Catalina Betancur
8PUBLICATIONS
63CO-AUTHORS
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Publications (8)
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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
|Oct 01, 2024
Phenome-wide profiling identifies genotype-phenotype associations in Phelan-McDermid syndrome using family-sourced data from an international registry.Rui Yin, Maxime Wack, Claire Hassen-Khodja
|Sep 29, 2023
Organic cation transporter 2 contributes to SSRI antidepressant efficacy by controlling tryptophan availability in the brain.Alejandro Orrico-Sanchez, Bruno P Guiard, Stella Manta
|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
|Apr 23, 2020
A framework for an evidence-based gene list relevant to autism spectrum disorder.Christian P Schaaf, Catalina Betancur, Ryan K C Yuen
|Dec 28, 2019
Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literature.Alexander Kolevzon, Elsa Delaby, Elizabeth Berry-Kravis
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Frequent Collaborators
4 joint publications
Joseph D Buxbaum
3 joint publications
Silvia De Rubeis
3 joint publications
Mark J Daly
2 joint publications
Rebecca Schmidt
2 joint publications
Ana Cristina Girardi
2 joint publications
Edwin H Cook
2 joint publications
Margaret Pericak-Vance
2 joint publications
Alexander Kolevzon
1 joint publications
Paige M Siper
1 joint publications
Danielle Halpern
