Author

Cristina Beltrami

University of Verona

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 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Organism:human· 1

Frequent Co-Authors

Barbara IadarolaiD· 2 shared Denise LavezzariiD· 2 shared Marzia RossatoiD· 2 shared Massimo DelledonneiD· 2 shared Alessandra ModiiD· 1 shared Alessandro SalviatiiD· 1 shared Annalisa VetroiD· 1 shared Chiara Degli Esposti· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Barbara IadarolaORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineScientific ReportsPeer-reviewedOct 26, 2021

Whole-exome sequencing of the mummified remains of Cangrande della Scala (1291-1329 CE) indicates the first known case of late-onset Pompe disease

Barbara Iadarola, Denise Lavezzari, Alessandra Modi…·Massimo Delledonne

The paper performs whole-exome sequencing on mummified remains to identify a genetic mutation associated with late-onset Pompe disease in a historical figure.

5 citations

humanwhole-exome sequencing

𝕏 PostBluesky

GenomicsScientific ReportsPeer-reviewedJun 10, 2020

Enhanced targeted resequencing by optimizing the combination of enrichment technology and DNA fragment length

Barbara Iadarola, Luciano Xumerle, Denise Lavezzari…·Massimo Delledonne

The paper evaluates how DNA fragment length and enrichment technology affect genotypability in whole-exome sequencing, finding that longer fragments improve callable bases and genotypability across different platforms.

22 citations

whole-exome sequencingstatistical model

𝕏 PostBluesky