Population- and family-based studies associate the MTHFR gene with idiopathic autism in simplex families (Q34149181)

31 July 2017

Population- and family-based studies associate the MTHFR gene with idiopathic autism in simplex families (English)

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31 July 2017

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Xudong Liu

1

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31 July 2017

Fatima Solehdin

2

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31 July 2017

Ira L Cohen

3

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31 July 2017

Maripaz G Gonzalez

4

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31 July 2017

Edmund C Jenkins

5

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31 July 2017

M E Suzanne Lewis

6

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31 July 2017

Jeanette J A Holden

7

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31 July 2017

language of work or name

English

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publication date

1 July 2011

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Journal of Autism and Developmental Disorders

31 July 2017

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31 July 2017

41

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31 July 2017

938-944

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31 July 2017

7

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https://scigraph.springernature.com/pub.10.1007/s10803-010-1120-x

31 July 2017

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Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives

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DNA methylation patterns and epigenetic memory

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Whole genome microarray analysis of gene expression in Prader-Willi syndrome.

21 January 2018

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5,10-methylenetetrahydrofolate reductase (MTHFR) 677C-->T and 1298A-->C mutations are associated with DNA hypomethylation

21 January 2018

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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

21 January 2018

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Parent PDD behavior inventory profiles of young children classified according to autism diagnostic observation schedule-generic and autism diagnostic interview-revised criteria.

21 January 2018

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Imprinted gene expression in the brain

21 January 2018

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The MTHFR 1298A>C polymorphism and genomic DNA methylation in human lymphocytes.

21 January 2018

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A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

21 January 2018

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Rett syndrome-causing mutations in human MeCP2 result in diverse structural changes that impact folding and DNA interactions.

21 January 2018

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15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders

21 January 2018

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Imprinted genes, cognition and behaviour.

21 January 2018

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Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism

21 January 2018

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Abnormal transmethylation/transsulfuration metabolism and DNA hypomethylation among parents of children with autism

21 January 2018

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A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A

21 January 2018

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Polymorphisms in folate metabolizing enzymes and transport proteins and the risk of breast cancer

21 January 2018

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

21 January 2018

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Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

21 January 2018

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Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

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Structural variation of chromosomes in autism spectrum disorder

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Aberrations in folate metabolic pathway and altered susceptibility to autism.

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High levels of homocysteine and low serum paraoxonase 1 arylesterase activity in children with autism.

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Phenomic determinants of genomic variation in autism spectrum disorders

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Genomic imprinting: parental influence on the genome

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A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

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Epigenetics of autism spectrum disorders

21 January 2018

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Strong association of de novo copy number mutations with autism

21 January 2018

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Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments.

21 January 2018

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A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

21 January 2018

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Multiplex PCR for simultaneous detection of 677 C-->T and 1298 A-->C polymorphisms in methylenetetrahydrofolate reductase gene for population studies of cancer risk

21 January 2018

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2LD, GENECOUNTING and HAP: Computer programs for linkage disequilibrium analysis

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12 December 2020

DNA hypomethylation and human diseases.

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12 December 2020

Methylenetetrahydrofolate reductase C677T polymorphism, folic acid and riboflavin are important determinants of genome stability in cultured human lymphocytes.

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12 December 2020

Functional inference of the methylenetetrahydrofolate reductase 677C > T and 1298A > C polymorphisms from a large-scale epidemiological study

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12 December 2020

X chromosome-inactivation patterns in patients with Rett syndrome

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12 December 2020

Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006

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12 December 2020

Methods of analysis and resources available for genetic trait mapping

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12 December 2020

Implementing a unified approach to family-based tests of association.

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12 December 2020

A comparative study of X-inactivation in Rett syndrome probands and control subjects

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12 December 2020

A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status.

1 reference

12 December 2020

10.1007/S10803-010-1120-X

Identifiers

DOI

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Dimensions Publication ID

31 July 2017

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