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Schizophrenia Research|January 28, 2019
P300 amplitude attenuation in high risk and early onset psychosis youthKelsey Graber, Michelle Bosquet Enlow, Frank H Duffy, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 18, 2007
Linkage analysis of attention deficit hyperactivity disorderStephen V Faraone, Alysa E Doyle, Jessica Lasky-Su, et al.
JAMA|June 4, 2009
Prevention of depression in at-risk adolescents: a randomized controlled trialJudy Garber, Gregory N Clarke, V Robin Weersing, et al.
Cerebellum (London, England)|March 21, 2025
Reduced Cerebellar Volumes Associate with P300 Amplitude Attenuation in Children with Clinical High Risk for Psychosis and Early Onset PsychosisHanne van der Heijden, Hesham M Hamoda, Aliza Ray, et al.
BMC Medical Genetics|November 15, 2018
De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case reportChrystal F Mavros, Catherine A Brownstein, Roshni Thyagrajan, et al.
Psychological Medicine|May 29, 2026
Evaluating psychosis-specific effects of trauma exposure in early-onset and adult-onset psychosisJimena Unzueta, Samuel Mathias, Nuria Lanzagorta, et al.
Neural Plasticity|February 17, 2016
N100 Repetition Suppression Indexes Neuroplastic Defects in Clinical High Risk and Psychotic YouthJoseph Gonzalez-Heydrich, Michelle Bosquet Enlow, Eugene D'Angelo, et al.
Schizophrenia Research|November 10, 2015
Early auditory processing evoked potentials (N100) show a continuum of blunting from clinical high risk to psychosis in a pediatric sampleJoseph Gonzalez-Heydrich, Michelle Bosquet Enlow, Eugene D'Angelo, et al.
Schizophrenia Research|September 27, 2025
The burden of early onset psychosis: Diagnostic complexity, high comorbidity, and poor functioning in patients and their relativesJosephine Mollon, Nuria Lanzagorta, Samuel R Mathias, et al.
Molecular Genetics and Metabolism Reports|June 21, 2018
De novo ATP1A3 and compound heterozygous NLRP3 mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndromeAlcy Torres, Catherine A Brownstein, Sahil K Tembulkar, et al.
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