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Items: 1 to 20 of 70

1.

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

Wang T, Guo H, Xiong B, Stessman HA, Wu H, Coe BP, Turner TN, Liu Y, Zhao W, Hoekzema K, Vives L, Xia L, Tang M, Ou J, Chen B, Shen Y, Xun G, Long M, Lin J, Kronenberg ZN, Peng Y, Bai T, Li H, Ke X, Hu Z, Zhao J, Zou X, Xia K, Eichler EE.

Nat Commun. 2016 Nov 8;7:13316. doi: 10.1038/ncomms13316.

2.

Expression of myogenes in longissimus dorsi muscle during prenatal development in commercial and local Piau pigs.

Reis EP, Paixão DM, Brustolini OJ, Silva FF, Silva W, Araújo FM, Salim AC, Oliveira G, Guimarães SE.

Genet Mol Biol. 2016 Oct-Dec;39(4):589-599. doi: 10.1590/1678-4685-GMB-2015-0295.

3.

A systematic variant annotation approach for ranking genes associated with autism spectrum disorders.

Larsen E, Menashe I, Ziats MN, Pereanu W, Packer A, Banerjee-Basu S.

Mol Autism. 2016 Oct 21;7:44.

4.

When size matters: CHD8 in autism.

Breuss MW, Gleeson JG.

Nat Neurosci. 2016 Oct 26;19(11):1430-1432. doi: 10.1038/nn.4431. No abstract available.

PMID:
27786184
5.

Chd8 mediates cortical neurogenesis via transcriptional regulation of cell cycle and Wnt signaling.

Durak O, Gao F, Kaeser-Woo YJ, Rueda R, Martorell AJ, Nott A, Liu CY, Watson LA, Tsai LH.

Nat Neurosci. 2016 Nov;19(11):1477-1488. doi: 10.1038/nn.4400.

PMID:
27694995
6.

CHD8 haploinsufficiency results in autistic-like phenotypes in mice.

Katayama Y, Nishiyama M, Shoji H, Ohkawa Y, Kawamura A, Sato T, Suyama M, Takumi T, Miyakawa T, Nakayama KI.

Nature. 2016 Sep 29;537(7622):675-679. doi: 10.1038/nature19357.

PMID:
27602517
7.

Identification of a rare variant in CHD8 that contributes to schizophrenia and autism spectrum disorder susceptibility.

Kimura H, Wang C, Ishizuka K, Xing J, Takasaki Y, Kushima I, Aleksic B, Uno Y, Okada T, Ikeda M, Mori D, Inada T, Iwata N, Ozaki N.

Schizophr Res. 2016 Dec;178(1-3):104-106. doi: 10.1016/j.schres.2016.08.023. No abstract available.

PMID:
27595554
8.

CHD8 intragenic deletion associated with autism spectrum disorder.

Stolerman ES, Smith B, Chaubey A, Jones JR.

Eur J Med Genet. 2016 Apr;59(4):189-94. doi: 10.1016/j.ejmg.2016.02.010.

PMID:
26921529
9.

Novel 14q11.2 microduplication including the CHD8 and SUPT16H genes associated with developmental delay.

Smyk M, Poluha A, Jaszczuk I, Bartnik M, Bernaciak J, Nowakowska B.

Am J Med Genet A. 2016 May;170A(5):1325-9. doi: 10.1002/ajmg.a.37579.

PMID:
26834018
10.

Genome-wide nucleosome specificity and function of chromatin remodellers in ES cells.

de Dieuleveult M, Yen K, Hmitou I, Depaux A, Boussouar F, Bou Dargham D, Jounier S, Humbertclaude H, Ribierre F, Baulard C, Farrell NP, Park B, Keime C, Carrière L, Berlivet S, Gut M, Gut I, Werner M, Deleuze JF, Olaso R, Aude JC, Chantalat S, Pugh BF, Gérard M.

Nature. 2016 Feb 4;530(7588):113-6. doi: 10.1038/nature16505.

11.

A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.

Merner N, Forgeot d'Arc B, Bell SC, Maussion G, Peng H, Gauthier J, Crapper L, Hamdan FF, Michaud JL, Mottron L, Rouleau GA, Ernst C.

Am J Med Genet A. 2016 May;170A(5):1225-35. doi: 10.1002/ajmg.a.37566.

PMID:
26789910
12.

Common BRAF(V600E)-directed pathway mediates widespread epigenetic silencing in colorectal cancer and melanoma.

Fang M, Hutchinson L, Deng A, Green MR.

Proc Natl Acad Sci U S A. 2016 Feb 2;113(5):1250-5. doi: 10.1073/pnas.1525619113.

13.

Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology.

Barnard RA, Pomaville MB, O'Roak BJ.

Front Neurosci. 2015 Dec 17;9:477. doi: 10.3389/fnins.2015.00477. Review.

14.

Cell cycle networks link gene expression dysregulation, mutation, and brain maldevelopment in autistic toddlers.

Pramparo T, Lombardo MV, Campbell K, Barnes CC, Marinero S, Solso S, Young J, Mayo M, Dale A, Ahrens-Barbeau C, Murray SS, Lopez L, Lewis N, Pierce K, Courchesne E.

Mol Syst Biol. 2015 Dec 14;11(12):841. doi: 10.15252/msb.20156108.

15.

NSD3-Short Is an Adaptor Protein that Couples BRD4 to the CHD8 Chromatin Remodeler.

Shen C, Ipsaro JJ, Shi J, Milazzo JP, Wang E, Roe JS, Suzuki Y, Pappin DJ, Joshua-Tor L, Vakoc CR.

Mol Cell. 2015 Dec 17;60(6):847-59. doi: 10.1016/j.molcel.2015.10.033.

16.

The Chromatin Regulator CHD8 Is a Context-Dependent Mediator of Cell Survival in Murine Hematopoietic Malignancies.

Shingleton JR, Hemann MT.

PLoS One. 2015 Nov 20;10(11):e0143275. doi: 10.1371/journal.pone.0143275.

17.

First glimpses of the neurobiology of autism spectrum disorder.

Sanders SJ.

Curr Opin Genet Dev. 2015 Aug;33:80-92. doi: 10.1016/j.gde.2015.10.002. Review.

PMID:
26547130
18.

CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment.

Wang P, Lin M, Pedrosa E, Hrabovsky A, Zhang Z, Guo W, Lachman HM, Zheng D.

Mol Autism. 2015 Oct 19;6:55. doi: 10.1186/s13229-015-0048-6.

19.

A genome-wide approach to link genotype to clinical outcome by utilizing next generation sequencing and gene chip data of 6,697 breast cancer patients.

Pongor L, Kormos M, Hatzis C, Pusztai L, Szabó A, Győrffy B.

Genome Med. 2015 Oct 16;7:104. doi: 10.1186/s13073-015-0228-1.

20.

Investigation of genes important in neurodevelopment disorders in adult human brain.

Maussion G, Diallo AB, Gigek CO, Chen ES, Crapper L, Théroux JF, Chen GG, Vasuta C, Ernst C.

Hum Genet. 2015 Oct;134(10):1037-53. doi: 10.1007/s00439-015-1584-z.

PMID:
26194112
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