(Q35345720)

7 August 2017

title

Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism (English)

1 reference

7 August 2017

0 references

1 reference

Michael Wigler

10

0 references

Jason Lerch

3

object named as

Jason P Lerch

1 reference

7 August 2017

7

Abba M Krieger

1 reference

7 August 2017

Guy Horev

1

1 reference

7 August 2017

Jacob Ellegood

2

1 reference

7 August 2017

Young-Eun E Son

4

1 reference

7 August 2017

Lakshmi Muthuswamy

5

1 reference

7 August 2017

Hannes Vogel

6

1 reference

7 August 2017

Andreas Buja

8

1 reference

7 August 2017

R Mark Henkelman

9

1 reference

7 August 2017

Alea A Mills

11

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7 August 2017

language of work or name

English

0 references

publication date

3 October 2011

1 reference

Proceedings of the National Academy of Sciences of the United States of America

7 August 2017

published in

1 reference

7 August 2017

volume

108

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7 August 2017

issue

41

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7 August 2017

page(s)

17076-17081

1 reference

Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications

7 August 2017

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1 reference

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12 July 2018

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12 July 2018

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Increased striatal injury and behavioral deficits after intracerebral hemorrhage in hemopexin knockout mice

12 July 2018

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Phenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse models

12 July 2018

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Expanding the clinical spectrum of the 16p11.2 chromosomal rearrangements: three patients with syringomyelia.

12 July 2018

1 reference

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A genome-wide scan for common alleles affecting risk for autism

12 July 2018

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Cognitive and behavioral characterization of 16p11.2 deletion syndrome

12 July 2018

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12 July 2018

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Ten ways to improve the quality of descriptions of whole-animal movement

12 July 2018

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A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.

12 July 2018

1 reference

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Structural variation in the human genome and its role in disease

12 July 2018

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Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice

12 July 2018

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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

12 July 2018

1 reference

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TAp63 induces senescence and suppresses tumorigenesis in vivo

12 July 2018

1 reference

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Microduplications of 16p11.2 are associated with schizophrenia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism

12 July 2018

1 reference

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Automated analysis of postoperative behaviour: assessment of HomeCageScan as a novel method to rapidly identify pain and analgesic effects in mice.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Large recurrent microdeletions associated with schizophrenia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Rare chromosomal deletions and duplications increase risk of schizophrenia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

High resolution three-dimensional brain atlas using an average magnetic resonance image of 40 adult C57Bl/6J mice

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

The possible interplay of synaptic and clock genes in autism spectrum disorders

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Medical genetics diagnostic evaluation of the child with global developmental delay or intellectual disability

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Structural variation of chromosomes in autism spectrum disorder

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Association between microdeletion and microduplication at 16p11.2 and autism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Recurrent 16p11.2 microdeletions in autism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

SIRT1 transgenic mice show phenotypes resembling calorie restriction

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

The Epidemiology of Autism Spectrum Disorders *

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Strong association of de novo copy number mutations with autism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

CHD5 is a tumor suppressor at human 1p36

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

The power of automated high-resolution behavior analysis revealed by its application to mouse models of Huntington's and prion diseases

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

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12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

High-resolution longitudinal screening with magnetic resonance imaging in a murine brain cancer model

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalance.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Controlling the false discovery rate in behavior genetics research

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

From mouse to man: generating megabase chromosome rearrangements

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Sensory Neglect Produced by Lateral Hypothalamic Damage

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Further analysis of sensory inattention following lateral hypothalamic damage in rats

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Nigrostriatal bundle damage and the lateral hypothalamic syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Stereotaxic mapping of the monoamine pathways in the rat brain.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

A proposed natural geometry of recovery from akinesia in the lateral hypothalamic rat

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Compulsive, Abnormal Walking Caused by Anticholinergics in Akinetic, 6-Hydroxydopamine-Treated Rats

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

A familial 593-kb microdeletion of 16p11.2 associated with mental retardation and hemivertebrae.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Estimating wall guidance and attraction in mouse free locomotor behavior

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

The lateral hypothalamic syndrome: recovery of feeding and drinking after lateral hypothalamic lesions.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3193230

Adaptive linear step-up procedures that control the false discovery rate

26 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.1114042108

Congenital heart disease in mice deficient for the DiGeorge syndrome region

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21969575

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.1114042108

1 reference

7 August 2017

0 references

1 reference

7 August 2017

1 reference