(Q48277609)

10 February 2018

http://europepmc.org/abstract/MED/28407358

title

Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder (English)

1 reference

10 February 2018

http://europepmc.org/abstract/MED/28407358

main subject

autism spectrum disorder

0 references

0 references

0 references

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Zhongsheng Sun

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Zhongsheng Sun

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Kun Xia

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

author name string

Jinchen Li

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Lin Wang

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Ping Yu

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Kun Zhang

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

publication date

13 April 2017

1 reference

10 February 2018

http://europepmc.org/abstract/MED/28407358

published in

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

volume

174

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

page(s)

568-577

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

6 June 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Schizophrenia and vitamin D related genes could have been subject to latitude-driven adaptation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Is high prevalence of Vitamin D deficiency evidence for autism disorder?: In a highly endogamous population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

From de novo mutations to personalized therapeutic interventions in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

What is the role of vitamin D in autism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Prevalence and Characteristics of Autism Spectrum Disorder Among Children Aged 8 Years--Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2012.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Megalin and cubilin: multifunctional endocytic receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Association of polymorphisms in the vitamin D receptor gene and serum 25-hydroxyvitamin D levels in children with autism spectrum disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Advancing the understanding of autism disease mechanisms through genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Synaptic, transcriptional and chromatin genes disrupted in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Review: the role of vitamin D in nervous system health and disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Vitamin D3 and brain development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Vitamin D, effects on brain development, adult brain function and the links between low levels of vitamin D and neuropsychiatric disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Serum levels of 25-hydroxyvitamin D in mothers of Swedish and of Somali origin who have children with and without autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Autism spectrum disorder and low vitamin D at birth: a sibling control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Coming of age: ten years of next-generation sequencing technologies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Vitamin D as a neurosteroid affecting the developing and adult brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Characterising and predicting haploinsufficiency in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

The contribution of de novo coding mutations to autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

De Novo Gene Disruptions in Children on the Autistic Spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Core symptoms of autism improved after vitamin D supplementation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

The chromatin-remodeling complex WINAC targets a nuclear receptor to promoters and is impaired in Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Vitamin d in the general population of young adults with autism in the faroe islands

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Toll-like receptor triggering of a vitamin D-mediated human antimicrobial response

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Vitamin D and Autism Spectrum Disorder: A Literature Review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Reduced serum levels of 25-hydroxy and 1,25-dihydroxy vitamin D in Egyptian children with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Reduced serum concentrations of 25-hydroxy vitamin D in children with autism: relation to autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Recurrent de novo mutations implicate novel genes underlying simplex autism risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Genic intolerance to functional variation and the interpretation of personal genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Autism spectrum disorders and autistic traits: a decade of new twin studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

The role of de novo mutations in the genetics of autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Vitamin D status in autism spectrum disorders and the efficacy of vitamin D supplementation in autistic children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

A framework for the interpretation of de novo mutation in human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

The familial risk of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Selected vitamin D metabolic gene variants and risk for autism spectrum disorder in the CHARGE Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Novel mechanism of negative regulation of 1,25-dihydroxyvitamin D3-induced 25-hydroxyvitamin D3 24-hydroxylase (Cyp24a1) Transcription: epigenetic modification involving cross-talk between protein-arginine methyltransferase 5 and the SWI/SNF complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Analysis of the SWI/SNF chromatin-remodeling complex during early heart development and BAF250a repression cardiac gene transcription during P19 cell differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Autism: Will vitamin D supplementation during pregnancy and early childhood reduce the recurrence rate of autism in newborn siblings?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

STRING v10: protein-protein interaction networks, integrated over the tree of life

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Low serum levels of 25-hydroxyvitamin D (25-OHD) in children with autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

De novo mutations in human genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Gestational vitamin D deficiency and autism-related traits: the Generation R Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

De novo genic mutations among a Chinese autism spectrum disorder cohort.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Serum concentration of 25-hydroxyvitamin D in autism spectrum disorder: a systematic review and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Large-scale in silico and microarray-based identification of direct 1,25-dihydroxyvitamin D3 target genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Genome-wide characteristics of de novo mutations in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

Whole-genome sequencing of quartet families with autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32543

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.32543

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28407358%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

1 reference