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Items: 1 to 20 of 178


Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder.

Garcia-Martínez I, Sánchez-Mora C, Soler Artigas M, Rovira P, Pagerols M, Corrales M, Calvo-Sánchez E, Richarte V, Bustamante M, Sunyer J, Cormand B, Casas M, Ramos-Quiroga JA, Ribasés M.

Sci Rep. 2017 Jul 14;7(1):5407. doi: 10.1038/s41598-017-05514-7.


Bio-collections in autism research.

Reilly J, Gallagher L, Chen JL, Leader G, Shen S.

Mol Autism. 2017 Jul 10;8:34. doi: 10.1186/s13229-017-0154-8. eCollection 2017. Review.


Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.

Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium.

Mol Autism. 2017 May 22;8:21. doi: 10.1186/s13229-017-0137-9. eCollection 2017.


Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general population.

Vojinovic D, Brison N, Ahmad S, Noens I, Pappa I, Karssen LC, Tiemeier H, van Duijn CM, Peeters H, Amin N.

Eur J Hum Genet. 2017 Aug;25(8):982-987. doi: 10.1038/ejhg.2017.82. Epub 2017 May 17.


Gene-set analysis shows association between FMRP targets and autism spectrum disorder.

Jansen A, Dieleman GC, Smit AB, Verhage M, Verhulst FC, Polderman TJC, Posthuma D.

Eur J Hum Genet. 2017 Jun;25(7):863-868. doi: 10.1038/ejhg.2017.55. Epub 2017 Apr 19.


NCAM Regulates Inhibition and Excitability in Layer 2/3 Pyramidal Cells of Anterior Cingulate Cortex.

Zhang X, Sullivan CS, Kratz MB, Kasten MR, Maness PF, Manis PB.

Front Neural Circuits. 2017 Mar 23;11:19. doi: 10.3389/fncir.2017.00019. eCollection 2017.


Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.

Chen R, Davis LK, Guter S, Wei Q, Jacob S, Potter MH, Cox NJ, Cook EH, Sutcliffe JS, Li B.

Mol Autism. 2017 Mar 21;8:14. doi: 10.1186/s13229-017-0130-3. eCollection 2017.


Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

Guo H, Peng Y, Hu Z, Li Y, Xun G, Ou J, Sun L, Xiong Z, Liu Y, Wang T, Chen J, Xia L, Bai T, Shen Y, Tian Q, Hu Y, Shen L, Zhao R, Zhang X, Zhang F, Zhao J, Zou X, Xia K.

Sci Rep. 2017 Mar 10;7:44155. doi: 10.1038/srep44155.


Social Isolation Alters Social and Mating Behavior in the R451C Neuroligin Mouse Model of Autism.

Burrows EL, Eastwood AF, May C, Kolbe SC, Hill T, McLachlan NM, Churilov L, Hannan AJ.

Neural Plast. 2017;2017:8361290. doi: 10.1155/2017/8361290. Epub 2017 Jan 31.


Widespread signatures of positive selection in common risk alleles associated to autism spectrum disorder.

Polimanti R, Gelernter J.

PLoS Genet. 2017 Feb 10;13(2):e1006618. doi: 10.1371/journal.pgen.1006618. eCollection 2017 Feb.


High-throughput screen detects calcium signaling dysfunction in typical sporadic autism spectrum disorder.

Schmunk G, Nguyen RL, Ferguson DL, Kumar K, Parker I, Gargus JJ.

Sci Rep. 2017 Feb 1;7:40740. doi: 10.1038/srep40740.


Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders.

Mitra I, Lavillaureix A, Yeh E, Traglia M, Tsang K, Bearden CE, Rauen KA, Weiss LA.

PLoS Genet. 2017 Jan 11;13(1):e1006516. doi: 10.1371/journal.pgen.1006516. eCollection 2017 Jan.


ATM induces MacroD2 nuclear export upon DNA damage.

Golia B, Moeller GK, Jankevicius G, Schmidt A, Hegele A, Preißer J, Tran ML, Imhof A, Timinszky G.

Nucleic Acids Res. 2017 Jan 9;45(1):244-254. doi: 10.1093/nar/gkw904. Epub 2016 Oct 7.


A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3.

Connolly S, Anney R, Gallagher L, Heron EA.

Eur J Hum Genet. 2017 Feb;25(2):234-239. doi: 10.1038/ejhg.2016.153. Epub 2016 Nov 23.


Pleiotropic Mechanisms Indicated for Sex Differences in Autism.

Mitra I, Tsang K, Ladd-Acosta C, Croen LA, Aldinger KA, Hendren RL, Traglia M, Lavillaureix A, Zaitlen N, Oldham MC, Levitt P, Nelson S, Amaral DG, Hertz-Picciotto I, Fallin MD, Weiss LA.

PLoS Genet. 2016 Nov 15;12(11):e1006425. doi: 10.1371/journal.pgen.1006425. eCollection 2016 Nov. Erratum in: PLoS Genet. 2017 Jun 7;13(6):e1006831.


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. doi: 10.1186/s13229-016-0103-y. eCollection 2016.


Brain enhancer activities at the gene-poor 5p14.1 autism-associated locus.

Inoue YU, Inoue T.

Sci Rep. 2016 Aug 9;6:31227. doi: 10.1038/srep31227.


Association between IRS1 Gene Polymorphism and Autism Spectrum Disorder: A Pilot Case-Control Study in Korean Males.

Park HJ, Kim SK, Kang WS, Park JK, Kim YJ, Nam M, Kim JW, Chung JH.

Int J Mol Sci. 2016 Jul 29;17(8). pii: E1227. doi: 10.3390/ijms17081227.


Enrichment of risk SNPs in regulatory regions implicate diverse tissues in Parkinson's disease etiology.

Coetzee SG, Pierce S, Brundin P, Brundin L, Hazelett DJ, Coetzee GA.

Sci Rep. 2016 Jul 27;6:30509. doi: 10.1038/srep30509.


Glycan susceptibility factors in autism spectrum disorders.

Dwyer CA, Esko JD.

Mol Aspects Med. 2016 Oct;51:104-14. doi: 10.1016/j.mam.2016.07.001. Epub 2016 Jul 11. Review.

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