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426 results on '"Chaffin, Mark"'

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1. Rare coding variant analysis for human diseases across biobanks and ancestries

4. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

7. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

9. Single-nucleus profiling of human dilated and hypertrophic cardiomyopathy

10. Genetic analysis of right heart structure and function in 40,000 people

11. Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

12. Deep learning enables genetic analysis of the human thoracic aorta

13. Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases

14. Single-cell meta-analysis of SARS-CoV-2 entry genes across tissues and demographics

15. Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

16. Genome-wide association study of peripheral artery disease in the Million Veteran Program

17. Implementation of an efficacious intervention for high risk women in Mexico: protocol for a multi-site randomized trial with a parallel study of organizational factors

18. Dynamic adaptation process to implement anevidence-based child maltreatment intervention

20. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

21. Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy

22. Abstract 14629: Rare Variants for Electrocardiographic Traits Identify Arrhythmia Susceptibility Genes

24. Transcriptional and Cellular Diversity of the Human Heart

28. Multi-ethnic genome-wide association study for atrial fibrillation

33. Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction

38. An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels

39. Heritability of Atrial Fibrillation

40. Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

41. Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

44. Changes in Parental Depression Symptoms during Family Preservation Services

45. A Combined Motivation and Parent-Child Interaction Therapy Package Reduces Child Welfare Recidivism in a Randomized Dismantling Field Trial

46. Change Trajectories for Parent-Child Interaction Sequences during Parent-Child Interaction Therapy for Child Physical Abuse

47. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

48. Randomized Trial of Treatment for Children with Sexual Behavior Problems: Ten-Year Follow-Up

49. Abstract 16514: Interpretation of Whole Genome Sequences for Risk of Early-Onset Myocardial Infarction

50. A Brief Form of the Child Abuse Potential Inventory: Development and Validation

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