Low risk of invasive lobular carcinoma of the breast in carriers of <i>BRCA1</i> (hereditary breast and ovarian cancer) and <i>TP53</i> (Li‐Fraumeni syndrome) germline mutations
Yoan Ditchi(Université Paris-Saclay), Patrick R. Benusiglio(Université Paris-Saclay), Donia Lejri(Université Paris-Saclay), Caroline Baynes(University of Cambridge), Pernelle Lavaud(Université Paris-Saclay), Olivier Caron(Université Paris-Saclay), Julia Salleron(Institut de Cancérologie de Lorraine), Marie‐Christine Mathieu(Université Paris-Saclay), Chloé Broudin(Assistance Publique – Hôpitaux de Paris), Yolla El Dakdouki(Université Paris-Saclay), Marie Müller(Assistance Publique – Hôpitaux de Paris)
Cited by 16
Related Papers
Association analysis identifies 65 new breast cancer risk loci
|Nature|2017|1.6k
A common coding variant in CASP8 is associated with breast cancer risk
|Nature Genetics|2007|612
Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline <i>CDH1</i> mutation carriers
|Journal of Medical Genetics|2015|567
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
|Nature Genetics|2013|544
Hereditary diffuse gastric cancer: updated clinical practice guidelines
|The Lancet Oncology|2020|493