Germline DNA Copy Number Aberrations Identified as Potential Prognostic Factors for Breast Cancer Recurrence

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

Genome-wide association analysis identifies three new breast cancer susceptibility loci

(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

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

(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