Adam S - Search Results

1

FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project.

Beaulieu CL, Majewski J, Schwartzentruber J, Samuels ME, Fernandez BA, Bernier FP, Brudno M, Knoppers B, Marcadier J, Dyment D, Adam S, Bulman DE, Jones SJ, Avard D, Nguyen MT, Rousseau F, Marshall C, Wintle RF, Shen Y, Scherer SW; FORGE Canada Consortium; Friedman JM, Michaud JL, Boycott KM. Beaulieu CL, et al. Among authors: adam s. Am J Hum Genet. 2014 Jun 5;94(6):809-17. doi: 10.1016/j.ajhg.2014.05.003. Am J Hum Genet. 2014. PMID: 24906018 Free PMC article.

2

Predictive testing for Huntington disease in Canada: the experience of those receiving an increased risk.

Bloch M, Adam S, Wiggins S, Huggins M, Hayden MR. Bloch M, et al. Among authors: adam s. Am J Med Genet. 1992 Feb 15;42(4):499-507. doi: 10.1002/ajmg.1320420416. Am J Med Genet. 1992. PMID: 1535177

3

Linkage disequilibrium and modification of risk for Huntington disease.

Adam S, Theilmann J, Buetow K, Hedrick A, Collins C, Weber B, Huggins M, Hayden M. Adam S, et al. Am J Hum Genet. 1991 Mar;48(3):595-603. Am J Hum Genet. 1991. PMID: 1671809 Free PMC article.

4

Proceed with care: direct predictive testing for Huntington disease.

Benjamin CM, Adam S, Wiggins S, Theilmann JL, Copley TT, Bloch M, Squitieri F, McKellin W, Cox S, Brown SA, et al. Benjamin CM, et al. Among authors: adam s. Am J Hum Genet. 1994 Oct;55(4):606-17. Am J Hum Genet. 1994. PMID: 7942838 Free PMC article. Clinical Trial.

5

Huntington disease without CAG expansion: phenocopies or errors in assignment?

Andrew SE, Goldberg YP, Kremer B, Squitieri F, Theilmann J, Zeisler J, Telenius H, Adam S, Almquist E, Anvret M, et al. Andrew SE, et al. Among authors: adam s. Am J Hum Genet. 1994 May;54(5):852-63. Am J Hum Genet. 1994. PMID: 8178825 Free PMC article.

6

Risk reversals in predictive testing for Huntington disease.

Almqvist E, Adam S, Bloch M, Fuller A, Welch P, Eisenberg D, Whelan D, Macgregor D, Meschino W, Hayden MR. Almqvist E, et al. Among authors: adam s. Am J Hum Genet. 1997 Oct;61(4):945-52. doi: 10.1086/514873. Am J Hum Genet. 1997. PMID: 9382108 Free PMC article.

7

"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.

Townsend A, Adam S, Birch PH, Lohn Z, Rousseau F, Friedman JM. Townsend A, et al. Among authors: adam s. Am J Med Genet A. 2012 Oct;158A(10):2519-25. doi: 10.1002/ajmg.a.35554. Epub 2012 Aug 17. Am J Med Genet A. 2012. PMID: 22903777

8

Genetics professionals' perspectives on reporting incidental findings from clinical genome-wide sequencing.

Lohn Z, Adam S, Birch P, Townsend A, Friedman J. Lohn Z, et al. Among authors: adam s. Am J Med Genet A. 2013 Mar;161A(3):542-9. doi: 10.1002/ajmg.a.35794. Epub 2013 Feb 7. Am J Med Genet A. 2013. PMID: 23401068

9

Autonomy and the patient's right 'not to know' in clinical whole-genomic sequencing.

Townsend A, Rousseau F, Friedman J, Adam S, Lohn Z, Birch P. Townsend A, et al. Among authors: adam s. Eur J Hum Genet. 2014 Jan;22(1):6. doi: 10.1038/ejhg.2013.94. Epub 2013 May 15. Eur J Hum Genet. 2014. PMID: 23674174 Free PMC article. No abstract available.

10

Paternalism and the ACMG recommendations on genomic incidental findings: patients seen but not heard.

Townsend A, Adam S, Birch PH, Friedman JM. Townsend A, et al. Among authors: adam s. Genet Med. 2013 Sep;15(9):751-2. doi: 10.1038/gim.2013.105. Genet Med. 2013. PMID: 24008256 Free article. No abstract available.

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