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Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01238250
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:27:43.542889+00:00
Published At
2025-06-06T00:00:00+00:00
Record Updated At
2025-06-06
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["16P11.2 Deletion Syndrome", "16p11.2 Duplications", "1Q21.1 Deletion", "1Q21.1 Microduplication Syndrome (Disorder)", "ACTL6B", "ADNP", "AHDC1", "ANK2", "ANKRD11", "ARID1B", "ASH1L", "BCL11A", "CHAMP1", "CHD2", "CHD8", "CSNK2A1", "CTBP1", "CTNNB1 Gene Mutation", "CUL3", "DDX3X", "DNMT3A", "DSCAM", "DYRK1A", "FOXP1", "GRIN2A", "GRIN2B", "HIVEP2-Related Intellectual Disability", "HNRNPH2", "KATNAL2", "KDM5B", "KDM6B", "KMT2C Gene Mutation", "KMT2E", "KMT5B", "MBD5", "MED13L", "PACS1", "PPP2R5D-Related Intellectual Disability", "PTCHD1", "REST", "SCN2A Encephalopathy", "SETBP1 Gene Mutation", "SETD5", "SMARCA4 Gene Mutation", "SMARCC2", "STXBP1 Encephalopathy With Epilepsy", "SYNGAP1-Related Intellectual Disability", "TBR1", "ARHGEF9", "HNRNPU", "PPP3CA", "PPP2R1A", "SLC6A1", "2p16.3 Deletions", "5q35 Deletions", "5q35 Duplications", "7q11.23 Duplications", "15Q13.3 Deletion Syndrome", "16p11.2 Triplications", "16P12.2 Microdeletion", "16P13.11 Microdeletion Syndrome (Disorder)", "17Q12 Microdeletion Syndrome (Disorder)", "17Q12 Duplication Syndrome", "17Q21.31 Deletion Syndrome", "17q21.3 Duplications", "ACTB", "ADSL", "AFF2", "ALDH5A1", "ANK3", "ARX", "ATRX Gene Mutation", "AUTS2 Syndrome", "BCKDK", "BRSK2", "CACNA1C", "CAPRIN1", "CASK", "CASZ1", "CHD3", "CIC", "CNOT3", "CREBBP Gene Mutation", "CSDE1", "CTCF", "DEAF1", "DHCR7", "DLG4", "EBF3", "EHMT1", "EP300 Gene Mutation", "GIGYF1", "GRIN1", "GRIN2D", "IQSEC2-Related Syndromic Intellectual Disability", "IRF2BPL", "KANSL1", "KCNB1", "KDM3B", "NEXMIF", "KMT2A", "MBOAT7", "MEIS2", "MYT1L", "NAA15", "NBEA", "NCKAP1", "NIPBL", "NLGN2", "NLGN3", "NLGN4X", "NR4A2", "NRXN1", "NRXN2", "NSD1 Gene Mutation", "PHF21A", "PHF3", "PHIP", "POMGNT1", "PSMD12", "RELN", "RERE", "RFX3", "RIMS1", "RORB", "SCN1A", "SETD2 Gene Mutation", "SHANK2", "SIN3A", "SLC9A6", "SON", "SOX5", "SPAST", "SRCAP", "TAOK1", "TANC2", "TCF20", "TLK2", "TRIO", "TRIP12", "UPF3B", "USP9X", "VPS13B", "WAC", "WDFY3", "ZBTB20", "ZNF292", "ZNF462", "2Q37 Deletion Syndrome", "9q34 Duplications", "15q15 Deletions", "15Q24 Deletion", "NR3C2", "SYNCRIP", "2q34 Duplication", "2q37.3 Deletion", "6q16 Deletion", "15q11.2 BP1-BP2 Deletion", "16p13.3 Deletion", "17Q11.2 Microduplication Syndrome (Disorder)", "17p13.3", "Xq28 Duplication", "CLCN4", "CSNK2B", "DYNC1H1", "EIF3F", "GNB1", "MED13", "MEF2C", "RALGAPB", "SCN1B", "YY1", "Xp11.22 Duplication", "PACS2", "MAOA", "MAOB", "HNRNPC", "HNRNPD", "HNRNPK", "HNRNPR", "HNRNPUL2", "5P Deletion Syndrome", "TCF7L2 Gene Mutation", "HECW2"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-06-06"
protocolSection.identificationModule.nctId
"NCT01238250"
protocolSection.identificationModule.officialTitle
"Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • 16P11.2 Deletion Syndrome (protocolSection.conditionsModule.conditions)
  • 16p11.2 Duplications (protocolSection.conditionsModule.conditions)
  • 1Q21.1 Deletion (protocolSection.conditionsModule.conditions)
  • 1Q21.1 Microduplication Syndrome (Disorder) (protocolSection.conditionsModule.conditions)
  • ACTL6B (protocolSection.conditionsModule.conditions)
  • ADNP (protocolSection.conditionsModule.conditions)
  • AHDC1 (protocolSection.conditionsModule.conditions)
  • ANK2 (protocolSection.conditionsModule.conditions)
