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Intellectual disability

Postoperative Adverse Outcomes in Intellectually Disabled Surgical Patients: A Nationwide Population-Based Study

Jui-An Lin, Chien-Chang Liao, [ ... ], Ta-Liang Chen

The Adaptor Function of TRAPPC2 in Mammalian TRAPPs Explains TRAPPC2-Associated SEDT and TRAPPC9-Associated Congenital Intellectual Disability

Min Zong, Xing-gang Wu, [ ... ], Sidney Yu

A Behavioral Comparison of Male and Female Adults with High Functioning Autism Spectrum Conditions

Meng-Chuan Lai, Michael V. Lombardo, [ ... ], Simon Baron-Cohen

Autism and Intellectual Disability Are Differentially Related to Sociodemographic Background at Birth

Helen Leonard, Emma Glasson, [ ... ], Fiona Stanley

DIA1R Is an X-Linked Gene Related to Deleted In Autism-1

Azhari Aziz, Sean P. Harrop, Naomi E. Bishop

Regulatory BC1 RNA and the Fragile X Mental Retardation Protein: Convergent Functionality in Brain

Jun Zhong, Shih-Chieh Chuang, [ ... ], Henri Tiedge

A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33

Ryan N. Traylor, Damien L. Bruno, [ ... ], Howard R. Slater

Lowering β-Amyloid Levels Rescues Learning and Memory in a Down Syndrome Mouse Model

William J. Netzer, Craig Powell, [ ... ], Paul Greengard

Array-Based FMR1 Sequencing and Deletion Analysis in Patients with a Fragile X Syndrome–Like Phenotype

Stephen C. Collins, Brad Coffee, [ ... ], Stephen T. Warren

COP9 Limits Dendritic Branching via Cullin3-Dependent Degradation of the Actin-Crosslinking BTB-Domain Protein Kelch

Inna Djagaeva, Sergey Doronkin

Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome

Jill A. Rosenfeld, Blake C. Ballif, [ ... ], Lisa G. Shaffer

Clinical Heterogeneity of Duchenne Muscular Dystrophy (DMD): Definition of Sub-Phenotypes and Predictive Criteria by Long-Term Follow-Up

Isabelle Desguerre, Christo Christov, [ ... ], Romain K. Gherardi

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