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You searched for: Author/Creator Christensen, Kurt D.

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1. When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing. Issue 2 (3rd April 2017)

2. Phenotypic Characterization of Individuals With Variants in Cardiovascular Genes in the Absence of a Primary Cardiovascular Indication for Testing. (March 2019)

3. How Can Psychological Science Inform Research About Genetic Counseling for Clinical Genomic Sequencing?. Issue 2 (9th December 2014)

4. P3‐407: Educating Patients and Care Partners about Mild Cognitive Impairment, APOE, and Alzheimer's Disease: Findings from the Reveal Study. (1st July 2016)

5. A randomized noninferiority trial of condensed protocols for genetic risk disclosure of Alzheimer's disease. Issue 10 (9th December 2014)

6. Do research participants share genomic screening results with family members?. Issue 2 (19th October 2021)

7. Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression. Issue 1 (26th July 2021)

8. The Reckoning: The Return of Genomic Results to 1444 Participants Across the eMERGE3 Network. Issue 11 (November 2022)

9. The impact of genetic counselors' use of facilitative strategies on cognitive and emotional processing of genetic risk disclosure for Alzheimer's disease. Issue 5 (May 2018)

10. Erratum to: How Can Psychological Science Inform Research About Genetic Counseling for Clinical Genomic Sequencing?. Issue 2 (25th December 2014)