Gillam L - Search Results

1

"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: gillam l. 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

2

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: gillam l. Genet Med. 2005 Jul-Aug;7(6):390-6. doi: 10.1097/01.gim.0000170775.39092.44. Genet Med. 2005. PMID: 16024970

3

"Holding your breath": interviews with young people who have undergone predictive genetic testing for Huntington disease.

Duncan RE, Gillam L, Savulescu J, Williamson R, Rogers JG, Delatycki MB. Duncan RE, et al. Among authors: gillam l. Am J Med Genet A. 2007 Sep 1;143A(17):1984-9. doi: 10.1002/ajmg.a.31720. Am J Med Genet A. 2007. PMID: 17663467

4

The challenge of developmentally appropriate care: predictive genetic testing in young people for familial adenomatous polyposis.

Duncan RE, Gillam L, Savulescu J, Williamson R, Rogers JG, Delatycki MB. Duncan RE, et al. Among authors: gillam l. Fam Cancer. 2010 Mar;9(1):27-35. doi: 10.1007/s10689-009-9294-0. Epub 2009 Sep 17. Fam Cancer. 2010. PMID: 19760114

5

Genetic selection for deafness: the views of hearing children of deaf adults.

Mand C, Duncan RE, Gillam L, Collins V, Delatycki MB. Mand C, et al. Among authors: gillam l. J Med Ethics. 2009 Dec;35(12):722-8. doi: 10.1136/jme.2009.030429. J Med Ethics. 2009. PMID: 19948926 Clinical Trial.

6

Predictive genetic testing in minors for late-onset conditions: a chronological and analytical review of the ethical arguments.

Mand C, Gillam L, Delatycki MB, Duncan RE. Mand C, et al. Among authors: gillam l. J Med Ethics. 2012 Sep;38(9):519-24. doi: 10.1136/medethics-2011-100055. Epub 2012 Mar 8. J Med Ethics. 2012. PMID: 22403084 Review.

7

"It was the missing piece": adolescent experiences of predictive genetic testing for adult-onset conditions.

Mand C, Gillam L, Duncan RE, Delatycki MB. Mand C, et al. Among authors: gillam l. Genet Med. 2013 Aug;15(8):643-9. doi: 10.1038/gim.2013.15. Epub 2013 Feb 28. Genet Med. 2013. PMID: 23448724 Free article.

8

"I'm scared of being like mum": The Experience of Adolescents Living in Families with Huntington Disease.

Mand CM, Gillam L, Duncan RE, Delatycki MB. Mand CM, et al. Among authors: gillam l. J Huntingtons Dis. 2015;4(3):209-17. doi: 10.3233/JHD-150148. J Huntingtons Dis. 2015. PMID: 26443924

9

Parents' experiences with requesting carrier testing for their unaffected children.

Vears DF, Delany C, Massie J, Gillam L. Vears DF, et al. Among authors: gillam l. Genet Med. 2016 Dec;18(12):1199-1205. doi: 10.1038/gim.2016.24. Epub 2016 Mar 24. Genet Med. 2016. PMID: 27011057 Free article.

10

Predictive genetic testing for neurodegenerative conditions: how should conflicting interests within families be managed?

Stark Z, Wallace J, Gillam L, Burgess M, Delatycki MB. Stark Z, et al. Among authors: gillam l. J Med Ethics. 2016 Oct;42(10):640-2. doi: 10.1136/medethics-2016-103400. Epub 2016 Jun 8. J Med Ethics. 2016. PMID: 27281798

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