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Candidate gene association study in pediatric acute lymphoblastic leukemia evaluated by Bayesian network based Bayesian multilevel analysis of relevance.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 42, doi. 10.1186/1755-8794-5-42
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Systematically characterizing and prioritizing chemosensitivity related gene based on Gene Ontology and protein interaction network.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 43, doi. 10.1186/1755-8794-5-43
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Structural, functional and molecular analysis of the effects of aging in the small intestine and colon of C57BL/6J mice.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 38, doi. 10.1186/1755-8794-5-38
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Integrative analysis of neuroblastoma and pheochromocytoma genomics data.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 48, doi. 10.1186/1755-8794-5-48
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Human breast cancer associated fibroblasts exhibit subtype specific gene expression profiles.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 39, doi. 10.1186/1755-8794-5-39
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Association of genetic polymorphisms with chronic obstructive pulmonary disease in the Chinese Han population: a case-control study.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 1, doi. 10.1186/1755-8794-5-64
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Histotype-specific copy-number alterations in ovarian cancer.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 1, doi. 10.1186/1755-8794-5-47
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Subtypes of primary colorectal tumors correlate with response to targeted treatment in colorectal cell lines.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 66, doi. 10.1186/1755-8794-5-66
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Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variants.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 65, doi. 10.1186/1755-8794-5-65
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Clinical and multiple gene expression variables in survival analysis of breast cancer: Analysis with the hypertabastic survival model.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 63, doi. 10.1186/1755-8794-5-63
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Mitochondrial proteomics of nasopharyngeal carcinoma metastasis.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 62, doi. 10.1186/1755-8794-5-62
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Adipose Co-expression networks across Finns and Mexicans identify novel triglyceride-associated genes.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 61, doi. 10.1186/1755-8794-5-61
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Soft tissue sarcoma subtypes exhibit distinct patterns of acquired uniparental disomy.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 60, doi. 10.1186/1755-8794-5-60
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Identification and characterization of alternative exon usage linked glioblastoma multiforme survival.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 59, doi. 10.1186/1755-8794-5-59
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A whole blood gene expression-based signature for smoking status.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 58, doi. 10.1186/1755-8794-5-58
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Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 57, doi. 10.1186/1755-8794-5-57
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Autworks: a cross-disease network biology application for Autism and related disorders.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 56, doi. 10.1186/1755-8794-5-56
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.An array CGH based genomic instability index (G2I) is predictive of clinical outcome in breast cancer and reveals a subset of tumors without lymph node involvement but with poor prognosis.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 54, doi. 10.1186/1755-8794-5-54
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Genomic signatures characterize leukocyte infiltration in myositis muscles.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 53, doi. 10.1186/1755-8794-5-53
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Genomic profiling of rectal adenoma and carcinoma by array-based comparative genomic hybridization.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 52, doi. 10.1186/1755-8794-5-52
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Cell Line Derived Multi-Gene Predictor of Pathologic Response to Neoadjuvant Chemotherapy in Breast Cancer: A Validation Study on US Oncology 02-103 Clinical Trial.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 51, doi. 10.1186/1755-8794-5-51
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A direct comparison of next generation sequencing enrichment methods using an aortopathy gene panel- clinical diagnostics perspective.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 50, doi. 10.1186/1755-8794-5-50
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Correlations of gene expression with ratings of inattention and hyperactivity/impulsivity in tourette syndrome: a pilot study.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 49, doi. 10.1186/1755-8794-5-49
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Completion of the swine genome will simplify the production of swine as a large animal biomedical model.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 55, doi. 10.1186/1755-8794-5-55
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Novel biomarker combination improves the diagnosis of serious bacterial infections in Malawian children.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 13, doi. 10.1186/1755-8794-5-13
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Screening significantly hypermethylated genes in fetal tissues compared with maternal blood using a methylated-CpG island recovery assay-based microarray.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 26, doi. 10.1186/1755-8794-5-26
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Batch correction of microarray data substantially improves the identification of genes differentially expressed in Rheumatoid Arthritis and Osteoarthritis.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 23, doi. 10.1186/1755-8794-5-23
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Saliva samples are a viable alternative to blood samples as a source of DNA for high throughput genotyping.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 19, doi. 10.1186/1755-8794-5-19
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MiRNAs associated with chemo-sensitivity in cell lines and in advanced bladder cancer.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 40, doi. 10.1186/1755-8794-5-40
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Association of differential gene expression with imatinib mesylate and omacetaxine mepesuccinate toxicity in lymphoblastoid cell lines.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 37, doi. 10.1186/1755-8794-5-37
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Defining the genomic signature of the parous breast.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 46, doi. 10.1186/1755-8794-5-46
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Approaches to informed consent for hypothesis-testing and hypothesis-generating clinical genomics research.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 45, doi. 10.1186/1755-8794-5-45
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PAM50 Breast Cancer Subtyping by RT-qPCR and Concordance with Standard Clinical Molecular Markers.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 44, doi. 10.1186/1755-8794-5-44
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Immune genes are associated with human glioblastoma pathology and patient survival.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 41, doi. 10.1186/1755-8794-5-41
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MicroRNA expression signature in human abdominal aortic aneurysms.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 25, doi. 10.1186/1755-8794-5-25
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Genetic and bioinformatic analyses of the expression and function of PI3K regulatory subunit PIK3R3 in an Asian patient gastric cancer library.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 34, doi. 10.1186/1755-8794-5-34
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Skeletal muscle alterations and exercise performance decrease in erythropoietin-deficient mice: a comparative study.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 29, doi. 10.1186/1755-8794-5-29
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Gankyrin gene deletion followed by proteomic analysis: insight into the roles of Gankyrin in Tumorigenesis and Metastasis.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 36, doi. 10.1186/1755-8794-5-36
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The effects of MicroRNA transfections on global patterns of gene expression in ovarian cancer cells are functionally coordinated.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 33, doi. 10.1186/1755-8794-5-33
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Genomic signatures for predicting survival and adjuvant chemotherapy benefit in patients with non-small-cell lung cancer.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 30, doi. 10.1186/1755-8794-5-30
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- Article
LINE-1 methylation status and its association with tetralogy of fallot in infants.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 20, doi. 10.1186/1755-8794-5-20
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- Article
Network analysis identifies a putative role for the PPAR and type 1 interferon pathways in glucocorticoid actions in asthmatics.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 27, doi. 10.1186/1755-8794-5-27
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- Article
MicroRNA profiling of a CD133+ spheroid-forming subpopulation of the OVCAR3 human ovarian cancer cell line.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 18, doi. 10.1186/1755-8794-5-18
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Relation between smoking history and gene expression profiles in lung adenocarcinomas.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 22, doi. 10.1186/1755-8794-5-22
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Patient-controlled encrypted genomic data: an approach to advance clinical genomics.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 31, doi. 10.1186/1755-8794-5-31
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Direct integration of intensity-level data from Affymetrix and Illumina microarrays improves statistical power for robust reanalysis.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 35, doi. 10.1186/1755-8794-5-35
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Genes associated with MUC5AC expression in small airway epithelium of human smokers and non-smokers.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 21, doi. 10.1186/1755-8794-5-21
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Fibroblasts from phenotypically normal palmar fascia exhibit molecular profiles highly similar to fibroblasts from active disease in Dupuytren's Contracture.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 15, doi. 10.1186/1755-8794-5-15
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- Article
Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 17, doi. 10.1186/1755-8794-5-17
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A target based approach identifies genomic predictors of breast cancer patient response to chemotherapy.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 16, doi. 10.1186/1755-8794-5-16
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