Author

Hélder Tedeschi

Universidade Estadual de Campinas (UNICAMP)ORCID 0000-0003-3347-3886Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:deconvolution· 1 Research Focus:differential expression· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Clarissa Lin YasudaiD· 2 shared Diogo F. T. VeigaiD· 2 shared Enrico GhizoniiD· 2 shared Fábio RogérioiD· 2 shared Fernando CendesiD· 2 shared Isabella C. GalvãoiD· 2 shared Íscia Lopes‐CendesiD· 2 shared Lauana Andrade Messias· 2 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersNeuroscience

Clarissa Lin YasudaORCID

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2 papers

Recent·Most cited

NeuroscienceiSciencePeer-reviewedNov 6, 2024

Multimodal single-cell profiling reveals neuronal vulnerability and pathological cell states in focal cortical dysplasia

Isabella C. Galvão, Manuela Lemoine, Lauana Andrade Messias…·Diogo F. T. Veiga

This study uses multi-omics single-cell profiling to identify chromatin and transcriptomic changes in FCD type II, revealing altered cell states and neuronal vulnerability.

17 citationstop 3%

humanscRNA-seq

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NeuroscienceScientific ReportsPeer-reviewedAug 16, 2023

Identifying cellular markers of focal cortical dysplasia type II with cell-type deconvolution and single-cell signatures

Isabella C. Galvão, Ludmyla Kandratavicius, Lauana Andrade Messias…·Diogo F. T. Veiga

This study uses cell-type deconvolution and single-cell signatures to analyze bulk RNA-seq data from FCD patients, revealing subtype-specific cellular changes, including astrogliosis in FCD IIb.

14 citations

humanbulk RNA-seq

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