Author

Michele Nicastro

ERN GUARD-HeartORCID 0000-0002-4136-2599Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Alex Vincent PostmaiD· 1 shared Alexa M.C. VermeeriD· 1 shared Antonio M. A. MirandaiD· 1 shared Arie O. VerkerkiD· 1 shared Arthur A.M. WildeiD· 1 shared Ástrós SkúladóttiriD· 1 shared Bitten AagaardiD· 1 shared Bo Gregers WinkeliD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alex Vincent PostmaORCID

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1 paper

Recent·Most cited

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

Michele Nicastro, Alexa M.C. Vermeer, Pieter Gerard Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir, Vinicius Tragante, Lukas Mach, Alex Vincent Postma, Elisabeth M. Lodder, Karel van Duijvenboden, Rob Zwart, Leander Beekman, Lingshuang Wu, Paul A. van der Zwaag, , Najim Lahrouchi

medRxiv · Jul 4, 2024 · PreprintGenetic & Genomic Medicine