  • ANKRD11 (protocolSection.conditionsModule.conditions)
  • ARID1B (protocolSection.conditionsModule.conditions)
  • ASH1L (protocolSection.conditionsModule.conditions)
  • BCL11A (protocolSection.conditionsModule.conditions)
  • CHAMP1 (protocolSection.conditionsModule.conditions)
  • CHD2 (protocolSection.conditionsModule.conditions)
  • CHD8 (protocolSection.conditionsModule.conditions)
  • CSNK2A1 (protocolSection.conditionsModule.conditions)
  • CTBP1 (protocolSection.conditionsModule.conditions)
  • CTNNB1 Gene Mutation (protocolSection.conditionsModule.conditions)
  • CUL3 (protocolSection.conditionsModule.conditions)
  • DDX3X (protocolSection.conditionsModule.conditions)
  • DNMT3A (protocolSection.conditionsModule.conditions)
  • DSCAM (protocolSection.conditionsModule.conditions)
  • DYRK1A (protocolSection.conditionsModule.conditions)
  • FOXP1 (protocolSection.conditionsModule.conditions)
  • GRIN2A (protocolSection.conditionsModule.conditions)
  • GRIN2B (protocolSection.conditionsModule.conditions)
  • HIVEP2-Related Intellectual Disability (protocolSection.conditionsModule.conditions)
  • HNRNPH2 (protocolSection.conditionsModule.conditions)
  • KATNAL2 (protocolSection.conditionsModule.conditions)
  • KDM5B (protocolSection.conditionsModule.conditions)
  • KDM6B (protocolSection.conditionsModule.conditions)
  • KMT2C Gene Mutation (protocolSection.conditionsModule.conditions)
  • KMT2E (protocolSection.conditionsModule.conditions)
  • KMT5B (protocolSection.conditionsModule.conditions)
  • MBD5 (protocolSection.conditionsModule.conditions)
  • MED13L (protocolSection.conditionsModule.conditions)
  • PACS1 (protocolSection.conditionsModule.conditions)
  • PPP2R5D-Related Intellectual Disability (protocolSection.conditionsModule.conditions)
  • PTCHD1 (protocolSection.conditionsModule.conditions)
  • REST (protocolSection.conditionsModule.conditions)
  • SCN2A Encephalopathy (protocolSection.conditionsModule.conditions)
  • SETBP1 Gene Mutation (protocolSection.conditionsModule.conditions)
  • SETD5 (protocolSection.conditionsModule.conditions)
  • SMARCA4 Gene Mutation (protocolSection.conditionsModule.conditions)
  • SMARCC2 (protocolSection.conditionsModule.conditions)
  • STXBP1 Encephalopathy With Epilepsy (protocolSection.conditionsModule.conditions)
  • SYNGAP1-Related Intellectual Disability (protocolSection.conditionsModule.conditions)
  • TBR1 (protocolSection.conditionsModule.conditions)
  • ARHGEF9 (protocolSection.conditionsModule.conditions)
  • HNRNPU (protocolSection.conditionsModule.conditions)
  • PPP3CA (protocolSection.conditionsModule.conditions)
  • PPP2R1A (protocolSection.conditionsModule.conditions)
  • SLC6A1 (protocolSection.conditionsModule.conditions)
  • 2p16.3 Deletions (protocolSection.conditionsModule.conditions)
  • 5q35 Deletions (protocolSection.conditionsModule.conditions)
  • 5q35 Duplications (protocolSection.conditionsModule.conditions)
  • 7q11.23 Duplications (protocolSection.conditionsModule.conditions)
  • 15Q13.3 Deletion Syndrome (protocolSection.conditionsModule.conditions)
  • 16p11.2 Triplications (protocolSection.conditionsModule.conditions)
  • 16P12.2 Microdeletion (protocolSection.conditionsModule.conditions)
  • 16P13.11 Microdeletion Syndrome (Disorder) (protocolSection.conditionsModule.conditions)
  • 17Q12 Microdeletion Syndrome (Disorder) (protocolSection.conditionsModule.conditions)
  • 17Q12 Duplication Syndrome (protocolSection.conditionsModule.conditions)
  • 17Q21.31 Deletion Syndrome (protocolSection.conditionsModule.conditions)
