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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  • Site-wide: 7,655
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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

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  • Site-wide: 989
  • In genomics: 93
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  • Site-wide: 1,349
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  • Site-wide: 1,213

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

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  • In genetics: 387
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  • Site-wide: None
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Identification of type 2 diabetes loci in 433,540 East Asian individuals

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  • Site-wide: 8,298
  • In genetics: 404
• Year to date:
  • Site-wide: 28,833
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  • Site-wide: 26,940

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

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  • Site-wide: 9,430
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Population sequencing data reveal a compendium of mutational processes in human germline

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  • Site-wide: 14,318
  • In genetics: 736
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  • Site-wide: 19,167
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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: 20,217
  • In genetic and genomic medicine: 61
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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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  • In genetics: 1,312
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  • Site-wide: 60,745

Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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  • In genetics: 1,348
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  • Site-wide: 42,952

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: 28,616
  • In gastroenterology: 20
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  • Site-wide: 23,969
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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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  • In genetics: 1,578
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  • Site-wide: 14,335
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  • Site-wide: 10,256

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

• Downloaded 709 times
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  • In genetics: 1,590
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  • Site-wide: 104,972
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  • Site-wide: 78,988

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: 71,075
  • In epidemiology: 2,953
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  • Site-wide: 110,258
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  • Site-wide: None

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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  • Site-wide: 86,381
  • In genetic and genomic medicine: 290
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Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization

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  • In genetics: 4,059
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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

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  • Site-wide: 101,916
  • In genomics: 6,014
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  • Site-wide: 99,026
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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: 112,344
  • In genetic and genomic medicine: 487
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  • Site-wide: 6,751
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  • Site-wide: 12,553