Abnormal Auditory Mismatch Fields in Children and Adolescents With 16p11.2 Deletion and 16p11.2 Duplication-Reference-Cited by-同舟云学术

Abnormal Auditory Mismatch Fields in Children and Adolescents With 16p11.2 Deletion and 16p11.2 Duplication

Published:2020-10 Issue:10 Volume:5 Page:942-950
ISSN:2451-9022
Container-title:Biological Psychiatry: Cognitive Neuroscience and Neuroimaging
language:en
Short-container-title:Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Author:

Matsuzaki Junko,Berman Jeffrey I.^ORCID,Blaskey Lisa,Kuschner Emily S.^ORCID,Gaetz Leah,Mukherjee Pratik,Buckner Randy L.,Nagarajan Srikantan S.,Chung Wendy K.^ORCID,Sherr Elliott H.,Roberts Timothy P.L.

Funder

Simons Foundation Autism Research Initiative

Publisher

Elsevier BV

Subject

Biological Psychiatry,Clinical Neurology,Cognitive Neuroscience,Radiology Nuclear Medicine and imaging

Reference43 articles.

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2. Association between microdeletion and microduplication at 16p11.2 and autism;Weiss;N Engl J Med,2008

3. Cognitive and behavioral characterization of 16p11.2 deletion syndrome;Hanson;J Dev Behav Pediatr,2010

4. Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioral problems, dysmorphism, epilepsy, and abnormal head size;Shinawi;J Med Genet,2010

5. A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders on behalf of the Simons VIP Consortium, on behalf of the 16p11.2 European Consortium;Zufferey;J Med Genet,2012

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1. Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication;BMC Pregnancy and Childbirth;2024-07-22

2. 16p11.2 deletion syndrome;Current Opinion in Genetics & Development;2021-06