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Page 1
Low penetrance alleles as risk modifiers in familial and sporadic breast cancer.
Esteban Cardeñosa E, de Juan Jiménez I, Palanca Suela S, Chirivella González I, Segura Huerta A, Santaballa Beltran A, Casals El Busto M, Barragán González E, Fuster Lluch O, Bermúdez Edo J, Bolufer Gilabert P. Esteban Cardeñosa E, et al. Among authors: chirivella gonzalez i. Fam Cancer. 2012 Dec;11(4):629-36. doi: 10.1007/s10689-012-9563-1. Fam Cancer. 2012. PMID: 22926736
Identification of a novel BRCA1 large genomic rearrangement in a Spanish breast/ovarian cancer family.
Palanca Suela S, Esteban Cardeñosa E, Barragán González E, Oltra Soler S, de Juan Jiménez I, Chirivella González I, Segura Huerta A, Guillén Ponce C, Martínez de Dueñas E, Bolufer Gilabert P; Group for Assessment of Hereditary Cancer of Valencia Community. Palanca Suela S, et al. Among authors: chirivella gonzalez i. Breast Cancer Res Treat. 2008 Nov;112(1):63-7. doi: 10.1007/s10549-007-9839-6. Epub 2007 Dec 1. Breast Cancer Res Treat. 2008. PMID: 18060491
Twenty-three novel BRCA1 and BRCA2 sequence alterations in breast and/or ovarian cancer families of Eastern Spain.
Esteban Cardeñosa E, Bolufer Gilabert P, Palanca Suela S, Oltra Soler S, Barragán González E, Velasco Sampedro E, Chirivella González I, Segura Huerta A, Guillén Ponce C, Martínez de Dueñas E; Group for Assessment of Hereditary Cancer of Valencia Community. Esteban Cardeñosa E, et al. Among authors: chirivella gonzalez i. Breast Cancer Res Treat. 2008 Nov;112(1):69-73. doi: 10.1007/s10549-007-9818-y. Epub 2007 Dec 1. Breast Cancer Res Treat. 2008. PMID: 18060494
[BRCA1 and BRCA2 mutations in families studied in the program of genetic counselling in cancer of the Valencian community (Spain)].
Esteban Cardeñosa E, Bolufer Gilabert P, Palanca Suela S, Barragán González E, Oltra Soler S, Chirivella González I, Segura Huerta A, Guillén Ponce C, Martínez de Dueñas E, Cuevas Cuerda D, Salas Trejo D; Grupo de Asesoramiento en Cáncer Hereditario de la Comunidad Valenciana. Esteban Cardeñosa E, et al. Among authors: chirivella gonzalez i. Med Clin (Barc). 2008 Feb 9;130(4):121-6. doi: 10.1157/13115767. Med Clin (Barc). 2008. PMID: 18279628 Spanish.
CASP8 D302H polymorphism delays the age of onset of breast cancer in BRCA1 and BRCA2 carriers.
Palanca Suela S, Esteban Cardeñosa E, Barragán González E, de Juan Jiménez I, Chirivella González I, Segura Huerta A, Guillén Ponce C, Martínez de Dueñas E, Montalar Salcedo J, Castel Sánchez V, Bolufer Gilabert P; Group for Assessment of Hereditary Cancer of Valencia Community. Palanca Suela S, et al. Among authors: chirivella gonzalez i. Breast Cancer Res Treat. 2010 Jan;119(1):87-93. doi: 10.1007/s10549-009-0316-2. Epub 2009 Feb 12. Breast Cancer Res Treat. 2010. PMID: 19214744
Broad BRCA1 and BRCA2 mutational spectrum and high incidence of recurrent and novel mutations in the eastern Spain population.
Esteban Cardeñosa E, Bolufer Gilabert P, de Juan Jimenez I, Palanca Suela S, Barragán González E, Chirivella González I, Segura Huerta A, Guillén Ponce C, Martínez de Dueñas E. Esteban Cardeñosa E, et al. Among authors: chirivella gonzalez i. Breast Cancer Res Treat. 2010 May;121(1):257-60. doi: 10.1007/s10549-009-0680-y. Epub 2009 Dec 24. Breast Cancer Res Treat. 2010. PMID: 20033483 No abstract available.
Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence.
Esteban Cardeñosa E, Bolufer Gilabert P, de Juan Jiménez I, Palanca Suela S, Barragán González E, González Anguix V, Lerma Alejos E, Chirivella González I, Segura Huerta A, Guillén Ponce C, Martínez de Dueñas E, Cuevas Cuerda D, Salas Trejo D; Group for Assessment for Hereditary Cancer of Valencian Community. Esteban Cardeñosa E, et al. Among authors: gonzalez anguix v, chirivella gonzalez i. Fam Cancer. 2010 Sep;9(3):291-5. doi: 10.1007/s10689-010-9327-8. Fam Cancer. 2010. PMID: 20711702
Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence.
de Juan Jiménez I, García Casado Z, Palanca Suela S, Esteban Cardeñosa E, López Guerrero JA, Segura Huerta Á, Chirivella González I, Sánchez Heras AB, Juan Fita MJ, Tena García I, Guillen Ponce C, Martínez de Dueñas E, Romero Noguera I, Salas Trejo D, Goicoechea Sáez M, Bolufer Gilabert P. de Juan Jiménez I, et al. Among authors: chirivella gonzalez i. Fam Cancer. 2013 Dec;12(4):767-77. doi: 10.1007/s10689-013-9622-2. Fam Cancer. 2013. PMID: 23479189
MicroRNA signatures in hereditary breast cancer.
Murria Estal R, Palanca Suela S, de Juan Jiménez I, Egoavil Rojas C, García-Casado Z, Juan Fita MJ, Sánchez Heras AB, Segura Huerta A, Chirivella González I, Sánchez-Izquierdo D, Llop García M, Barragán González E, Bolufer Gilabert P. Murria Estal R, et al. Among authors: chirivella gonzalez i. Breast Cancer Res Treat. 2013 Nov;142(1):19-30. doi: 10.1007/s10549-013-2723-7. Epub 2013 Oct 16. Breast Cancer Res Treat. 2013. PMID: 24129975
Relationship of immunohistochemistry, copy number aberrations and epigenetic disorders with BRCAness pattern in hereditary and sporadic breast cancer.
Murria Estal R, Palanca Suela S, de Juan Jiménez I, Alenda Gonzalez C, Egoavil Rojas C, García-Casado Z, López Guerrero JA, Juan Fita MJ, Sánchez Heras AB, Segura Huerta Á, Santaballa Bertrán A, Chirivella González I, Llop García M, Pérez Simó G, Barragán González E, Bolufer Gilabert P. Murria Estal R, et al. Among authors: chirivella gonzalez i. Fam Cancer. 2016 Apr;15(2):193-200. doi: 10.1007/s10689-015-9864-2. Fam Cancer. 2016. PMID: 26723934
22 results