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Leila Kushan

Biographic Data

ID1935688
NAMELeila Kushan
GIVEN NAMESLeila
FAMILY NAMEKushan
SIGNATUREKUSHAN L
AFFILIATIONSUniversity of California, Los Angeles
ORCID0000-0002-2650-7147
VERIFIEDYes
TOTAL WORKS3
TOTAL CITATIONS1
WORKS AS AUTHOR3
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2022
LATEST PUBLICATION YEAR2023
H-INDEX1
  • Neurobehavioral risk factors influence prevalence and severity of hazardous substance use in youth at genetic and clinical high risk for psychosis

    Open Access•Chaya Amir, Carolyn M Amir et al.•ARTICLE•Frontiers in Psychiatry•2023

    Individuals at genetic and CHR-P have strikingly different patterns of substance use. Factors such as increased neurodevelopmental symptoms (lower IQ, higher rates of ASD) and poorer social functioning in 22qDel may help explain this distinction from substance use patterns observed in CHR-P individuals

  • Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence

    Open Access•Jakub Kopal, Kuldeep Kumar et al.•ARTICLE•Nature Human Behaviour•2023•Cited by: 1•References: 72

  • Neurobehavioral Dimensions of Prader Willi Syndrome

    Open Access•Kathleen P O’Hora, Kathleen P O'Hora et al.•ARTICLE•Frontiers in Psychiatry•2022

    PWS is associated with a high prevalence of distressing psychosis-risk symptoms, which are associated with sleep disturbance. Findings indicate that self/parent-reported neurobehavioral symptoms and cognition can be assessed remotely in individuals with PWS, which has implications for future large-scale investigations of rare neurogenetic disorders

  • Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence

    Open Access•Jakub Kopal, Kuldeep Kumar et al.•ARTICLE•Nature Human Behaviour•2023•Cited by: 1•References: 72

  • Neurobehavioral Dimensions of Prader Willi Syndrome

    Open Access•Kathleen P O’Hora, Kathleen P O'Hora et al.•ARTICLE•Frontiers in Psychiatry•2022

    PWS is associated with a high prevalence of distressing psychosis-risk symptoms, which are associated with sleep disturbance. Findings indicate that self/parent-reported neurobehavioral symptoms and cognition can be assessed remotely in individuals with PWS, which has implications for future large-scale investigations of rare neurogenetic disorders

  • Neurobehavioral risk factors influence prevalence and severity of hazardous substance use in youth at genetic and clinical high risk for psychosis

    Open Access•Chaya Amir, Carolyn M Amir et al.•ARTICLE•Frontiers in Psychiatry•2023

    Individuals at genetic and CHR-P have strikingly different patterns of substance use. Factors such as increased neurodevelopmental symptoms (lower IQ, higher rates of ASD) and poorer social functioning in 22qDel may help explain this distinction from substance use patterns observed in CHR-P individuals

  • Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence

    Open Access•Jakub Kopal, Kuldeep Kumar et al.•ARTICLE•Nature Human Behaviour•2023•Cited by: 1•References: 72

Clinical Psychology (2 works) · Clinical Psychology (2 works) · Congenital heart defects research (2 works) · Genetics and Neurodevelopmental Disorders (2 works) · Medicine (2 works) · Psychiatry (2 works) · Psychology (2 works) · Psychosis (2 works) · Anhedonia (1 work) · Autism Spectrum Disorder Research (1 work)

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