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Breast Cancer Research and Treatment|December 2, 2009
Two founder BRCA2 mutations predispose to breast cancer in young womenMar Infante, Mercedes Durán, Adriana Lasa, et al.
Breast Cancer Research and Treatment|December 7, 2007
Twenty-three novel BRCA1 and BRCA2 sequence alterations in breast and/or ovarian cancer families of Eastern SpainEva Esteban Cardeñosa, Pascual Bolufer Gilabert, Sarai Palanca Suela, et al.
Breast Cancer Research and Treatment|December 7, 2007
Identification of a novel BRCA1 large genomic rearrangement in a Spanish breast/ovarian cancer familySarai Palanca Suela, Eva Esteban Cardeñosa, Eva Barragán González, et al.
Medicina Clinica|February 19, 2008
[BRCA1 and BRCA2 mutations in families studied in the program of genetic counselling in cancer of the Valencian community (Spain)]Eva Esteban Cardeñosa, Pascual Bolufer Gilabert, Sarai Palanca Suela, et al.
Breast Cancer Research and Treatment|February 14, 2009
CASP8 D302H polymorphism delays the age of onset of breast cancer in BRCA1 and BRCA2 carriersSarai Palanca Suela, Eva Esteban Cardeñosa, Eva Barragán González, et al.
Familial Cancer|August 29, 2012
Low penetrance alleles as risk modifiers in familial and sporadic breast cancerEva Esteban Cardeñosa, Inmaculada de Juan Jiménez, Sarai Palanca Suela, et al.
Familial Cancer|August 17, 2010
Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidenceEva Esteban Cardeñosa, Pascual Bolufer Gilabert, Inmaculada de Juan Jiménez, et al.
Familial Cancer|September 16, 2011
Low prevalence of BRCA1 and BRCA2 mutations in the sporadic breast cancer of Spanish populationInmaculada de Juan Jiménez, Eva Esteban Cardeñosa, Sarai Palanca Suela, et al.
Carcinogenesis|August 10, 2013
The highly prevalent BRCA2 mutation c.2808_2811del (3036delACAA) is located in a mutational hotspot and has multiple originsMar Infante, Mercedes Durán, Alberto Acedo, et al.
Familial Cancer|March 13, 2013
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 prevalenceInmaculada de Juan Jiménez, Zaida García Casado, Sarai Palanca Suela, et al.
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