Medicina Xenómica
GMX - USC
Javier
Benítez Ortiz
Publicacións nas que colabora con Javier Benítez Ortiz (20)
2023
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A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry
Breast cancer research : BCR, Vol. 25, Núm. 1, pp. 93
2021
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Breast cancer risk genes - Association analysis in more than 113,000 women
New England Journal of Medicine, Vol. 384, Núm. 5, pp. 428-439
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Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk
Journal of the National Cancer Institute, Vol. 113, Núm. 3, pp. 329-337
2019
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Genome-wide association study of germline variants and breast cancer-specific mortality
British Journal of Cancer, Vol. 120, Núm. 6, pp. 647-657
2017
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Association analysis identifies 65 new breast cancer risk loci
Nature, Vol. 551, Núm. 7678, pp. 92-94
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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Nature Genetics, Vol. 49, Núm. 12, pp. 1767-1778
2015
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Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors
International Journal of Cancer, Vol. 136, Núm. 6, pp. E685-E696
2014
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FAS system deregulation in T-cell lymphoblastic lymphoma
Cell Death and Disease, Vol. 5, Núm. 3
2013
2012
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Detection of a large rearrangement in PALB2 in Spanish breast cancer families with male breast cancer
Breast Cancer Research and Treatment, Vol. 132, Núm. 1, pp. 307-315
2009
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Evaluating new candidate SNPs as low penetrance risk factors in sporadic breast cancer: A two-stage Spanish case-control study
Gynecologic Oncology, Vol. 112, Núm. 1, pp. 210-214
2008
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Is mitochondrial DNA variation associated with sporadic breast cancer risk?
Cancer Research
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The ‘Pokemon’ (ZBTB7) gene: No evidence of association with sporadic breast cancer
Clinical Medicine: Oncology, Vol. 2, pp. 357-362
2007
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Association study of 69 genes in the ret pathway identifies low-penetrance loci in sporadic medullary thyroid carcinoma
Cancer Research, Vol. 67, Núm. 19, pp. 9561-9567
2006
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ERCC4 associated with breast cancer risk: A two-stage case-control study using high-throughput genotyping
Cancer Research, Vol. 66, Núm. 19, pp. 9420-9427
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Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genes
Human Genetics, Vol. 118, Núm. 6, pp. 669-679
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Genomic rearrangements at the BRCA1 locus in Spanish families with breast/ovarian cancer
Clinical Chemistry, Vol. 52, Núm. 8, pp. 1480-1485
2004
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The variant E233G of the rad51d gene could be a low-penetrance allele in high-risk breast cancer families without BRCA1/2 mutations
International Journal of Cancer, Vol. 110, Núm. 6, pp. 845-849
2003
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Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: A high proportion of mutations unique to Spain and evidence of founder effects
Human Mutation, Vol. 22, Núm. 4, pp. 301-312
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Over-representation of two specific haplotypes among chromosomes harbouring BRCA1 mutations
European Journal of Human Genetics