Author

Christina Fenger

FiladelfiaORCID 0009-0001-7288-4787Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Assay:ATAC-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Allan BayatiD· 2 shared Alena Jahodová· 1 shared Allyn McConkie‐RoselliD· 1 shared Andrea Paras· 1 shared Andrew T. FerenbachiD· 1 shared Anita DattaiD· 1 shared Anju ShuklaiD· 1 shared Barbara K. BurtoniD· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersMolecular Biology

Allan BayatORCID

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2 papers

Recent·Most cited

Molecular BiologybioRxivPreprintMar 13, 2023

An O-GlcNAc transferase pathogenic variant that affects pluripotent stem cell self-renewal

Michaela Omelková, Christina Fenger, Marta Murray…·Daan M. F. van Aalten

The paper shows that an OGT variant causes reduced pluripotent stem cell self-renewal and lower stem cell marker levels in mouse embryonic stem cells.

3 citations

mouseATAC-seq

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Genetic & Genomic MedicinemedRxivPreprintApr 26, 2022

Missense variants in the voltage sensing and pore domain of KCNH5 cause neurodevelopmental phenotypes including epilepsy

Hannah C. Happ, Lynette Grant Sadleir, Matthew Zemel…·Gemma L. Carvill

The paper reports a cohort of 17 patients with pathogenic KCNH5 variants causing neurodevelopmental disorders and epilepsy, identifying genotype-phenotype correlations.

DOI 10.1101/2022.04.26.22274147

humanstatistical model

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