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Items: 1 to 20 of 77


Autistic, Aberrant, and Food-Related Behaviors in Adolescents and Young Adults with Prader-Willi Syndrome: The Effects of Age and Genotype.

Ishii A, Ihara H, Ogata H, Sayama M, Gito M, Murakami N, Ayabe T, Oto Y, Takahashi A, Nagai T.

Behav Neurol. 2017;2017:4615451. doi: 10.1155/2017/4615451. Epub 2017 Dec 26.


The Default Mode Network in Autism.

Padmanabhan A, Lynch CJ, Schaer M, Menon V.

Biol Psychiatry Cogn Neurosci Neuroimaging. 2017 Sep;2(6):476-486. doi: 10.1016/j.bpsc.2017.04.004.


GABAA receptor subunit gene polymorphisms predict symptom-based and developmental deficits in Chinese Han children and adolescents with autistic spectrum disorders.

Yang S, Guo X, Dong X, Han Y, Gao L, Su Y, Dai W, Zhang X.

Sci Rep. 2017 Jun 12;7(1):3290. doi: 10.1038/s41598-017-03666-0.


Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy.

Robert C, Pasquier L, Cohen D, Fradin M, Canitano R, Damaj L, Odent S, Tordjman S.

Int J Mol Sci. 2017 Mar 12;18(3). pii: E618. doi: 10.3390/ijms18030618. Review.


Williams Syndrome and 15q Duplication: Coincidence versus Association.

Khokhar A, Agarwal S, Perez-Colon S.

Mol Syndromol. 2017 Jan;8(1):50-54. doi: 10.1159/000452360. Epub 2016 Nov 15.


A Rare Inherited 15q11.2-q13.1 Interstitial Duplication with Maternal Somatic Mosaicism, Renal Carcinoma, and Autism.

Urraca N, Potter B, Hundley R, Pivnick EK, McVicar K, Thibert RL, Ledbetter C, Chamberlain R, Miravalle L, Sirois CL, Chamberlain S, Reiter LT.

Front Genet. 2016 Nov 25;7:205. eCollection 2016.


Topoisomerase 1 Regulates Gene Expression in Neurons through Cleavage Complex-Dependent and -Independent Mechanisms.

Mabb AM, Simon JM, King IF, Lee HM, An LK, Philpot BD, Zylka MJ.

PLoS One. 2016 May 27;11(5):e0156439. doi: 10.1371/journal.pone.0156439. eCollection 2016.


Identification of a distinct developmental and behavioral profile in children with Dup15q syndrome.

DiStefano C, Gulsrud A, Huberty S, Kasari C, Cook E, Reiter LT, Thibert R, Jeste SS.

J Neurodev Disord. 2016 May 6;8:19. doi: 10.1186/s11689-016-9152-y. eCollection 2016.


New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.

Cappuccio G, Vitiello F, Casertano A, Fontana P, Genesio R, Bruzzese D, Ginocchio VM, Mormile A, Nitsch L, Andria G, Melis D.

Ital J Pediatr. 2016 Apr 12;42:39. doi: 10.1186/s13052-016-0246-7.


Significant neuronal soma volume deficit in the limbic system in subjects with 15q11.2-q13 duplications.

Wegiel J, Flory M, Schanen NC, Cook EH, Nowicki K, Kuchna I, Imaki H, Ma SY, Wegiel J, London E, Casanova MF, Wisniewski T, Brown WT.

Acta Neuropathol Commun. 2015 Oct 13;3:63. doi: 10.1186/s40478-015-0241-z.


Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism.

Li J, Zhao L, You Y, Lu T, Jia M, Yu H, Ruan Y, Yue W, Liu J, Lu L, Zhang D, Wang L.

PLoS One. 2015 Jul 23;10(7):e0133247. doi: 10.1371/journal.pone.0133247. eCollection 2015.


The Human Model: Changing Focus on Autism Research.

Muotri AR.

Biol Psychiatry. 2016 Apr 15;79(8):642-9. doi: 10.1016/j.biopsych.2015.03.012. Epub 2015 Mar 17. Review.


GABAB Receptor Agonist R-Baclofen Reverses Social Deficits and Reduces Repetitive Behavior in Two Mouse Models of Autism.

Silverman JL, Pride MC, Hayes JE, Puhger KR, Butler-Struben HM, Baker S, Crawley JN.

Neuropsychopharmacology. 2015 Aug;40(9):2228-39. doi: 10.1038/npp.2015.66. Epub 2015 Mar 10.


Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1.

Germain ND, Chen PF, Plocik AM, Glatt-Deeley H, Brown J, Fink JJ, Bolduc KA, Robinson TM, Levine ES, Reiter LT, Graveley BR, Lalande M, Chamberlain SJ.

Mol Autism. 2014 Aug 20;5:44. doi: 10.1186/2040-2392-5-44. eCollection 2014.


GABA receptor subunit distribution and FMRP-mGluR5 signaling abnormalities in the cerebellum of subjects with schizophrenia, mood disorders, and autism.

Fatemi SH, Folsom TD.

Schizophr Res. 2015 Sep;167(1-3):42-56. doi: 10.1016/j.schres.2014.10.010. Epub 2014 Nov 26. Review.


Gene × Environment interactions in autism spectrum disorders: role of epigenetic mechanisms.

Tordjman S, Somogyi E, Coulon N, Kermarrec S, Cohen D, Bronsard G, Bonnot O, Weismann-Arcache C, Botbol M, Lauth B, Ginchat V, Roubertoux P, Barburoth M, Kovess V, Geoffray MM, Xavier J.

Front Psychiatry. 2014 Aug 4;5:53. doi: 10.3389/fpsyt.2014.00053. eCollection 2014. Review.


Genetic aspects of autism spectrum disorders: insights from animal models.

Banerjee S, Riordan M, Bhat MA.

Front Cell Neurosci. 2014 Feb 24;8:58. doi: 10.3389/fncel.2014.00058. eCollection 2014. Review.


Prevalence of selected genomic deletions and duplications in a French-Canadian population-based sample of newborns.

Tucker T, Giroux S, Clément V, Langlois S, Friedman JM, Rousseau F.

Mol Genet Genomic Med. 2013 Jul;1(2):87-97. doi: 10.1002/mgg3.12. Epub 2013 May 21.


Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism.

Warrier V, Baron-Cohen S, Chakrabarti B.

Mol Autism. 2013 Dec 9;4(1):48. doi: 10.1186/2040-2392-4-48.


Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.

Roberts JL, Hovanes K, Dasouki M, Manzardo AM, Butler MG.

Gene. 2014 Feb 1;535(1):70-8. doi: 10.1016/j.gene.2013.10.020. Epub 2013 Nov 2.

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