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Molecular Oncology
Volume 4, Issue 3
, Pages 174-191
, June 2010
Genetic susceptibility to breast cancer
References
- . Gene expression profiling predicts clinical outcome of breast cancer. Nature. 2002;415:530–536
- . BEK and FLG, two receptors to members of the FGF family, are amplified in subsets of human breast cancers. Oncogene. 1991;6:659–663
- . Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Nat. Genet. 2009;41:585–590
- . Breast cancer in African-American women: differences in tumor biology from European-American women. Cancer Res. 2006;66:8327–8330
- . Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear family. PLoS Med. 2004;1:e65;229–236
- . Estrogen receptor breast cancer phenotypes in the surveillance, epidemiology, and end results database. Breast Cancer Res. Treat. 2002;76:27–36
- . Breast cancer heterogeneity: a mixture of at least two main types?. J. Natl. Cancer Inst. 2006;98:948–951
- . Pregnancies, breast-feeding, and breast cancer risk in the International BRCA1/2 Carrier Cohort Study (IBCCS). J. Natl. Cancer Inst. 2006;98:535–544
- . Models of genetic susceptibility to breast cancer. Oncogene. 2006;25:5898–5905
- . A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes. Br. J. Cancer. 2002;86:76–83
- . Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. Am. J. Hum. Genet. 2003;72:1117–1130
- . The BOADICEA model of genetic susceptibility to breast and ovarian cancer. Br. J. Cancer. 2004;91:1580–1590
- . RAD51 135G→C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies. Am. J. Hum. Genet. 2007;81:1186–1200
- . The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions. Br. J. Cancer. 2008;98:1457–1466
- . Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. Am. J. Hum. Genet. 2008;82:937–948
- . Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. Hum. Mol. Genet. 2009;18:4442–4456
- . The histologic phenotypes of breast carcinoma occurring before age 40 years in women with and without BRCA1 or BRCA2 germline mutations: a population-based study. Cancer. 1998;83:2335–2345
- . Distinct molecular pathogeneses of early-onset breast cancers in BRCA1 and BRCA2 mutation carriers: a population-based study. Cancer Res. 1999;59:2011–2017
- . The death effector domain protein family. Oncogene. 2003;22:8634–8644
- . Aberrations of the MRE11-RAD50-NBS1 DNA damage sensor complex in human breast cancer: MRE11 as a candidate familial cancer-predisposing gene. Mol. Oncol. 2008;2:296–316
- . On the use of familial aggregation in population-based case probands for calculating penetrance. J. Natl. Cancer Inst. 2002;94:1221–1226
- . Variation of breast cancer risk among BRCA1/2 carriers. JAMA. 2008;299:194–201
- . Relative frequency and morphology of cancers in carriers of germline TP53 mutations. Oncogene. 2001;20:4621–4628
- . Association between the CHEK2*1100delC germ line mutation and estrogen receptor status. Int. J. Gynecol. Cancer. 2006;16(Suppl. 2):552–555
- Commonly studied single-nucleotide polymorphisms and breast cancer: results from the Breast Cancer Association Consortium. J Natl Cancer Inst 2006, 98:1382–1396.
- . Race, breast cancer subtypes, and survival in the Carolina breast cancer study. JAMA. 2006;295:2492–2502
- . The small subunit of the mammalian mitochondrial ribosome. Identification of the full complement of ribosomal proteins present. J. Biol. Chem. 2001;276:19363–19374
- . A new face on apoptosis: death-associated protein 3 and PDCD9 are mitochondrial ribosomal proteins. FEBS Lett. 2001;492:166–170
- CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies. Am J Hum Genet 2004, 74:1175–1182.
