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Brain Research|December 7, 2010
Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still countingCatalina Betancur
Current Opinion in Genetics & Development|June 30, 2020
Gene constraint and genotype-phenotype correlations in neurodevelopmental disordersCatalina Betancur, Joseph D Buxbaum
Molecular Autism|June 14, 2013
SHANK3 haploinsufficiency: a "common" but underdiagnosed highly penetrant monogenic cause of autism spectrum disordersCatalina Betancur, Joseph D Buxbaum
Trends in Neurosciences|June 23, 2009
The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disordersCatalina Betancur, Takeshi Sakurai, Joseph D Buxbaum
The European Journal of Neuroscience|June 28, 2005
The reinforcing effects of chronic D-amphetamine and morphine are impaired in a line of memory-deficient mice overexpressing calcineurinGrazyna Biala, Catalina Betancur, Isabelle M Mansuy, et al.
Medecine Sciences : M/S|December 4, 2003
[Genetics of autism: from genome scans to candidate genes]Stéphane Jamain, Catalina Betancur, Bruno Giros, et al.
Neurobiology of Aging|March 28, 2006
Altered expression of vesicular glutamate transporters VGLUT1 and VGLUT2 in Parkinson diseaseAlireza Kashani, Catalina Betancur, Bruno Giros, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 14, 2012
Network- and attribute-based classifiers can prioritize genes and pathways for autism spectrum disorders and intellectual disabilityYan Kou, Catalina Betancur, Huilei Xu, et al.
Molecular Autism|December 28, 2019
Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literatureAlexander Kolevzon, Elsa Delaby, Elizabeth Berry-Kravis, et al.
Journal of Neurodevelopmental Disorders|February 14, 2020
Psychiatric illness and regression in individuals with Phelan-McDermid syndromeTeresa M Kohlenberg, M Pilar Trelles, Brittany McLarney, et al.
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