Ghent University Academic Bibliography

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- Journal Article
- A2
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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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- 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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Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer

Daniel R. Barnes, Jonathan P. Tyrer, Joe Dennis, Goska Leslie, Manjeet K. Bolla, Michael Lush, Amber M. Aeilts, Kristiina Aittomaeki, Nadine Andrieu, Irene L. Andrulis, et al.

(2025) NPJ GENOMIC MEDICINE. 10(1).
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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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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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Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2

Denise G. O’Mahony, Susan J. Ramus, Melissa C. Southey, Nicola S. Meagher, Andreas Hadjisavvas, Esther M. John, Ute Hamann, Evgeny N. Imyanitov, Irene L. Andrulis, Priyanka Sharma, et al.

(2023) BRITISH JOURNAL OF CANCER. 128(12). p.2283-2294
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Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

Christopher Hakkaart, John F. Pearson, Louise Marquart, Joe Dennis, George A. R. Wiggins, Daniel R. Barnes, Bridget A. Robinson, Peter D. Mace, Kristiina Aittomäki, Irene L. Andrulis, et al.

(2022) COMMUNICATIONS BIOLOGY. 5(1).
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Breast and prostate cancer risks for male BRCA1 and BRCA2 pathogenic variant carriers using polygenic risk scores

Daniel R Barnes, Valentina Silvestri, Goska Leslie, Lesley McGuffog, Joe Dennis, Xin Yang, Julian Adlard, Bjarni A Agnarsson, Munaza Ahmed, Kristiina Aittomäki, et al.

(2022) JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE. 114(1). p.109-122
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Polygenic risk modeling for prediction of epithelial ovarian cancer risk

Eileen O. Dareng, Jonathan P. Tyrer, Daniel R. Barnes, Michelle R. Jones, Xin Yang, Katja K. H. Aben, Muriel A. Adank, Simona Agata, Irene L. Andrulis, Hoda Anton-Culver, et al.

(2022) EUROPEAN JOURNAL OF HUMAN GENETICS. 30(3). p.349-362

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)

Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer

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

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

Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2

Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

Breast and prostate cancer risks for male BRCA1 and BRCA2 pathogenic variant carriers using polygenic risk scores

Polygenic risk modeling for prediction of epithelial ovarian cancer risk

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