Wright CF - Search Results

1

Informatics and clinical genome sequencing: opening the black box.

Moorthie S, Hall A, Wright CF. Moorthie S, et al. Among authors: wright cf. Genet Med. 2013 Mar;15(3):165-71. doi: 10.1038/gim.2012.116. Epub 2012 Sep 13. Genet Med. 2013. PMID: 22975759 Free article. Review.

2

Size of the direct-to-consumer genomic testing market.

Wright CF, Gregory-Jones S. Wright CF, et al. Genet Med. 2010 Sep;12(9):594. doi: 10.1097/GIM.0b013e3181ead743. Genet Med. 2010. PMID: 20697288 Free article.

3

Regulating direct-to-consumer genetic tests: what is all the fuss about?

Wright CF, Hall A, Zimmern RL. Wright CF, et al. Genet Med. 2011 Apr;13(4):295-300. doi: 10.1097/GIM.0b013e3181f69dd2. Genet Med. 2011. PMID: 20921893 Free article.

4

Extending the reach of public health genomics: what should be the agenda for public health in an era of genome-based and “personalized” medicine?

Burke W, Burton H, Hall AE, Karmali M, Khoury MJ, Knoppers B, Meslin EM, Stanley F, Wright CF, Zimmern RL; Ickworth Group. Burke W, et al. Among authors: wright cf. Genet Med. 2010 Dec;12(12):785-91. doi: 10.1097/GIM.0b013e3182011222. Genet Med. 2010. PMID: 21189494 Free article.

5

Review of massively parallel DNA sequencing technologies.

Moorthie S, Mattocks CJ, Wright CF. Moorthie S, et al. Among authors: wright cf. Hugo J. 2011 Dec;5(1-4):1-12. doi: 10.1007/s11568-011-9156-3. Epub 2011 Oct 27. Hugo J. 2011. PMID: 23205160 Free PMC article.

6

Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders.

Wright CF, McRae JF, Clayton S, Gallone G, Aitken S, FitzGerald TW, Jones P, Prigmore E, Rajan D, Lord J, Sifrim A, Kelsell R, Parker MJ, Barrett JC, Hurles ME, FitzPatrick DR, Firth HV; DDD Study. Wright CF, et al. Genet Med. 2018 Oct;20(10):1216-1223. doi: 10.1038/gim.2017.246. Epub 2018 Jan 11. Genet Med. 2018. PMID: 29323667 Free PMC article.

7

Genomic variant sharing: a position statement.

Wright CF, Ware JS, Lucassen AM, Hall A, Middleton A, Rahman N, Ellard S, Firth HV. Wright CF, et al. Wellcome Open Res. 2019 Feb 5;4:22. doi: 10.12688/wellcomeopenres.15090.2. eCollection 2019. Wellcome Open Res. 2019. PMID: 31886409 Free PMC article.

8

Assessing performance of pathogenicity predictors using clinically relevant variant datasets.

Gunning AC, Fryer V, Fasham J, Crosby AH, Ellard S, Baple EL, Wright CF. Gunning AC, et al. Among authors: wright cf. J Med Genet. 2021 Aug;58(8):547-555. doi: 10.1136/jmedgenet-2020-107003. Epub 2020 Aug 25. J Med Genet. 2021. PMID: 32843488 Free PMC article.

9

Community Corner: Opening the Pandora's box of prenatal genetic testing.

Wright C, Quake SR, Bianchi D, Wald NJ. Wright C, et al. Nat Med. 2011 Mar;17(3):250-1. doi: 10.1038/nm0311-250. Nat Med. 2011. PMID: 21383717 No abstract available.

10

Policy challenges of clinical genome sequencing.

Wright CF, Middleton A, Burton H, Cunningham F, Humphries SE, Hurst J, Birney E, Firth HV. Wright CF, et al. BMJ. 2013 Nov 22;347:f6845. doi: 10.1136/bmj.f6845. BMJ. 2013. PMID: 24270507 No abstract available.

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