Author

Shlomi Constantini

Tel Aviv UniversityORCID 0000-0002-3170-5295Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:imaging· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:spatial domain detection· 1

Frequent Co-Authors

Alexandra KavushanskyiD· 2 shared Ben ShoftyiD· 2 shared Itamar KahniD· 2 shared Jad AslehiD· 2 shared Alejandro López‐JuáreziD· 1 shared Eyal BergmanniD· 1 shared F. Xavier CastellanosiD· 1 shared Gil ZuriD· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersNeuroscience

Alexandra KavushanskyORCID

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2 papers

Recent·Most cited

Brain-wide structural and functional disruption in mice with oligodendrocyte specific Nf1 deletion is rescued by inhibition of NOS

Jad Asleh, Ben Shofty, Nadav Cohen, Alexandra Kavushansky, Alejandro López‐Juárez, Shlomi Constantini, Nancy Ratner, Itamar Kahn

This paper shows that Nf1 deletion in oligodendrocytes causes brain structural and functional disruptions in mice, which are rescued by NOS inhibition.

Proceedings of the National Academy of Sciences · Aug 24, 2020Peer-reviewedNeuroscience

Loss of function in the autism and learning disabilities associated gene Nf1 disrupts corticocortical and corticostriatal functional connectivity in human and mouse

Ben Shofty, Eyal Bergmann, Gil Zur, Jad Asleh, Noam Bosak, Alexandra Kavushansky, F. Xavier Castellanos, Liat Ben‐Sira, Roger J. Packer, Gilbert Vézina, Shlomi Constantini, Maria T. Acosta, Itamar Kahn

This study shows that Nf1 loss-of-function disrupts corticocortical and corticostriatal functional connectivity in both human NF1 patients and Nf1+/- mice.

Neurobiology of Disease · May 22, 2019Peer-reviewedNeuroscience