Selective Genomic Copy Number Imbalances and Probability of Recurrence in Early-Stage Breast Cancer
暂无分享,去创建一个
Mary E. Edgerton | Veerabhadran Baladandayuthapani | Gordon B. Mills | Patricia A. Thompson | Li Zhang | Bradley M. Broom | G. Mills | G. Hortobagyi | B. Broom | V. Baladandayuthapani | J. Murray | A. Sahin | Yuker Wang | M. Bondy | M. Edgerton | P. Thompson | A. Brewster | S. Tsavachidis | Melissa L. Bondy | Aysegul Sahin | Gabriel N. Hortobagyi | Yuker Wang | James L. Murray | Spyros Tsavachidis | Abenaa M. Brewster | Do Kim-Anh | Karin M. Hahn | K. Hahn | Do Kim-Anh | Li Zhang
[1] Daniel Birnbaum,et al. Gene expression profiling shows medullary breast cancer is a subgroup of basal breast cancers. , 2006, Cancer research.
[2] R. Tibshirani,et al. Repeated observation of breast tumor subtypes in independent gene expression data sets , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[3] D. Madigan,et al. Bayesian Model Averaging in Proportional Hazard Models: Assessing the Risk of a Stroke , 1997 .
[4] M. Ringnér,et al. High-resolution genomic and expression analyses of copy number alterations in HER2-amplified breast cancer , 2010, Breast Cancer Research.
[5] Yudong D. He,et al. Gene expression profiling predicts clinical outcome of breast cancer , 2002, Nature.
[6] Y. Nakamura,et al. Allelic losses of loci at 3p25.1, 8p22, 13q12, 17p13.3, and 22q13 correlate with postoperative recurrence in breast cancer. , 2001, Clinical cancer research : an official journal of the American Association for Cancer Research.
[7] Harald Binder,et al. Allowing for mandatory covariates in boosting estimation of sparse high-dimensional survival models , 2008, BMC Bioinformatics.
[8] Robert Tibshirani,et al. Distinct patterns of DNA copy number alteration are associated with different clinicopathological features and gene‐expression subtypes of breast cancer , 2006, Genes, chromosomes & cancer.
[9] James Ireland,et al. Analysis of molecular inversion probe performance for allele copy number determination , 2007, Genome Biology.
[10] Harald Binder,et al. Boosting for high-dimensional time-to-event data with competing risks , 2009, Bioinform..
[11] R. Gray. Modeling Survival Data: Extending the Cox Model , 2002 .
[12] Yusuke Nakamura,et al. Association of allelic loss at 8p22 with poor prognosis among breast cancer cases treated with high-dose adjuvant chemotherapy. , 2002, Cancer letters.
[13] S. Tavaré,et al. High-resolution aCGH and expression profiling identifies a novel genomic subtype of ER negative breast cancer , 2007, Genome Biology.
[14] Yusuke Nakamura,et al. Allelic loss at the 8p22 region as a prognostic factor in large and estrogen receptor negative breast carcinomas , 2000, Cancer.
[15] C. Sotiriou,et al. Taking gene-expression profiling to the clinic: when will molecular signatures become relevant to patient care? , 2007, Nature Reviews Cancer.
[16] A. Nobel,et al. Supervised risk predictor of breast cancer based on intrinsic subtypes. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[17] E. S. Venkatraman,et al. A faster circular binary segmentation algorithm for the analysis of array CGH data , 2007, Bioinform..
[18] Wonshik Han,et al. DNA copy number alterations and expression of relevant genes in triple‐negative breast cancer , 2008, Genes, chromosomes & cancer.
[19] John M S Bartlett,et al. Guidelines for human epidermal growth factor receptor 2 testing: biologic and methodologic considerations. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[20] G. Hortobagyi,et al. Ki‐67 immunostaining in node‐negative stage I/II breast carcinoma. Significant correlation with prognosis , 1991, Cancer.
[21] D. Madigan,et al. Correction to: ``Bayesian model averaging: a tutorial'' [Statist. Sci. 14 (1999), no. 4, 382--417; MR 2001a:62033] , 2000 .
[22] Toshima Z. Parris,et al. High-resolution genomic profiling to predict 10-year overall survival in node-negative breast cancer. , 2010, Cancer genetics and cytogenetics.