  • 17q21.3 Duplications (protocolSection.conditionsModule.conditions)
  • ACTB (protocolSection.conditionsModule.conditions)
  • ADSL (protocolSection.conditionsModule.conditions)
  • AFF2 (protocolSection.conditionsModule.conditions)
  • ALDH5A1 (protocolSection.conditionsModule.conditions)
  • ANK3 (protocolSection.conditionsModule.conditions)
  • ARX (protocolSection.conditionsModule.conditions)
  • ATRX Gene Mutation (protocolSection.conditionsModule.conditions)
  • AUTS2 Syndrome (protocolSection.conditionsModule.conditions)
  • BCKDK (protocolSection.conditionsModule.conditions)
  • BRSK2 (protocolSection.conditionsModule.conditions)
  • CACNA1C (protocolSection.conditionsModule.conditions)
  • CAPRIN1 (protocolSection.conditionsModule.conditions)
  • CASK (protocolSection.conditionsModule.conditions)
  • CASZ1 (protocolSection.conditionsModule.conditions)
  • CHD3 (protocolSection.conditionsModule.conditions)
  • CIC (protocolSection.conditionsModule.conditions)
  • CNOT3 (protocolSection.conditionsModule.conditions)
  • CREBBP Gene Mutation (protocolSection.conditionsModule.conditions)
  • CSDE1 (protocolSection.conditionsModule.conditions)
  • CTCF (protocolSection.conditionsModule.conditions)
  • DEAF1 (protocolSection.conditionsModule.conditions)
  • DHCR7 (protocolSection.conditionsModule.conditions)
  • DLG4 (protocolSection.conditionsModule.conditions)
  • EBF3 (protocolSection.conditionsModule.conditions)
  • EHMT1 (protocolSection.conditionsModule.conditions)
  • EP300 Gene Mutation (protocolSection.conditionsModule.conditions)
  • GIGYF1 (protocolSection.conditionsModule.conditions)
  • GRIN1 (protocolSection.conditionsModule.conditions)
  • GRIN2D (protocolSection.conditionsModule.conditions)
  • IQSEC2-Related Syndromic Intellectual Disability (protocolSection.conditionsModule.conditions)
  • IRF2BPL (protocolSection.conditionsModule.conditions)
  • KANSL1 (protocolSection.conditionsModule.conditions)
  • KCNB1 (protocolSection.conditionsModule.conditions)
  • KDM3B (protocolSection.conditionsModule.conditions)
  • NEXMIF (protocolSection.conditionsModule.conditions)
  • KMT2A (protocolSection.conditionsModule.conditions)
  • MBOAT7 (protocolSection.conditionsModule.conditions)
  • MEIS2 (protocolSection.conditionsModule.conditions)
  • MYT1L (protocolSection.conditionsModule.conditions)
  • NAA15 (protocolSection.conditionsModule.conditions)
  • NBEA (protocolSection.conditionsModule.conditions)
  • NCKAP1 (protocolSection.conditionsModule.conditions)
  • NIPBL (protocolSection.conditionsModule.conditions)
  • NLGN2 (protocolSection.conditionsModule.conditions)
  • NLGN3 (protocolSection.conditionsModule.conditions)
  • NLGN4X (protocolSection.conditionsModule.conditions)
  • NR4A2 (protocolSection.conditionsModule.conditions)
  • NRXN1 (protocolSection.conditionsModule.conditions)
  • NRXN2 (protocolSection.conditionsModule.conditions)
  • NSD1 Gene Mutation (protocolSection.conditionsModule.conditions)
  • PHF21A (protocolSection.conditionsModule.conditions)
  • PHF3 (protocolSection.conditionsModule.conditions)
  • PHIP (protocolSection.conditionsModule.conditions)
  • POMGNT1 (protocolSection.conditionsModule.conditions)
  • PSMD12 (protocolSection.conditionsModule.conditions)
  • RELN (protocolSection.conditionsModule.conditions)
  • RERE (protocolSection.conditionsModule.conditions)
  • RFX3 (protocolSection.conditionsModule.conditions)
  • RIMS1 (protocolSection.conditionsModule.conditions)
  • RORB (protocolSection.conditionsModule.conditions)
