362 results on '"Strug, Lisa J."'
Search Results
2. Language and Reading Impairments Are Associated with Increased Prevalence of Non-Right-Handedness
3. SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy
4. Identification of brain cell types underlying genetic association with word reading and correlated traits
5. Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder.
6. The X Factor: A Robust and Powerful Approach to X-chromosome-Inclusive Whole-genome Association Studies
7. High-quality read-based phasing of cystic fibrosis cohort informs genetic understanding of disease modification
8. Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities
9. Genetic evidence supports the development of SLC26A9 targeting therapies for the treatment of lung disease
10. Sex-specific disease modifiers in juvenile myoclonic epilepsy
11. Positive epistasis between disease-causing missense mutations and silent polymorphism with effect on mRNA translation velocity
12. Cystic fibrosis–related diabetes onset can be predicted using biomarkers measured at birth
13. Annotation of nuclear lncRNAs based on chromatin interactions.
14. AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestations
15. The CF Canada-Sick Kids Program in individual CF therapy: A resource for the advancement of personalized medicine in CF
16. Canadian COVID-19 host genetics cohort replicates known severity associations.
17. Translational research to enable personalized treatment of cystic fibrosis
18. Visceral fat-related systemic inflammation and the adolescent brain: a mediating role of circulating glycerophosphocholines
19. Endoplasmic Reticulum Stress and Chemokine Production in Cystic Fibrosis Airway Cells: Regulation by STAT3 Modulation
20. A robust association test leveraging unknown genetic interactions: Application to cystic fibrosis lung disease
21. Leveraging Hardy–Weinberg disequilibrium for association testing in case-control studies
22. Gene copy number variation and pediatric mental health/neurodevelopment in a general population
23. RoPE: A robust profile likelihood method for differential gene expression analysis
24. Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole Genome Analysis of 7,840 Patients
25. Language and reading impairments are associated with increased prevalence of non‐right‐handedness
26. Variants in Solute Carrier SLC26A9 Modify Prenatal Exocrine Pancreatic Damage in Cystic Fibrosis
27. Genomic architecture of autism from comprehensive whole-genome sequence annotation
28. Prioritizing Rare Variants with Conditional Likelihood Ratios
29. The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants
30. Gene copy number variation in pediatric mental illness in a general population
31. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people
32. Expression of cystic fibrosis lung disease modifier genes in human airway models
33. Airway Mucosal Host Defense Is Key to Genomic Regulation of Cystic Fibrosis Lung Disease Severity
34. Variation in prognosis and treatment outcome in juvenile myoclonic epilepsy: a Biology of Juvenile Myoclonic Epilepsy Consortium proposal for a practical definition and stratified medicine classifications.
35. Improving imputation in disease-relevant regions: lessons from cystic fibrosis
36. Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation
37. SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy
38. Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients
39. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people
40. A cystic fibrosis lung disease modifier locus harbors tandem repeats associated with gene expression
41. High Quality Phasing Using Linked-Read Whole Genome Sequencing of Patient Cohorts Informs Genetic Understanding of Complex Traits
42. Non-right handedness is associated with language and reading impairments
43. A flexible summary statistics-based colocalization method with application to the mucin cystic fibrosis lung disease modifier locus
44. Using Parametric Multipoint Lods and Mods for Linkage Analysis Requires a Shift in Statistical Thinking
45. An Introduction to Evidential Sample Size Calculations
46. Leveraging TOPMed Imputation Server and Constructing a Cohort-Specific Imputation Reference Panel to Enhance Genotype Imputation among Cystic Fibrosis Patients
47. Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people
48. Genetic evidence supports the development of SLC26A9 targeting therapies for the treatment of lung disease
49. An Alternative Foundation for the Planning and Evaluation of Linkage Analysis : I. Decoupling ‘Error Probabilities’ from ‘Measures of Evidence’
50. An Alternative Foundation for the Planning and Evaluation of Linkage Analysis : II. Implications for Multiple Test Adjustments
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.