[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100061146":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":8,"centralContacts":13,"locations":22,"responsibleParty":41,"collaborators":44,"id":50,"slug":51,"hasResults":52,"nctId":53,"briefTitle":54,"officialTitle":54,"acronym":7,"eligibilityCriteria":55,"healthyVolunteers":52,"sex":56,"minAge":7,"maxAge":7,"enrollmentInfo":57,"targetDuration":7,"studyType":60,"phases":7,"briefSummary":61,"conditions":62,"keywords":67,"overallStatus":25,"whyStopped":7,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":88},{"fullName":5,"class":6},"Harvard University Faculty of Medicine","OTHER",null,[9],{"name":10,"affiliation":11,"role":12},"Christopher A. Walsh, M.D., Ph.D.","Harvard Institutes of Medicine","PRINCIPAL_INVESTIGATOR",[14,19],{"name":15,"role":16,"phone":17,"phoneExt":7,"email":18},"Jennifer Neil, MS","CONTACT","617-919-2865","walshresearch@childrens.harvard.edu",{"name":20,"role":16,"phone":21,"phoneExt":7,"email":7},"Abbe Lai, MS","617-919-4371",[23],{"facility":24,"status":25,"city":26,"state":27,"zip":28,"country":29,"countryCode":30,"cosmosGeoPoint":31,"geoPoint":36,"contacts":37},"Boston Children's Hospital, Walsh Laboratory","RECRUITING","Boston","Massachusetts","02115","United States","US",{"type":32,"coordinates":33},"Point",[34,35],-71.05977,42.35843,{"lat":35,"lon":34},[38,39,40],{"name":15,"role":16,"phone":17,"phoneExt":7,"email":18},{"name":20,"role":16,"phone":21,"phoneExt":7,"email":7},{"name":10,"role":12,"phone":7,"phoneExt":7,"email":7},{"type":12,"investigatorFullName":42,"investigatorTitle":43,"investigatorAffiliation":5,"oldNameTitle":7,"oldOrganization":7},"Dr. Chris Walsh","Investigator",[45,48],{"name":46,"class":47},"National Institute of Neurological Disorders and Stroke (NINDS)","NIH",{"name":49,"class":6},"Howard Hughes Medical Institute","100061146","human-epilepsy-genetics--neuronal-migration-disorders-study-100061146",false,"NCT00041600","Human Epilepsy Genetics--Neuronal Migration Disorders Study","INCLUSION:\n\n* Males and females of any age.\n* Persons with a brain malformation or disorder of cognition (familial intellectual disability \\[previously known as mental retardation\\] or autism).\n\nEXCLUSION:\n\n* Persons without a brain malformation or disorder of cognition (familial intellectual disability (previously known as mental retardation\\] or autism).","ALL",{"count":58,"type":59},3500,"ESTIMATED","OBSERVATIONAL","The purpose of this study is to identify genes responsible for epilepsy, brain malformations and disorders of human cognition.",[63,64,65,66],"Brain Malformation","Neuronal Migration Disorder","Cognition Disorder","Epilepsy",[68,69,70,71,72,73,74,75,76,77,78],"epilepsy","seizures","disorders of human cognition","neuronal migration","neuronal migration disorders","lissencephaly","schizencephaly","polymicrogyria","heterotopia","microcephaly","pachygyria","2023-09-20",{"date":81,"type":82},"2023-09-21","ACTUAL",{"date":84,"type":7},"1996-04",{"date":86,"type":59},"2030-06",{"name":5,"class":6},1]