Last Updated: 09/26/2026
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Found 22 publications
Clinical, cellular, and genomic consequences of a population-enriched SETD1A missense variant.
Journal: Research square
Published: July 29, 2026
Clinical, cellular, and genomic consequences of a population-enriched SETD1A missense variant.
Journal: Research square
Published: July 29, 2026
Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental Disorders.
Journal: bioRxiv : the preprint server for biology
Published: June 26, 2025
A rare variant in GPR156 associated with depression in a Mennonite pedigree causes habenula hyperactivity and stress sensitivity in mice.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 14, 2025
Genomic and Transcriptomic Signatures of SETD1A Disruption in Human Excitatory Neuron Development and Psychiatric Disease Risk.
Journal: bioRxiv : the preprint server for biology
Published: April 08, 2025
Prevalence and incidence measures for schizophrenia among commercial health insurance and medicaid enrollees.
Journal: Schizophrenia (Heidelberg, Germany)
Published: May 17, 2024
Aberrant pace of cortical neuron development in brain organoids from patients with 22q11.2 deletion syndrome-associated schizophrenia.
Journal: Nature communications
Published: October 26, 2023
Aberrant pace of cortical neuron development in brain organoids from patients with 22q11.2 deletion syndrome-associated schizophrenia.
Journal: bioRxiv : the preprint server for biology
Published: October 24, 2023
Inhibition of Abl Kinase by Imatinib Can Rescue the Compromised Barrier Function of 22q11.2DS Patient-iPSC-Derived Blood-Brain Barriers.
Journal: Cells
Published: December 08, 2022
High-impact rare genetic variants in severe schizophrenia.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: November 04, 2021
Last Updated: 09/26/2026