Ghent University Academic Bibliography

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Your filters: cql: author="Foulkes, William D*" or (type exact bookEditor and editor="Foulkes, William D*")

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Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient cases

Dörthe Holdhof, Pascal D. Johann, Michael Spohn, Michael Bockmayr, Sepehr Safaei, Piyush Joshi, Julien Masliah-Planchon, Ben Ho, Mamy Andrianteranagna, Franck Bourdeaut, et al.

(2021) ACTA NEUROPATHOLOGICA. 141(2). p.291-301
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Embryonal rhabdomyosarcoma of the uterine corpus : a clinicopathological and molecular analysis of 21 cases highlighting a frequent association with DICER1 mutations

Jennifer A. Bennett, Zehra Ordulu, Robert H. Young, Andre Pinto, Koen Van de Vijver (UGent) , Eike Burandt, Pankhuri Wanjari, Rajeev Shah, Leanne de Kock, William D. Foulkes, et al.

(2021) MODERN PATHOLOGY. 34(9). p.1750-1762
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Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

Xin Yang, Goska Leslie, Alicja Doroszuk, Sandra Schneider, Jamie Allen, Brennan Decker, Alison M. Dunning, James Redman, James Scarth, Inga Plaskocinska, et al.

(2020) Journal of Clinical Oncology. 38(7). p.674-687
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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).
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The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Gisella Figlioli, Massimo Bogliolo, Irene Catucci, Laura Caleca, Sandra Viz Lasheras, Roser Pujol, Johanna I Kiiski, Taru A Muranen, Daniel R Barnes, Joe Dennis, et al.

(2019) NPJ BREAST CANCER. 5.
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Thorough in silico and in vitro cDNA analysis of 21 putative BRCA1 and BRCA2 splice variants and a complex tandem duplication in BRCA2 allowing the identification of activated cryptic splice donor sites in BRCA2 exon 11

Annelot Baert (UGent) , Eva Machackova, Ilse Coene (UGent) , Carol Cremin, Kristin Turner, Cheryl Portigal-Todd, Marie Jill Asrat, Jennifer Nuk, Allison Mindlin, Sean Young, et al.

(2018) HUMAN MUTATION. 39(4). p.515-526
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Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Catherine M Phelan, Karoline B Kuchenbaecker, Jonathan P Tyrer, Siddhartha P Kar, Kate Lawrenson, Stacey J Winham, Joe Dennis, Ailith Pirie, Marjorie J Riggan, Ganna Chornokur, et al.

(2017) NATURE GENETICS. 49(5). p.680-691
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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Roger L Milne, Karoline B Kuchenbaecker, Kyriaki Michailidou, Jonathan Beesley, Siddhartha Kar, Sara Lindström, Shirley Hui, Audrey Lemaçon, Penny Soucy, Joe Dennis, et al.

(2017) NATURE GENETICS. 49(12). p.1767-1778
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Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression : identification of a modifier of breast cancer risk at locus 11q22.3

Yosr Hamdi, Penny Soucy, Karoline B. Kuchenbaeker, Tomi Pastinen, Arnaud Droit, Audrey Lemacon, Julian Adlard, Kristiina Aittomaki, Irene L. Andrulis, Adalgeir Arason, et al.

(2017) BREAST CANCER RESEARCH AND TREATMENT. 161(1). p.117-134
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PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

Melissa Southey, David E Goldgar, Robert Winqvist, Katri Pylkäs, Fergus Couch, Marc Tischkowitz, William D Foulkes, Joe Dennis, Kyriaki Michailidou, Elizabeth J van Rensburg, et al.

(2016) JOURNAL OF MEDICAL GENETICS. 53(12). p.800-811
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Functional redundancy of Exon 12 of BRCA2 revealed by a comprehensive analysis of the c.6853A > G (p.I2285V) variant

Li LL Li, Kajal Biswas, Laura Anne Habib, Sergey G Kuznetsov, Nancy Hamel, Tomas Kirchhoff, Nora Wong, Susan Armel, George Chong, SA Narod, et al.

(2009) HUMAN MUTATION. 30(11). p.1543-1550

Academic Bibliography

Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient cases

Embryonal rhabdomyosarcoma of the uterine corpus : a clinicopathological and molecular analysis of 21 cases highlighting a frequent association with DICER1 mutations

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

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

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Thorough in silico and in vitro cDNA analysis of 21 putative BRCA1 and BRCA2 splice variants and a complex tandem duplication in BRCA2 allowing the identification of activated cryptic splice donor sites in BRCA2 exon 11

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression : identification of a modifier of breast cancer risk at locus 11q22.3

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

Functional redundancy of Exon 12 of BRCA2 revealed by a comprehensive analysis of the c.6853A > G (p.I2285V) variant

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