Author

Seung‐Tae Lee

Yonsei UniversityORCID 0000-0003-1047-1415Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Daniela NachmansoniD· 1 shared Hyunki KimiD· 1 shared Jae Eun LeeiD· 1 shared Jae‐Ho CheongiD· 1 shared Jeong-Hyeon Jo· 1 shared Ji Soo ParkiD· 1 shared Lisa MadlenskyiD· 1 shared Olivier HarismendyiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Daniela NachmansonORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineScientific ReportsPeer-reviewedJul 20, 2021

Prevalence of cancer susceptibility variants in patients with multiple Lynch syndrome related cancers

Yoon Young Choi, Su‐Jin Shin, Jae Eun Lee…·Olivier Harismendy

The paper identifies pathogenic variants in Lynch Syndrome genes in patients with multiple cancers and finds higher prevalence of non-LS gene variants in early-onset cases.

8 citations

humanwhole-exome sequencing

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