- . BRCA1, BRCA2, and Rad51 operate in a common DNA damage response pathway. Cancer Res. 1999;59:1752s–1756s
- . Differential expression of novel tyrosine kinase substrates during breast cancer development. Mol. Cell Proteomics. 2007;6:2072–2087
- . Ethnicity and breast cancer: factors influencing differences in incidence and outcome. J. Natl. Cancer Inst. 2005;97:439–448
- . Rates for breast cancer characteristics by estrogen and progesterone receptor status in the major racial/ethnic groups. Breast Cancer Res. Treat. 2002;74:199–211
- . Prediction and interaction in complex disease genetics: experience in type 1 diabetes. PLoS Genet. 2009;5:e1000540;1–6
- . Risk factors for breast cancer according to estrogen and progesterone receptor status. J. Natl. Cancer Inst. 2004;96:218–228
- . Comparison between genotype and phenotype identifies a high-risk population carrying BRCA1 mutations. Genes Chromosomes Cancer. 2000;27:130–135
- . Hormonal factors and the risk of breast cancer according to estrogen- and progesterone-receptor subgroup. Cancer Epidemiol. Biomarkers Prev. 2003;12:1053–1060
- . AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 study. Cancer Epidemiol. Biomarkers Prev. 2007;16:1416–1421
- . A common coding variant in CASP8 is associated with breast cancer risk. Nat. Genet. 2007;39:352–358
- . Effect of pregnancy as a risk factor for breast cancer in BRCA1/BRCA2 mutation carriers. Int. J. Cancer. 2005;117:988–991
- Cunningham, J.E., Montero, A.J., Garrett-Mayer, E., Berkel, H.J., Ely, B, 2009. Racial differences in the incidence of breast cancer subtypes defined by combined histologic grade and hormone receptor status. Cancer Causes Control.
- . A six-nucleotide deletion in the CASP8 promoter is not associated with a susceptibility to breast and prostate cancers in the Polish population. Breast Cancer Res. Treat. 2008;112:367–368
- . Estrogen receptor status in CHEK2-positive breast cancers: implications for chemoprevention. Clin. Genet. 2009;75:72–78
- . Evidences for association of the CASP8 -652 6N del promoter polymorphism with age at diagnosis in familial breast cancer cases. Breast Cancer Res. Treat. 2009;113:607–608
- . Tyrosine kinase signalling in breast cancer: fibroblast growth factors and their receptors. Breast Cancer Res. 2000;2:191–196
- . Familial risks of breast cancer. Breast Cancer Res. 2002;4:179–181
- . Genome-wide association studies in cancer. Hum. Mol. Genet. 2008;17:R109–R115
- . Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. Breast Cancer Linkage Consortium. Am. J. Hum. Genet. 1993;52:678–701
- . Genome-wide association study identifies novel breast cancer susceptibility loci. Nature. 2007;447:1087–1093
- . Novel indications for BRCA1 screening using individual clinical and morphological features. Int. J. Cancer. 1999;84:263–267
- Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease, 2001. Lancet, 358, 1389–1399.
- . An admixture scan in 1484 African American women with breast cancer. Cancer Epidemiol. Biomarkers Prev. 2009;18:3110–3117
- . Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Breast Cancer Linkage Consortium. Am. J. Hum. Genet. 1998;62:676–689
- . Estrogen receptor status in BRCA1- and BRCA2-related breast cancer: the influence of age, grade, and histological type. Clin. Cancer Res. 2004;10:2029–2034
- . The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter study. Breast Cancer Res. Treat. 2008;111:139–144
- . Bilateral prophylactic oophorectomy and bilateral prophylactic mastectomy in a prospective cohort of unaffected BRCA1 and BRCA2 mutation carriers. Clin. Breast Cancer. 2007;7:875–882
- . Caspase-8 in cancer biology and therapy. Cancer Lett. 2009;281:128–133
- . Value of adding single-nucleotide polymorphism genotypes to a breast cancer risk model. J. Natl. Cancer Inst. 2009;101:959–963
- . Follow-up study of twenty-four families with Li-Fraumeni syndrome. Cancer Res. 1991;51:6094–6097
- . Genetic susceptibility loci for breast cancer by estrogen receptor status. Clin. Cancer Res. 2008;14:8000–8009
- . Established breast cancer risk factors by clinically important tumour characteristics. Br. J. Cancer. 2006;95:123–129
- . Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics. PLoS Genet. 2008;4:e1000054;1–10.
