Tjitske Kleefstra

4PUBLICATIONS
51CO-AUTHORS
Cell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesEnglish as a second language
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Publications (4)

|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

|Jan 10, 2024
Arrhythmias including atrial fibrillation and congenital heart disease in Kleefstra syndrome: a possible epigenetic link.

Sunil K Vasireddi, Tanja Zdolsek Draksler, Arianne Bouman

|May 18, 2022
Human KCNQ5 de novo mutations underlie epilepsy and intellectual disability.

Aguan D Wei, Paul Wakenight, Theresa A Zwingman

|Jul 09, 2021
Speech-language profiles in the context of cognitive and adaptive functioning in SATB2-associated syndrome.

Lot Snijders Blok, Y Max Goosen, Leenke van Haaften

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