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2021
Mark Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers : an international cohort study
Schrijver, Lieske H ; Antoniou, Antonis C ; Olsson, Håkan ^LU ; Mooij, Thea M ; Roos-Blom, Marie-José ; Azarang, Leyla ; Adlard, Julian ; Ahmed, Munaza ; Barrowdale, Daniel and Davidson, Rosemarie , et al. (2021) In American Journal of Obstetrics and Gynecology 225(1). p.1-51
- Contribution to journal › Article
2020
Mark Alcohol consumption, cigarette smoking, and risk of breast cancer for BRCA1 and BRCA2 mutation carriers : Results from the BRCA1 and BRCA2 cohort consortium
Li, Hongyan ; Terry, Mary Beth ; Antoniou, Antonis C. ; Phillips, Kelly Anne ; Kast, Karin ; Mooij, Thea M. ; Engel, Christoph ; Nogues, Catherine ; Stoppa-Lyonnet, Dominique and Lasset, Christine , et al. (2020) In Cancer Epidemiology Biomarkers and Prevention 29(2). p.368-378
- Contribution to journal › Article
2018
Mark Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility
Catucci, Irene ; Osorio, Ana ; Arver, Brita ; Neidhardt, Guido ; Bogliolo, Massimo ; Zanardi, Federica ; Riboni, Mirko ; Minardi, Simone ; Pujol, Roser and Azzollini, Jacopo , et al. (2018) In Genetics in Medicine 20. p.452-457
- Contribution to journal › Article
2016
Mark Efficacy and safety of olaparib monotherapy in germline BRCA1/2 mutation carriers with advanced ovarian cancer and three or more lines of prior therapy.
Domchek, Susan M ; Aghajanian, Carol ; Shapira-Frommer, Ronnie ; Schmutzler, Rita K ; Audeh, M William ; Friedlander, Michael ; Balmaña, Judith ; Mitchell, Gillian ; Fried, Georgeta and Stemmer, Salomon M , et al. (2016) In Gynecologic Oncology 140(2). p.199-203
- Contribution to journal › Article
Mark Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
Couch, Fergus J ; Kuchenbaecker, Karoline B. ; Michailidou, Kyriaki ; Mendoza-Fandino, Gustavo A. ; Nord, Silje ; Lilyquist, Janna ; Olswold, Curtis ; Hallberg, Emily ; Agata, Simona and Ahsan, Habibul , et al. (2016) In Nature Communications 7.
- Contribution to journal › Article
Mark Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
Dunning, Alison M ; Michailidou, Kyriaki ; Kuchenbaecker, Karoline B ; Thompson, Deborah ; French, Juliet D ; Beesley, Jonathan ; Healey, Catherine S ; Kar, Siddhartha ; Pooley, Karen A and Lopez-Knowles, Elena , et al. (2016) In Nature Genetics
- Contribution to journal › Article
Mark No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
Hollestelle, Antoinette ; Van Der Baan, Frederieke H. ; Berchuck, Andrew ; Johnatty, Sharon E. ; Aben, Katja K. ; Agnarsson, Bjarni A. ; Aittomäki, Kristiina ; Alducci, Elisa ; Andrulis, Irene L. and Anton-Culver, Hoda , et al. (2016) In Gynecologic Oncology 141(2). p.386-401
- Contribution to journal › Article
Mark Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Lawrenson, Kate ; Kar, Siddhartha ; McCue, Karen ; Kuchenbaeker, Karoline ; Michailidou, Kyriaki ; Tyrer, Jonathan ; Beesley, Jonathan ; Ramus, Susan J. ; Li, Qiyuan and Delgado, Melissa K. , et al. (2016) In Nature Communications 7.
- Contribution to journal › Article
2015
Mark Olaparib Monotherapy in Patients With Advanced Cancer and a Germline BRCA1/2 Mutation.
Kaufman, Bella ; Shapira-Frommer, Ronnie ; Schmutzler, Rita K ; Audeh, M William ; Friedlander, Michael ; Balmaña, Judith ; Mitchell, Gillian ; Fried, Georgeta ; Stemmer, Salomon M and Hubert, Ayala , et al. (2015) In Journal of Clinical Oncology 33(3). p.134-244
- Contribution to journal › Article
Mark FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
Peterlongo, Paolo ; Catucci, Irene ; Colombo, Mara ; Caleca, Laura ; Mucaki, Eliseos ; Bogliolo, Massimo ; Marin, Maria ; Damiola, Francesca ; Bernard, Loris and Pensotti, Valeria , et al. (2015) In Human Molecular Genetics 24(18). p.5345-5355
- Contribution to journal › Article

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