Gabriele da Silva Campos

5PUBLICATIONS
43CO-AUTHORS
Developmental genetics (incl. sex determination)NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|Dec 21, 2025
Catatonia and regression in an autism spectrum disorder patient harbouring a BRSK2 frameshift mutation.

Andrea Laurato Sertié, Raphaella Josino, Vitória Rezende Goll

|Mar 06, 2025
Understanding rare variant contributions to autism: lessons from dystrophin-deficient model.

Claudia Ismania Samogy Costa, Luciana Madanelo, Jaqueline Yu Ting Wang

|Jun 06, 2023
Three generation families: Analysis of de novo variants in autism.

Claudia I Samogy Costa, Gabriele da Silva Campos, Eduarda Morgana da Silva Montenegro

|Aug 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.

Jack M Fu, F Kyle Satterstrom, Minshi Peng

|May 02, 2022
Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in Drosophila.

Angelina Palacios-Muñoz, Danielle de Paula Moreira, Valeria Silva

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Frequent Collaborators

4 joint publications

Maria Rita Passos-Bueno

2 joint publications

Stephen W Scherer

2 joint publications

Ana Cristina Girardi

1 joint publications

Angelina Palacios-Muñoz