrum Disorder

Top Venues

Clinical genetics

European journal of human genetics : EJHG

Journal of medical genetics

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

Publications

Venceslas Douillard, Nayane Dos Santos Brito Silva, Sonia Bourguiba-Hachemi, Michel Satya Naslavsky, Marilia O Scliar, Yeda Aparecida de Oliveira Duarte, Mayana Zatz, Maria Rita Passos-Bueno, Sophie Limou, Pierre-Antoine Gourraud, Elise Launay, Erick da Cruz Castelli, Nicolas Vince, null null
Optimal population-specific HLA imputation with dimension reduction. HLA (2023)
Lucas Alvizi, Diogo Nani, Luciano Abreu Brito, Gerson Shigeru Kobayashi, Maria Rita Passos-Bueno, Roberto Mayor
Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene-environment interaction. Nature communications 14 (1) (2023)
Claudia I Samogy Costa, Gabriele Campos, Eduarda Morgana da Silva Montenegro, Jaqueline Yu Ting Wang, Marília Scliar, Frederico Monfardini, Elaine Cristina Zachi, Naila C V Lourenço, Ada J S Chan, Sergio L Pereira, Worrawat Engchuan, Bhooma Thiruvahindrapuram, Mehdi Zarrei, Stephen W Scherer, Maria Rita Passos-Bueno
Three generation families: Analysis of de novo variants in autism. European journal of human genetics : EJHG (2023)
Maria Rita Passos-Bueno, Claudia Ismania Samogy Costa, Mayana Zatz
Dystrophin genetic variants and autism. Discover mental health 2 (1) (2022)
Angelina Palacios-Muñoz, Danielle de Paula Moreira, Valeria Silva, Isaac E García, Francisco Aboitiz, Mehdi Zarrei, Gabriele Campos, Olivia Rennie, Jennifer L Howe, Evdokia Anagnostou, Patricia Ambrozewic, Stephen W Scherer, Maria Rita Passos-Bueno, John Ewer
Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in Drosophila. Molecular psychiatry 27 (8) (2022)
Claudia Ismania Samogy Costa, Eduarda Morgana da Silva Montenegro, Mehdi Zarrei, Eloísa de Sá Moreira, Isabela Maya Wahys Silva, Marília de Oliveira Scliar, Jaqueline Yu Ting Wang, Elaine Cristina Zachi, Elisa Varella Branco, Silvia Souza da Costa, Naila Cristina Vilaça Lourenço, Angela Maria Vianna-Morgante, Carla Rosenberg, Ana Cristina Victorino Krepischi, Stephen W Scherer, Maria Rita Passos-Bueno
Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes. Clinical genetics 101 (1) (2021)
Letícia Alves da Rocha, Lucas Vieira Lacerda Pires, Guilherme Lopes Yamamoto, José Ricardo Magliocco Ceroni, Rachel Sayuri Honjo, Edgard de Novaes França Bisneto, Luiz Antônio Nunes Oliveira, Carla Rosenberg, Ana Cristina Victorino Krepischi, Maria Rita Passos-Bueno, Chong Ae Kim, Debora Romeo Bertola
Congenital limb deficiency: Genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms. Clinical genetics 100 (5) (2021)
Vanessa Luiza Romanelli Tavares, Sofia Ligia Guimarães-Ramos, Yan Zhou, Cibele Masotti, Suzana Ezquina, Danielle de Paula Moreira, Henk Buermans, Renato S Freitas, Johan T Den Dunnen, Stephen R F Twigg, Maria Rita Passos-Bueno
New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements. Journal of medical genetics (2021)