Pages that link to "Q81290124"
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The following pages link to Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia--a comparative study of four differently designed, high resolution microarray platforms (Q81290124):
Displaying 50 items.
- Republished: Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetime (Q28385687) (← links)
- Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetime (Q28392579) (← links)
- Quantification of normal cell fraction and copy number neutral LOH in clinical lung cancer samples using SNP array data (Q28752458) (← links)
- The pitfalls of platform comparison: DNA copy number array technologies assessed (Q30967336) (← links)
- Concordance of copy number alterations using a common analytic pipeline for genome-wide analysis of Illumina and Affymetrix genotyping data: a report from the Children's Oncology Group (Q30979681) (← links)
- Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios (Q33373518) (← links)
- Potential predictive markers of chemotherapy resistance in stage III ovarian serous carcinomas (Q33511042) (← links)
- Characterization of the genomic features and expressed fusion genes in micropapillary carcinomas of the breast (Q33579776) (← links)
- Evaluation of high-resolution microarray platforms for genomic profiling of bone tumours (Q33651757) (← links)
- Integrative molecular profiling of triple negative breast cancers identifies amplicon drivers and potential therapeutic targets (Q33780945) (← links)
- High-resolution genomic and expression analyses of copy number alterations in HER2-amplified breast cancer (Q34048024) (← links)
- Progressive but previously untreated CLL patients with greater array CGH complexity exhibit a less durable response to chemoimmunotherapy (Q34519192) (← links)
- Evaluation of chronic lymphocytic leukemia by BAC-based microarray analysis (Q34608117) (← links)
- LPL is the strongest prognostic factor in a comparative analysis of RNA-based markers in early chronic lymphocytic leukemia (Q35143479) (← links)
- Novel copy number variants in children with autism and additional developmental anomalies (Q35187237) (← links)
- Intra-tumor genetic heterogeneity and alternative driver genetic alterations in breast cancers with heterogeneous HER2 gene amplification (Q35633666) (← links)
- Age-related somatic structural changes in the nuclear genome of human blood cells (Q35748382) (← links)
- Landscape of somatic allelic imbalances and copy number alterations in HER2-amplified breast cancer (Q35889655) (← links)
- DNA Copy Number Aberrations, and Human Papillomavirus Status in Penile Carcinoma. Clinico-Pathological Correlations and Potential Driver Genes (Q35931316) (← links)
- Functional characterization of the 19q12 amplicon in grade III breast cancers (Q36245567) (← links)
- Comparison of familial and sporadic chronic lymphocytic leukaemia using high resolution array comparative genomic hybridization (Q36644914) (← links)
- Genomic variation by whole-genome SNP mapping arrays predicts time-to-event outcome in patients with chronic lymphocytic leukemia: a comparison of CLL and HapMap genotypes (Q36651908) (← links)
- Genomic approaches to chronic lymphocytic leukemia (Q36737322) (← links)
- Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays (Q36993047) (← links)
- Prognostic impact of epigenetic classification in chronic lymphocytic leukemia: The case of subset #2. (Q37082635) (← links)
- Immunophenotypic and genomic characterization of papillary carcinomas of the breast (Q37130628) (← links)
- Genomic and mutational profiling of ductal carcinomas in situ and matched adjacent invasive breast cancers reveals intra-tumour genetic heterogeneity and clonal selection (Q37155717) (← links)
- Expression, mutation and copy number analysis of platelet-derived growth factor receptor A (PDGFRA) and its ligand PDGFA in gliomas. (Q37345320) (← links)
- Genome-wide profiling of chromosomal alterations in renal cell carcinoma using high-density single nucleotide polymorphism arrays (Q37401031) (← links)
- Large-scale genomic analysis of ovarian carcinomas (Q37453861) (← links)
- Statistical issues in the analysis of DNA Copy Number Variations (Q37601955) (← links)
- Clinical application of targeted and genome-wide technologies: can we predict treatment responses in chronic lymphocytic leukemia? (Q37618663) (← links)
- Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk (Q37659388) (← links)
- The Basis and Rational Use of Molecular Genetic Testing in Mature B-cell Lymphomas (Q37781972) (← links)
- Dysregulated TRK signalling is a therapeutic target in CYLD defective tumours (Q38493679) (← links)
- Integrative molecular and functional profiling of ERBB2-amplified breast cancers identifies new genetic dependencies (Q39207741) (← links)
- Amplifications of NCOA3 gene in colorectal cancers in a Chinese population (Q41520032) (← links)
- Coexistence of copy number increases of ZNF217 and CYP24A1 in colorectal cancers in a Chinese population (Q41881597) (← links)
- Genomic and immunohistochemical analysis of adenosquamous carcinoma of the breast (Q42471198) (← links)
- 450K-array analysis of chronic lymphocytic leukemia cells reveals global DNA methylation to be relatively stable over time and similar in resting and proliferative compartments (Q43939577) (← links)
- Loss of 16q in high grade breast cancer is associated with estrogen receptor status: Evidence for progression in tumors with a luminal phenotype? (Q44606345) (← links)
- ERBB2 gene amplification in oral squamous cell malignancies: a correlation with tumor progression and gene expression (Q45179853) (← links)
- Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study (Q46168265) (← links)
- TP53 Mutations are infrequent in newly diagnosed chronic lymphocytic leukemia (Q54409519) (← links)
- Copy-number increase of AURKA in gastric cancers in a Chinese population: a correlation with tumor progression. (Q54422162) (← links)
- American College of Medical Genetics and Genomics technical standards and guidelines: microarray analysis for chromosome abnormalities in neoplastic disorders (Q57783666) (← links)
- Genome-wide high-resolution analysis of DNA copy number alterations in NF1-associated malignant peripheral nerve sheath tumors using 32K BAC array (Q60305038) (← links)
- The rewards and challenges of array-based karyotyping for clinical oncology applications (Q83815683) (← links)
- Large but not small copy-number alterations correlate to high-risk genomic aberrations and survival in chronic lymphocytic leukemia: a high-resolution genomic screening of newly diagnosed patients (Q84537035) (← links)
- Oligonucleotide array-CGH identifies genomic subgroups and prognostic markers for tumor stage mycosis fungoides (Q84566867) (← links)