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1. Genetic risk factors for COVID-19 and influenza are largely distinct

2. Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis

3. Common and rare variant associations with clonal haematopoiesis phenotypes

4. Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From Sepsis

5. Whole-genome sequencing reveals host factors underlying critical COVID-19

6. Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease

7. Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes

8. Exome sequencing and analysis of 454,787 UK Biobank participants

9. Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes

10. Exome-wide evaluation of rare coding variants using electronic health records identifies new gene–phenotype associations

11. Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4

13. Whole-genome sequencing reveals host factors underlying critical COVID-19

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

15. Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative

17. Suggestive Linkage of the Child Behavior Checklist Juvenile Bipolar Disorder Phenotype to 1p21, 6p21, and 8q21

18. Exome-wide association study to identify rare variants influencing COVID-19 outcomes : Results from the Host Genetics Initiative

19. Whole-genome sequencing reveals host factors underlying critical COVID-19

20. Targeting the P2Y13 Receptor Suppresses IL-33 and HMGB1 Release and Ameliorates Experimental Asthma

21. Mapping the human genetic architecture of COVID-19

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

24. Age-of-onset information helps identify 76 genetic variants associated with allergic disease

27. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

29. Eleven loci with new reproducible genetic associations with allergic disease risk.

32. PAG1 limits allergen‐induced type 2 inflammation in the murine lung

33. PAG1 limits allergen‐induced type 2 inflammation in the murine lung.

35. Cohort profile: The Childhood Asthma Prevention Study (CAPS)

38. Meta-analysis identifies seven susceptibility loci involved in the atopic march

40. Is Schizophrenia a Risk Factor for Breast Cancer?—Evidence From Genetic Data.

42. Telomere length in circulating leukocytes is associated with lung function and disease

46. Genome-Wide Association Studies of Asthma in Population-Based Cohorts Confirm Known and Suggested Loci and Identify an Additional Association near HLA

47. Genome-Wide Association Studies of Asthma in Population-Based Cohorts Confirm Known and Suggested Loci and Identify an Additional Association near HLA

48. Correction: Genome-Wide Association Studies of Asthma in Population-Based Cohorts Confirm Known and Suggested Loci and Identify an Additional Association near HLA

50. Erratum: Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

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