Ghent University Academic Bibliography

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Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes : a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes

José Garcia-Pelaez, Rita Barbosa-Matos, Silvana Lobo, Alexandre Dias, Luzia Garrido, Sérgio Castedo, Sónia Sousa, Hugo Pinheiro, Liliana Sousa, Rita Monteiro, et al.

(2023) LANCET ONCOLOGY. 24(1). p.91-106
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- Journal Article
- A1
- open access
Two years of genomic surveillance in Belgium during the SARS-CoV-2 pandemic to attain country-wide coverage and monitor the introduction and spread of emerging variants

Lize Cuypers, Simon Dellicour, Samuel L. Hong, Barney I. Potter, Bruno Verhasselt (UGent) , Nick Vereecke (UGent) , Laurens Lambrechts (UGent) , Keith Durkin, Vincent Bours, Sofieke Klamer, et al.

(2022) VIRUSES-BASEL. 14(10).
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- Journal Article
- A1
- open access
PCIP-seq : simultaneous sequencing of integrated viral genomes and their insertion sites with long reads

Maria Artesi, Vincent Hahaut, Basiel Cole, Laurens Lambrechts (UGent) , Fereshteh Ashrafi, Ambroise Marçais, Olivier Hermine, Philip Griebel, Natasa Arsic, Frank van der Meer, et al.

(2021) GENOME BIOLOGY. 22(1).
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Outcome of publicly funded nationwide first-tier noninvasive prenatal screening

Kris Van den Bogaert, Lore Lannoo, Nathalie Brison, Vincent Gatinois, Machteld Baetens (UGent) , Bettina Blaumeiser, Francois Boemer, Laura Bourlard, Vincent Bours, Anne De Leener, et al.

(2021) GENETICS IN MEDICINE. 23(6). p.1137-1142
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Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy

François-Guillaume Debray, Claudia Stümpfig, Arnaud Vanlander (UGent) , Vinciane Dideberg, Claire Josse, Jean-Hubert Caberg, François Boemer, Vincent Bours, René Stevens, Sara Seneca, et al.

(2015) JOURNAL OF INHERITED METABOLIC DISEASE. 38(6). p.1147-1153

Academic Bibliography

Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes : a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes

Two years of genomic surveillance in Belgium during the SARS-CoV-2 pandemic to attain country-wide coverage and monitor the introduction and spread of emerging variants

PCIP-seq : simultaneous sequencing of integrated viral genomes and their insertion sites with long reads

Outcome of publicly funded nationwide first-tier noninvasive prenatal screening

Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy

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