Author

Celeste Sassi

Humboldt-Universität zu BerlinORCID 0000-0002-2837-1765Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Organism:human· 1 Assay:imaging· 1 Research Focus:spatial domain detection· 1 Research Focus:variant calling· 1

Frequent Co-Authors

José BrásiD· 2 shared Marco FoddisiD· 2 shared Rita João GuerreiroiD· 2 shared Susanne G. MuelleriD· 2 shared Ulrich DirnagliD· 2 shared Alistair T. PagnamentaiD· 1 shared Andreas MeiseliD· 1 shared Andrew SingletoniD· 1 shared

Activity by Year

2018-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetics

José BrásORCID

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3 papers

Recent·Most cited

GeneticsbioRxivPreprintMay 15, 2024

Ide copy number variant does not influence lesion size and mortality in two C57BL/6J mouse models of cerebrovascular ischemia nor in human cerebrovascular disease. An exploratory study

Marco Foddis, Sonja Blumenau, Susanne G. Mueller…·Celeste Sassi

The paper investigates whether Ide copy number variants influence vascular phenotypes in mice and humans, finding no significant association.

DOI 10.1101/2024.05.15.593342

mousebulk RNA-seq

𝕏 PostBluesky

NeurosciencebioRxivPreprintNov 4, 2020

Vascular cognitive impairment in the mouse reshapes visual, spatial network functional connectivity.

Gerard R. Hall, Philipp Boehm‐Sturm, Ulrich Dirnagl…·Tracy D. Farr

The paper examines structural and functional connectivity changes in a mouse model of vascular cognitive impairment, finding altered network connectivity and behavioural deficits.

DOI 10.1101/2020.11.04.366294

𝕏 PostBluesky

GenomicsbioRxivPreprintFeb 23, 2018

A comprehensive assessment of benign genetic variability for neurodegenerative disorders

Rita João Guerreiro, Celeste Sassi, Jesse Raphael Gibbs…·José Brás

The paper assesses benign genetic variability in elderly individuals without neurodegenerative disease to aid in distinguishing pathogenic mutations.

19 citations

humanwhole-exome sequencing

𝕏 PostBluesky