Author

Myung K. Shin

Merck & Co., Inc., Rahway, NJ, USA (United States)ORCID 0009-0001-6458-6296Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2

Signature Assays, Organisms & Methods

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Approach:Bayesian inference· 2 Research Focus:GWAS / association mapping· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:eQTL / molecular QTL mapping· 1 Assay:GWAS summary statistics· 1 Assay:scATAC-seq· 1 Approach:statistical model· 1

Frequent Co-Authors

Adrián CortésiD· 1 shared Adriana M. HungiD· 1 shared Benjamin F. VoightiD· 1 shared Chengxiang QiuiD· 1 shared Chris WallaceiD· 1 shared Christopher D. BrowniD· 1 shared Guillermo RealesiD· 1 shared Hongbo LiuiD· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Adrián CortésORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintJun 29, 2023

CoPheScan: phenome-wide association studies accounting for linkage disequilibrium

Ichcha Manipur, Guillermo Reales, Jae Hoon Sul…·Chris Wallace

CoPheScan improves PheWAS by accounting for linkage disequilibrium, identifying causal associations and reducing false positives in genetic variant analyses.

1 citation

humanGWAS summary statistics

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GeneticsNature GeneticsPeer-reviewedAug 12, 2021

Mapping the genetic architecture of human traits to cell types in the kidney identifies mechanisms of disease and potential treatments

Xin Sheng, Yuting Guan, Ziyuan Ma…·Katalin Suszták

The paper maps genetic variants to cell types in the kidney to identify disease mechanisms and drug targets.

161 citationstop 1%

humanbulk RNA-seq

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