Search Results - "Bull, Shelley B"
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Met induces mammary tumors with diverse histologies and is associated with poor outcome and human basal breast cancer
Published in Proceedings of the National Academy of Sciences - PNAS (04-08-2009)“…Elevated MET receptor tyrosine kinase correlates with poor outcome in breast cancer, yet the reasons for this are poorly understood. We thus generated a…”
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Genome-Wide Association Scan for Diabetic Nephropathy Susceptibility Genes in Type 1 Diabetes
Published in Diabetes (New York, N.Y.) (01-06-2009)“…Genome-Wide Association Scan for Diabetic Nephropathy Susceptibility Genes in Type 1 Diabetes Marcus G. Pezzolesi 1 , G. David Poznik 1 , Josyf C. Mychaleckyj…”
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Osteosarcoma and soft-tissue sarcomas with an immune infiltrate express PD-L1: relation to clinical outcome and Th1 pathway activation
Published in Oncoimmunology (01-01-2020)“…Immune checkpoint proteins, such as PD-L1 and PD-1, are important in several cancers; however, their role in osteosarcoma (OSA) and soft tissue sarcoma (STS)…”
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Tumoral BRD4 expression in lymph node-negative breast cancer: association with T-bet+ tumor-infiltrating lymphocytes and disease-free survival
Published in BMC cancer (20-07-2018)“…We previously observed that T-bet+ tumor-infiltrating T lymphocytes (T-bet+ TILs) in primary breast tumors were associated with adverse clinicopathological…”
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Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identification
Published in PLoS genetics (01-08-2013)“…Next generation sequencing has dramatically increased our ability to localize disease-causing variants by providing base-pair level information at costs…”
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Insights From Mixture Cure Modeling of Molecular Markers for Prognosis in Breast Cancer
Published in Journal of clinical oncology (01-06-2013)“…With the ultimate aim of improving clinical management of breast cancer, investigators have sought to identify molecular genetic markers that stratify newly…”
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A Genome-Wide Association Study Identifies a Novel Major Locus for Glycemic Control in Type 1 Diabetes, as Measured by Both A1C and Glucose
Published in Diabetes (New York, N.Y.) (01-02-2010)“…A Genome-Wide Association Study Identifies a Novel Major Locus for Glycemic Control in Type 1 Diabetes, as Measured by Both A1C and Glucose Andrew D. Paterson…”
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Statistical power in COVID-19 case-control host genomic study design
Published in Genome medicine (28-12-2020)“…The identification of genetic variation that directly impacts infection susceptibility to SARS-CoV-2 and disease severity of COVID-19 is an important step…”
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Penalized maximum likelihood inference under the mixture cure model in sparse data
Published in Statistics in medicine (15-06-2023)“…Introduction When a study sample includes a large proportion of long‐term survivors, mixture cure (MC) models that separately assess biomarker associations…”
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Integrating epigenetic, genetic, and phenotypic data to uncover gene-region associations with triglycerides in the GOLDN study
Published in BMC proceedings (17-09-2018)“…There has been significant interest in investigating genome-wide and epigenome-wide associations with lipids. Testing at the gene or region level may improve…”
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Prognostic Effect of Basal-Like Breast Cancers Is Time Dependent: Evidence from Tissue Microarray Studies on a Lymph Node–Negative Cohort
Published in Clinical cancer research (01-07-2008)“…Purpose: To determine whether data obtained from tissue microarrays (TMA) of a prospectively accrued node-negative breast cancer cohort are prognostically…”
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Expression profiling of familial breast cancers demonstrates higher expression of FGFR2 in BRCA2-associated tumors
Published in Breast cancer research and treatment (01-09-2009)“…Background BRCA1- and BRCA2-associated tumors appear to have distinct molecular signatures. BRCA1-associated tumors are predominantly basal-like cancers,…”
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A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits
Published in Frontiers in genetics (20-10-2014)“…Genetic pleiotropy refers to the situation in which a single gene influences multiple traits and so it is considered as a major factor that underlies genetic…”
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Gene-based multiple regression association testing for combined examination of common and low frequency variants in quantitative trait analysis
Published in Frontiers in genetics (2013)“…Multi-marker methods for genetic association analysis can be performed for common and low frequency SNPs to improve power. Regression models are an intuitive…”
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TP53 Mutations and Outcome in Osteosarcoma: A Prospective, Multicenter Study
Published in Journal of clinical oncology (01-03-2005)“…Mutations of the TP53 gene have been associated with resistance to chemotherapy as well as poor prognosis in many different malignancies. This is the first…”
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CK8/18 expression, the basal phenotype, and family history in identifying BRCA1‐associated breast cancer in the Ontario site of the Breast Cancer Family Registry
Published in Cancer (01-04-2011)“…BACKGROUND. BRCA1‐associated breast cancer had been shown to be morphologically and genetically distinct from sporadic cancers. The aim of this study was to…”
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gpart: human genome partitioning and visualization of high-density SNP data by identifying haplotype blocks
Published in Bioinformatics (01-11-2019)“…Abstract Summary For the analysis of high-throughput genomic data produced by next-generation sequencing (NGS) technologies, researchers need to identify…”
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Characterization of direct and/or indirect genetic associations for multiple traits in longitudinal studies of disease progression
Published in Genetics (Austin) (31-08-2023)“…Abstract When quantitative longitudinal traits are risk factors for disease progression and subject to random biological variation, joint model analysis of…”
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Human leucocyte antigen risk alleles for psoriatic arthritis among patients with psoriasis
Published in Annals of the rheumatic diseases (01-01-2012)“…Aim Genes that differentiate patients with psoriatic arthritis (PsA) from those with cutaneous psoriasis (PsC) may serve as markers for the development of PsA…”
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A new haplotype block detection method for dense genome sequencing data based on interval graph modeling of clusters of highly correlated SNPs
Published in Bioinformatics (01-02-2018)“…Abstract Motivation Linkage disequilibrium (LD) block construction is required for research in population genetics and genetic epidemiology, including…”
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