Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders (Q28655713)

21 June 2017

title

Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders (English)

1 reference

Bhooma Thiruvahindrapuram

21 June 2017

main subject

autism spectrum disorder

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author

14

Bhooma Thiruvahindrapuram

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21 June 2017

20

Daniel H Geschwind

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21 June 2017

19

Stephen W Scherer

1 reference

21 June 2017

Ana F Sequeira

6

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Frederico Duque

Frederico Duque

9

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Susana Mouga

Susana Mouga

10

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Dalila Pinto

Dalila Pinto

17

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Guiomar Oliveira

Guiomar Oliveira

21

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Astrid M. Vicente

Astrid M Vicente

22

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John I. Nurnberger

John I Nurnberger

18

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Wendy Roberts

11

Wendy Roberts

1 reference

21 June 2017

2

Inês C Conceição

1 reference

21 June 2017

16

Christian R Marshall

1 reference

21 June 2017

8

Cátia Café

1 reference

21 June 2017

Catarina T Correia

1

1 reference

21 June 2017

Bárbara Oliveira

3

1 reference

21 June 2017

Joana Coelho

4

1 reference

21 June 2017

Inês Sousa

5

1 reference

21 June 2017

Joana Almeida

7

1 reference

21 June 2017

Kun Gao

12

1 reference

21 June 2017

Jennifer K Lowe

13

1 reference

21 June 2017

Susan Walker

15

1 reference

21 June 2017

language of work or name

English

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publication date

10 April 2014

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21 June 2017

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21 June 2017

volume

5

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21 June 2017

issue

1

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21 June 2017

page(s)

28

1 reference

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

21 June 2017

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17 March 2017

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Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability

17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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Common genetic variants on 5p14.1 associate with autism spectrum disorders

17 March 2017

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Annexin A1 and glucocorticoids as effectors of the resolution of inflammation

17 March 2017

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17 March 2017

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17 March 2017

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Strong association of de novo copy number mutations with autism

17 March 2017

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

17 March 2017

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17 March 2017

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Intergenerational transmission of subthreshold autistic traits in the general population

17 March 2017

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17 March 2017

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17 March 2017

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Estimate of the mutation rate per nucleotide in humans

17 March 2017

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17 March 2017

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Individual common variants exert weak effects on the risk for autism spectrum disorders

17 March 2017

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

17 March 2017

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

17 March 2017

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6 April 2017

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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

7 April 2017

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Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting

7 April 2017

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7 April 2017

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7 April 2017

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7 April 2017

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Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders

7 April 2017

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Autism: where genetics meets the immune system

3 June 2018

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Autism genetics: searching for specificity and convergence

3 June 2018

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Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

3 June 2018

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Detection and characterization of copy number variation in autism spectrum disorder

3 June 2018

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Investigation of the serum levels of anterior pituitary hormones in male children with autism

3 June 2018

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2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

Annexin A1: a central player in the anti-inflammatory and neuroprotective role of microglia.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

Mutation spectrum revealed by breakpoint sequencing of human germline CNVs

3 June 2018

1 reference

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A genome-wide association study of alcohol dependence

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

The immune system's role in the biology of autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

Novel proteins regulated by mTOR in subependymal giant cell astrocytomas of patients with tuberous sclerosis complex and new therapeutic implications

3 June 2018

1 reference

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A genome-wide linkage and association scan reveals novel loci for autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

Comparing cortisol, stress, and sensory sensitivity in children with autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

Human Splicing Finder: an online bioinformatics tool to predict splicing signals

3 June 2018

1 reference

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3 June 2018

1 reference

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Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history

3 June 2018

1 reference

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Familial aggregation of quantitative autistic traits in multiplex versus simplex autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

Recurrent 16p11.2 microdeletions in autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

Annexin 1, glucocorticoids, and the neuroendocrine-immune interface

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

Lack of annexin 1 results in an increase in corticotroph number in male but not female mice

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

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3 June 2018

1 reference

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Immunity, neuroglia and neuroinflammation in autism

3 June 2018

1 reference

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Subtypes of autism by cluster analysis based on structural MRI data.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

Neuropathological findings in autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

Annexin 1 and the regulation of endocrine function

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

A novel calcium-dependent proapoptotic effect of annexin 1 on human neutrophils.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098665

Annexin 1: an endogenous anti-inflammatory protein

3 June 2018

1 reference

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Neurofunctional mechanisms in autism

3 June 2018

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3 June 2018

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Macrocortin: a polypeptide causing the anti-phospholipase effect of glucocorticoids

3 June 2018

1 reference

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Urinary cortisol circadian rhythm in a group of high-functioning children with autism

3 June 2018

1 reference

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Anti-inflammatory steroids induce biosynthesis of a phospholipase A2 inhibitor which prevents prostaglandin generation

3 June 2018

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Kinesin family member 6 variant Trp719Arg does not associate with angiographically defined coronary artery disease in the Ottawa Heart Genomics Study

3 June 2018

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Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions.

21 January 2018

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The broad autism phenotype questionnaire

21 January 2018

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Vitamin D receptor variants in 192 patients with schizophrenia and other psychiatric diseases

21 January 2018

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Penetrance for copy number variants associated with schizophrenia

21 January 2018

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Variable expression of the autism broader phenotype: findings from extended pedigrees

21 January 2018

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Annexin-1 is abnormally expressed in fragile X syndrome: two-dimensional electrophoresis study in lymphocytes.

21 January 2018

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Autoantibody repertoires to brain tissue in autism nuclear families

21 January 2018

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MRI volumes of amygdala and hippocampus in non-mentally retarded autistic adolescents and adults

21 January 2018

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Neurosteroids, brain damage, and mental illness

21 January 2018

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Hippocampus and amygdala volumes in parents of children with autistic disorder

21 January 2018

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Cortisol circadian rhythms and response to stress in children with autism

21 January 2018

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Lower cortisol and higher ACTH levels in individuals with autism

21 January 2018

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21 January 2018

Identifiers

DOI

10.1186/2040-2392-5-28

1 reference

Dimensions Publication ID

21 June 2017

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/2040-2392-5-28

PMC publication ID

4098665

0 references

1 reference