Frank Sleutels
7PUBLICATIONS
63CO-AUTHORS
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Publications (7)
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|Mar 30, 2026
Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.Daniel Greene, Rodrigo Mendez, Jon Lees
|Oct 20, 2025
Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision making.Daphne J Smits, Federico Ferraro, Mark Drost
|Jul 29, 2025
Clinical utility of DNA-methylation signatures in routine diagnostics for neurodevelopmental disorders.Daphne J Smits, Christophe Debuy, Alice S Brooks
|Apr 10, 2025
Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy.Daniel Greene, Koenraad De Wispelaere, Jon Lees
|Jul 30, 2021
CTCF chromatin residence time controls three-dimensional genome organization, gene expression and DNA methylation in pluripotent cells.Widia Soochit, Frank Sleutels, Gregoire Stik
|Apr 03, 2018
UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population.Dewi A Wisnumurti, Yunia Sribudiani, Robert M Porsch
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Frequent Collaborators
5 joint publications
Tahsin Stefan Barakat
5 joint publications
Rachel Schot
4 joint publications
Federico Ferraro
3 joint publications
Ernest Turro
3 joint publications
Kathleen Freson
2 joint publications
Lies H Hoefsloot
2 joint publications
Wilfred F J van Ijcken
2 joint publications
Matthew T Wheeler
2 joint publications
Tjakko J van Ham
2 joint publications
Hennie T Brüggenwirth
