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Items: 14

1.

Exonic deletion of SLC9A9 in autism with epilepsy.

Cardon M, Evankovich KD, Holder JL Jr.

Neurol Genet. 2016 Feb 25;2(2):e62. doi: 10.1212/NXG.0000000000000062. eCollection 2016 Apr.

2.

Autism spectrum disorder traits in Slc9a9 knock-out mice.

Yang L, Faraone SV, Zhang-James Y.

Am J Med Genet B Neuropsychiatr Genet. 2016 Apr;171B(3):363-76. doi: 10.1002/ajmg.b.32415. Epub 2016 Jan 11.

PMID:
26755066
3.

Genome-wide analysis of attention deficit hyperactivity disorder in Norway.

Zayats T, Athanasiu L, Sonderby I, Djurovic S, Westlye LT, Tamnes CK, Fladby T, Aase H, Zeiner P, Reichborn-Kjennerud T, Knappskog PM, Knudsen GP, Andreassen OA, Johansson S, Haavik J.

PLoS One. 2015 Apr 13;10(4):e0122501. doi: 10.1371/journal.pone.0122501. eCollection 2015.

4.

An inside job: how endosomal Na(+)/H(+) exchangers link to autism and neurological disease.

Kondapalli KC, Prasad H, Rao R.

Front Cell Neurosci. 2014 Jun 23;8:172. doi: 10.3389/fncel.2014.00172. eCollection 2014. Review.

5.

Can sodium/hydrogen exchange inhibitors be repositioned for treating attention deficit hyperactivity disorder? An in silico approach.

Faraone SV, Zhang-James Y.

Am J Med Genet B Neuropsychiatr Genet. 2013 Oct;162B(7):711-7. doi: 10.1002/ajmg.b.32155.

PMID:
24132903
6.

Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.

Ebejer JL, Duffy DL, van der Werf J, Wright MJ, Montgomery G, Gillespie NA, Hickie IB, Martin NG, Medland SE.

Twin Res Hum Genet. 2013 Apr;16(2):560-74. doi: 10.1017/thg.2013.12.

PMID:
23527680
7.

Differential expression of SLC9A9 and interacting molecules in the hippocampus of rat models for attention deficit/hyperactivity disorder.

Zhang-James Y, Middleton FA, Sagvolden T, Faraone SV.

Dev Neurosci. 2012;34(2-3):218-27. Epub 2012 Jul 6.

8.

SLC9A9 mutations, gene expression, and protein-protein interactions in rat models of attention-deficit/hyperactivity disorder.

Zhang-James Y, DasBanerjee T, Sagvolden T, Middleton FA, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(7):835-43. doi: 10.1002/ajmg.b.31229. Epub 2011 Aug 19.

9.

Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.

Mick E, Todorov A, Smalley S, Hu X, Loo S, Todd RD, Biederman J, Byrne D, Dechairo B, Guiney A, McCracken J, McGough J, Nelson SF, Reiersen AM, Wilens TE, Wozniak J, Neale BM, Faraone SV.

J Am Acad Child Adolesc Psychiatry. 2010 Sep;49(9):898-905.e3. doi: 10.1016/j.jaac.2010.02.014. Epub 2010 May 14.

10.

Genetic variants in SLC9A9 are associated with measures of attention-deficit/hyperactivity disorder symptoms in families.

Markunas CA, Quinn KS, Collins AL, Garrett ME, Lachiewicz AM, Sommer JL, Morrissey-Kane E, Kollins SH, Anastopoulos AD, Ashley-Koch AE.

Psychiatr Genet. 2010 Apr;20(2):73-81. doi: 10.1097/YPG.0b013e3283351209.

11.

Genome-wide association studies in ADHD.

Franke B, Neale BM, Faraone SV.

Hum Genet. 2009 Jul;126(1):13-50. doi: 10.1007/s00439-009-0663-4. Epub 2009 Apr 22. Review.

12.

Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.

Lasky-Su J, Anney RJ, Neale BM, Franke B, Zhou K, Maller JB, Vasquez AA, Chen W, Asherson P, Buitelaar J, Banaschewski T, Ebstein R, Gill M, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Taylor E, Daly M, Laird N, Lange C, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1355-8. doi: 10.1002/ajmg.b.30869.

13.

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.

Lasky-Su J, Neale BM, Franke B, Anney RJ, Zhou K, Maller JB, Vasquez AA, Chen W, Asherson P, Buitelaar J, Banaschewski T, Ebstein R, Gill M, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Taylor E, Daly M, Laird N, Lange C, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1345-54. doi: 10.1002/ajmg.b.30867.

PMID:
18821565
14.

Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype.

de Silva MG, Elliott K, Dahl HH, Fitzpatrick E, Wilcox S, Delatycki M, Williamson R, Efron D, Lynch M, Forrest S.

J Med Genet. 2003 Oct;40(10):733-40.

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