Similar articles for PMID: 14569117

Year	Number of Results
1978	1
2000	2
2001	2
2002	2
2003	4
2004	2
2005	3
2006	6
2007	2
2008	4
2009	1
2010	4
2011	5
2012	2
2013	7
2014	2
2015	2
2016	5
2017	5
2018	3
2019	2
2020	1
2024	0

1

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. de Silva MG, et al. J Med Genet. 2003 Oct;40(10):733-40. doi: 10.1136/jmg.40.10.733. J Med Genet. 2003. PMID: 14569117 Free PMC article.

2

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. Markunas CA, et al. Psychiatr Genet. 2010 Apr;20(2):73-81. doi: 10.1097/YPG.0b013e3283351209. Psychiatr Genet. 2010. PMID: 20032819 Free PMC article.

3

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. Zhang-James Y, et al. Dev Neurosci. 2012;34(2-3):218-27. doi: 10.1159/000338813. Epub 2012 Jul 6. Dev Neurosci. 2012. PMID: 22777493 Free PMC article.

4

Effect of disease-associated SLC9A9 mutations on protein-protein interaction networks: implications for molecular mechanisms for ADHD and autism.

Zhang-James Y, Vaudel M, Mjaavatten O, Berven FS, Haavik J, Faraone SV. Zhang-James Y, et al. Atten Defic Hyperact Disord. 2019 Mar;11(1):91-105. doi: 10.1007/s12402-018-0281-x. Epub 2019 Mar 29. Atten Defic Hyperact Disord. 2019. PMID: 30927234

5

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. Zhang-James Y, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(7):835-43. doi: 10.1002/ajmg.b.31229. Epub 2011 Aug 19. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21858920 Free PMC article.

6

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. Zayats T, et al. PLoS One. 2015 Apr 13;10(4):e0122501. doi: 10.1371/journal.pone.0122501. eCollection 2015. PLoS One. 2015. PMID: 25875332 Free PMC article.

7

A novel pericentric inversion of chromosome 3 cosegregates with a developmental-behavioural phenotype.

Efron D, Delatycki MB, de Silva MG, Langbein A, Slaghuis W, Larson A, Dahl HH, Forrest SM. Efron D, et al. J Med Genet. 2003 Feb;40(2):E15. doi: 10.1136/jmg.40.2.e15. J Med Genet. 2003. PMID: 12566533 Free PMC article. No abstract available.

8

Sodium hydrogen exchanger 9 NHE9 (SLC9A9) and its emerging roles in neuropsychiatric comorbidity.

Patak J, Faraone SV, Zhang-James Y. Patak J, et al. Am J Med Genet B Neuropsychiatr Genet. 2020 Jul;183(5):289-305. doi: 10.1002/ajmg.b.32787. Epub 2020 May 13. Am J Med Genet B Neuropsychiatr Genet. 2020. PMID: 32400953

9

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. Lasky-Su J, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1355-8. doi: 10.1002/ajmg.b.30869. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18937294 Free PMC article.

10

Biallelic loss-of-function variants in DOCK3 cause muscle hypotonia, ataxia, and intellectual disability.

Helbig KL, Mroske C, Moorthy D, Sajan SA, Velinov M. Helbig KL, et al. Clin Genet. 2017 Oct;92(4):430-433. doi: 10.1111/cge.12995. Epub 2017 Mar 30. Clin Genet. 2017. PMID: 28195318

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