[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100061146":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":8,"centralContacts":13,"locations":22,"responsibleParty":40,"collaborators":43,"id":49,"slug":7,"hasResults":50,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":7,"eligibilityCriteria":53,"healthyVolunteers":50,"sex":54,"minAge":7,"maxAge":7,"enrollmentInfo":55,"targetDuration":7,"studyType":58,"phases":7,"briefSummary":59,"conditions":60,"keywords":65,"overallStatus":25,"whyStopped":7,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"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,"cosmosGeoPoint":30,"geoPoint":35,"contacts":36},"Boston Children's Hospital, Walsh Laboratory","RECRUITING","Boston","Massachusetts","02115","United States",{"type":31,"coordinates":32},"Point",[33,34],-71.05977,42.35843,{"lat":34,"lon":33},[37,38,39],{"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":41,"investigatorTitle":42,"investigatorAffiliation":5,"oldNameTitle":7,"oldOrganization":7},"Dr. Chris Walsh","Investigator",[44,47],{"name":45,"class":46},"National Institute of Neurological Disorders and Stroke (NINDS)","NIH",{"name":48,"class":6},"Howard Hughes Medical Institute","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":56,"type":57},3500,"ESTIMATED","OBSERVATIONAL","The purpose of this study is to identify genes responsible for epilepsy, brain malformations and disorders of human cognition.",[61,62,63,64],"Brain Malformation","Neuronal Migration Disorder","Cognition Disorder","Epilepsy",[66,67,68,69,70,71,72,73,74,75,76],"epilepsy","seizures","disorders of human cognition","neuronal migration","neuronal migration disorders","lissencephaly","schizencephaly","polymicrogyria","heterotopia","microcephaly","pachygyria","2023-09-20",{"date":79,"type":80},"2023-09-21","ACTUAL",{"date":82,"type":7},"1996-04",{"date":84,"type":57},"2030-06",{"name":5,"class":6},1]