- . Polygenic susceptibility to breast cancer: current state-of-the-art. Future Oncol. 2009;5:689–701
- . Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33. Proc. Natl. Acad. Sci. USA. 2008;105:4340–4345
- . A promoter polymorphism in the CASP8 gene is not associated with cancer risk. Nat. Genet. 2008;40:259–260
- . Linkage of early-onset familial breast cancer to chromosome 17q21. Science. 1990;250:1684–1689
- . Efficacy of bilateral prophylactic mastectomy in BRCA1 and BRCA2 gene mutation carriers. J. Natl. Cancer Inst. 2001;93:1633–1637
- . Gene-expression profiles in hereditary breast cancer. N. Engl. J. Med. 2001;344:539–548
- . The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype. Clin. Cancer Res. 2009;15:3214–3222
- . A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Nature. 1998;391:184–187
- . Differences in estrogen receptor subtype according to family history of breast cancer among Hispanic, but not non-Hispanic White women. Cancer Epidemiol. Biomarkers Prev. 2008;17:2700–2706
- . Expression of keratinocyte growth factor and its receptor in human breast cancer: its inhibitory role in the induction of apoptosis possibly through the overexpression of Bcl-2. Arch. Histol. Cytol. 2004;67:455–464
- . Familial aggregation of a disease consequent upon correlation between relatives in a risk factor measured on a continuous scale. Am. J. Epidemiol. 1992;136:1138–1147
- . Biallelic inactivation of BRCA2 in Fanconi anemia. Science. 2002;297:606–609
- . Hormone-related factors and risk of breast cancer in relation to estrogen receptor and progesterone receptor status. Am. J. Epidemiol. 2000;151:703–714
- . Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Nat. Genet. 1998;18:38–43
- . Tumour biological features of BRCA1-induced breast and ovarian cancer. Eur. J. Cancer. 1997;33:362–371
- . No evidence that GATA3 rs570613 SNP modifies breast cancer risk. Breast Cancer Res. Treat. 2009;117:371–379
- . Hormone receptors in breast cancer: racial differences in distribution and survival. Breast Cancer Res. Treat. 2002;73:45–59
- . Influence of BRCA1 mutations on nuclear grade and estrogen receptor status of breast carcinoma in Ashkenazi Jewish women. Cancer. 1997;80:435–441
- . Risk-reducing salpingo-oophorectomy for the prevention of BRCA1- and BRCA2-associated breast and gynecologic cancer: a multicenter, prospective study. J. Clin. Oncol. 2008;26:1331–1337
- . Endogenous sex hormones and breast cancer in postmenopausal women: reanalysis of nine prospective studies. J. Natl. Cancer Inst. 2002;94:606–616
- . Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2. Science. 2003;302:643–646
- . The 6q22.33 locus and breast cancer susceptibility. Cancer Epidemiol. Biomarkers Prev. 2009;18:2468–2475
- . Parental origin of sequence variants associated with complex diseases. Nature. 2009;462:868–874
- . Variants in DNA double-strand break repair genes and breast cancer susceptibility. Hum. Mol. Genet. 2002;11:1399–1407
- . Genomic instability in breast cancer: pathogenesis and clinical implications. Mol. Oncol. 2010;4(3):255–266
- . The pathology of familial breast cancer: morphological aspects. Breast Cancer Res. 1999;1:31–35
- . Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations. J. Natl. Cancer Inst. 1998;90:1138–1145
- . The pathology of familial breast cancer: histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2. Clin. Cancer Res. 2000;6:782–789
- . The pathology of familial breast cancer: predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2. J. Clin. Oncol. 2002;20:2310–2318
- . Pathology of ovarian cancers in BRCA1 and BRCA2 carriers. Clin. Cancer Res. 2004;10:2473–2481
- . Major improvement in the efficacy of BRCA1 mutation screening using morphoclinical features of breast cancer. Cancer Res. 2000;60:1206–1210
- . Steroid receptors in hereditary breast carcinomas associated with BRCA1 or BRCA2 mutations or unknown susceptibility genes. Cancer. 1998;83:310–319
- . Expression of basic fibroblast growth factor, FGFR1 and FGFR2 in normal and malignant human breast, and comparison with other normal tissues. Br. J. Cancer. 1992;66:273–280
- . Molecular basis for therapy resistance. Mol. Oncol. 2010;4(3):284–300
- . Germline p53 mutations and heritable cancer. Annu. Rev. Genet. 1994;28:443–465
- . Germline E-cadherin mutations in familial lobular breast cancer. J. Med. Genet. 2007;44:726–731
- . Common genetic variation in candidate genes and susceptibility to subtypes of breast cancer. Cancer Epidemiol. Biomarkers Prev. 2009;18:255–259
