Benítez J - Search Results

1

A common SNP in the UNG gene decreases ovarian cancer risk in BRCA2 mutation carriers.

Baquero JM, Benítez-Buelga C, Fernández V, Urioste M, García-Giménez JL, Perona R; CIMBA Consortium; Benítez J, Osorio A. Baquero JM, et al. Among authors: benitez j, benitez buelga c. Mol Oncol. 2019 May;13(5):1110-1120. doi: 10.1002/1878-0261.12470. Epub 2019 Mar 1. Mol Oncol. 2019. PMID: 30747491 Free PMC article.

2

Association between BRCA1 and BRCA2 mutations and cancer phenotype in Spanish breast/ovarian cancer families: implications for genetic testing.

de la Hoya M, Osorio A, Godino J, Sulleiro S, Tosar A, Perez-Segura P, Fernandez C, Rodríguez R, Díaz-Rubio E, Benítez J, Devilee P, Caldés T. de la Hoya M, et al. Among authors: benitez j. Int J Cancer. 2002 Feb 1;97(4):466-71. doi: 10.1002/ijc.1627. Int J Cancer. 2002. PMID: 11802208

3

Loss of heterozygosity analysis at the BRCA loci in tumor samples from patients with familial breast cancer.

Osorio A, de la Hoya M, Rodríguez-López R, Martínez-Ramírez A, Cazorla A, Granizo JJ, Esteller M, Rivas C, Caldés T, Benítez J. Osorio A, et al. Among authors: benitez j. Int J Cancer. 2002 May 10;99(2):305-9. doi: 10.1002/ijc.10337. Int J Cancer. 2002. PMID: 11979449

4

Clustering of cancer-related mutations in a subset of BRCA1 alleles: a study in the Spanish population.

de la Hoya M, Sulleiro S, Osorio A, Díez O, Baiget M, Benítez J, Díaz-Rubio E, Caldés T. de la Hoya M, et al. Among authors: benitez j. Int J Cancer. 2002 Aug 10;100(5):618-9. doi: 10.1002/ijc.10527. Int J Cancer. 2002. PMID: 12124814

5

A rapid and easy method for multiple endocrine neoplasia type 1 mutation detection using conformation-sensitive gel electrophoresis.

Arancha C, Ruíz-Llorente S, Cascón A, Osorio A, Martínez-Delgado B, Benítez J, Robledo M. Arancha C, et al. Among authors: benitez j. J Hum Genet. 2002;47(4):190-5. doi: 10.1007/s100380200022. J Hum Genet. 2002. PMID: 12166655

6

No mutations in the XRCC2 gene in BRCA1/2-negative high-risk breast cancer families.

Rodríguez-López R, Osorio A, Sánchez-Pulido L, De La Hoya M, Barroso A, Caldés T, Benítez J. Rodríguez-López R, et al. Among authors: benitez j. Int J Cancer. 2003 Jan 1;103(1):136-7. doi: 10.1002/ijc.10766. Int J Cancer. 2003. PMID: 12455067 No abstract available.

7

Molecular study of a new family with hereditary renal cell carcinoma and a translocation t(3;8)(p13;q24.1).

Meléndez B, Rodríguez-Perales S, Martínez-Delgado B, Otero I, Robledo M, Martínez-Ramírez A, Ruiz-Llorente S, Urioste M, Cigudosa JC, Benítez J. Meléndez B, et al. Among authors: benitez j. Hum Genet. 2003 Feb;112(2):178-85. doi: 10.1007/s00439-002-0848-6. Epub 2002 Nov 13. Hum Genet. 2003. PMID: 12522559

8

De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19.

Cigudosa JC, Odero MD, Calasanz MJ, Solé F, Salido M, Arranz E, Martínez-Ramirez A, Urioste M, Alvarez S, Cervera JV, MacGrogan D, Sanz MA, Nimer SD, Benitez J. Cigudosa JC, et al. Among authors: benitez j. Genes Chromosomes Cancer. 2003 Apr;36(4):406-12. doi: 10.1002/gcc.10180. Genes Chromosomes Cancer. 2003. PMID: 12619165 Free article.

9

Haplotype analysis of the BRCA2 9254delATCAT recurrent mutation in breast/ovarian cancer families from Spain.

Campos B, Díez O, Odefrey F, Domènech M, Moncoutier V, Martínez-Ferrandis JI, Osorio A, Balmaña J, Barroso A, Armengod ME, Benítez J, Alonso C, Stoppa-Lyonnet D, Goldgar D, Baiget M. Campos B, et al. Among authors: benitez j. Hum Mutat. 2003 Apr;21(4):452. doi: 10.1002/humu.9133. Hum Mutat. 2003. PMID: 12655574

10

Over-representation of two specific haplotypes among chromosomes harbouring BRCA1 mutations.

Osorio A, de la Hoya M, Rodríguez-López R, Granizo JJ, Díez O, Vega A, Durán M, Carracedo A, Baiget M, Caldés T, Benítez J. Osorio A, et al. Among authors: benitez j. Eur J Hum Genet. 2003 Jun;11(6):489-92. doi: 10.1038/sj.ejhg.5200969. Eur J Hum Genet. 2003. PMID: 12774043

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