Author: Yii-Der Ida Chen

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Preprints

An open resource of structural variation for medical and population genetics

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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Identification of type 2 diabetes loci in 433,540 East Asian individuals

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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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Population sequencing data reveal a compendium of mutational processes in human germline

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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

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Trans-ethnic genome-wide association study provides insight into effector genes and molecular mechanisms for kidney function and highlights a causal effect on kidney-specific disease aetiologies

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rs641738C>T near MBOAT7 promotes steatosis, NASH, fibrosis and hepatocellular carcinoma in non-alcoholic fatty liver disease: a meta-analysis

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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Multi-ethnic genome-wide association study of decomposed cardioelectric phenotypes illustrates strategies to identify and characterize evidence of shared genetic effects for complex traits

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Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization

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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

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Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes: Trans-Omics for Precision Medicine (TOPMed) Program

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