Ana Cristina Girardi
5PUBLICATIONS
41CO-AUTHORS
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Publications (5)
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|Mar 30, 2026
Deleterious coding variation associated with autism is shared across ancestries.Marina Natividad Avila, Seulgi Jung, F Kyle Satterstrom
|Jan 31, 2026
"SHANK3 deficiency alters early progenitor dynamics and reveals shared pathways with neurodegeneration".Elisa Varella-Branco, Elizabeth Shephard, Victor H C Toledo
|Mar 06, 2025
Understanding rare variant contributions to autism: lessons from dystrophin-deficient model.Claudia Ismania Samogy Costa, Luciana Madanelo, Jaqueline Yu Ting Wang
|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
|Jan 04, 2022
FMR1 premutation in children with autism spectrum disorders: Should additional diagnostic tests be performed?Ana Cristina De Sanctis Girardi, Vanessa Naomi van Opstal Takahashi, Estevão Vadasz
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Frequent Collaborators
2 joint publications
Edwin H Cook
2 joint publications
Gabriele da Silva Campos
2 joint publications
Catalina Betancur
2 joint publications
Silvia De Rubeis
2 joint publications
Maria Rita Passos-Bueno
2 joint publications
Joseph D Buxbaum
2 joint publications
Mark J Daly
2 joint publications
Margaret Pericak-Vance
2 joint publications
Rebecca Schmidt
1 joint publications
Elizabeth Shephard
