Author

Ningning Hu

Vanderbilt University Medical Center

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 Genetics· 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 Approach:experimental assay· 1 Assay:scRNA-seq· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alexander G. BickiD· 1 shared Alexander James SilveriD· 1 shared Alyssa ParkeriD· 1 shared Ayesha Ahmad· 1 shared Bian LiiD· 1 shared Brian SharberiD· 1 shared Caitlyn VlasschaertiD· 1 shared Chad R. PottsiD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Alexander G. BickORCID

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2 papers

Recent·Most cited

Multiomic Profiling of Human Clonal Hematopoiesis Reveals Genotype and Cell-Specific Inflammatory Pathway Activation

Jonathan Brett Heimlich, Pawan K. Bhat, Alyssa Parker, Matthew T. Jenkins, Caitlyn Vlasschaert, Jessica Ulloa, Joseph C. Van Amburg, Chad R. Potts, Sydney S. Olson, Alexander James Silver, Ayesha Ahmad, Brian Sharber, Donovan J. Brown, Ningning Hu, Peter van Galen, , Paul Brent Ferrell

This study profiles single-cell multiomic data from clonal hematopoiesis patients and controls, revealing pro-inflammatory profiles in monocytes and T cell dysfunction.

Blood Advances · Mar 20, 2024Peer-reviewedGenetics

Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

Souhrid Mukherjee, Thomas A. Cassini, Ningning Hu, Tao Yang, Bian Li, Wangzhen Shen, Christopher W. Moth, David C. Rinker, Jonathan H. Sheehan, Joy D. Cogan, Undiagnosed Diseases Network, John H. Newman, Rizwan Hamid, Robert L. Macdonald, Dan M. Roden, , John A. Capra

The paper uses personalized structural biology to analyze de novo KCNC2 variants in a DEE patient, revealing distinct functional effects of two nearby variants.

Human Genetics and Genomics Advances · Jul 18, 2022Peer-reviewedGenetic & Genomic Medicine