Correction to: Breast Cancer Res
https://doi.org/10.1186/s13058-020-1247-4
After publication of the original article [1], we were notified that columns in Table 2 were erroneously displayed.
The correction version of Table 2 is shown below.
Reference
Mavaddat, et al. Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers. Breast Cancer Res. 2020;22:8. https://doi.org/10.1186/s13058-020-1247-4.
Author information
Nadine Andrieu and Douglas F. Easton contributed equally to this work.
Authors and Affiliations
Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, Strangeways Research Laboratory, Worts Causeway, University of Cambridge, Cambridge, CBI 8RN, UK
Nasim Mavaddat, Antonis C. Antoniou, Daniel Barrowdale, Debra Frost & Douglas F. Easton
Department of Epidemiology, Netherlands Cancer Institute, P.O. Box 90203, 1006 BE, Amsterdam, The Netherlands
Thea M. Mooij, Marie-José Roos-Blom, Flora E. Van Leeuwen & Matti A. Rookus
Department of Medical Oncology, Family Center Clinic, Erasmus MC Cancer Institute, Rotterdam, The Netherlands
Maartje J. Hooning & Bernadette A. Heemskerk-Gerritsen
DASC, Oncogénétique Clinique, Institut Paoli-Calmettes, Marseille, France
Catherine Noguès
Institut Curie, Service de Génétique, Paris, France
Marion Gauthier-Villars
Département de Médecine Oncologique, Gustave Roussy Hôpital Universitaire, Villejuif, France
Olivier Caron
Centre Hospitalier, Service Régional d’Oncologie Génétique Poitou-Charentes, Niort, France
Paul Gesta
Unité d’Oncogénétique, CHU Arnaud de Villeneuve, Montpellier, France
Pascal Pujol
Centre Catherine de Sienne, Service d’Oncologie Médicale, Nantes, France
Alain Lortholary
Genomic Medicine, Manchester Academic Health Sciences Centre, Division of Evolution and Genomic Sciences, Manchester University, Central Manchester, University Hospitals NHS Foundation Trust, Manchester, UK
D. Gareth Evans
Clinical Genetics, Guy’s and St Thomas’ NHS Foundation Trust, London, UK
Louise Izatt
Yorkshire Regional Genetics Service, Chapel Allerton Hospital and University of Leeds, Leeds, UK
Julian Adlard
Oncogenetics Team, The Institute of Cancer Research and Royal Marsden NHS Foundation Trust, London, UK
Ros Eeles
Department of Clinical Genetics, Royal Devon & Exeter Hospital, Exeter, UK
Carole Brewer
Academic Department of Medical Genetics, National Institute for Health Research Cambridge Biomedical Research Centre, University of Cambridge, Cambridge, UK
Marc Tischkowitz
Institute of Genetic Medicine, Centre for Life, Newcastle Upon Tyne Hospitals NHS Trust, Newcastle upon Tyne, UK
Alex Henderson
Sheffield Clinical Genetics Service, Sheffield Children’s Hospital, Sheffield, UK
Jackie Cook
University of Southampton Faculty of Medicine, Southampton University Hospitals NHS Trust, Southampton, UK
Diana Eccles
Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands
Klaartje van Engelen
Department of Gynaecological Oncology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
Marian J. E. Mourits
Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands
Margreet G. E. M. Ausems
Department of Surgical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands
Linetta B. Koppert
Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, 3010, Australia
John L. Hopper, Kelly-Anne Phillips & Roger L. Milne
Department of Medicine and Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, USA
Esther M. John
Departments of Pediatrics and Medicine, Columbia University Medical Center, New York, NY, USA
Wendy K. Chung
Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, NY, USA
Wendy K. Chung & Mary Beth Terry
Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada
Irene L. Andrulis
Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada
Irene L. Andrulis
Department of Clinical Genetics, Fox Chase Cancer Center, Philadelphia, PA, USA
Mary B. Daly
Department of Medicine, Huntsman Cancer Institute, University of Utah Health Sciences Center, Salt Lake City, UT, USA
Saundra S. Buys
The Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Australia
Kelly-Anne Phillips
Human Genetics Group and Genotyping Unit, CEGEN, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain
Javier Benitez
Molecular Oncology Laboratory, Hospital Clinico San Carlos, IdISSC, CIBERONC (ISCIII), Madrid, Spain
Trinidad Caldes
Department of Genetics and Pathology, Pomeranian Medical University, Unii Lubelskiej 1, Szczecin, Poland
Anna Jakubowska
Independent Laboratory of Molecular Biology and Genetic Diagnostics, Pomeranian Medical University, Unii Lubelskiej 1, Szczecin, Poland
Anna Jakubowska
Genomics Center, Centre Hospitalier Universitaire de Québec, Université Laval Research Center, 2705 Laurier Boulevard, Quebec City, Quebec, Canada
Jacques Simard
Department of OB/GYN and Comprehensive Cancer Center, Medical University of Vienna, Waehringer Guertel 18-20, A 1090, Vienna, Austria
Christian F. Singer & Yen Tan
Department of Molecular Genetics, National Institute of Oncology, Budapest, Hungary
Edith Olah
Department of Cancer Epidemiology and Genetics, Masaryk Memorial Cancer Institute, Zluty kopec 7, 65653, Brno, Czech Republic
Marie Navratilova & Lenka Foretova
Department of Clinical Genetics, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
Anne-Marie Gerdes
The Department of Oncology and Pathology, Karolinska Institute, 171 76, Stockholm, Sweden
Brita Arver
Department of Oncology, Lund University Hospital, Lund, Sweden
Brita Arver & Håkan Olsson
Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), Medical Faculty, University Hospital Cologne, Cologne, Germany
Rita K. Schmutzler
Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany
Rita K. Schmutzler
Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany
Christoph Engel
Department of Gynecology and Obstetrics, Medical Faculty and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany
Karin Kast
National Center for Tumor Diseases (NCT), Partner Site Dresden, Dresden, Germany
Karin Kast
German Cancer Consortium (DKTK), Dresden and German Cancer Research Center (DKFZ), Heidelberg, Germany
Karin Kast
Department of Medical Oncology Peter MacCallum Cancer Centre, Locked Bag 1, A’Beckett St, East Melbourne, Victoria, 8006, Australia
Kelly-Anne Phillips
Department of Epidemiology, Columbia University, New York, NY, USA
Mary Beth Terry
Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, Victoria, Australia
Roger L. Milne
Precision Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, Victoria, Australia
Roger L. Milne
Department of Dermatology, University of Utah School of Medicine, 30 North 1900 East, SOM 4B454, Salt Lake City, UT, 841232, USA
David E. Goldgar
INSERM, U900, Paris, France
Nadine Andrieu
Institut Curie, Paris, France
Nadine Andrieu
Mines Paris Tech, Fontainebleau, France
Nadine Andrieu
PSL Research University, Paris, France
Nadine Andrieu
Centre for Cancer Genetic Epidemiology, Department of Oncology, Strangeways Research Laboratory, Worts Causeway, University of Cambridge, Cambridge, CBI 8RN, UK
Douglas F. Easton
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Correspondence to Nasim Mavaddat.
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Mavaddat, N., Antoniou, A.C., Mooij, T.M. et al. Correction to: Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers. Breast Cancer Res 22, 25 (2020). https://doi.org/10.1186/s13058-020-01259-w
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DOI: https://doi.org/10.1186/s13058-020-01259-w
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