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Translational Psychiatry|January 22, 2019
Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.Journal of Autism and Developmental Disorders|November 18, 2016
The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 DuplicationsM A Gillentine, L N Berry, R P Goin-Kochel, et al.Translational Psychiatry|March 7, 2019
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2015
Clinical phenotype of the recurrent 1q21.1 copy-number variantRaphael Bernier, Kyle J Steinman, Beau Reilly, et al.Biological Psychiatry|July 28, 2014
The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained populationEllen Hanson, Raphael Bernier, Ken Porche, et al.Biological Psychiatry|January 9, 2016
The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and InhibitionLoyse Hippolyte, Anne M Maillard, Borja Rodriguez-Herreros, et al.American Journal on Intellectual and Developmental Disabilities|November 19, 2020
Person Ability Scores as an Alternative to Norm-Referenced Scores as Outcome Measures in Studies of Neurodevelopmental DisordersCristan A Farmer, Aaron J Kaat, Audrey Thurm, et al.Archives of General Psychiatry|November 9, 2011
A multisite study of the clinical diagnosis of different autism spectrum disordersCatherine Lord, Eva Petkova, Vanessa Hus, et al.Journal of Medical Genetics|October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersFlore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.The American Journal of Psychiatry|January 1, 2021
A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number VariantsSamuel J R A Chawner, Joanne L Doherty, Richard J L Anney, et al.Pageof 7