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1. Opportunities, resources, and techniques for implementing genomics in clinical care. Issue 10197 (10th August 2019)

2. 163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease. (31st May 2014)

3. Genetic nondiscrimination legislation: a critical prerequisite for pharmacogenomics data sharing. (May 2007)

5. Quantifying the phenome‐wide disease burden of obesity using electronic health records and genomics. Issue 12 (13th November 2022)

6. Comparing medical history data derived from electronic health records and survey answers in the All of Us Research Program. (9th April 2022)

7. Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for the Use of Potent Volatile Anesthetic Agents and Succinylcholine in the Context of RYR1 or CACNA1S Genotypes. Issue 6 (24th January 2019)

8. KCNQ1 and Long QT Syndrome in 1/45 Amish: The Road From Identification to Implementation of Culturally Appropriate Precision Medicine. (December 2020)

9. Real-time clinical note monitoring to detect conditions for rapid follow-up: A case study of clinical trial enrollment in drug-induced torsades de pointes and Stevens-Johnson syndrome. (29th October 2020)

10. An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels. Issue 13 (25th September 2018)