Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors von Mensenkamp, Arjen R, Vogelaar, Ingrid P, van Zelst–Stams, Wendy A.G, Goossens, Monique, Ouchene, Hicham, Hendriks–Cornelissen, Sandra J.B, Kwint, Michael P, Hoogerbrugge, Nicoline, Nagtegaal, Iris D, Ligtenberg, Marjolijn J.L

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Universal Tumor DNA BRCA1/2 Testing of Ovarian Cancer: Prescreening PARPi Treatment and Genetic Predisposition von Vos, Janet R, Fakkert, Ingrid E, de Hullu, Joanne A, van Altena, Anne M, Sie, Aisha S, Ouchene, Hicham, Willems, Riki W, Nagtegaal, Iris D, Jongmans, Marjolijn C J, Mensenkamp, Arjen R, Woldringh, Gwendolyn H, Bulten, Johan, Leter, Edward M, Kets, C Marleen, Simons, Michiel, Ligtenberg, Marjolijn J L, Hoogerbrugge, Nicoline

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Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas von Weren, Robbert D.A., Mensenkamp, Arjen R., Simons, Michiel, Eijkelenboom, Astrid, Sie, Aisha S., Ouchene, Hicham, Asseldonk, Monique, Gomez‐Garcia, Encarna B., Blok, Marinus J., Hullu, Joanne A., Nelen, Marcel R., Hoischen, Alexander, Bulten, Johan, Tops, Bastiaan B.J., Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J.L.

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BRCA 1/2 mutations by next-generation sequencing testing in 200 Romanian high-risk patients with breast cancer von Eniu, Alexandru E., Antone, Nicoleta Zenovia, Stoian, Andrei, Dronca, Eleonora, Matei, Ramona DOINA, Ligtenberg, Marjolijn, Ouchene, Hicham, Eniu, Rares, Pop, Laura

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Are young breast cancer patients' clinico-pathological characteristic different when comparing populations from developing countries? Analysis of two cohorts of patients from Roman... von Campos Gomez, Saul, Antone, Nicoleta Zenovia, Pop, Laura, Campos Gomez, Karen Angelica, Stoian, Andrei, Pacheco-Cuéllar, Guillermo, Dronca, Eleonora, Valdes Andrade, Juan, Matei, Ramona DOINA, Ligtenberg, Marjolijn, Ouchene, Hicham, Onisim, Andrea, Rotaru, Olivia, Eniu, Rares, Eniu, Alexandru E.

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