Lisa J. Strug, Ph.D.
Affiliations: | 2003 | University of Toronto, Toronto, ON, Canada |
Area:
Biostatistics BiologyGoogle:
"Lisa Strug"Parents
Sign in to add mentor| Paul Corey | grad student | 2003 | University of Toronto | |
| (Evidential sample size.) | ||||
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Publications
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| Garg E, Arguello-Pascualli P, Vishnyakova O, et al. (2024) Canadian COVID-19 host genetics cohort replicates known severity associations. Plos Genetics. 20: e1011192 |
| Price KM, Wigg KG, Eising E, et al. (2022) Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. Translational Psychiatry. 12: 495 |
| Sun Q, Liu W, Rosen JD, et al. (2022) Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients. Hgg Advances. 3: 100090 |
| Wang F, Panjwani N, Wang C, et al. (2022) A flexible summary statistics-based colocalization method with application to the mucin cystic fibrosis lung disease modifier locus. American Journal of Human Genetics |
| Burton CL, Lemire M, Xiao B, et al. (2021) Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder. Translational Psychiatry. 11: 91 |
| Laselva O, Moraes TJ, He G, et al. (2020) The CFTR Mutation c.3453G > C (D1152H) Confers an Anion Selectivity Defect in Primary Airway Tissue that Can Be Rescued by Ivacaftor. Journal of Personalized Medicine. 10 |
| Lorè NI, Sipione B, He G, et al. (2020) Collaborative Cross Mice Yield Genetic Modifiers for Pseudomonas aeruginosa Infection in Human Lung Disease. Mbio. 11 |
| Price KM, Wigg KG, Feng Y, et al. (2020) Genome-Wide Association Study of Word Reading: Overlap with Risk Genes for Neurodevelopmental Disorders. Genes, Brain, and Behavior. e12648 |
| Saferali A, Tang AC, Strug LJ, et al. (2020) Immunomodulatory function of the cystic fibrosis modifier gene BPIFA1. Plos One. 15: e0227067 |
| Baskurt Z, Mastromatteo S, Gong J, et al. (2019) VikNGS: A C ++ Variant Integration Kit for Next Generation Sequencing Association Analysis. Bioinformatics (Oxford, England) |