- . Familial relative risks for breast cancer by pathological subtype: a population-based cohort study. Breast Cancer Res. 2010;12:R10;1--2
- . Breast cancer after prophylactic bilateral mastectomy in women with a BRCA1 or BRCA2 mutation. N. Engl. J. Med. 2001;345:159–164
- . Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat. Genet. 2002;31:55–59
- . Allele-specific up-regulation of FGFR2 increases susceptibility to breast cancer. PLoS Biol. 2008;6:e108
- . Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042. J. Natl. Cancer Inst. 2009;101:1012–1018
- . Parity and the risk of breast and ovarian cancer in BRCA1 and BRCA2 mutation carriers. Breast Cancer Res. Treat. 2010;119:221–232
- . Transforming potential of alternatively spliced variants of fibroblast growth factor receptor 2 in human mammary epithelial cells. Mol. Cancer Res. 2004;2:643–652
- . Modifiers of risk of hereditary breast and ovarian cancer. Nat. Rev. Cancer. 2002;2:113–123
- . Tracing the tumor lineage. Mol. Oncol. 2010;4(3):267–283
- . Localization of the gene for Cowden disease to chromosome 10q22-23. Nat. Genet. 1996;13:114–116
- . TOX defines a conserved subfamily of HMG-box proteins. BMC Genomics. 2003;4:13-
- . The pathology of familial breast cancer: immunohistochemistry and molecular analysis. Breast Cancer Res. 1999;1:36–40
- . Loss of heterozygosity analysis at the BRCA loci in tumor samples from patients with familial breast cancer. Int. J. Cancer. 2002;99:305–309
- . Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA). Br. J. Cancer. 2009;101:2048–2054
- . Immunohistochemical characteristics defined by tissue microarray of hereditary breast cancer not attributable to BRCA1 or BRCA2 mutations: differences from breast carcinomas arising in BRCA1 and BRCA2 mutation carriers. Clin. Cancer Res. 2003;9:3606–3614
- . Cancer Incidence in Five Continents. vol. VIII. 2002;
- Pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases. Breast Cancer Linkage Consortium, 1997. Lancet, 349, 1505–1510.
- Molecular portraits of human breast tumours. Nature. 2000;406:747–752
- . High constant incidence in twins and other relatives of women with breast cancer. Nat. Genet. 2000;26:411–414
- . Familial predisposition to breast cancer in a British population: implications for prevention. Eur. J. Cancer. 2000;36:773–779
- . Polygenic susceptibility to breast cancer and implications for prevention. Nat. Genet. 2002;31:33–36
- . Polygenes, risk prediction, and targeted prevention of breast cancer. N. Engl. J. Med. 2008;358:2796–2803
- . Immunophenotypic and pathologic differences between BRCA1 and BRCA2 hereditary breast cancers. J. Clin. Oncol. 2000;18:107S–112S
- . Triple-negative breast cancer: Present challenges and new perspectives. Mol. Oncol. 2010;4(3):209–229
- . Progesterone and estrogen receptors and mammary neoplasia in the Iowa women’s health study: how many kinds of breast cancer are there?. Cancer Epidemiol. Biomarkers Prev. 1995;4:319–326
- . PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nat. Genet. 2007;39:165–167
- . Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations. N. Engl. J. Med. 2002;346:1616–1622
- . Bilateral prophylactic mastectomy reduces breast cancer risk in BRCA1 and BRCA2 mutation carriers: the PROSE Study Group. J. Clin. Oncol. 2004;22:1055–1062
- . No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort study. Breast Cancer Res. Treat. 2009;115:185–192
- . Meta-analysis of risk reduction estimates associated with risk-reducing salpingo-oophorectomy in BRCA1 or BRCA2 mutation carriers. J. Natl. Cancer Inst. 2009;101:80–87
- . ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles. Nat. Genet. 2006;38:873–875
- . Medullary carcinoma of the breast: a clinicopathologic study with 10 year follow-up. Cancer. 1977;40:1365–1385
- . Risk factors for hormone receptor-defined breast cancer in postmenopausal women. Cancer Epidemiol. Biomarkers Prev. 2006;15:2482–2488
- . Genetic variants on chromosome 5p12 are associated with risk of breast cancer in African American women: the black women’s health study. Breast Cancer Res. Treat. 2010;
- . Breast cancer risk factors according to joint estrogen receptor and progesterone receptor status. Cancer Detect Prev. 2005;29:419–426
- . Association of BRCA1 with Rad51 in mitotic and meiotic cells. Cell. 1997;88:265–275
- . Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat. Genet. 2006;38:1239–1241
- Surveillance, Epidemiology, and End Results (SEER) Program Limited-Use Data (1973–2006), National Cancer Institute, DCCPS, Surveillance Research Program, Cancer Statistics Branch, Released April 2009, based on the November 2008 submission. <www.seer.cancer.gov> 9 A.D