[23] E. Milgrom,et al. Ligand-controlled interaction of histone acetyltransferase binding to ORC-1 (HBO1) with the N-terminal transactivating domain of progesterone receptor induces steroid receptor coactivator 1-dependent coactivation of transcription. , 2006, Molecular endocrinology.
[24] Ronald W. Davis,et al. Multiplexed genotyping with sequence-tagged molecular inversion probes , 2003, Nature Biotechnology.
[25] Thomas D. Wu,et al. Genetic Alterations and Oncogenic Pathways Associated with Breast Cancer Subtypes , 2009, Molecular Cancer Research.
[26] Christopher W. Wong,et al. RCP is a human breast cancer-promoting gene with Ras-activating function. , 2009, The Journal of clinical investigation.
[27] Adrian E. Raftery,et al. Bayesian model averaging: a tutorial (with comments by M. Clyde, David Draper and E. I. George, and a rejoinder by the authors , 1999 .
[28] Jude Kendall,et al. Oncogenic cooperation and coamplification of developmental transcription factor genes in lung cancer , 2007, Proceedings of the National Academy of Sciences.
[29] G. Mills,et al. The RAB25 small GTPase determines aggressiveness of ovarian and breast cancers , 2004, Nature Medicine.
[30] P. Nederlof,et al. Array-CGH and breast cancer , 2006, Breast Cancer Research.
[31] H. Dressman,et al. Characterizing the developmental pathways TTF-1, NKX2–8, and PAX9 in lung cancer , 2009, Proceedings of the National Academy of Sciences.
[32] Marcel J T Reinders,et al. Imaging , Diagnosis , Prognosis Clinical Cancer Research Integration of DNA Copy Number Alterations and Prognostic Gene Expression Signatures in Breast Cancer Patients , 2010 .
[33] G. Hortobagyi,et al. Relationship between epidemiologic risk factors and breast cancer recurrence. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[34] P. Spellman,et al. High quality copy number and genotype data from FFPE samples using Molecular Inversion Probe (MIP) microarrays , 2009, BMC Medical Genomics.
[35] A. Vincent-Salomon,et al. Identification of typical medullary breast carcinoma as a genomic sub-group of basal-like carcinomas, a heterogeneous new molecular entity , 2007, Breast Cancer Research.
[36] D. Haber,et al. Cancer: Drivers and passengers , 2007, Nature.
[37] Ajay N. Jain,et al. Genomic and transcriptional aberrations linked to breast cancer pathophysiologies. , 2006, Cancer cell.
[38] R. Tibshirani,et al. Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[39] C. Perou,et al. Race, breast cancer subtypes, and survival in the Carolina Breast Cancer Study. , 2006, JAMA.
[40] Tianji Chen,et al. Dppa2 knockdown-induced differentiation and repressed proliferation of mouse embryonic stem cells. , 2010, Journal of biochemistry.
[41] Christos Hatzis,et al. Commercialized multigene predictors of clinical outcome for breast cancer. , 2008, The oncologist.
[42] T. Lumley,et al. Time‐Dependent ROC Curves for Censored Survival Data and a Diagnostic Marker , 2000, Biometrics.
[43] J. Haerting,et al. Gene-expression signatures in breast cancer. , 2003, The New England journal of medicine.
[44] M. Wigler,et al. Circular binary segmentation for the analysis of array-based DNA copy number data. , 2004, Biostatistics.
[45] Y. Nakamura,et al. Allelic losses as prognostic markers for breast cancers , 2001, International Journal of Clinical Oncology.
[46] Daniel Birnbaum,et al. Integrated profiling of basal and luminal breast cancers. , 2007, Cancer research.
[47] Philippe Dessen,et al. Molecular Characterization of Breast Cancer with High-Resolution Oligonucleotide Comparative Genomic Hybridization Array , 2009, Clinical Cancer Research.
[48] Christian A. Rees,et al. Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[49] Jorma Isola,et al. Patterns of chromosomal imbalances defines subgroups of breast cancer with distinct clinical features and prognosis. A study of 305 tumors by comparative genomic hybridization. , 2003, Cancer research.
[50] Luke Hughes-Davies,et al. Amplification of the BRCA2 Pathway Gene EMSY in Sporadic Breast Cancer Is Related to Negative Outcome , 2004, Clinical Cancer Research.