Last Updated: 09/26/2026
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Found 32 publications
The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait.
Journal: Genes
Published: July 21, 2023
Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments.
Journal: International journal of molecular sciences
Published: June 17, 2023
Common genetic risk factors in ASD and ADHD co-occurring families.
Journal: Human genetics
Published: August 02, 2022
Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses.
Journal: Stem cell reports
Published: July 13, 2022
Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses.
Journal: Stem cell reports
Published: June 26, 2020
Characterization hiPSC-derived neural progenitor cells and neurons to investigate the role of NOS1AP isoforms in human neuron dendritogenesis.
Journal: Molecular and cellular neurosciences
Published: May 04, 2020
Childhood maltreatment, serotonin transporter gene, and risk for callous and unemotional traits: A prospective investigation.
Journal: Psychiatry research
Published: January 16, 2020
Social (Pragmatic) Communication Disorder: Another name for the Broad Autism Phenotype?
Journal: Autism : the international journal of research and practice
Published: April 02, 2019
Within-task variability on standardized language tests predicts autism spectrum disorder: a pilot study of the Response Dispersion Index.
Journal: Journal of neurodevelopmental disorders
Published: February 12, 2019
Last Updated: 09/26/2026