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| 37601974 | Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries. | Cell Genom | 2023 |
| 37461573 | Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank. | medRxiv | 2023 |
| 37425708 | Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program. | medRxiv | 2023 |
| 37296406 | Triglyceride-glucose index as a marker of adverse cardiovascular prognosis in patients with coronary heart disease and hypertension. | | 2023 |
| 37280429 | Publisher Correction: Explainable artificial intelligence incorporated with domain knowledge diagnosing early gastric neoplasms under white light endoscopy. | | 2023 |
| 37163978 | Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytes. | Stem Cell Reports | 2023 |
| 37019109 | Scalable mixed model methods for set-based association studies on large-scale categorical data analysis and its application to exome-sequencing data in UK Biobank. | | 2023 |
| 36929173 | Clinical characteristics and outcomes of Chinese patients with coronary heart disease and resistant hypertension. | | 2023 |
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| 36726384 | A Hospital-Based and Cross-Sectional Investigation on Clinical Characteristics of Pediatric Isolates in Beijing from 2015 to 2021. | | 2023 |
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| 36653479 | Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. | Nat Med | 2023 |
| 36154123 | Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors. | Circulation | 2022 |
| 35945607 | Enhanced rare disease mapping for phenome-wide genetic association in the UK Biobank. | Genome Medicine | 2022 |
| 35876838 | Incorporating family disease history and controlling case-control imbalance for population-based genetic association studies. | | 2022 |
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| 35652341 | Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension. | Hypertension | 2022 |
| 35396580 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia. | Nature | 2022 |
| 35144019 | Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variant. | Heart Rhythm | 2022 |
| 36777998 | The HUNT study: A population-based cohort for genetic research. | Cell Genom | 2022 |
| 36477530 | Genetic diversity fuels gene discovery for tobacco and alcohol use. | Nature | 2022 |
| 36200066 | Erratum: Co-delivery of 5-fluorouracil and miRNA-34a mimics by host-guest self-assembly nanocarriers for efficacious targeted therapy in colorectal cancer patient-derived tumor xenografts: Erratum. | Theranostics | 2022 |
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| 32056457 | Mitochondrial genome-wide association study of migraine - the HUNT Study. | Cephalalgia | 2020 |
| 33381146 | Aberrantly Methylated-Differentially Expressed Genes Identify Novel Atherosclerosis Risk Subtypes. | Frontiers in Genetics | 2020 |
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| 32058015 | Clinical and functional reappraisal of alleged type 5 long QT syndrome: Causative genetic variants in the KCNE1-encoded minK β-subunit. | Heart Rhythm | 2020 |
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| 30061737 | Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. | Nat Genet | 2018 |
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| 29290336 | Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development. | Am J Hum Genet | 2018 |
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