Microsatellite instability correlates with negative expression of estrogen and progesterone receptors in sporadic breast cancerCALDES, Trinidad; PEREZ-SEGURA, Pedro; TOSAR, Alicia et al.Teratogenesis, carcinogenesis, and mutagenesis. 2000, Vol 20, Num 5, pp 283-291, issn 0270-3211Article

Clustering of cancer-related mutations in a subset of BRCAI alleles: A study in the Spanish populationDE LA HOYA, Miguel; SULLEIRO, Sara; OSORIO, Ana et al.International journal of cancer. 2002, Vol 100, Num 5, pp 618-619, issn 0020-7136Article

Alternative Splicing and Molecular Characterization of Splice Site Variants: BRCA1 c.591C>T as a Case StudyDOSIL, Vanesa; TOSAR, Alicia; CANADAS, Carmen et al.Clinical chemistry (Baltimore, Md.). 2010, Vol 56, Num 1, pp 53-61, issn 0009-9147, 9 p.Article

No mutations in the XRCC2 gene in BRCA1/2-negative high-risk breast cancer familiesRODRIGUEZ-LOPEZ, Raquel; OSORIO, Ana; SANCHEZ-PULIDO, Luis et al.International journal of cancer. 2003, Vol 103, Num 1, pp 136-137, issn 0020-7136, 2 p.Article

Mutation analysis of the SHFM1 gene in breast/ovarian cancer familiesBONACHE, Sandra; DE LA HOYA, Miguel; GUTIERREZ-ENRIQUEZ, Sara et al.Journal of cancer research and clinical oncology. 2013, Vol 139, Num 3, pp 529-532, issn 0171-5216, 4 p.Article

A HRM-based screening method detects RAD51C germ-line deleterious mutations in Spanish breast and ovarian cancer familiesROMERO, Atocha; PEREZ-SEGURA, Pedro; TOSAR, Alicia et al.Breast cancer research and treatment. 2011, Vol 129, Num 3, pp 939-946, issn 0167-6806, 8 p.Article

Shorter telomere length is associated with increased ovarian cancer risk in both familial and sporadic casesMARTINEZ-DELGADO, Beatriz; YANOWSKY, Kira; ROBLEDO, Mercedes et al.Journal of medical genetics. 2012, Vol 49, Num 5, pp 341-344, issn 0022-2593, 4 p.Article

Increased frequency of disease-causing MYH mutations in colon cancer familiesPETERLONGO, Paolo; MITRA, Nandita; OFFIT, Kenneth et al.Carcinogenesis (New York. Print). 2006, Vol 27, Num 11, pp 2243-2249, issn 0143-3334, 7 p.Article

The breast cancer low-penetrance allele 1100DELC in the chek2 gene is not present in spanish familial breast cancer populationOSORIO, Ana; RODRIGUEZ-LOPEZ, Raquel; DIEZ, Orland et al.International journal of cancer. 2004, Vol 108, Num 1, pp 54-56, issn 0020-7136, 3 p.Article

International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutationPEIXOTO, Ana; SANTOS, Catarina; THOMASSEN, Mads et al.Breast cancer research and treatment. 2011, Vol 127, Num 3, pp 671-679, issn 0167-6806, 9 p.Article

Parity and the risk of breast and ovarian cancer in BRCA1 and BRCA2 mutation carriersMILNE, Roger L; OSORIO, Ana; BLANCO, Ignacio et al.Breast cancer research and treatment. 2010, Vol 119, Num 1, pp 221-232, issn 0167-6806, 12 p.Article

Analysis of FANCB and FANCN/PALB2 Fanconi Anemia genes in BRCA1/2-negative Spanish breast cancer familiesGARCIA, Maria J; FERNANDEZ, Victoria; ALONSO, Carmen et al.Breast cancer research and treatment. 2009, Vol 113, Num 3, pp 545-551, issn 0167-6806, 7 p.Article

The variant E233G of the RAD51D gene could be a low-penetrance allele in high-risk breast cancer families without BRCA1/2 mutationsRODRIGUEZ-LOPEZ, Raquel; OSORIO, Ana; VEGA, Ana et al.International journal of cancer. 2004, Vol 110, Num 6, pp 845-849, issn 0020-7136, 5 p.Article

