Author

Bryan H. Louie

Stanford MedicineORCID 0000-0001-6922-5396Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:machine learning (classical)· 1 Assay:scATAC-seq· 1

Frequent Co-Authors

Anna ShcherbinaiD· 1 shared Anshul Bharat KundajeiD· 1 shared Boxiang LiuiD· 1 shared Howard Y. ChangiD· 1 shared Jeffrey M. GranjaiD· 1 shared Kathleen S. MontineiD· 1 shared Laure FrésardiD· 1 shared M. Ryan CorcesiD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Anna ShcherbinaORCID

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1 paper

Recent·Most cited

Single-cell epigenomic identification of inherited risk loci in Alzheimer's and Parkinson's disease

M. Ryan Corces, Anna Shcherbina, Soumya Kundu, Michael J. Gloudemans, Laure Frésard, Jeffrey M. Granja, Bryan H. Louie, Tiffany Y. Eulalio, Shadi Shams, S. Tansu Bagdatli, Maxwell R. Mumbach, Boxiang Liu, Kathleen S. Montine, William James Greenleaf, Anshul Bharat Kundaje, , Thomas Jude Montine

The paper uses single-cell epigenomic data to identify functional SNPs associated with Alzheimer's and Parkinson's disease, revealing novel gene-disease associations and regulatory mechanisms.

Nature Genetics · Oct 26, 2020Peer-reviewedGenomics