Inter-rater reliability of subthreshold psychotic symptoms in individuals with 22q11.2 deletion syndrome

被引:0
|
作者
Tyler M. Moore
Deby Salzer
Carrie E. Bearden
Monica E. Calkins
Wendy R. Kates
Leila Kushan
Robert Sean Gallagher
Dafna Sofrin Frumer
Ronnie Weinberger
Donna M. McDonald-McGinn
Raquel E. Gur
Doron Gothelf
机构
[1] University of Pennsylvania,Department of Psychiatry, Perelman School of Medicine
[2] Lifespan Brain Institute of Penn Medicine and the Children’s Hospital of Philadelphia (CHOP),The Behavioral Neurogenetics Center, Edmond and Lily Safra Children’s Hospital
[3] Sheba Medical Center,Semel Institute for Neuroscience and Human Behavior
[4] University of California,Department of Psychiatry and Behavioral Sciences
[5] State University of New York at Upstate Medical University,22q and You Center
[6] CHOP,Department of Child and Adolescent Psychiatry and Behavioral Sciences
[7] CHOP,Sackler Faculty of Medicine and the Sagol School of Neuroscience
[8] Tel Aviv University,undefined
关键词
Velocardiofacial syndrome; DiGeorge; Subthreshold psychotic symptoms; Structured Interview for Prodromal Syndromes (SIPS); Scale of Prodromal Symptoms (SOPS); Inter-rater reliability; Psychosis risk syndrome;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
  • [21] Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndrome
    Yuen, Tracy
    Chow, Eva W. C.
    Silversides, Candice K.
    Bassett, Anne S.
    SCHIZOPHRENIA RESEARCH, 2013, 151 (1-3) : 221 - 225
  • [22] Psychotic symptoms influence the development of anterior cingulate BOLD variability in 22q11.2 deletion syndrome
    Zoller, Daniela
    Padula, Maria Carmela
    Sandini, Corrado
    Schneider, Maude
    Scariati, Elisa
    Van de Ville, Dimitri
    Schaer, Marie
    Eliez, Stephan
    SCHIZOPHRENIA RESEARCH, 2018, 193 : 319 - 328
  • [23] LONGITUDINAL COGNITIVE DEVELOPMENT AND ASSOCIATION WITH PRODROMAL PSYCHOTIC SYMPTOMS IN ADOLESCENTS WITH 22Q11.2 DELETION SYNDROME
    Morrison, Sinead
    Chawner, Samuel
    Owen, Michael
    van den Bree, Marianne
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2019, 29 : 1253 - 1253
  • [24] The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome
    Chawner, Samuel J. R. A.
    Niarchou, Maria
    Doherty, Joanne L.
    Moss, Hayley
    Owen, Michael J.
    van den Bree, Marianne B. M.
    JOURNAL OF PSYCHIATRIC RESEARCH, 2019, 109 : 10 - 17
  • [25] Longitudinal predictors of psychotic symptoms during adolescence in 22q11.2 deletion syndrome (22q11DS)
    Schneider, Maude
    EUROPEAN CHILD & ADOLESCENT PSYCHIATRY, 2013, 22 : S204 - S204
  • [26] Negative subthreshold psychotic symptoms distinguish 22q11.2 deletion syndrome from other neurodevelopmental disorders: A two-site study
    Mekori-Domachevsky, Ehud
    Guri, Yael
    Yi, James
    Weisman, Omri
    Calkins, Monica E.
    Tang, Sunny X.
    Gross, Raz
    McDonald-McGinn, Donna M.
    Emanuel, Beverly S.
    Zackai, Elaine H.
    Zalsman, Gil
    Weizman, Abraham
    Gur, Ruben C.
    Gur, Raquel E.
    Gothelf, Doron
    SCHIZOPHRENIA RESEARCH, 2017, 188 : 42 - 49
  • [27] Predictors of Subthreshold Psychotic Features in 22q11.2 Deletion Syndrome: A Longitudinal Study of Neuropsychiatric Factors of Psychosis Risk
    Yi, James J.
    Calkins, Monica E.
    Tang, Sunny X.
    Ruparel, Kosha S.
    McDonald-McGinn, Donna M.
    Zackai, Elaine H.
    Gur, Ruben C.
    Emanuel, Beverly S.
    Gur, Raquel E.
    BIOLOGICAL PSYCHIATRY, 2016, 79 (09) : 369S - 369S
  • [28] 22q11.2 deletion syndrome and schizophrenia
    Qin, Xianzheng
    Chen, Jiang
    Zhou, Tian
    ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2020, 52 (11) : 1181 - 1190
  • [29] Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome
    Heung, Tracy
    Conroy, Brigid
    Malecki, Sarah
    Ha, Joanne
    Boot, Erik
    Corral, Maria
    Bassett, Anne S.
    GENES, 2022, 13 (11)
  • [30] Camptodactyly and the 22q11.2 deletion syndrome
    Couser, Natario L.
    Pande, Chetna K.
    Walsh, Jonathan M.
    Tepperberg, James
    Aylsworth, Arthur S.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (02) : 515 - 518