Author

Kishore R. Kumar

The University of SydneyORCID 0000-0002-9917-3379Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Approach:graph neural network· 1 Research Focus:GWAS / association mapping· 1 Assay:long-read sequencing· 1

Frequent Co-Authors

Ai Huey TaniD· 1 shared Alice SteeliD· 1 shared Andrew Leslie LeeiD· 1 shared Anis Nadhirah Khairul AnuariD· 1 shared Azlina Ahmad‐AnnuariD· 1 shared Beomseok JeoniD· 1 shared Charles M. KingiD· 1 shared Cheng‐Hsuan LiiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ai Huey TanORCID

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2 papers

Recent·Most cited

Lineage-specific X chromosome inactivation escape and skew underlie sex-biased immune gene dosage and deleterious variant exposure

Daisy Kavanagh, Alice Steel, Helen E. King, Helaine Graziele Santos Vieira, Kishore R. Kumar, Etienne Masle‐Farquhar, Charles M. King, Robert J. Weatheritt, Ksenia Skvortsova

This paper introduces scDaisyChain to analyze X chromosome inactivation escape and skew in immune cells, revealing lineage-specific effects on gene dosage and variant exposure in healthy and autoimmune disease contexts.

bioRxiv · Aug 31, 2026 · PreprintBioinformatics

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations

Yi Wen Tay, Andrew Leslie Lee, Jie Ping Schee, Chin Hsien Lin, Eng‐King Tan, Jung Hwan Shin, Pin‐Shiuan Chen, Sung‐Pin Fan, Cheng‐Hsuan Li, Ebonne Yu Lin Ng, Han‐Joon Kim, Beomseok Jeon, Sulev Kõks, Kin Ying Mok, Yi Ting Lim, , Ai Huey Tan

The paper identifies the GCH1 p.Ser80Asn variant as a rare, East Asian-enriched risk factor for Parkinson's disease with increased odds ratio and specific clinical features.

medRxiv · Jun 22, 2026 · PreprintGenetic & Genomic Medicine