Author

Raquel Sofia Silva

Human TechnopoleORCID 0000-0002-1455-3082Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:experimental assay· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Assay:long-read sequencing· 1 Assay:spatial transcriptomics· 1

Frequent Co-Authors

Ivano LegniniiD· 2 shared Rodrigo PracanaiD· 2 shared Alessandra Zappulo· 1 shared Alice LamboleziD· 1 shared Ambreen KalhoroiD· 1 shared Ana KotteiD· 1 shared Andre SimiD· 1 shared Andrew R. WebsteriD· 1 shared

Activity by Year

2017-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersMolecular Biology

Ivano LegniniORCID

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3 papers

Recent·Most cited

Molecular BiologybioRxivPreprintJul 6, 2026

Insulin synthesis is sustained by Tent5 poly(A) polymerases

Ana Kotte, Fabio Marcuccio, Linda Masante…·Ivano Legnini

The paper identifies Tent5 poly(A) polymerases as stabilizers of insulin mRNA, showing their specific activity regulated by glucose and localization.

DOI 10.64898/2026.07.04.736497

humanbulk RNA-seq

𝕏 PostBluesky

GenomicsbioRxivPreprintOct 31, 2024

Genomic codes governing enhancer RNA fate

Chi Wai Yip, Callum Parr, Hazuki Takahashi…·Piero Carninci

This paper introduces CFC-seq and SALA to sequence non-poly(A) RNAs, identifies 39,425 novel transcriptional units, and reveals a genomic code governing enhancer RNA fate based on promoter architecture.

5 citations

humanlong-read sequencing

𝕏 PostBluesky

GenomicsScientific ReportsPeer-reviewedAug 2, 2017

Duplication events downstream of IRX1 cause North Carolina macular dystrophy at the MCDR3 locus

Valentina Cipriani, Raquel Sofia Silva, Gavin Arno…·Anthony T. Moore

The paper identifies two duplications at the MCDR3 locus associated with North Carolina macular dystrophy, refining the disease-causing region and showing expression of IRX1 and ADAMTS16 in fetal retina.

29 citations

humanwhole-genome sequencing

𝕏 PostBluesky