Author

Sabrina Gade Ellesøe

University of CopenhagenORCID 0000-0002-0846-6409Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Organism:zebrafish· 1

Frequent Co-Authors

Alejandro SifrimiD· 1 shared Anna WilsdoniD· 1 shared Bernard ThienpontiD· 1 shared Canan DoğanlıiD· 1 shared Competence Network for Congenital Heart Defects, Germany· 1 shared Enrique AudainiD· 1 shared Gregor DombrowskyiD· 1 shared J. David BrookiD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Alejandro SifrimORCID

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1 paper

Recent·Most cited

Systems genetics analysis identify calcium signalling defects as novel cause of congenital heart disease

José M. G. Izarzugaza, Sabrina Gade Ellesøe, Canan Doğanlı, Natasja Spring Ehlers, Marlene Dalgaard, Enrique Audain, Gregor Dombrowsky, Alejandro Sifrim, Anna Wilsdon, Bernard Thienpont, Jeroen Breckpot, Marc H. M. L. Gewillig, Competence Network for Congenital Heart Defects, Germany, J. David Brook, Marc‐Phillip Hitz, , Søren Brunak

The paper identifies calcium signalling defects as a novel cause of congenital heart disease through whole exome sequencing and functional validation in zebrafish.

bioRxiv · Dec 11, 2019 · PreprintGenetics