Author

Fiona Wang

Massachusetts Institute of Technology

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

Biology Disciplines

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Genetic & Genomic Medicine· 1 Immunology· 1 Pathology· 1

Signature Assays, Organisms & Methods

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Approach:deep learning· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Assay:imaging· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Adam T. HigginsiD· 1 shared Anant MadabhushiiD· 1 shared Andrea CasiraghiiD· 1 shared Andrew H. SongiD· 1 shared Angela N. KoehleriD· 1 shared Ann J. Johnston· 1 shared Arturo J. VegasiD· 1 shared Becky S. LeiferiD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam T. HigginsORCID

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Author profile →

3 papers

Recent·Most cited

Surveying the target tractability of cytokines with small molecules

Raavi, Sean P. Quinnell, Andrea Casiraghi, Becky S. Leifer, Benjamin Leu, Morgan Stilgenbauer, Fiona Wang, Haoyi Hou, Angela N. Koehler, Arturo J. Vegas

This study identifies small-molecule ligands and inhibitors for 32 cytokines, showing their tractability for small-molecule modulation and providing insights into chemical structures that enable cytokine inhibition.

bioRxiv · Apr 23, 2026 · PreprintImmunology

Deep-learning triage of 3D pathology datasets for comprehensive and efficient pathologist assessments

Gan Gao, Renao Yan, Andrew H. Song, Huai-Ching Hsieh, Lindsey A. Erion Barner, Fiona Wang, David Brenes, Sarah S. L. Chow, Rui Wang, Kevin W. Bishop, Yongjun Liu, Xavier Farré, Mukul K. Divatia, Michelle R. Downes, Funda Vakar‐Lopez, , Jonathan T.C. Liu

CARP3D uses deep learning to prioritize high-risk 2D sections in 3D pathology data, improving disease detection while reducing pathologist workload.

bioRxiv · Jul 20, 2025 · PreprintPathology

A synonymous SLC2A1 variant causes familial epilepsy and paroxysmal exercise-induced dyskinesia by creating aberrant mosaic splicing patterns

Adam T. Higgins, Fiona Wang, William Owen Pickrell, Ann J. Johnston, Jeya Natarajan, Khalid Hamandi, Johann te Water Naudé, Mary Chebib, Mark I. Rees, Phil E M Smith, Seo‐Kyung Chung

This paper identifies a synonymous SLC2A1 variant causing GLUT1-DS through mosaic splicing, leading to variable haploinsufficiency and phenotypic diversity.

medRxiv · Apr 5, 2025 · PreprintGenetic & Genomic Medicine