- . Variation in breast cancer hormone receptor and HER2 levels by etiologic factors: a population-based analysis. Int. J. Cancer. 2007;121:1079–1085
- . The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. Br. J. Cancer. 2009;101:1456–1460
- . Genes associated with breast cancer metastatic to bone. J. Clin. Oncol. 2006;24:2261–2267
- . A genome wide linkage search for breast cancer susceptibility genes. Genes Chromosomes Cancer. 2006;45:646–655
- . A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. Nat. Genet. 2009;41:996–1000
- . Repeated observation of breast tumor subtypes in independent gene expression data sets. Proc. Natl. Acad. Sci. U S A. 2003;100:8418–8423
- . The AIB1 polyglutamine repeat does not modify breast cancer risk in BRCA1 and BRCA2 mutation carriers. Cancer Epidemiol. Biomarkers Prev. 2006;15:76–79
- . No evidence that CDKN1B (p27) polymorphisms modify breast cancer risk in BRCA1 and BRCA2 mutation carriers. Breast Cancer Res. Treat. 2009;115:307–313
- . Pooled analysis indicates that the GSTT1 deletion, GSTM1 deletion, and GSTP1 Ile105Val polymorphisms do not modify breast cancer risk in BRCA1 and BRCA2 mutation carriers. Breast Cancer Res. Treat. 2009;
- . Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. Nat. Genet. 2007;39:865–869
- . Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer. Nat. Genet. 2008;40:703–706
- . A six-nucleotide insertion-deletion polymorphism in the CASP8 promoter is associated with susceptibility to multiple cancers. Nat. Genet. 2007;39:605–613
- . Estrogen receptor-associated expression of keratinocyte growth factor and its possible role in the inhibition of apoptosis in human breast cancer. Lab. Invest. 2004;84:1460–1471
- . Methodological challenges of genome-wide association analysis in Africa. Nat. Rev. Genet. 2010;11:149–160
- . A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). Nat. Genet. 2009;41:579–584
- . Variation in cancer risks, by mutation position, in BRCA2 mutation carriers. Am. J. Hum. Genet. 2001;68:410–419
- . Variation in BRCA1 cancer risks by mutation position. Cancer Epidemiol. Biomarkers Prev. 2002;11:329–336
- . The genetic epidemiology of breast cancer genes. J. Mammary Gland Biol. Neoplasia. 2004;9:221–236
- . Genetic predisposition to breast cancer: past, present, and future. Annu. Rev. Genomics Hum. Genet. 2008;9:321–345
- . Association between family history of cancer and breast cancer defined by estrogen and progesterone receptor status. Genet. Epidemiol. 1996;13:207–221
- . FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation. Hum. Mol. Genet. 2009;18:1692–1703
- . Performance of common genetic variants in breast-cancer risk models. N. Engl. J. Med. 2010;362:986–993
- . Double-strand break repair gene polymorphisms and risk of breast or ovarian cancer. Cancer Epidemiol. Biomarkers Prev. 2005;14:319–323
- . Histological types of breast cancer: How special are they?. Mol. Oncol. 2010;4(3):192–208
- . Population-based estimates of the relation between breast cancer risk, tumor subtype, and family history. Breast Cancer Res. Treat. 2009;114:549–558
- . RAD51 interacts with the evolutionarily conserved BRC motifs in the human breast cancer susceptibility gene brca2. J. Biol. Chem. 1997;272:31941–31944
- . Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science. 1994;265:2088–2090
- . Hormonal markers in breast cancer: coexpression, relationship with pathologic characteristics, and risk factor associations in a population-based study. Cancer Res. 2007;67:10608–10617
- . Deconstructing the molecular portrait of basal-like breast cancer. Trends Mol. Med. 2006;12:537–544
- . Keratinocyte growth factor-induced motility of breast cancer cells. Clin. Exp. Metastasis. 2000;18:573–580
- . Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat. Genet. 2008;40:638–645
- . Keratinocyte growth factor (KGF) induces aromatase activity in cultured MCF-7 human breast cancer cells. Anticancer Res. 1998;18:2541–2546
- . Estrogen-induced keratinocyte growth factor mRNA expression in normal and cancerous human breast cells. Oncol. Rep. 1998;5:577–583
- . Evaluation of 11 breast cancer susceptibility loci in African-American women. Cancer Epidemiol. Biomarkers Prev. 2009;18:2761–2764
- . Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. Nat. Genet. 2009;41:324–328
PII: S1574-7891(10)00033-5
doi: 10.1016/j.molonc.2010.04.011
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Molecular Oncology
Volume 4, Issue 3
, Pages 174-191
, June 2010

