Author

Filomena Pirozzi

Case Western Reserve UniversityORCID 0000-0002-7603-662XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Assay:scRNA-seq· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Andrew E. TimmsiD· 1 shared Anthony J. Wynshaw-BorisiD· 1 shared Christina M. LockwoodiD· 1 shared Colin C. PritchardiD· 1 shared Edward John NovotnyiD· 1 shared Emily Pao· 1 shared Emily S Doherty· 1 shared Francesca ForzanoiD· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Andrew E. TimmsORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintDec 29, 2022

MOPD I patient-derived cerebral organoids model microcephaly showing premature neurogenesis due to disrupted mitotic spindle orientation.

Jagjit Singh, Noah J. Daniels, Filomena Pirozzi…·Richard A. Padgett

This study uses patient-derived cerebral organoids to show that MOPD I mutations cause disrupted mitotic spindle orientation, leading to premature neurogenesis and cortical layering defects.

1 citation

humanscRNA-seq

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Genetic & Genomic MedicineBrainPeer-reviewedOct 6, 2021

Analysis of common PI3K-AKT-MTOR mutations in pediatric surgical epilepsy by droplet digital PCR reveals novel clinical and molecular insights

Filomena Pirozzi, Matthew Berkseth, Rylee Shear…·Ghayda Mirzaa

The paper uses ddPCR to analyze PI3K-AKT-MTOR mutations in pediatric epilepsy cases, finding associations between specific mutations and clinical phenotypes.

54 citationstop 1%

humanDNA methylation

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