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2. Genomic architecture of autism from comprehensive whole-genome sequence annotation.

3. A Genomic Counseling Model for Population-Based Sequencing: A Pre-Post Intervention Study

4. Language and Reading Impairments Are Associated with Increased Prevalence of Non-Right-Handedness

5. SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy

8. Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder.

9. Genome screening, reporting, and genetic counseling for healthy populations

10. High-quality read-based phasing of cystic fibrosis cohort informs genetic understanding of disease modification

11. The X Factor: A Robust and Powerful Approach to X-chromosome-Inclusive Whole-genome Association Studies

13. Genetic evidence supports the development of SLC26A9 targeting therapies for the treatment of lung disease

14. Sex-specific disease modifiers in juvenile myoclonic epilepsy

16. A composite likelihood ratio approach to the analysis of correlated binary data in genetic association studies

17. Cystic fibrosis–related diabetes onset can be predicted using biomarkers measured at birth

18. A novel joint location-scale testing framework for improved detection of variants with main or interaction effects

20. The CF Canada-Sick Kids Program in individual CF therapy: A resource for the advancement of personalized medicine in CF

21. Annotation of nuclear lncRNAs based on chromatin interactions.

22. Canadian COVID-19 host genetics cohort replicates known severity associations.

26. Characterizing Risk Factors for Hospitalization and Clinical Characteristics in a Cohort of COVID-19 Patients Enrolled in the GENCOV Study

29. P733: Comparative analysis of DNA variant classifications between the GENCOV COVID-19 genome study and the ClinVar database

30. P710: Phenome-wide association study (PheWAS) for the Canadian HostSeq Biobank

31. P709: Self reported vs genetic ancestry from the GENCOV COVID-19 genomic sequencing study

32. P574: Summary of findings from comprehensive genome sequencing performed in a healthy population cohort*

33. Gene copy number variation and pediatric mental health/neurodevelopment in a general population

35. Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis

36. Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole Genome Analysis of 7,840 Patients

37. A second update on mapping the human genetic architecture of COVID-19

38. Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis

39. P436: Population genome screening identifies previously undiagnosed disease: A case series

40. P357: Replication of genetic variation associated with COVID-19 clinical outcomes: The GENCOV Prospective Cohort Study

43. The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants

44. Genome screening, reporting, and genetic counseling for healthy populations

45. Gene copy number variation in pediatric mental illness in a general population

46. Airway Mucosal Host Defense Is Key to Genomic Regulation of Cystic Fibrosis Lung Disease Severity

48. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

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