Literature DB >> 17420674

Autism in children with 22q11.2 deletion syndrome.

Stephan Eliez1.   

Abstract

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Year:  2007        PMID： 17420674     DOI： 10.1097/CHI.0b013e31802f5490

Source DB:  PubMed          Journal:  J Am Acad Child Adolesc Psychiatry        ISSN： 0890-8567            Impact factor:   8.829


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  14 in total

Review 1.  22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.

Authors:  Maria Karayiorgou; Tony J Simon; Joseph A Gogos
Journal:  Nat Rev Neurosci       Date:  2010-06       Impact factor: 34.870

2.  Categorical versus dimensional approaches to autism-associated intermediate phenotypes in 22q11.2 microdeletion syndrome.

Authors:  Maria Jalbrzikowski; Khwaja Hamzah Ahmed; Arati Patel; Rachel Jonas; Leila Kushan; Carolyn Chow; Carrie E Bearden
Journal:  Biol Psychiatry Cogn Neurosci Neuroimaging       Date:  2017-01

3.  Autism Spectrum and psychosis risk in the 22q11.2 deletion syndrome. Findings from a prospective longitudinal study.

Authors:  A M Fiksinski; E J Breetvelt; S N Duijff; A S Bassett; R S Kahn; J A S Vorstman
Journal:  Schizophr Res       Date:  2017-01-21       Impact factor: 4.939

4.  Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype?

Authors:  Kathleen Angkustsiri; Beth Goodlin-Jones; Lesley Deprey; Khyati Brahmbhatt; Susan Harris; Tony J Simon
Journal:  J Autism Dev Disord       Date:  2014-04

Review 5.  Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia.

Authors:  Bernard Crespi; Philip Stead; Michael Elliot
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-01       Impact factor: 11.205

6.  Care of Children with DiGeorge Before and After Cultured Thymus Tissue Implantation.

Authors:  Stephanie E Gupton; Elizabeth A McCarthy; M Louise Markert
Journal:  J Clin Immunol       Date:  2021-05-18       Impact factor: 8.542

Review 7.  Clinical evaluation of patients with a neuropsychiatric risk copy number variant.

Authors:  Samuel Jra Chawner; Cameron J Watson; Michael J Owen
Journal:  Curr Opin Genet Dev       Date:  2021-01-15       Impact factor: 4.665

8.  Prader-Willi syndrome and autism spectrum disorders: an evolving story.

Authors:  Elisabeth M Dykens; Evon Lee; Elizabeth Roof
Journal:  J Neurodev Disord       Date:  2011-08-20       Impact factor: 4.025

9.  Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome.

Authors:  Liang Zhan; Lisanne M Jenkins; Aifeng Zhang; Giorgio Conte; Angus Forbes; Danielle Harvey; Kathleen Angkustsiri; Naomi J Goodrich-Hunsaker; Courtney Durdle; Aaron Lee; Cyndi Schumann; Owen Carmichael; Kristopher Kalish; Alex D Leow; Tony J Simon
Journal:  Hum Brain Mapp       Date:  2017-10-08       Impact factor: 5.038

10.  Association testing of copy number variants in schizophrenia and autism spectrum disorders.

Authors:  Bernard J Crespi; Helen J Crofts
Journal:  J Neurodev Disord       Date:  2012-05-30       Impact factor: 4.025
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