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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  • Site-wide: 1,175
  • In genomics: 96
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  • Site-wide: 3,661
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Identification of type 2 diabetes loci in 433,540 East Asian individuals

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  • Site-wide: 9,563
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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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  • Site-wide: 9,587
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  • Site-wide: 100,017
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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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  • Site-wide: 10,867
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A trans-ancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.

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  • Site-wide: 10,975
  • In genetic and genomic medicine: 45
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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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  • Site-wide: 14,198
  • In genetic and genomic medicine: 60
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  • Site-wide: 6,285
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  • Site-wide: 13,265

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

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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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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  • Site-wide: 28,609
  • In gastroenterology: 26
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  • Site-wide: 8,196

Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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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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  • Site-wide: 38,431
  • In genetics: 1,738
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  • Site-wide: 143,188
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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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  • In genetic and genomic medicine: 277
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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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  • Site-wide: 77,967
  • In epidemiology: 3,319
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Bidirectional Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of intermediate potential

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  • Site-wide: 91,616
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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

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  • Site-wide: 100,202
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Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits - the Hispanic/Latino Anthropometry Consortium

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Whole Genome Sequence Association Analysis of Fasting Glucose and Fasting Insulin Levels in Diverse Cohorts from the NHLBI TOPMed Program

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  • Site-wide: 101,944
  • In genetic and genomic medicine: 478
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Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization

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  • Site-wide: 103,495
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  • Site-wide: 148,376
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Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL Study

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  • Site-wide: 140,497
  • In genetic and genomic medicine: 779
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Amerind ancestry predicts the impact of FADS genetic variation on omega-3 PUFA deficiency, cardiometabolic and inflammatory risk in Hispanic populations

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  • Site-wide: 142,535
  • In genetic and genomic medicine: 800
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  • Site-wide: 59,386
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