  • SCN1A (protocolSection.conditionsModule.conditions)
  • SETD2 Gene Mutation (protocolSection.conditionsModule.conditions)
  • SHANK2 (protocolSection.conditionsModule.conditions)
  • SIN3A (protocolSection.conditionsModule.conditions)
  • SLC9A6 (protocolSection.conditionsModule.conditions)
  • SON (protocolSection.conditionsModule.conditions)
  • SOX5 (protocolSection.conditionsModule.conditions)
  • SPAST (protocolSection.conditionsModule.conditions)
  • SRCAP (protocolSection.conditionsModule.conditions)
  • TAOK1 (protocolSection.conditionsModule.conditions)
  • TANC2 (protocolSection.conditionsModule.conditions)
  • TCF20 (protocolSection.conditionsModule.conditions)
  • TLK2 (protocolSection.conditionsModule.conditions)
  • TRIO (protocolSection.conditionsModule.conditions)
  • TRIP12 (protocolSection.conditionsModule.conditions)
  • UPF3B (protocolSection.conditionsModule.conditions)
  • USP9X (protocolSection.conditionsModule.conditions)
  • VPS13B (protocolSection.conditionsModule.conditions)
  • WAC (protocolSection.conditionsModule.conditions)
  • WDFY3 (protocolSection.conditionsModule.conditions)
  • ZBTB20 (protocolSection.conditionsModule.conditions)
  • ZNF292 (protocolSection.conditionsModule.conditions)
  • ZNF462 (protocolSection.conditionsModule.conditions)
  • 2Q37 Deletion Syndrome (protocolSection.conditionsModule.conditions)
  • 9q34 Duplications (protocolSection.conditionsModule.conditions)
  • 15q15 Deletions (protocolSection.conditionsModule.conditions)
  • 15Q24 Deletion (protocolSection.conditionsModule.conditions)
  • NR3C2 (protocolSection.conditionsModule.conditions)
  • SYNCRIP (protocolSection.conditionsModule.conditions)
  • 2q34 Duplication (protocolSection.conditionsModule.conditions)
  • 2q37.3 Deletion (protocolSection.conditionsModule.conditions)
  • 6q16 Deletion (protocolSection.conditionsModule.conditions)
  • 15q11.2 BP1-BP2 Deletion (protocolSection.conditionsModule.conditions)
  • 16p13.3 Deletion (protocolSection.conditionsModule.conditions)
  • 17Q11.2 Microduplication Syndrome (Disorder) (protocolSection.conditionsModule.conditions)
  • 17p13.3 (protocolSection.conditionsModule.conditions)
  • Xq28 Duplication (protocolSection.conditionsModule.conditions)
  • CLCN4 (protocolSection.conditionsModule.conditions)
  • CSNK2B (protocolSection.conditionsModule.conditions)
  • DYNC1H1 (protocolSection.conditionsModule.conditions)
  • EIF3F (protocolSection.conditionsModule.conditions)
  • GNB1 (protocolSection.conditionsModule.conditions)
  • MED13 (protocolSection.conditionsModule.conditions)
  • MEF2C (protocolSection.conditionsModule.conditions)
  • RALGAPB (protocolSection.conditionsModule.conditions)
  • SCN1B (protocolSection.conditionsModule.conditions)
  • YY1 (protocolSection.conditionsModule.conditions)
  • Xp11.22 Duplication (protocolSection.conditionsModule.conditions)
  • PACS2 (protocolSection.conditionsModule.conditions)
  • MAOA (protocolSection.conditionsModule.conditions)
  • MAOB (protocolSection.conditionsModule.conditions)
  • HNRNPC (protocolSection.conditionsModule.conditions)
  • HNRNPD (protocolSection.conditionsModule.conditions)
  • HNRNPK (protocolSection.conditionsModule.conditions)
  • HNRNPR (protocolSection.conditionsModule.conditions)
  • HNRNPUL2 (protocolSection.conditionsModule.conditions)
  • 5P Deletion Syndrome (protocolSection.conditionsModule.conditions)
  • TCF7L2 Gene Mutation (protocolSection.conditionsModule.conditions)
  • HECW2 (protocolSection.conditionsModule.conditions)

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