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1. Contrasting Nav1.8 Activity in Scn10a−/− Ventricular Myocytes and the Intact Heart. Issue 11 (2nd November 2016)

2. Contrasting Nav1.8 Activity in Scn10a−/− Ventricular Myocytes and the Intact Heart. Issue 11 (November 2016)

3. Examining Rare and Low-Frequency Genetic Variants Previously Associated With Lone or Familial Forms of Atrial Fibrillation in an Electronic Medical Record System. (February 2015)

4. Examining Rare and Low-Frequency Genetic Variants Previously Associated With Lone or Familial Forms of Atrial Fibrillation in an Electronic Medical Record System: A Cautionary Note. (February 2015)

5. Genetic Susceptibility for Atrial Fibrillation in Patients Undergoing Atrial Fibrillation Ablation. (March 2020)

6. Genome‐Wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol. Issue 3 (23rd May 2019)

7. Genotype and risk of major bleeding during warfarin treatment. (December 2014)

8. Population‐specific single‐nucleotide polymorphism confers increased risk of venous thromboembolism in African Americans. Issue 5 (21st June 2016)

9. The relationship between high density lipoprotein cholesterol and sepsis: A clinical and genetic approach. Issue 3 (16th January 2023)

10. Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization. Issue 10 (16th December 2022)