Germline DNA Copy Number Aberrations Identified as Potential Prognostic Factors for Breast Cancer Recurrence
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Title
Germline DNA Copy Number Aberrations Identified as Potential Prognostic Factors for Breast Cancer Recurrence
Authors
Keywords
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Journal
PLoS One
Volume 8, Issue 1, Pages e53850
Publisher
Public Library of Science (PLoS)
Online
2013-01-17
DOI
10.1371/journal.pone.0053850
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Related references
Note: Only part of the references are listed.- Cancer statistics, 2012
- (2012) Rebecca Siegel et al. CA-A CANCER JOURNAL FOR CLINICIANS
- Novel Genetic Markers of Breast Cancer Survival Identified by a Genome-Wide Association Study
- (2012) X. O. Shu et al. CANCER RESEARCH
- A two-stage association study identifies methyl-CpG-binding domain protein 2 gene polymorphisms as candidates for breast cancer susceptibility
- (2012) Yadav Sapkota et al. EUROPEAN JOURNAL OF HUMAN GENETICS
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- (2012) Maya Ghoussaini et al. NATURE GENETICS
- The consequences of uniparental disomy and copy number neutral loss-of-heterozygosity during human development and cancer
- (2011) Pablo Lapunzina et al. BIOLOGY OF THE CELL
- Comprehensive SNP array study of frequently used neuroblastoma cell lines; copy neutral loss of heterozygosity is common in the cell lines but uncommon in primary tumors
- (2011) Hanna Kryh et al. BMC GENOMICS
- LOH and copy neutral LOH (cnLOH) act as alternative mechanism in sporadic colorectal cancers with chromosomal and microsatellite instability
- (2011) R. Melcher et al. CARCINOGENESIS
- Copy-Neutral Loss of Heterozygosity at the p53 Locus in Carcinogenesis of Esophageal Squamous Cell Carcinomas Associated with p53 Mutations
- (2011) H. Saeki et al. CLINICAL CANCER RESEARCH
- Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility
- (2011) Badan Sehrawat et al. HUMAN GENETICS
- Characterization of the nonallelic homologous recombination hotspot PRS3 associated with type-3NF1deletions
- (2011) Antje M. Zickler et al. HUMAN MUTATION
- A role for XRCC2 gene polymorphisms in breast cancer risk and survival
- (2011) W.-Y. Lin et al. JOURNAL OF MEDICAL GENETICS
- Receptors, Associations, and Risk Factor Differences by Breast Cancer Subtypes: Positive or Negative?
- (2011) L. Bernstein et al. JNCI-Journal of the National Cancer Institute
- A refined molecular taxonomy of breast cancer
- (2011) M Guedj et al. ONCOGENE
- Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies
- (2010) C. O'Keefe et al. BLOOD
- Influence of pharmacogenetics on response and toxicity in breast cancer patients treated with doxorubicin and cyclophosphamide
- (2010) J Bray et al. BRITISH JOURNAL OF CANCER
- Functional Genetic Polymorphisms in the Aromatase Gene CYP19 Vary the Response of Breast Cancer Patients to Neoadjuvant Therapy with Aromatase Inhibitors
- (2010) L. Wang et al. CANCER RESEARCH
- Germline copy number variation and cancer risk
- (2010) Roland P Kuiper et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Germline copy number variations in BRCA1-associated ovarian cancer patients
- (2010) Kosuke Yoshihara et al. GENES CHROMOSOMES & CANCER
- Breast Cancer Subtypes and the Risk of Local and Regional Relapse
- (2010) K. David Voduc et al. JOURNAL OF CLINICAL ONCOLOGY
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- (2010) NATURE
- HIV-1/AIDS susceptibility and copy number variation in CCL3L1, a gene encoding a natural ligand for HIV-1 co-receptor CCR5
- (2009) T. Nakajima et al. CYTOGENETIC AND GENOME RESEARCH
- Copy number variants, diseases and gene expression
- (2009) C. N. Henrichsen et al. HUMAN MOLECULAR GENETICS
- Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer
- (2008) Simon N Stacey et al. NATURE GENETICS
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