Author

Christine W. Gao

Johns Hopkins UniversityORCID 0000-0003-2298-2239Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:gene regulatory network inference· 3 Organism:mouse· 3 Approach:statistical model· 3 Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Assay:ATAC-seq· 1

Frequent Co-Authors

Hans Tomas BjornssoniD· 3 shared Jill A. FahrneriD· 3 shared Kasper D. HanseniD· 2 shared Leandros BoukasiD· 2 shared Ryan C. RiddleiD· 2 shared Wanying LiniD· 2 shared Agnar HelgasoniD· 1 shared Ana S.A. CoheniD· 1 shared

Activity by Year

2023-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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3 shared papersGenetics

Hans Tomas BjornssonORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineThe American Journal of Human GeneticsPeer-reviewedSep 1, 2026

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome

Kimberley Jade Anderson, Eirny Tholl Thorolfsdottir, Ilana M. Nodelman…·Hans Tomas Bjornsson

The paper investigates sex-specific penetrance in PILBOS, showing male overrepresentation and androgen-mediated sexual dimorphism through genetic and mouse model studies.

2 citations

mousehuman

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GeneticsJCI InsightPeer-reviewedNov 28, 2023

Novel mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition

Christine W. Gao, Wanying Lin, Ryan C. Riddle…·Jill A. Fahrner

The paper creates a mouse model of Weaver syndrome and shows that inhibiting KDM6A/6B can reverse excessive osteogenesis caused by an EZH2 mutation.

29 citations

mouseATAC-seq

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GeneticsbioRxivPreprintOct 15, 2023

Growth retardation in a mouse model of Kabuki syndrome 2 bears mechanistic similarities to Kabuki syndrome 1

Christine W. Gao, Wanying Lin, Ryan C. Riddle…·Jill A. Fahrner

This study compares growth retardation in mouse models of Kabuki syndrome 1 and 2, finding similar transcriptional profiles in their chondrocyte models.

1 citation

mousebulk RNA-seq

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