ABOUT OUR RESEARCH
Developmental disorders of the human brain can cause epilepsy, intellectual disability and/or autism. We study the genetics and molecular biology of the developing cerebral cortex, the brain's largest structure, to advance the understanding, diagnosis and management of human neurological disease.
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PUBLICATIONS
Our research achievements are peer-reviewed and published in collaboration with other scientists and clinicians around the world.

METTL23, a transcriptional partner of GABPA, is essential for human cognition

Inherited mutations of SLC25A22.
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PARTICIPATE IN RESEARCH
The generous participation of many families makes our research possible. Their involvement helps us better understand disorders of the human brain and leads us to gene discovery, a key step toward improving clinical care.

Please contact us about your eligibility.
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SPECIALTY CLINICS
The Brain Development and Genetics Clinic offers consultation for children with developmental brain disorders and their families. Our physicians will review brain MRIs and medical history to help provide the best diagnosis and management options available.

Christopher Walsh, MD, PhD
Annapurna Poduri, MD, MPH
Mustafa Sahin, MD, PhD
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