Ghent University Academic Bibliography

HRAS-related epidermal nevus syndromes : expansion of the spectrum with first branchial arch defects

Aude Beyens (UGent) , Charlotte Lietaer, Kathleen Claes (UGent) , Elfride De Baere (UGent) , Marleen Goeteyn (UGent) , Bob Lerut, Hannes Syryn (UGent) , Olivier Vanakker (UGent) , Joni Van der Meulen (UGent) , Lieve Vanwalleghem, et al.

(2023) CLINICAL GENETICS. 103(6). p.709-713

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Application of an ultrasensitive NGS-based blood test for the diagnosis of early-stage lung cancer : sensitivity, a hurdle still difficult to overcome

Malaïka Van der Linden (UGent) , Bram Van Gaever (UGent) , Lennart Raman, Karim Vermaelen (UGent) , Ingel Demedts (UGent) , Veerle Surmont (UGent) , Ulrike Himpe, Yolande Lievens (UGent) , Liesbeth Ferdinande (UGent) , Franceska Dedeurwaerdere, et al.

(2022) CANCERS. 14(8).

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OMEN : network-based driver gene identification using mutual exclusivity

Dries Van Daele, Bram Weytjens (UGent) , Luc De Raedt and Kathleen Marchal (UGent)

(2022) BIOINFORMATICS. 38(12). p.3245-3251

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European experts consensus : BRCA/homologous recombination deficiency testing in first-line ovarian cancer

I. Vergote, A. González-Martín, I. Ray-Coquard, P. Harter, N. Colombo, P. Pujol, D. Lorusso, M.R. Mirza, B. Brasiuniene, R. Madry, et al.

(2022) ANNALS OF ONCOLOGY. 33(3). p.276-287

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Network-based analysis to identify drivers of metastatic prostate cancer using GoNetic

Louise de Schaetzen van Brienen (UGent) , Giles Miclotte (UGent) , Maarten Larmuseau (UGent) , Jimmy Van den Eynden (UGent) and Kathleen Marchal (UGent)

(2021) CANCERS. 13(21).

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Pan-cancer analysis of whole genomes

Peter J. Campbell, Gad Getz, Jan O. Korbel, Joshua M. Stuart, Jennifer L. Jennings, Lincoln D. Stein, Marc D. Perry, Hardeep K. Nahal-Bose, B. F. Francis Ouellette, Constance H. Li, et al.

(2020) NATURE. 578(7793). p.82-93

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Prevalence of cytoplasmic actin mutations in diffuse large B-cell lymphoma and multiple myeloma : a functional assessment based on actin three-dimensional structures

Laura Witjes, Marleen Van Troys (UGent) , Bruno Verhasselt (UGent) and Christophe Ampe (UGent)

(2020) INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 21(9).

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Pathway and network analysis of more than 2500 whole cancer genomes

Matthew A Reyna, David Haan, Marta Paczkowska, Lieven Verbeke (UGent) , Miguel Vazquez, Abdullah Kahraman, Sergio Pulido-Tamayo, Jonathan Barenboim, Lina Wadi, Priyanka Dhingra, et al.

(2020) NATURE COMMUNICATIONS. 11(1).

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Incorporating PARP-inhibitors into clinical routine : a tailored treatment strategy to tackle ovarian cancer

Emiel De Jaeghere (UGent) , Katrien Vandecasteele (UGent) , Kathleen Claes (UGent) , Amin Makar (UGent) , Philippe Tummers (UGent) , Veronique Cocquyt (UGent) and Hannelore Denys (UGent)

(2017) ACTA CLINICA BELGICA. 72(1). p.6-11

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Performance of four modern whole genome amplification methods for copy number variant detection in single cells

Lieselot Deleye (UGent) , Laurentijn Tilleman (UGent) , Ann-Sophie Vander Plaetsen, Senne Cornelis (UGent) , Dieter Deforce (UGent) and Filip Van Nieuwerburgh (UGent)

(2017) SCIENTIFIC REPORTS. 7.

Academic Bibliography

HRAS-related epidermal nevus syndromes : expansion of the spectrum with first branchial arch defects

Application of an ultrasensitive NGS-based blood test for the diagnosis of early-stage lung cancer : sensitivity, a hurdle still difficult to overcome

OMEN : network-based driver gene identification using mutual exclusivity

European experts consensus : BRCA/homologous recombination deficiency testing in first-line ovarian cancer

Network-based analysis to identify drivers of metastatic prostate cancer using GoNetic

Pan-cancer analysis of whole genomes

Prevalence of cytoplasmic actin mutations in diffuse large B-cell lymphoma and multiple myeloma : a functional assessment based on actin three-dimensional structures

Pathway and network analysis of more than 2500 whole cancer genomes

Incorporating PARP-inhibitors into clinical routine : a tailored treatment strategy to tackle ovarian cancer

Performance of four modern whole genome amplification methods for copy number variant detection in single cells

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