Association between BRCA1 mutations and ratio of female to male births in offspring of families with breast cancer, ovarian cancer, or bothDE LA HOYA, Miguel; FERNANDEZ, Juan M; TOSAR, Alicia et al.JAMA, the journal of the American Medical Association. 2003, Vol 290, Num 7, pp 929-931, issn 0098-7484, 3 p.Article

About 1% of the breast and ovarian Spanish families testing negative for BRCA1 and BRCA2 are carriers of RAD51D pathogenic variantsGUTIERREZ-ENRIQUEZ, Sara; BONACHE, Sandra; MONTALBAN, Gemma et al.International journal of cancer (Print). 2014, Vol 134, Num 9, pp 2088-2097, issn 0020-7136, 10 p.Article

Characterization of four novel BRCA2 large genomic rearrangements in Spanish breast/ovarian cancer families: review of the literature, and reevaluation of the genetic mechanisms involved in their originDE GARIBAY, Gorka Ruiz; GUTIERREZ-ENRIQUEZ, Sara; DIAZ-RUBIO, Eduardo et al.Breast cancer research and treatment. 2012, Vol 133, Num 1, pp 273-283, issn 0167-6806, 11 p.Article

Assessment of Topoisomerase II α Status in Breast Cancer by Quantitative PCR, Gene Expression Microarrays, Immunohistochemistry, and Fluorescence in Situ HybridizationROMERO, Atocha; MARTIN, Miguel; PEROU, Charles M et al.The American journal of pathology. 2011, Vol 178, Num 4, pp 1453-1460, issn 0002-9440, 8 p.Article

Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancerPITTMAN, Alan M; WEBB, Emily; TWISS, Philip et al.Human molecular genetics (Print). 2008, Vol 17, Num 23, pp 3720-3727, issn 0964-6906, 8 p.Article

Detection of a large rearrangement in PALB2 in Spanish breast cancer families with male breast cancerBLANCO, Ana; DE LA HOYA, Miguel; TEJADA, Maria-Isabel et al.Breast cancer research and treatment. 2012, Vol 132, Num 1, pp 307-315, issn 0167-6806, 9 p.Article

Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer familiesOSORIO, Ana; ENDT, Daniela; FERNANDEZ, Fernando et al.Human molecular genetics (Print). 2012, Vol 21, Num 13, pp 2889-2898, issn 0964-6906, 10 p.Article

Molecularanalysis of colorectal cancer tumors from patients with mismatch repair : Proficient hereditary nonpolyposis colorectal cancer suggests novel carcinogenic pathwaysSANCHEZ-DE-ABAJO, Ana; DE LA HOYA, Miguel; VAN PUIJENBROEK, Marjo et al.Clinical cancer research. 2007, Vol 13, Num 19, pp 5729-5735, issn 1078-0432, 7 p.Article

Screening for large rearrangements of the BRCA2 gene in Spanish families with breast/ovarian cancerGUTIERREZ-ENRIQUEZ, Sara; DE LA HOYA, Miguel; TEJADA, Maria-Isabel et al.Breast cancer research and treatment. 2007, Vol 103, Num 1, pp 103-107, issn 0167-6806, 5 p.Article

Association between BRCA1 and BRCA2 mutations and cancer phenotype in Spanish breast/ovarian cancer families: Implications for genetic testingDE LA HOYA, Miguel; OSORIO, Ana; DEVILEE, Peter et al.International journal of cancer. 2002, Vol 97, Num 4, pp 466-471, issn 0020-7136Article

Changes in the expression of plasma proteins associated with thrombosis in BRCA1 mutation carriersCUSTODIO, Ana; LOPEZ-FARRE, Antonio J; PEREZ-SEGURA, Pedro et al.Journal of cancer research and clinical oncology. 2012, Vol 138, Num 5, pp 867-875, issn 0171-5216, 9 p.Article

Two founder BRCA2 mutations predispose to breast cancer in young womenINFANTE, Mar; DURAN, Mercedes; VELASCO, Eladio A et al.Breast cancer research and treatment. 2010, Vol 122, Num 2, pp 567-571, issn 0167-6806, 5 p.Article