Author

Emma Delanote

Ghent University Hospital

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 3

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

Frequent Co-Authors

Frans P.M. CremersiD· 3 shared Frauke CoppietersiD· 3 shared Alfredo Dueñas ReyiD· 2 shared Barbara FerrariiD· 2 shared Erik de VriezeiD· 2 shared Merel StemerdinkiD· 2 shared Michael P. KwintiD· 2 shared Peter A.C. ’t HoeniD· 2 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

Frans P.M. CremersORCID

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Author profile →

3 papers

Recent·Most cited

RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs)

Mathieu Quinodoz, Elifnaz Çelik, Dhryata Kamdar, Francesca Cancellieri, Karolina Kamińska, Mukhtar Ullah, Pilar Barberán-Martínez, Manon Bouckaert, Marta Cortón, Emma Delanote, Lidia Fernández‐Caballero, Gema García‐García, Lara K. Holtes, Marianthi Karali, Irma López, , Carlo Rivolta

RetiGene provides a curated gene atlas for inherited retinal diseases, integrating variant data and RNA sequencing to support gene prioritization and therapeutic development.

bioRxiv · Jun 8, 2025 · PreprintGenetics

A proteogenomic atlas of the human neural retina

Tabea Riepe, Merel Stemerdink, Renee Salz, Alfredo Dueñas Rey, Suzanne E. de Bruijn, Erica G. M. Boonen, Tomasz Z. Tomkiewicz, Michael P. Kwint, Jolein Gloerich, Hans J. C. T. Wessels, Emma Delanote, Elfride B. W. De Baere, Filip Van Nieuwerburgh, Sarah De Keulenaer, Barbara Ferrari, , Peter A.C. ’t Hoen

The paper generates a proteogenomic atlas of the human neural retina using long-read RNA-sequencing and mass spectrometry, identifying novel transcript isoforms and peptides.

Frontiers in Genetics · Sep 19, 2024Peer-reviewedGenetics

Pushing the limits of single molecule transcript sequencing to uncover the largest disease-associated transcript isoforms in the human neural retina

Merel Stemerdink, Tabea Riepe, Nick Zomer, Renee Salz, Michael P. Kwint, Raoul Timmermans, Barbara Ferrari, Stefano Ferrari, Alfredo Dueñas Rey, Emma Delanote, Suzanne E. de Bruijn, Hannie Kremer, Susanne Roosing, Frauke Coppieters, Alexander Hoischen, , Erik de Vrieze

The paper uses long-read sequencing and cDNA capture to sequence large transcripts associated with Usher syndrome in the human neural retina, identifying novel isoforms and splicing events.

bioRxiv · Sep 10, 2024 · PreprintGenetics