Academic Bibliography

Search 200 years of publications by Ghent University researchers.

Jilke De Wilde

Faculty of Medicine and Health Sciences > Department of Biomolecular Medicine

Work address: C. Heymanslaan 10, ingang 34 (MRB)
9000 Gent
Email: Jilke.DeWilde@UGent.be
ORCID iD: 0000-0003-0392-7162

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The long non-coding RNA SAMMSON is essential for uveal melanoma cell survival

Shanna Dewaele (UGent) , Louis Delhaye (UGent) , Boel De Paepe (UGent) , Eric de Bony de Lavergne (UGent) , Jilke De Wilde (UGent) , Katrien Vanderheyden (UGent) , Jasper Anckaert (UGent) , Nurten Yigit (UGent) , Justine Nuytens (UGent) , Eveline Vanden Eynde (UGent) , et al.

(2021) ONCOGENE.
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mTor inhibitor GDC-0349 improves ASO induced SAMMSON knock down resulting in enhanced anti-tumor efficacy in uveal melanoma

Shanna Dewaele (UGent) , Boel De Paepe (UGent) , Louis Delhaye (UGent) , Eric de Bony de Lavergne (UGent) , Jilke De Wilde (UGent) , Katrien Vanderheyden (UGent) , Jasper Anckaert (UGent) , Nurten Yigit (UGent) , Eveline Vanden Eynde (UGent) , Fariba Nemati, et al.

(2020) IEEE International Conference on Bioinformatics and Biomedicine (BIBM 2020), Abstracts.
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mTor inhibitor GDC-0349 improves ASO induced SAMMSON knock down resulting in enhanced anti-tumor efficacy in uveal melanoma

Shanna Dewaele (UGent) , Boel De Paepe (UGent) , Louis Delhaye (UGent) , Eric de Bony de Lavergne (UGent) , Jilke De Wilde (UGent) , Katrien Vanderheyden, Jasper Anckaert (UGent) , Nurten Yigit (UGent) , Eveline Vanden Eynde (UGent) , Fariba Nemati, et al.

(2020) OncoDot.1 symposium, Abstracts.
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Faster, cheaper and more accurate diagnosis of cancer of unknown primary (CUP) by using methylation profiling.

Jilke De Wilde (UGent) , Ruben Van Paemel (UGent) , Charlotte Vandeputte (UGent) , Andries De Koker (UGent) , Joni Van der Meulen (UGent) , Malaïka Van Der Linden (UGent) , Nico Callewaert (UGent) , Jo Van Dorpe (UGent) , David Creytens (UGent) , Bram De Wilde (UGent) , et al.

(2019) OncoPoint, 7th Research seminar, Abstracts.
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A fast, affordable and minimally-invasive diagnostic test for Cancer of Unknown Primary (CUP) using DNA methylation profiling

Jilke De Wilde (UGent) , Ruben Van Paemel (UGent) , Charlotte Vandeputte (UGent) , Andries De Koker (UGent) , Joni Van der Meulen (UGent) , Malaïka Van Der Linden (UGent) , Nico Callewaert (UGent) , Jo Van Dorpe (UGent) , David Creytens (UGent) , Bram De Wilde (UGent) , et al.

(2019)
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Shallow whole genome sequencing on circulating cell-free DNA in pediatric cancer patients

Charlotte Vandeputte (UGent) , Jolien Van Thorre, Ruben Van Paemel (UGent) , Andries De Koker (UGent) , Leen Willems (UGent) , Jo Van Dorpe (UGent) , Malaïka Van Der Linden (UGent) , Jilke De Wilde (UGent) , Björn Menten (UGent) , L. van Zogchel, et al.

(2019) PEDIATRIC BLOOD & CANCER. 66. p.S505-S506
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Successful copy number alteration profiling using circulating cell-free tumor DNA as a non-invasive alternative for tissue biopsies in pediatric cancer patients

Charlotte Vandeputte (UGent) , Jolien Van Thorre, Ruben Van Paemel (UGent) , Andries De Koker (UGent) , Leen Willems (UGent) , Jo Van Dorpe (UGent) , Malaïka Van Der Linden (UGent) , Jilke De Wilde (UGent) , Björn Menten (UGent) , Lieke van Zogchel, et al.

(2019) cell free DNA, 3de Nederlandse dag, Abstracts.
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Shallow whole genome sequencing on circulating cell-free DNA in pediatric cancer patients

Charlotte Vandeputte (UGent) , Jolien Van Thorre, Ruben Van Paemel (UGent) , Andries De Koker (UGent) , Leen Willems (UGent) , Jo Van Dorpe (UGent) , Malaïka Van Der Linden (UGent) , Jilke De Wilde (UGent) , Björn Menten (UGent) , Lieke van Zogchel, et al.

(2019) OncoPoint, 7th Research seminar, Abstracts.
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- Conference Paper
- C3
Shallow whole genome sequencing on circulating cell-free DNA in pediatric cancer patients

Charlotte Vandeputte (UGent) , Jolien Van Thorre, Ruben Van Paemel (UGent) , Andries De Koker (UGent) , Leen Willems (UGent) , Jo Van Dorpe (UGent) , Malaïka Van Der Linden (UGent) , Jilke De Wilde (UGent) , Björn Menten (UGent) , Lieke van Zogchel, et al.

(2019) Belgian Society for Human Genetics, 19th Annual meeting, Abstracts.