Human Epilepsy Genetics--Neuronal Migration Disorders Study
RecruitingObservational study
Who can join
All ages · All sexes
Full eligibility criteria
INCLUSION: * Males and females of any age. * Persons with a brain malformation or disorder of cognition (familial intellectual disability \[previously known as mental retardation\] or autism). EXCLUSION: * Persons without a brain malformation or disorder of cognition (familial intellectual disability (previously known as mental retardation\] or autism).
About the study
The purpose of this study is to identify genes responsible for epilepsy, brain malformations and disorders of human cognition.
Sponsor: Harvard University Faculty of Medicine · Participants: 3,500 · Started: 1996-04
Contact the study team
- Jennifer Neil, MS · Phone: 617-919-2865
- Abbe Lai, MS · Phone: 617-919-4371
Official record on ClinicalTrials.gov — NCT00041600
Locations in the U.S.
| Massachusetts | Boston Children's Hospital, Walsh Laboratory, Boston |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.