De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder (Q34324641)

25284784

1 August 2017

title

De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder (English)

1 reference

25284784

1 August 2017

main subject

autism spectrum disorder

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Adam Yongxin Ye

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author name string

Michael F Walker

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Michael DiCola

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A Jeremy Willsey

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Zainulabedin Waqar

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Luis E Gonzalez

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John D Overton

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Nicole A Teran

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language of work or name

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2 October 2014

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1 August 2017

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4 June 2020

volume

9

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issue

1

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4 June 2020

page(s)

16-23

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De novo mutations in schizophrenia implicate synaptic networks

4 June 2020

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1 reference

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Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

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6 July 2018

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A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

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RIM genes differentially contribute to organizing presynaptic release sites

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De Novo Gene Disruptions in Children on the Autistic Spectrum

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Patterns and rates of exonic de novo mutations in autism spectrum disorders

6 July 2018

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

6 July 2018

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism

6 July 2018

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Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

6 July 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/25284784

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12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.CELREP.2014.08.068

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4 June 2020

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4 June 2020

25284784

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