Thomas Naert

Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder

Maria del Rocio Pérez Baca (UGent) , María Palomares-Bralo, Michiel Vanhooydonck (UGent) , Lisa Hamerlinck (UGent) , Eva D'haene (UGent) , Sebastian Leimbacher (UGent) , Eva Jacobs, Laurenz De Cock (UGent) , Erika D'haenens (UGent) , Annelies Dheedene (UGent) , et al.

(2025) AMERICAN JOURNAL OF HUMAN GENETICS. 112(6). p.1388-1414

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CRISPR/Cas9 mediated disruption of an evolutionary conserved putative enhancer in the mab21l2 locus induces developmental eye anomalies in Xenopus tropicalis

Münevver Burcu Cicekdal (UGent) , Fabiola Ceroni, Richard Holt, Thomas Naert (UGent) , Soeren S. Lienkamp, Elena Sorokin, Elena Semina, Nicolas Chassaing, Nicola Ragge, Elfride De Baere (UGent) , et al.

(2024) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 32(Supplement 1). p.247-247

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Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development

Fabiola Ceroni, Münevver Burcu Cicekdal (UGent) , Richard Holt, Elena Sorokina, Nicolas Chassaing, Samuel Clokie, Thomas Naert (UGent) , Lidiya V. Talbot, Sanaa Muheisen, Dorine A. Bax, et al.

(2024) NATURE COMMUNICATIONS. 15(1).

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Benchtop mesoSPIM : a next-generation open-source light-sheet microscope for cleared samples

Nikita Vladimirov, Fabian F. Voigt, Thomas Naert (UGent) , Gabriela R. Araujo, Ruiyao Cai, Anna Maria Reuss, Shan Zhao, Patricia Schmid, Sven Hildebrand, Martina Schaettin, et al.

(2024) NATURE COMMUNICATIONS. 15(1).

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Reflective multi-immersion microscope objectives inspired by the Schmidt telescope

Fabian F. Voigt, Anna Maria Reuss, Thomas Naert (UGent) , Sven Hildebrand, Martina Schaettin, Adriana L. Hotz, Lachlan Whitehead, Armin Bahl, Stephan C. F. Neuhauss, Alard Roebroeck, et al.

(2024) NATURE BIOTECHNOLOGY. 42(1). p.65-71

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Mutations in the histone methyltransferase Ezh2 drive context-dependent leukemia in Xenopus tropicalis

Dieter Tulkens, Marthe Boelens (UGent) , Thomas Naert (UGent) , Marjolein Carron (UGent) , Suzan Demuynck (UGent) , Sylviane Dewaele (UGent) , Gert Van Isterdael (UGent) , David Creytens (UGent) , Tim Pieters (UGent) , Steven Goossens (UGent) , et al.

(2023) LEUKEMIA. 37. p.2404-2413

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HNF1B alters an evolutionarily conserved nephrogenic program of target genes

Kelli Grand, Martine Stoltz, Ludovica Rizzo, Ruth Roeck, Michael M. Kaminski, Gabriela Salinas, Maike Getwan, Thomas Naert (UGent) , Roman Pichler and Soeren S. Lienkamp

(2023) JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY. 34(3). p.412-432

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Genetic variants in ARHGEF6 cause congenital anomalies of the kidneys and urinary tract in humans, mice, and frogs

V. Klämbt, F. Buerger, C. Wang, Thomas Naert (UGent) , K. Richter, T. Nauth, A. C. Weiss, T. Sieckmann, E. Lai, D. Connaughton, et al.

(2023) JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY. 34(2). p.273-290

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Identifying and characterizing EZH2 as a druggable dependency factor for desmoid tumors in a genetic Xenopus tropicalis model for Gardner's Syndrome

Thomas Naert (UGent) , Dieter Tulkens, Tom Van Nieuwenhuysen (UGent) , Joanna Przybyl, Suzan Demuynck (UGent) , Mushriq Al-Jazrawe, Matt van de Rijn, Benjamin Alman, Kim De Leenheer, Paul Coucke (UGent) , et al.

(2022) EUROPEAN JOURNAL OF HUMAN GENETICS. 30(SUPPL 1). p.71-72

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Deep learning is widely applicable to phenotyping embryonic development and disease

Thomas Naert (UGent) , Ozgun Cicek, Paulina Ogar, Max Burgi, Nikko-Ideen Shaidani, Michael M. Kaminski, Yuxiao Xu, Kelli Grand, Marko Vujanovic, Daniel Prata, et al.

(2021) DEVELOPMENT. 148(21).

Academic Bibliography

Thomas Naert

Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder

CRISPR/Cas9 mediated disruption of an evolutionary conserved putative enhancer in the mab21l2 locus induces developmental eye anomalies in Xenopus tropicalis

Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development

Benchtop mesoSPIM : a next-generation open-source light-sheet microscope for cleared samples

Reflective multi-immersion microscope objectives inspired by the Schmidt telescope

Mutations in the histone methyltransferase Ezh2 drive context-dependent leukemia in Xenopus tropicalis

HNF1B alters an evolutionarily conserved nephrogenic program of target genes

Genetic variants in ARHGEF6 cause congenital anomalies of the kidneys and urinary tract in humans, mice, and frogs

Identifying and characterizing EZH2 as a druggable dependency factor for desmoid tumors in a genetic Xenopus tropicalis model for Gardner's Syndrome

Deep learning is widely applicable to phenotyping embryonic development and disease

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