Author

Karl E. Pfeifer

National Institutes of HealthORCID 0000-0002-0254-682XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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

Frequent Co-Authors

Apratim MitraiD· 2 shared Claudia M. GebertiD· 2 shared Connor M. KeaniD· 2 shared Jacob A. NoekeriD· 2 shared Anne L. CalofiD· 1 shared Arthur D. LanderiD· 1 shared Beenish RahatiD· 1 shared Beth A. KozeliD· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersGenetics

Apratim MitraORCID

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2 papers

Recent·Most cited

Decreasing Wapl dosage partially corrects transcriptome phenotypes in Nipbl-/+ embryonic mouse brain

Connor M. Kean, Christopher J. Tracy, Apratim Mitra, Matthew T. Van Winkle, Claudia M. Gebert, Jacob A. Noeker, Anne L. Calof, Arthur D. Lander, Judith A. Kassis, Karl E. Pfeifer

This study shows that reducing Wapl dosage partially corrects transcriptome and growth defects in Nipbl-/+ embryonic mouse brains, suggesting cohesin dynamics regulate gene expression.

bioRxiv · May 31, 2022 · PreprintGenetics

Cardiac pathologies in mouse loss of imprinting models are due to misexpression of H19 long noncoding RNA

Ki-Sun Park, Beenish Rahat, Hyung Chul Lee, Zu‐Xi Yu, Jacob A. Noeker, Apratim Mitra, Connor M. Kean, Russell H. Knutsen, Danielle Springer, Claudia M. Gebert, Beth A. Kozel, Karl E. Pfeifer

The paper shows that maternal loss of imprinting at the H19/IGF2 locus causes cardiac pathologies in mice, with Igf2 driving transient hypertrophy and H19 causing progressive fibrosis and reduced ventricular function.

eLife · Aug 17, 2021Peer-reviewedDevelopmental Biology