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| 37758436 | Genetic Insights on the Relation of Vascular Risk Factors and Cervical Artery Dissection. | J Am Coll Cardiol | 2023 |
| 37923804 | Identification of circulating proteins associated with general cognitive function among middle-aged and older adults. | Commun Biol | 2023 |
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| 37038246 | Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study. | Eur Heart J | 2023 |
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| 34700051 | Genomic Studies Across the Lifespan Point to Early Mechanisms Determining Subcortical Volumes. | Biol Psychiatry Cogn Neurosci Neuroimaging | 2022 |
| 35585611 | Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature. | Clin Epigenetics | 2022 |
| 35511193 | Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate. | Brain | 2022 |
| 36327219 | Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. | PLoS Genet | 2022 |
| 35314756 | Author Correction: Integrated genomics point to immune vulnerabilities in pleural mesothelioma. | Sci Rep | 2022 |
| 35273064 | Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA). | BMJ Open | 2022 |
| 34886679 | Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries. | Circ Res | 2022 |
| 34700051 | Genomic Studies Across the Lifespan Point to Early Mechanisms Determining Subcortical Volumes. | Biol Psychiatry Cogn Neurosci Neuroimaging | 2022 |
| 35585611 | Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature. | Clin Epigenetics | 2022 |
| 35511193 | Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate. | Brain | 2022 |
| 36327219 | Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. | PLoS Genet | 2022 |
| 35314756 | Author Correction: Integrated genomics point to immune vulnerabilities in pleural mesothelioma. | Sci Rep | 2022 |
| 34886679 | Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries. | Circ Res | 2022 |
| 35273064 | Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA). | BMJ Open | 2022 |
| 33403511 | Morphological findings in frozen non-neoplastic kidney tissues of patients with kidney cancer from large-scale multicentric studies on renal cancer. | Virchows Arch | 2021 |
| 34127738 | Y disruption, autosomal hypomethylation and poor male lung cancer survival. | Sci Rep | 2021 |
| 34115965 | Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. | Am J Hum Genet | 2021 |
| 34043590 | Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19. | J Clin Invest | 2021 |
| 33655273 | A catalog of associations between rare coding variants and COVID-19 outcomes. | medRxiv | 2021 |
| 33403511 | Morphological findings in frozen non-neoplastic kidney tissues of patients with kidney cancer from large-scale multicentric studies on renal cancer. | Virchows Arch | 2021 |
| 34580349 | Integrated genomics point to immune vulnerabilities in pleural mesothelioma. | Sci Rep | 2021 |
| 34737286 | An innate contribution of human nicotinic receptor polymorphisms to COPD-like lesions. | Nat Commun | 2021 |
| 34706766 | A small number of early introductions seeded widespread transmission of SARS-CoV-2 in Québec, Canada. | Genome Med | 2021 |
| 33655273 | A catalog of associations between rare coding variants and COVID-19 outcomes. | medRxiv | 2021 |
| 34737286 | An innate contribution of human nicotinic receptor polymorphisms to COPD-like lesions. | Nat Commun | 2021 |
| 34706766 | A small number of early introductions seeded widespread transmission of SARS-CoV-2 in Québec, Canada. | Genome Med | 2021 |
| 34580349 | Integrated genomics point to immune vulnerabilities in pleural mesothelioma. | Sci Rep | 2021 |
| 34043590 | Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19. | J Clin Invest | 2021 |
| 34127738 | Y disruption, autosomal hypomethylation and poor male lung cancer survival. | Sci Rep | 2021 |
| 34115965 | Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. | Am J Hum Genet | 2021 |
| 31158522 | Association of a single nucleotide polymorphism in the ubxn6 gene with long-term non-progression phenotype in HIV-positive individuals. | Clin Microbiol Infect | 2020 |
| 32429735 | Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. | Circulation | 2020 |
| 32075738 | The Natural Metabolite 4-Cresol Improves Glucose Homeostasis and Enhances β-Cell Function. | Cell Rep | 2020 |
| 31792077 | ZBTB7B (ThPOK) Is Required for Pathogenesis of Cerebral Malaria and Protection against Pulmonary Tuberculosis. | Infect Immun | 2020 |
| 32186652 | Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis. | JAMA Cardiol | 2020 |
| 32173762 | Dominant gut Prevotella copri in gastrectomised non-obese diabetic Goto-Kakizaki rats improves glucose homeostasis through enhanced FXR signalling. | Diabetologia | 2020 |
| 32390008 | Dysregulation at multiple points of the kynurenine pathway is a ubiquitous feature of renal cancer: implications for tumour immune evasion. | Br J Cancer | 2020 |
| 32702748 | Independent risk factors for simvastatin-related myopathy and relevance to different types of muscle symptom. | Eur Heart J | 2020 |
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