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Items: 1 to 20 of 128

1.

A Novel Human CAMK2A Mutation Disrupts Dendritic Morphology and Synaptic Transmission, and Causes ASD-Related Behaviors.

Stephenson JR, Wang X, Perfitt TL, Parrish WP, Shonesy BC, Marks CR, Mortlock DP, Nakagawa T, Sutcliffe JS, Colbran RJ.

J Neurosci. 2017 Feb 22;37(8):2216-2233. doi: 10.1523/JNEUROSCI.2068-16.2017.

PMID:
28130356
2.

Maternal BMI as a predictor of methylation of obesity-related genes in saliva samples from preschool-age Hispanic children at-risk for obesity.

Oelsner KT, Guo Y, To SB, Non AL, Barkin SL.

BMC Genomics. 2017 Jan 9;18(1):57. doi: 10.1186/s12864-016-3473-9.

3.

The emerging landscape of dynamic DNA methylation in early childhood.

Xu CJ, Bonder MJ, Söderhäll C, Bustamante M, Baïz N, Gehring U, Jankipersadsing SA, van der Vlies P, van Diemen CC, van Rijkom B, Just J, Kull I, Kere J, Antó JM, Bousquet J, Zhernakova A, Wijmenga C, Annesi-Maesano I, Sunyer J, Melén E, Li Y, Postma DS, Koppelman GH.

BMC Genomics. 2017 Jan 5;18(1):25. doi: 10.1186/s12864-016-3452-1.

4.

Chromosome 11q13 deletion syndrome.

Kim YS, Kim GH, Byeon JH, Eun SH, Eun BL.

Korean J Pediatr. 2016 Nov;59(Suppl 1):S10-S13. doi: 10.3345/kjp.2016.59.11.S10.

5.

Knowledge-Guided Bioinformatics Model for Identifying Autism Spectrum Disorder Diagnostic MicroRNA Biomarkers.

Shen L, Lin Y, Sun Z, Yuan X, Chen L, Shen B.

Sci Rep. 2016 Dec 21;6:39663. doi: 10.1038/srep39663.

6.

A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.

Lin YC, Frei JA, Kilander MB, Shen W, Blatt GJ.

Front Cell Neurosci. 2016 Nov 17;10:263. Review.

7.

The Neurobiological Basis for Social Affiliation in Autism Spectrum Disorder and Schizophrenia.

Crider A, Pillai A.

Curr Behav Neurosci Rep. 2016 Jun;3(2):154-164.

PMID:
27695666
8.

Dysfunctional cerebellar Purkinje cells contribute to autism-like behaviour in Shank2-deficient mice.

Peter S, Ten Brinke MM, Stedehouder J, Reinelt CM, Wu B, Zhou H, Zhou K, Boele HJ, Kushner SA, Lee MG, Schmeisser MJ, Boeckers TM, Schonewille M, Hoebeek FE, De Zeeuw CI.

Nat Commun. 2016 Sep 1;7:12627. doi: 10.1038/ncomms12627.

9.

Recording Mouse Ultrasonic Vocalizations to Evaluate Social Communication.

Ferhat AT, Torquet N, Le Sourd AM, de Chaumont F, Olivo-Marin JC, Faure P, Bourgeron T, Ey E.

J Vis Exp. 2016 Jun 5;(112). doi: 10.3791/53871.

10.

Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders.

Kim KC, Gonzales EL, Lázaro MT, Choi CS, Bahn GH, Yoo HJ, Shin CY.

Biomol Ther (Seoul). 2016 May 1;24(3):207-43. doi: 10.4062/biomolther.2016.061. Review.

11.

Advancing the understanding of autism disease mechanisms through genetics.

de la Torre-Ubieta L, Won H, Stein JL, Geschwind DH.

Nat Med. 2016 Apr;22(4):345-61. doi: 10.1038/nm.4071. Review.

12.

Whole-genome sequencing in multiplex families with psychoses reveals mutations in the SHANK2 and SMARCA1 genes segregating with illness.

Homann OR, Misura K, Lamas E, Sandrock RW, Nelson P, McDonough SI, DeLisi LE.

Mol Psychiatry. 2016 Dec;21(12):1690-1695. doi: 10.1038/mp.2016.24.

13.

Brain connectivity in autism spectrum disorder.

Mohammad-Rezazadeh I, Frohlich J, Loo SK, Jeste SS.

Curr Opin Neurol. 2016 Apr;29(2):137-47. doi: 10.1097/WCO.0000000000000301. Review.

14.

Reduction in parvalbumin expression not loss of the parvalbumin-expressing GABA interneuron subpopulation in genetic parvalbumin and shank mouse models of autism.

Filice F, Vörckel KJ, Sungur AÖ, Wöhr M, Schwaller B.

Mol Brain. 2016 Jan 27;9:10. doi: 10.1186/s13041-016-0192-8.

15.

Monogenic mouse models of autism spectrum disorders: Common mechanisms and missing links.

Hulbert SW, Jiang YH.

Neuroscience. 2016 May 3;321:3-23. doi: 10.1016/j.neuroscience.2015.12.040. Review.

PMID:
26733386
16.

Genome-wide disruption of 5-hydroxymethylcytosine in a mouse model of autism.

Papale LA, Zhang Q, Li S, Chen K, Keleş S, Alisch RS.

Hum Mol Genet. 2015 Dec 15;24(24):7121-31. doi: 10.1093/hmg/ddv411.

17.

Behavioral phenotypes of genetic mouse models of autism.

Kazdoba TM, Leach PT, Crawley JN.

Genes Brain Behav. 2016 Jan;15(1):7-26. doi: 10.1111/gbb.12256. Review.

18.

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.

Sanders SJ, He X, Willsey AJ, Ercan-Sencicek AG, Samocha KE, Cicek AE, Murtha MT, Bal VH, Bishop SL, Dong S, Goldberg AP, Jinlu C, Keaney JF 3rd, Klei L, Mandell JD, Moreno-De-Luca D, Poultney CS, Robinson EB, Smith L, Solli-Nowlan T, Su MY, Teran NA, Walker MF, Werling DM, Beaudet AL, Cantor RM, Fombonne E, Geschwind DH, Grice DE, Lord C, Lowe JK, Mane SM, Martin DM, Morrow EM, Talkowski ME, Sutcliffe JS, Walsh CA, Yu TW; Autism Sequencing Consortium., Ledbetter DH, Martin CL, Cook EH, Buxbaum JD, Daly MJ, Devlin B, Roeder K, State MW.

Neuron. 2015 Sep 23;87(6):1215-33. doi: 10.1016/j.neuron.2015.09.016.

19.

Phelan McDermid Syndrome: From Genetic Discoveries to Animal Models and Treatment.

Harony-Nicolas H, De Rubeis S, Kolevzon A, Buxbaum JD.

J Child Neurol. 2015 Dec;30(14):1861-70. doi: 10.1177/0883073815600872. Review.

20.

Fmr1 deficiency promotes age-dependent alterations in the cortical synaptic proteome.

Tang B, Wang T, Wan H, Han L, Qin X, Zhang Y, Wang J, Yu C, Berton F, Francesconi W, Yates JR 3rd, Vanderklish PW, Liao L.

Proc Natl Acad Sci U S A. 2015 Aug 25;112(34):E4697-706. doi: 10.1073/pnas.1502258112.

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