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1. EndoPRS: Incorporating Endophenotype Information to Improve Polygenic Risk Scores for Clinical Endpoints

2. The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeup

3. Determinants of mosaic chromosomal alteration fitness

4. Carriers of rare damaging CCR2 genetic variants are at lower risk of atherosclerotic disease

5. The Relationship of Duffy Gene Polymorphism, High Sensitivity C-Reactive Protein, and Long-term Outcomes

7. Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

8. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications

9. Mosaic chromosomal alterations in blood across ancestries via whole-genome sequencing

10. Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-specific effects via GAUDI

11. The power of TOPMed imputation for the discovery of Latino enriched rare variants associated with type 2 diabetes

12. Expression quantitative trait methylation analysis elucidates gene regulatory effects of DNA methylation: The Framingham Heart Study

13. Genetic Examination of Hematological Parameters in SARS-CoV-2 Infection and COVID-19

14. Clonal hematopoiesis is driven by aberrant activation of TCL1A

17. A large-scale transcriptome-wide association study (TWAS) of ten blood cell phenotypes reveals complexities of TWAS fine-mapping

21. A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

22. Association of mitochondrial DNA copy number with cardiometabolic diseases in a large cross-sectional study of multiple ancestries

23. Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations

24. Common genetic risk variants identified in the SPARK cohort implicate DDHD2 as a novel autism risk gene

25. Novel genetic determinants of telomere length from a multi-ethnic analysis of 75,000 whole genome sequences in TOPMed

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