Author

Bin Ye

Regeneron (United States)ORCID 0000-0002-9544-6907Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2

Frequent Co-Authors

Alan R. ShuldineriD· 2 shared Aris BarasiD· 2 shared Aris N. EconomidesiD· 2 shared John D. OvertoniD· 2 shared Alexander H. LiiD· 1 shared Anthony MarckettaiD· 1 shared Asif Rasheed· 1 shared Ayeesha Kamran KamaliD· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Alan R. ShuldinerORCID

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2 papers

Recent·Most cited

NOTCH3 p.Arg1231Cys is Markedly Enriched in South Asians and Associated with Stroke

Juan L. Rodríguez-Flores, Shareef Khalid, Neelroop Parikshak, Asif Rasheed, Bin Ye, Manav Kapoor, Joshua Backman, Farshid Sepehrband, Silvio Alessandro Di Gioia, Sahar Gelfman, Tanima De, Nilanjana Banerjee, Deepika Sharma, Hector Martinez, Sofia Castaneda, , Danish Saleheen

The paper identifies a NOTCH3 variant, p.Arg1231Cys, enriched in South Asians and strongly associated with stroke risk, highlighting the importance of genetic diversity in stroke research.

medRxiv · Oct 5, 2023 · PreprintGenetic & Genomic Medicine

Exome-wide association studies in general and long-lived populations identify genetic variants related to human age

Patrick Sin‐Chan, Nehal Gosalia, Chuan Gao, Cristopher V. Van Hout, Bin Ye, Anthony Marcketta, Alexander H. Li, Colm T. O’Dushlaine, Dadong Li, John D. Overton, Jeffrey D. Reid, Aris Baras, David J. Carey, David H. Ledbetter, Daniel James Rader, , Alan R. Shuldiner

The paper performs exome-wide association studies in large cohorts to identify genetic variants linked to human age, finding new candidates and confirming known ones.

bioRxiv · Jul 19, 2020 · PreprintGenetics