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Results: 1 to 20 of 44

References for PMC Articles for PubMed (Select 20139767)

1.

Disclosure of APOE genotype for risk of Alzheimer's disease.

Green RC, Roberts JS, Cupples LA, Relkin NR, Whitehouse PJ, Brown T, Eckert SL, Butson M, Sadovnick AD, Quaid KA, Chen C, Cook-Deegan R, Farrer LA; REVEAL Study Group.

N Engl J Med. 2009 Jul 16;361(3):245-54. doi: 10.1056/NEJMoa0809578.

2.

A systematic review of the impact of genetic counseling on risk perception accuracy.

Smerecnik CM, Mesters I, Verweij E, de Vries NK, de Vries H.

J Genet Couns. 2009 Jun;18(3):217-28. doi: 10.1007/s10897-008-9210-z. Epub 2009 Mar 17. Review.

PMID:
19291376
3.

Anchoring-and-adjustment bias in communication of disease risk.

Senay I, Kaphingst KA.

Med Decis Making. 2009 Mar-Apr;29(2):193-201. doi: 10.1177/0272989X08327395. Epub 2009 Mar 11. Review.

4.

Putting science over supposition in the arena of personalized genomics.

McBride CM, Alford SH, Reid RJ, Larson EB, Baxevanis AD, Brody LC.

Nat Genet. 2008 Aug;40(8):939-42. doi: 10.1038/ng0808-939.

5.

Incorporating ethnicity into genetic risk assessment for Alzheimer disease: the REVEAL study experience.

Christensen KD, Roberts JS, Royal CD, Fasaye GA, Obisesan T, Cupples LA, Whitehouse PJ, Butson MB, Linnenbringer E, Relkin NR, Farrer L, Cook-Deegan R, Green RC.

Genet Med. 2008 Mar;10(3):207-14. doi: 10.1097/GIM.0b013e318164e4cf.

6.

The feasibility of online genetic testing for lung cancer susceptibility: uptake of a web-based protocol and decision outcomes.

O'Neill SC, White DB, Sanderson SC, Lipkus IM, Bepler G, Bastian LA, McBride CM.

Genet Med. 2008 Feb;10(2):121-30. doi: 10.1097/GIM.0b013e31815f8e06. Erratum in: Genet Med. 2008 Mar;10(3):228.

PMID:
18281920
7.

How risk is perceived, constructed and interpreted by clients in clinical genetics, and the effects on decision making: systematic review.

Sivell S, Elwyn G, Gaff CL, Clarke AJ, Iredale R, Shaw C, Dundon J, Thornton H, Edwards A.

J Genet Couns. 2008 Feb;17(1):30-63. Epub 2007 Oct 30. Review.

PMID:
17968638
8.

Genetic testing in cardiovascular disease.

Robin NH, Tabereaux PB, Benza R, Korf BR.

J Am Coll Cardiol. 2007 Aug 21;50(8):727-37. Epub 2007 Aug 6. Review.

9.

Information processing in the context of genetic risk: implications for genetic-risk communication.

Etchegary H, Perrier C.

J Genet Couns. 2007 Aug;16(4):419-32. Epub 2007 May 1. Review.

PMID:
17473961
10.

Recall of disclosed apolipoprotein E genotype and lifetime risk estimate for Alzheimer's disease: the REVEAL Study.

Eckert SL, Katzen H, Roberts JS, Barber M, Ravdin LD, Relkin NR, Whitehouse PJ, Green RC.

Genet Med. 2006 Dec;8(12):746-51.

PMID:
17172937
11.

Illness representations, self-regulation, and genetic counseling: a theoretical review.

Shiloh S.

J Genet Couns. 2006 Oct;15(5):325-37. Review.

PMID:
16972194
12.

Genetic susceptibility testing for Alzheimer disease: motivation to obtain information and control as precursors to coping with increased risk.

Gooding HC, Linnenbringer EL, Burack J, Roberts JS, Green RC, Biesecker BB.

Patient Educ Couns. 2006 Dec;64(1-3):259-67. Epub 2006 Jul 21.

PMID:
16860524
13.

A definition and operational framework for health numeracy.

Golbeck AL, Ahlers-Schmidt CR, Paschal AM, Dismuke SE.

Am J Prev Med. 2005 Nov;29(4):375-6.

PMID:
16242604
14.

Predictive genetic testing for Alzheimer's disease: impact upon risk perception.

Marteau TM, Roberts S, LaRusse S, Green RC.

Risk Anal. 2005 Apr;25(2):397-404.

PMID:
15876213
15.
16.

Is family history related to preventive health behaviors and medical management in breast cancer patients?

Madlensky L, Flatt SW, Bardwell WA, Rock CL, Pierce JP; WHEL Study group.

Breast Cancer Res Treat. 2005 Mar;90(1):47-54.

PMID:
15770526
17.

Patients' resistance to risk information in genetic counseling for BRCA1/2.

Gurmankin AD, Domchek S, Stopfer J, Fels C, Armstrong K.

Arch Intern Med. 2005 Mar 14;165(5):523-9.

PMID:
15767527
18.

Genetic susceptibility testing versus family history-based risk assessment: Impact on perceived risk of Alzheimer disease.

LaRusse S, Roberts JS, Marteau TM, Katzen H, Linnenbringer EL, Barber M, Whitehouse P, Quaid K, Brown T, Green RC, Relkin NR.

Genet Med. 2005 Jan;7(1):48-53.

PMID:
15654228
19.

Using the common sense model to understand perceived cancer risk in individuals testing for BRCA1/2 mutations.

Kelly K, Leventhal H, Andrykowski M, Toppmeyer D, Much J, Dermody J, Marvin M, Baran J, Schwalb M.

Psychooncology. 2005 Jan;14(1):34-48.

PMID:
15386791
20.
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