NIH-funded research R01 grant

Context-dependent disease mechanisms in neurodevelopmental disorders (16p11.2)

Official title: Context-dependent disease mechanisms of neurodevelopmental disorders

Funded at University of California Los Angeles · NIH-11366753 · Data updated 2026-11-12

A human-cell study from UCLA will explore how genetic risk for autism and ADHD affects early brain development, using patient-derived stem cells to test how cells respond to developmental signals.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of California Los Angeles
NIH-funded
Lab location1 site (Los Angeles, United States)
Project startJuly 16, 2026
Project endApril 30, 2031
Funding year2026
Award (this year)$764,785
NIH project number1R01MH140813-01A1
Project IDNIH-11366753 on NIH RePORTER

Who could benefit from this research

Could help

Individuals with neurodevelopmental disorders, including autism and ADHD, who carry the 16p11.2 deletion or related genetic risk factors.

Less likely to help

Patients without the 16p11.2 deletion or similar genetic risk may not directly benefit from this mechanistic study.

What this research studies

This project uses a novel stem cell platform called the cell village to study fetal brain cells carrying the 16p11.2 risk deletion. Researchers will expose these cells to key developmental signals and measure molecular and cellular responses to understand context-dependent disease mechanisms. The goal is to uncover signatures and pathways that underlie neurodevelopmental disorders like autism and ADHD, with a focus on how genetic risk shapes early brain development. The work is designed to connect basic biology to potential future interventions by revealing when and how these pathways go awry.

Why it matters

Potential benefit: Understanding context-specific brain development in people with 16p11.2 deletions could guide new approaches to early diagnosis and targeted therapies for autism and ADHD.

How similar studies have gone: Previous work has linked 16p11.2 deletions to neurodevelopmental changes; this project builds on that by testing responses to developmental signals in a high-throughput human cell platform.

Where this research is happening

  • University of California Los Angeles
    Los Angeles, United States
    Active

Researchers

  • Principal investigator: Wells, Michael Frederick — University of California Los Angeles
  • Study coordinator: Wells, Michael Frederick

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.