Search

Your search keyword '"Fuller, Erin D."' showing total 23 results

Search Constraints

Start Over You searched for: Author "Fuller, Erin D." Remove constraint Author: "Fuller, Erin D."
23 results on '"Fuller, Erin D."'

Search Results

1. “PMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black Patients”

2. Genetic Susceptibility to Mood Disorders and Risk of Stroke: A Polygenic Risk Score and Mendelian Randomization Study

3. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

4. PMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black patients

5. Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female‐Specific Health Conditions

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

7. Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle‐aged and older adults: A population‐based cohort study

8. A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease

9. Thrombotic risk determined by rare and common SERPINA1 variants in a population‐based cohort study

10. Performance of polygenic risk scores for cancer prediction in a racially diverse academic biobank

11. Classic Thrombophilias and Thrombotic Risk Among Middle‐Aged and Older Adults: A Population‐Based Cohort Study

12. Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581]

13. Thrombotic Risk Determined by STAB 2 Variants in a Population-Based Cohort Study

14. An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs

15. Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

16. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

17. Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals

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

19. Suptavumab for the Prevention of Medically Attended Respiratory Syncytial Virus Infection in Preterm Infants

20. Suptavumab for the Prevention of Medically Attended Respiratory Syncytial Virus Infection in Preterm Infants.

21. Thrombotic risk determined by rare and common SERPINA1variants in a population‐based cohort study

22. A Protein-TruncatingHSD17B13Variant and Protection from Chronic Liver Disease

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

Catalog

Books, media, physical & digital resources