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Items: 18

1.

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.

2.

GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans.

Chittoor G, Kent JW Jr, Almeida M, Puppala S, Farook VS, Cole SA, Haack K, Göring HH, MacCluer JW, Curran JE, Carless MA, Johnson MP, Moses EK, Almasy L, Mahaney MC, Lehman DM, Duggirala R, Comuzzie AG, Blangero J, Voruganti VS.

BMC Genomics. 2016 Apr 2;17:276. doi: 10.1186/s12864-016-2594-5.

3.

Limited impact of Cntn4 mutation on autism-related traits in developing and adult C57BL/6J mice.

Molenhuis RT, Bruining H, Remmelink E, de Visser L, Loos M, Burbach JP, Kas MJ.

J Neurodev Disord. 2016 Mar 2;8:6. doi: 10.1186/s11689-016-9140-2.

4.

CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders.

Hu J, Liao J, Sathanoori M, Kochmar S, Sebastian J, Yatsenko SA, Surti U.

J Neurodev Disord. 2015;7(1):26. doi: 10.1186/s11689-015-9122-9.

5.

Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints.

Newman S, Hermetz KE, Weckselblatt B, Rudd MK.

Am J Hum Genet. 2015 Feb 5;96(2):208-20. doi: 10.1016/j.ajhg.2014.12.017.

6.

Proper migration and axon outgrowth of zebrafish cranial motoneuron subpopulations require the cell adhesion molecule MDGA2A.

Ingold E, Vom Berg-Maurer CM, Burckhardt CJ, Lehnherr A, Rieder P, Keller PJ, Stelzer EH, Greber UF, Neuhauss SC, Gesemann M.

Biol Open. 2015 Jan 8;4(2):146-54. doi: 10.1242/bio.20148482.

7.

Association of NCAM1 polymorphisms with autism and parental age at conception in a Chinese Han population.

Zhang J, Wang A, Li Y, Lu X, Wang F, Fang F.

Genet Test Mol Biomarkers. 2014 Oct;18(10):690-4. doi: 10.1089/gtmb.2014.0055.

8.

Intercellular protein-protein interactions at synapses.

Yang X, Hou D, Jiang W, Zhang C.

Protein Cell. 2014 Jun;5(6):420-44. doi: 10.1007/s13238-014-0054-z. Review.

9.

Family-based clinical associations and functional characterization of the serotonin 2A receptor gene (HTR2A) in autism spectrum disorder.

Smith RM, Banks W, Hansen E, Sadee W, Herman GE.

Autism Res. 2014 Aug;7(4):459-67. doi: 10.1002/aur.1383.

10.

ChIP-seq analysis of histone H3K9 trimethylation in peripheral blood mononuclear cells of membranous nephropathy patients.

Sui WG, He HY, Yan Q, Chen JJ, Zhang RH, Dai Y.

Braz J Med Biol Res. 2014 Jan;47(1):42-9. doi: 10.1590/1414-431X20132809.

11.

Common DNA methylation alterations in multiple brain regions in autism.

Ladd-Acosta C, Hansen KD, Briem E, Fallin MD, Kaufmann WE, Feinberg AP.

Mol Psychiatry. 2014 Aug;19(8):862-71. doi: 10.1038/mp.2013.114.

12.

Contactin 4, -5 and -6 differentially regulate neuritogenesis while they display identical PTPRG binding sites.

Mercati O, Danckaert A, André-Leroux G, Bellinzoni M, Gouder L, Watanabe K, Shimoda Y, Grailhe R, De Chaumont F, Bourgeron T, Cloëz-Tayarani I.

Biol Open. 2013 Mar 15;2(3):324-34. doi: 10.1242/bio.20133343.

13.

Genetic schizophrenia risk variants jointly modulate total brain and white matter volume.

Terwisscha van Scheltinga AF, Bakker SC, van Haren NE, Derks EM, Buizer-Voskamp JE, Boos HB, Cahn W, Hulshoff Pol HE, Ripke S, Ophoff RA, Kahn RS; Psychiatric Genome-wide Association Study Consortium..

Biol Psychiatry. 2013 Mar 15;73(6):525-31. doi: 10.1016/j.biopsych.2012.08.017.

14.

Autism genetics: searching for specificity and convergence.

Berg JM, Geschwind DH.

Genome Biol. 2012 Jul 31;13(7):247. doi: 10.1186/gb4034. Review.

15.

Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways.

Griswold AJ, Ma D, Cukier HN, Nations LD, Schmidt MA, Chung RH, Jaworski JM, Salyakina D, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Martin ER, Haines JL, Gilbert JR, Cuccaro ML, Pericak-Vance MA.

Hum Mol Genet. 2012 Aug 1;21(15):3513-23. doi: 10.1093/hmg/dds164.

16.

Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics.

Ghani M, Pinto D, Lee JH, Grinberg Y, Sato C, Moreno D, Scherer SW, Mayeux R, St George-Hyslop P, Rogaeva E.

G3 (Bethesda). 2012 Jan;2(1):71-8. doi: 10.1534/g3.111.000869.

17.

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.

Leblond CS, Heinrich J, Delorme R, Proepper C, Betancur C, Huguet G, Konyukh M, Chaste P, Ey E, Rastam M, Anckarsäter H, Nygren G, Gillberg IC, Melke J, Toro R, Regnault B, Fauchereau F, Mercati O, Lemière N, Skuse D, Poot M, Holt R, Monaco AP, Järvelä I, Kantojärvi K, Vanhala R, Curran S, Collier DA, Bolton P, Chiocchetti A, Klauck SM, Poustka F, Freitag CM, Waltes R, Kopp M, Duketis E, Bacchelli E, Minopoli F, Ruta L, Battaglia A, Mazzone L, Maestrini E, Sequeira AF, Oliveira B, Vicente A, Oliveira G, Pinto D, Scherer SW, Zelenika D, Delepine M, Lathrop M, Bonneau D, Guinchat V, Devillard F, Assouline B, Mouren MC, Leboyer M, Gillberg C, Boeckers TM, Bourgeron T.

PLoS Genet. 2012 Feb;8(2):e1002521. doi: 10.1371/journal.pgen.1002521.

18.

Inositol 1,4,5-trisphosphate receptor 1 mutation perturbs glucose homeostasis and enhances susceptibility to diet-induced diabetes.

Ye R, Ni M, Wang M, Luo S, Zhu G, Chow RH, Lee AS.

J Endocrinol. 2011 Aug;210(2):209-17. doi: 10.1530/JOE-11-0012.

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