Author

Eren Shin

Broad Institute

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:long-read sequencing· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Alba Sanchis‐JuaniD· 2 shared Arthur S. LeeiD· 2 shared Harrison BrandiD· 2 shared Michael E. TalkowskiiD· 2 shared Nehir Edibe KurtasiD· 2 shared Xuefang ZhaoiD· 2 shared Akanksha KhorgadeiD· 1 shared Alan H. BeggsiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Alba Sanchis‐JuanORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencing

Alba Sanchis‐Juan, Yulia Mostovoy, Sarah L. Stenton, Vijay S Ganesh, Ben Weisburd, Alex Yenkin, Nehir Edibe Kurtas, Xuefang Zhao, Eren Shin, Philip M. Boone, Hang Su, Arthur S. Lee, Rachita Yadav, Kirsten Allan, Emanuela Argilli, , Michael E. Talkowski

This study evaluates the diagnostic yield of short-read and long-read sequencing in rare diseases, finding limited added value from long-read sequencing despite increased variant discovery.

medRxiv · Jun 24, 2026 · PreprintGenetic & Genomic Medicine

Comprehensive analysis of de novo variants across 2,497 orofacial cleft trios reveals novel genetic drivers of disease

Nehir Edibe Kurtas, Alba Sanchis‐Juan, Eren Shin, Sarah W. Curtis, Kelsey R. Robinson, Arthur S. Lee, Azeez Arisekola Alade, Xuefang Zhao, Jack M. Fu, Kimberly K. Diaz Perez, Lord Jephthah Joojo Gowans, Mekonen A. Eshete, WasiuL Adeyemo, Carmen J. Buxó, Carmencita D. Padilla, , Harrison Brand

This study identifies novel genetic drivers of orofacial clefts by analyzing de novo variants in 2,497 trios and integrating findings across subtypes and syndromic status.

medRxiv · May 24, 2026 · PreprintGenetic & Genomic Medicine