Cox D - Search Results

1

NPAS3 variants in schizophrenia: a neuroimaging study.

Bernier D, Macintyre G, Bartha R, Hanstock CC, McAllindon D, Cox D, Purdon S, Aitchison KJ, Rusak B, Tibbo PG. Bernier D, et al. Among authors: cox d. BMC Med Genet. 2014 Mar 27;15:37. doi: 10.1186/1471-2350-15-37. BMC Med Genet. 2014. PMID: 24674381 Free PMC article.

2

Association of NPAS3 exonic variation with schizophrenia.

Macintyre G, Alford T, Xiong L, Rouleau GA, Tibbo PG, Cox DW. Macintyre G, et al. Schizophr Res. 2010 Jul;120(1-3):143-9. doi: 10.1016/j.schres.2010.04.002. Epub 2010 May 14. Schizophr Res. 2010. PMID: 20466522

3

New mutations in the Wilson disease gene, ATP7B: implications for molecular testing.

Davies LP, Macintyre G, Cox DW. Davies LP, et al. Genet Test. 2008 Mar;12(1):139-45. doi: 10.1089/gte.2007.0072. Genet Test. 2008. PMID: 18373411

4

A child with deletion (14)(q24.3q32.13) and auditory neuropathy.

Schlade-Bartusiak K, Macintyre G, Zunich J, Cox DW. Schlade-Bartusiak K, et al. Am J Med Genet A. 2008 Jan 1;146A(1):117-23. doi: 10.1002/ajmg.a.32064. Am J Med Genet A. 2008. PMID: 18074379

5

A minigene approach for analysis of ATP7B splice variants in patients with Wilson disease.

Wilson AM, Schlade-Bartusiak K, Tison JL, Macintyre G, Cox DW. Wilson AM, et al. Biochimie. 2009 Oct;91(10):1342-5. doi: 10.1016/j.biochi.2009.06.008. Epub 2009 Jun 21. Biochimie. 2009. PMID: 19540904

6

Functional analysis of mutations in the ATP loop of the Wilson disease copper transporter, ATP7B.

Luoma LM, Deeb TM, Macintyre G, Cox DW. Luoma LM, et al. Hum Mutat. 2010 May;31(5):569-77. doi: 10.1002/humu.21228. Hum Mutat. 2010. PMID: 20333758

7

Value of an enzymatic assay for the determination of serum ceruloplasmin.

Macintyre G, Gutfreund KS, Martin WR, Camicioli R, Cox DW. Macintyre G, et al. J Lab Clin Med. 2004 Dec;144(6):294-301. doi: 10.1016/j.lab.2004.08.005. J Lab Clin Med. 2004. PMID: 15614251

8

Sequence variation in the ATP-binding domain of the Wilson disease transporter, ATP7B, affects copper transport in a yeast model system.

Hsi G, Cullen LM, Macintyre G, Chen MM, Glerum DM, Cox DW. Hsi G, et al. Among authors: cox dw. Hum Mutat. 2008 Apr;29(4):491-501. doi: 10.1002/humu.20674. Hum Mutat. 2008. PMID: 18203200

9

Disruption of the neuronal PAS3 gene in a family affected with schizophrenia.

Kamnasaran D, Muir WJ, Ferguson-Smith MA, Cox DW. Kamnasaran D, et al. Among authors: cox dw. J Med Genet. 2003 May;40(5):325-32. doi: 10.1136/jmg.40.5.325. J Med Genet. 2003. PMID: 12746393 Free PMC article.

10

Molecular analysis of three patients with interstitial deletions of chromosome band 14q31.

Byth BC, Costa MT, Teshima IE, Wilson WG, Carter NP, Cox DW. Byth BC, et al. Among authors: cox dw. J Med Genet. 1995 Jul;32(7):564-7. doi: 10.1136/jmg.32.7.564. J Med Genet. 1995. PMID: 7562974 Free PMC article.

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