Judith L. Rapoport

National Institute of Mental Health — United States

Medicine · Health Sciences

126h-index71.1kcitations560works0.72yr avg
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Research Topics

Schizophrenia research and treatment(118), Attention Deficit Hyperactivity Disorder(116), Functional Brain Connectivity Studies(95), Obsessive-Compulsive Spectrum Disorders(78), Child and Adolescent Psychosocial and Emotional Development(69)

Publications559 total

The Infraslow Fluctuation of Sigma Power During Sleep in Young Individuals with Schizophrenia
Sleep Medicine·2026
The infraslow fluctuation of sigma power during sleep in young individuals with schizophrenia
Schizophrenia Research·2025· 1 citedOpen Access
The Infraslow Fluctuation of Sigma Power During Sleep in Young Individuals with Schizophrenia
2025· 1 citedOpen Access
Activity-Dependent Transcriptional Program in NGN2+ Neurons Enriched for Genetic Risk for Brain-Related Disorders
Biological Psychiatry·2023· 13 citedOpen Access
Sleep spindles across youth affected by schizophrenia or anti-N-methyl-D-aspartate-receptor encephalitis
Frontiers in Psychiatry·2023· 3 citedOpen Access
Neuronal defects in a human cellular model of 22q11.2 deletion syndrome
Nature Medicine·2020· 195 citedOpen Access
Sleep spindle activity in childhood onset schizophrenia: Diminished and associated with clinical symptoms
Schizophrenia Research·2020· 29 citedOpen Access
Sleep neurophysiology in childhood onset schizophrenia
Journal of Sleep Research·2020· 9 cited
Aetiology of intellectual disability and its clinical features
2020
Neuronal impact of patient-specific aberrant NRXN1α splicing
Nature Genetics·2019· 125 citedOpen Access
Childhood-Onset Schizophrenia and Early-onset Schizophrenia Spectrum Disorders
Child and Adolescent Psychiatric Clinics of North America·2019· 117 cited
NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis
Translational Psychiatry·2019· 36 citedOpen Access
Dysregulated protocadherin-pathway activity as an intrinsic defect in induced pluripotent stem cell–derived cortical interneurons from subjects with schizophrenia
Nature Neuroscience·2019· 116 cited
51IDENTIFICATION OF NEW GENES ASSOCIATED WITH CHILDHOOD-ONSET SCHIZOPHRENIA: ATP1A3 AND THE FXYD GENE FAMILY
European Neuropsychopharmacology·2019
21ABERRANT NRXN1α SPLICING ARISING FROM 2P16.3 HETEROZYGOUS DELETIONS IMPACTS NEURONAL FUNCTION
European Neuropsychopharmacology·2019
TRANSCRIPTIONAL SIGNATURES OF CHILDHOOD ONSET SCHIZOPHRENIA IN HIPSC-DERIVED NPCS AND NEURONS ARE CONCORDANT WITH SIGNATURES FROM POST MORTEM ADULT BRAINS
European Neuropsychopharmacology·2019
Exome sequencing of sporadic childhood‐onset schizophrenia suggests the contribution of X‐linked genes in males
American Journal of Medical Genetics Part B Neuropsychiatric Genetics·2018· 13 cited
3.68 Missense Variants in the ATP1A3 and FXYD Gene Family are Associated With Childhood-Onset Schizophrenia
Journal of the American Academy of Child & Adolescent Psychiatry·2018· 2 cited
7 T MRI reveals hippocampal structural abnormalities associated with memory intrusions in childhood-onset schizophrenia
Schizophrenia Research·2018· 2 citedOpen Access
Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia
Molecular Psychiatry·2018· 46 cited
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Frequent Co-authors

Jay N. Giedd(30), F. Xavier Castellanos(11), Alan C. Evans(10), Nitin Gogtay(10), Deanna Greenstein(8), A. Catherine Vaituzis(8), Liv Clasen(7), Anjené Addington(7), Philip Shaw(7), Susan D. Hamburger(7), Jonathan D. Blumenthal(6), Debra Kaysen(6), Wendy Sharp(5), Jagath C. Rajapakse(5), Alex Zijdenbos(4), Tomáš Paus(4), Arthur W. Toga(4), Paul M. Thompson(4), Jason P. Lerch(4), B. J. Casey(4)