Christensen KD - Search Results

1

Providers' knowledge of genetics: A survey of 5915 individuals and families with genetic conditions.

Harvey EK, Fogel CE, Peyrot M, Christensen KD, Terry SF, McInerney JD. Harvey EK, et al. Among authors: christensen kd. Genet Med. 2007 May;9(5):259-67. doi: 10.1097/GIM.0b013e31805002f2. Genet Med. 2007. PMID: 17505202 Free article.

2

Direct-to-consumer genetic testing: an assessment of genetic counselors' knowledge and beliefs.

Hock KT, Christensen KD, Yashar BM, Roberts JS, Gollust SE, Uhlmann WR. Hock KT, et al. Among authors: christensen kd. Genet Med. 2011 Apr;13(4):325-32. doi: 10.1097/GIM.0b013e3182011636. Genet Med. 2011. PMID: 21233722 Free PMC article.

3

Adopting genetics: motivations and outcomes of personal genomic testing in adult adoptees.

Baptista NM, Christensen KD, Carere DA, Broadley SA, Roberts JS, Green RC. Baptista NM, et al. Among authors: christensen kd. Genet Med. 2016 Sep;18(9):924-32. doi: 10.1038/gim.2015.192. Epub 2016 Jan 28. Genet Med. 2016. PMID: 26820063 Free PMC article.

4

Family health history reporting is sensitive to small changes in wording.

Conway-Pearson LS, Christensen KD, Savage SK, Huntington NL, Weitzman ER, Ziniel SI, Bacon P, Cacioppo CN, Green RC, Holm IA. Conway-Pearson LS, et al. Among authors: christensen kd. Genet Med. 2016 Dec;18(12):1308-1311. doi: 10.1038/gim.2016.45. Epub 2016 May 5. Genet Med. 2016. PMID: 27148937 Free PMC article.

5

Patient understanding of, satisfaction with, and perceived utility of whole-genome sequencing: findings from the MedSeq Project.

Roberts JS, Robinson JO, Diamond PM, Bharadwaj A, Christensen KD, Lee KB, Green RC, McGuire AL; MedSeq Project team. Roberts JS, et al. Among authors: christensen kd. Genet Med. 2018 Sep;20(9):1069-1076. doi: 10.1038/gim.2017.223. Epub 2018 Jan 4. Genet Med. 2018. PMID: 29300387 Free PMC article.

6

Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings.

Christensen KD, Bernhardt BA, Jarvik GP, Hindorff LA, Ou J, Biswas S, Powell BC, Grundmeier RW, Machini K, Karavite DJ, Pennington JW, Krantz ID, Berg JS, Goddard KAB. Christensen KD, et al. Genet Med. 2018 Oct;20(10):1186-1195. doi: 10.1038/gim.2017.243. Epub 2018 Feb 1. Genet Med. 2018. PMID: 29388940 Free PMC article.

7

Improved provider preparedness through an 8-part genetics and genomic education program.

Hajek C, Hutchinson AM, Galbraith LN, Green RC, Murray MF, Petry N, Preys CL, Zawatsky CLB, Zoltick ES, Christensen KD; Imagenetics METRICS Team. Hajek C, et al. Among authors: christensen kd. Genet Med. 2022 Jan;24(1):214-224. doi: 10.1016/j.gim.2021.08.008. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906462 Free PMC article.

8

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. Christensen KD, et al. Genet Med. 2008 Mar;10(3):207-14. doi: 10.1097/GIM.0b013e318164e4cf. Genet Med. 2008. PMID: 18344711 Free PMC article. Clinical Trial.

9

Changes to perceptions of the pros and cons of genetic susceptibility testing after APOE genotyping for Alzheimer disease risk.

Christensen KD, Roberts JS, Uhlmann WR, Green RC. Christensen KD, et al. Genet Med. 2011 May;13(5):409-14. doi: 10.1097/GIM.0b013e3182076bf1. Genet Med. 2011. PMID: 21270636 Free PMC article.

10

A randomized controlled trial of disclosing genetic risk information for Alzheimer disease via telephone.

Christensen KD, Uhlmann WR, Roberts JS, Linnenbringer E, Whitehouse PJ, Royal CDM, Obisesan TO, Cupples LA, Butson MB, Fasaye GA, Hiraki S, Chen CA, Siebert U, Cook-Deegan R, Green RC. Christensen KD, et al. Genet Med. 2018 Jan;20(1):132-141. doi: 10.1038/gim.2017.103. Epub 2017 Jul 20. Genet Med. 2018. PMID: 28726810 Free PMC article. Clinical Trial.

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