Williamson R - Search Results

1

Implementation of HaemScreen, a workplace-based genetic screening program for hemochromatosis.

Nisselle AE, Delatycki MB, Collins V, Metcalfe S, Aitken MA, du Sart D, Halliday J, Macciocca I, Wakefield A, Hill V, Gason A, Warner B, Calabro V, Williamson R, Allen KJ. Nisselle AE, et al. Among authors: williamson r. Clin Genet. 2004 May;65(5):358-67. doi: 10.1111/j.1399-0004.2004.0239.x. Clin Genet. 2004. PMID: 15099342

2

Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis.

Delatycki MB, Allen KJ, Nisselle AE, Collins V, Metcalfe S, du Sart D, Halliday J, Aitken MA, Macciocca I, Hill V, Wakefield A, Ritchie A, Gason AA, Nicoll AJ, Powell LW, Williamson R. Delatycki MB, et al. Among authors: williamson r. Lancet. 2005 Jul 23-29;366(9482):314-6. doi: 10.1016/S0140-6736(05)63012-7. Lancet. 2005. PMID: 16039334

3

Assessment of education and counselling offered by a familial colorectal cancer clinic.

Collins V, Halliday J, Warren R, Williamson R. Collins V, et al. Among authors: williamson r. Clin Genet. 2000 Jan;57(1):48-55. doi: 10.1034/j.1399-0004.2000.570107.x. Clin Genet. 2000. PMID: 10733235

4

Cancer worries, risk perceptions and associations with interest in DNA testing and clinic satisfaction in a familial colorectal cancer clinic.

Collins V, Halliday J, Warren R, Williamson R. Collins V, et al. Among authors: williamson r. Clin Genet. 2000 Dec;58(6):460-8. doi: 10.1034/j.1399-0004.2000.580606.x. Clin Genet. 2000. PMID: 11149615

5

An international survey of predictive genetic testing in children for adult onset conditions.

Duncan RE, Savulescu J, Gillam L, Williamson R, Delatycki MB. Duncan RE, et al. Among authors: williamson r. Genet Med. 2005 Jul-Aug;7(6):390-6. doi: 10.1097/01.gim.0000170775.39092.44. Genet Med. 2005. PMID: 16024970

6

"You're one of us now": young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP).

Duncan RE, Gillam L, Savulescu J, Williamson R, Rogers JG, Delatycki MB. Duncan RE, et al. Among authors: williamson r. Am J Med Genet C Semin Med Genet. 2008 Feb 15;148C(1):47-55. doi: 10.1002/ajmg.c.30158. Am J Med Genet C Semin Med Genet. 2008. PMID: 18189288

7

Asymptomatic individuals at genetic risk of haemochromatosis take appropriate steps to prevent disease related to iron overload.

Allen KJ, Nisselle AE, Collins VR, Williamson R, Delatycki MB. Allen KJ, et al. Among authors: williamson r. Liver Int. 2008 Mar;28(3):363-9. doi: 10.1111/j.1478-3231.2008.01661.x. Liver Int. 2008. PMID: 18290779

8

Providing services for families with a genetic condition: a contrast between cystic fibrosis and Down syndrome.

Collins V, Williamson R. Collins V, et al. Among authors: williamson r. Pediatrics. 2003 Nov;112(5):1177-80. doi: 10.1542/peds.112.5.1177. Pediatrics. 2003. PMID: 14595065 No abstract available.

9

Friedreich ataxia: an overview.

Delatycki MB, Williamson R, Forrest SM. Delatycki MB, et al. Among authors: williamson r. J Med Genet. 2000 Jan;37(1):1-8. doi: 10.1136/jmg.37.1.1. J Med Genet. 2000. PMID: 10633128 Free PMC article. Review.

10

Should we genetically test everyone for haemochromatosis?

Allen K, Williamson R. Allen K, et al. Among authors: williamson r. J Med Ethics. 1999 Apr;25(2):209-14. doi: 10.1136/jme.25.2.209. J Med Ethics. 1999. PMID: 10226930 Free PMC article.

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