Ghent University Academic Bibliography

Your filters: cql: author="Colas, Chrystelle" or (type any "bookEditor issueEditor" and editor="Colas, Chrystelle")

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- Journal Article
- A2
- open access
Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS) : a European cohort study

Linda A. J. Hendricks, Katja C. J. Verbeek, Janneke H. M. Schuurs-Hoeijmakers, Robin de Putter (UGent) , Hilde Brems, Sien H. Van Daele, Violetta C. Anastasiadou, Lenka Foretová, Patrick R. Benusiglio, Anna Gerasimenko, et al.

(2025) BJC REPORTS. 3(1).
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- Journal Article
- A1
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The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)

Linda A.J. Hendricks, Katja C.J. Verbeek, Janneke H.M. Schuurs-Hoeijmakers, Mirjam M. de Jong, Thera P. Links, Hilde Brems, Mio Aerden, Joan Brunet, Roser Lleuger-Pujol, Robert Hüneburg, et al.

(2025) GENETICS IN MEDICINE. 27(10).
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- Conference Paper
- C3
Cancer prognosis in PTEN Hamartoma Tumor Syndrome : a European cohort study

Linda Hendricks, Katja Verbeek, Hilde Brems, Robin de Putter (UGent) , Lenka Foretova, Chrystelle Colas, Patrick Benusiglio, Claude Houdayer, Arne Jahn, Verena Steinke-Lange, et al.

(2024) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 32(Supplement 1). p.563-564
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- Journal Article
- A1
- open access
Genetic counselling legislation and practice in cancer in EU Member States

J. Matt McCrary, Els Van Valckenborgh, Helene A. Poirel, Robin de Putter (UGent) , Jeroen van Rooij, Denis Horgan, Marie-Luise Dierks, Olga Antonova, Joan Brunet, Adela Chirita-Emandi, et al.

(2024) EUROPEAN JOURNAL OF PUBLIC HEALTH. 34(4). p.666-675
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- Journal Article
- A1
- open access
Clinical practice guidelines for the diagnosis and surveillance of BAP1 tumour predisposition syndrome

Fiona Lalloo, Anju Kulkarni, Cindy Chau, Maartje Nielsen, Michael Sheaff, Jeremy Steele, Remco van Doorn, Karin Wadt, Monica Hamill, Beth Torr, et al.

(2023) EUROPEAN JOURNAL OF HUMAN GENETICS. 31(11). p.1261-1269
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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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Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe

David Humberto Marmolejo, Mark Yu Zheng Wong, Svetlana Bajalica-Lagercrantz, Marc Tischkowitz, Judith Balmaña, Attila Balázs Patócs, Pierre Chappuis, Chrystelle Colas, Maurizio Genuardi, Maria Haanpää, et al.

(2021) EUROPEAN JOURNAL OF MEDICAL GENETICS. 64(12).
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- Journal Article
- A1
- open access
Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

Marc Tischkowitz, Chrystelle Colas, Sjaak Pouwels, Nicoline Hoogerbrugge, on behalf of European Reference Network GENTURI, on behalf of PHTS Guideline Dev Grp, Kathleen Claes (UGent) , Bruce Poppe (UGent) and Robin de Putter (UGent)

(2020) EUROPEAN JOURNAL OF HUMAN GENETICS. 28(10). p.1387-1393
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- Journal Article
- A1
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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

Daniel R. Barnes, Matti A. Rookus, Lesley McGuffog, Goska Leslie, Thea M. Mooij, Joe Dennis, Nasim Mavaddat, Julian Adlard, Munaza Ahmed, Kristiina Aittomäki, et al.

(2020) GENETICS IN MEDICINE. 22(10). p.1653-1666
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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Laura Fachal, Hugues Aschard, Jonathan Beesley, Daniel R. Barnes, Jamie Allen, Siddhartha Kar, Karen A. Pooley, Joe Dennis, Kyriaki Michailidou, Constance Turman, et al.

(2020) NATURE GENETICS. 52(1).

Academic Bibliography

Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS) : a European cohort study

The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)

Cancer prognosis in PTEN Hamartoma Tumor Syndrome : a European cohort study

Genetic counselling legislation and practice in cancer in EU Member States

Clinical practice guidelines for the diagnosis and surveillance of BAP1 tumour predisposition syndrome

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

Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe

Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

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