Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder-Reference-Cited by-同舟云学术

Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder

Published:2010-11-29 Issue:5 Volume:80 Page:435-443
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Carter MT,Nikkel SM,Fernandez BA,Marshall CR,Noor A,Lionel AC,Prasad A,Pinto D,Joseph-George AM,Noakes C,Fairbrother-Davies C,Roberts W,Vincent J,Weksberg R,Scherer SW

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2010.01578.x/fullpdf

Reference20 articles.

1. Mapping autism risk loci using genetic linkage and chromosomal rearrangements.;Szatmari;Nat Genet,2007

2. Strong association of de novo copy number mutations with autism.;Sebat;Science,2007

3. Structural variation of chromosomes in autism spectrum disorder.;Marshall;Am J Hum Genet,2008

4. Functional impact of global rare copy number variation in autism spectrum disorders.;Pinto;Nature,2010

5. Copy-number variations associated with neuropsychiatric conditions.;Cook;Nature,2008

Cited by 65 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Review of Neurologic and Developmental Conditions Associated with Pediatric Dihydropyrimidine Dehydrogenase Deficiency;Advances in Molecular Pathology;2024-08

2. DPYD Genotyping Recommendations;The Journal of Molecular Diagnostics;2024-07

3. Generation and transcriptomic characterization of MIR137 knockout miniature pig model for neurodevelopmental disorders;Cell & Bioscience;2024-06-28

4. Metabolomic changes in children with autism;World Journal of Clinical Pediatrics;2024-06-09

5. ARID1B controls transcriptional programs of axon projection in an organoid model of the human corpus callosum;Cell Stem Cell;2024-06