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210 results on '"Puckelwartz, Megan J."'

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1. The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young

2. Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

3. Susceptibility to innate immune activation in genetically mediated myocarditis

4. Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network

6. Returning integrated genomic risk and clinical recommendations: The eMERGE study

8. Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure

9. Prelamin A causes aberrant myonuclear arrangement and results in muscle fiber weakness.

10. Neptune: an environment for the delivery of genomic medicine

11. Identification of Clinical Drivers of Left Atrial Enlargement Through Genomics of Left Atrial Size

12. Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network

15. Risk factors affecting polygenic score performance across diverse cohorts

16. Returning integrated genomic risk and clinical recommendations: The eMERGE study

17. The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young

19. Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index

26. South Asian-Specific MYBPC3Δ25bp Deletion Carriers Display Hypercontraction and Impaired Diastolic Function Under Exercise Stress

29. Genomic Autopsy of Sudden Deaths in Young Individuals

31. Genetic mutations and mechanisms in dilated cardiomyopathy

32. Identification of Cardiac Fibrosis in Young Adults With a Homozygous Frameshift Variant in SERPINE1

34. Mitochondrial cardiomyopathy and ventricular arrhythmias associated with biallelic variants inC1QBP

35. Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics Network

37. Genomic Context Differs Between Human Dilated Cardiomyopathy and Hypertrophic Cardiomyopathy

39. The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype

41. Abstract 439: Trajectory Analysis of Left Ventricular Dimensions From Biobank Data Uncovers Novel Genetic Associations

43. Trajectory analysis of cardiovascular phenotypes from biobank data uncovers novel genetic associations

48. Abstract 469: Genomic Context Predicts Dilated but Not Hypertrophic Cardiomyopathy

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