Ghent University Academic Bibliography

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Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility gene

E Dicks, H Song, SJ Ramus, Elke Van Oudenhove (UGent) , JP Tyrer, MP Intermaggio, S Kar, P Harrington, DD Bowtell, AS Group, et al.

(2017) ONCOTARGET. 8(31). p.50930-50940
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Fine-scale mapping at 9p22.2 identifies candidate causal variants that modify ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

E Vigorito, KB Kuchenbaecker, J Beesley, J Adlard, BA Agnarsson, IL Andrulis, BK Arun, L Barjhoux, M Belotti, J Benitez, et al.

(2016) PLOS ONE. 11(7).
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Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

C Zeng, XY Guo, JR Long, KB Kuchenbaecker, A Droit, K Michailidou, M Ghoussaini, S Kar, A Freeman, JL Hopper, et al.

(2016) BREAST CANCER RESEARCH. 18.
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Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

FJ Couch, KB Kuchenbaecker, K Michailidou, GA Mendoza-Fandino, S Nord, J Lilyquist, C Olswold, E Hallberg, S Agata, H Ahsan, et al.

(2016) NATURE COMMUNICATIONS. 7.
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Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

K Lawrenson, S Kar, K McCue, K Kuchenbaeker, K Michailidou, J Tyrer, J Beesley, SJ Ramus, QY Li, MK Delgado, et al.

(2016) NATURE COMMUNICATIONS. 7.
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Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

P Peterlongo, J Chang-Claude, KB Moysich, A Rudolph, RK Schmutzler, J Simard, P Soucy, RA Eeles, DF Easton, U Hamann, et al.

(2015) CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION. 24(1). p.308-316
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Identification of six new susceptibility loci for invasive epithelial ovarian cancer

KB Kuchenbaecker, SJ Ramus, J Tyrer, A Lee, HC Shen, J Beesley, K Lawrenson, L McGuffog, S Healey, JM Lee, et al.

(2015) NATURE GENETICS. 47(2). p.164-171

Academic Bibliography

Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility gene

Fine-scale mapping at 9p22.2 identifies candidate causal variants that modify ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

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