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The Psychiatric Hospital|February 5, 1984
The child abuse program in a child guidance centerB B Burnett, P Feinstein, F Pescosolido, et al.
Dialogues in Clinical Neuroscience|December 11, 2012
Lighting a path: genetic studies pinpoint neurodevelopmental mechanisms in autism and related disordersMatthew F Pescosolido, Unikora Yang, Mark Sabbagh, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|April 16, 2013
Distribution of disease-associated copy number variants across distinct disorders of cognitive developmentMatthew F Pescosolido, Ece D Gamsiz, Shailender Nagpal, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 16, 2021
Loss of Christianson Syndrome Na+/H+ Exchanger 6 (NHE6) Causes Abnormal Endosome Maturation and Trafficking Underlying Lysosome Dysfunction in NeuronsMatthew F Pescosolido, Qing Ouyang, Judy S Liu, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 10, 2023
Live-Imaging Detection of Multivesicular Body-Plasma Membrane Fusion and Exosome Release in Cultured Primary NeuronsMatthew F Pescosolido, Qing Ouyang, Judy S Liu, et al.
Expert Review of Neurotherapeutics|November 19, 2011
Translational neuroscience in pediatric bipolar disorderDaniel P Dickstein, Brooke L Reidy, Matthew F Pescosolido, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytomaHassan M Minhas, Matthew F Pescosolido, Matthew Schwede, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|April 30, 2013
Emotional face identification in youths with primary bipolar disorder or primary attention-deficit/hyperactivity disorderKaren E Seymour, Matthew F Pescosolido, Brooke L Reidy, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|June 25, 2015
Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental MechanismsEce D Gamsiz, Laura N Sciarra, Abbie M Maguire, et al.
American Journal of Medical Genetics. Part A|November 5, 2011
A novel familial 11p15.4 microduplication associated with intellectual disability, dysmorphic features, and obesity with involvement of the ZNF214 geneElvera Sofos, Matthew F Pescosolido, Jose B Quintos, et al.
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