Supplemental material
Epigenetics
Volume 10, 2015 - Issue 12
Related Research Data
Pyrosequencing protocol using a universal biotinylated primer for mutation detection and SNP genotyping
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Analysis of cancer risk and BRCA1 and BRCA2mutation prevalence in the kConFab familial breast cancer resource
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Molecular subtypes of breast cancer are associated with characteristic DNA methylation patterns
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Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working Group
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Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?
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DNA methylome of familial breast cancer identifies distinct profiles defined by mutation status
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The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups
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A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes
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20q11.1 amplification in giant-cell tumor of bone: Array CGH, FISH, and association with outcome
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Genome-wide DNA methylation analysis of archival formalin-fixed paraffin-embedded tissue using the Illumina Infinium HumanMethylation27 BeadChip.
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DNA methylation epigenotypes in breast cancer molecular subtypes
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Adjusting batch effects in microarray expression data using empirical Bayes methods
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Oxford University Press (OUP)
DNA methylome of familial breast cancer identifies distinct profiles defined by mutation status
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Comprehensive molecular portraits of human breast tumours
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Springer Science and Business Media LLC
Genome-wide Methylation Analysis Identifies Genes Specific to Breast Cancer Hormone Receptor Status and Risk of Recurrence
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American Association for Cancer Research (AACR)
The effects of fixation, processing and evaluation criteria on immunohistochemical detection of hormone receptors in breast cancer
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Springer Nature
Structure and mechanism of BRCA1 BRCT domain recognition of phosphorylated BACH1 with implications for cancer
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A Methyl-Deviator Epigenotype of Estrogen Receptor–Positive Breast Carcinoma Is Associated with Malignant Biology
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Elsevier BV
Genetic evidence and integration of various data sources for classifying uncertain variants into a single model
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Wiley
BRCA1/2 Sequence Variants of Uncertain Significance: A Primer for Providers to Assist in Discussions and in Medical Management
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Alphamed Press
A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2genes based on cancer family history
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Springer Nature
A multiplex PCR predictor for aCGH success of FFPE samples
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Springer Nature
Consistency of staining and reporting of oestrogen receptor immunocytochemistry within the European Union—an inter-laboratory study
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Springer Nature
Multinational study of oestrogen and progesterone receptor immunocytochemistry on breast carcinoma fine needle aspirates
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Wiley-Blackwell
DNA methylation profiling to assess pathogenicity of BRCA1 unclassified variants in breast cancer
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Figshare
Estrogen receptor positive breast cancers in BRCA1 mutation carriers: clinical risk factors and pathologic features
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Maximum Entropy Modeling of Short Sequence Motifs with Applications to RNA Splicing Signals
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Mary Ann Liebert Inc
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