Author

Dario Ronchi

University of MilanORCID 0000-0002-6093-9816Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2

Frequent Co-Authors

Francesco FortunatoiD· 2 shared Alex Vincent PostmaiD· 1 shared Alexa M.C. VermeeriD· 1 shared Amalia GastaldelliiD· 1 shared Anna AlisiiD· 1 shared Anna Ludovica FracanzaniiD· 1 shared Antonio M. A. MirandaiD· 1 shared Arie O. VerkerkiD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Francesco FortunatoORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 4, 2024

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…·Najim Lahrouchi

DOI 10.1101/2024.07.04.24309755

humanbulk RNA-seq

𝕏 PostBluesky

GeneticsDigestive and Liver DiseasePeer-reviewedFeb 23, 2021

TM6SF2/PNPLA3/MBOAT7 loss-of-function genetic variants impact on NAFLD development and progression both in patients and in in vitro models

M. Longo, M. Meroni, Veronica Erconi…·Paola Dongiovanni

The paper investigates the combined effect of three genetic variants on NAFLD progression in patients and in vitro models, finding increased HCC risk and altered lipid and mitochondrial metabolism.

9 citations

humanbulk RNA-seq

𝕏 PostBluesky