Author

Silvia Caroselli

IgenomixORCID 0009-0009-2496-6647Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:scRNA-seq· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Antonio CapalboiD· 2 shared Ajuna AzadiD· 1 shared António PelliceriD· 1 shared Antonio RequenaiD· 1 shared Beril Yüksel· 1 shared Carlos Marin Vallejo· 1 shared Carlos SimóniD· 1 shared Chaim JalasiD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Antonio CapalboORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 23, 2025

PGT-A Mosaicism Reporting Lacks Clinical Predictive Value: Evidence from a Multisite, Double-Blinded Study with Independent Validation Across 15,315 Single-Embryo Transfers

P. Gill, Xin Tao, Yiping Zhan…·Antonio Capalbo

This study shows that reporting mosaicism in PGT-A based on intermediate copy number (ICN) does not improve clinical outcomes in embryo selection.

DOI 10.1101/2025.06.23.25329758

humanstatistical model

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Genetic & Genomic MedicineReproductive BioMedicine OnlinePeer-reviewedMay 21, 2022

A standardized approach for case selection and genomic data analysis of maternal exomes for the diagnosis of oocyte maturation and early embryonic developmental arrest in IVF

Antonio Capalbo, Silvia Buonaiuto, Matteo Figliuzzi…·Semra Kahraman

The paper develops a methodology for selecting IVF cases with oocyte maturation defects and preimplantation embryo lethality, using whole-exome sequencing and bioinformatics to identify causative genetic variants.

18 citations

humanwhole-exome sequencing

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