Author

Daniel M. DeLaughter

Harvard UniversityORCID 0000-0002-5352-2502Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:scRNA-seq· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Christine E. SeidmaniD· 2 shared Daniel ReichartiD· 2 shared Jonathan G. SeidmaniD· 2 shared Anissa ViveirosiD· 1 shared Barbara A. McDonoughiD· 1 shared Carlos N. Talavera-LópeziD· 1 shared Catherine L. WorthiD· 1 shared Danielle MurashigeiD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenomics

Christine E. SeidmanORCID

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2 papers

Recent·Most cited

Genes of the fatty acid oxidation pathway are upregulated in female as compared to male cardiomyocytes

Maya Talukdar, Lukáš Chmátal, Linyong Mao, Daniel Reichart, Danielle Murashige, Helen Skaletsky, Daniel M. DeLaughter, Zoltan Pierre Arany, Jonathan G. Seidman, Christine E. Seidman, David C. Page

The paper identifies sex differences in cardiac metabolism, showing female hearts have higher fatty acid oxidation gene expression and energy utilization compared to male hearts.

Circulation · Feb 17, 2025Peer-reviewedGenomics

Cells and gene expression programs in the adult human heart

Monika Litviňuková, Carlos N. Talavera-López, Henrike Maatz, Daniel Reichart, Catherine L. Worth, Eric L. Lindberg, Masatoshi Kanda, Krzysztof Polański, Eirini Sofia Fasouli, Sara Samari, Kenny Roberts, Elizabeth J. Tuck, Matthias Heinig, Daniel M. DeLaughter, Barbara A. McDonough, , Sarah Amalia Teichmann

The paper characterizes the cellular composition and gene expression of the adult human heart using single-cell transcriptomics, identifying distinct cell types and their functional roles.

bioRxiv · Apr 3, 2020 · PreprintGenomics