Search Results - "Hopper, John L."
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Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
Published in JAMA : the journal of the American Medical Association (20-06-2017)“…IMPORTANCE: The clinical management of BRCA1 and BRCA2 mutation carriers requires accurate, prospective cancer risk estimates. OBJECTIVES: To estimate…”
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Cost-effectiveness of Population-Based BRCA1, BRCA2, RAD51C, RAD51D, BRIP1, PALB2 Mutation Testing in Unselected General Population Women
Published in JNCI : Journal of the National Cancer Institute (01-07-2018)“…The cost-effectiveness of population-based panel testing for high- and moderate-penetrance ovarian cancer (OC)/breast cancer (BC) gene mutations is unknown. We…”
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Determining Risk of Colorectal Cancer and Starting Age of Screening Based on Lifestyle, Environmental, and Genetic Factors
Published in Gastroenterology (New York, N.Y. 1943) (01-06-2018)“…Guidelines for initiating colorectal cancer (CRC) screening are based on family history but do not consider lifestyle, environmental, or genetic risk factors…”
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4
Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer
Published in Cancer epidemiology, biomarkers & prevention (01-03-2017)“…Although high-risk mutations in identified major susceptibility genes (DNA mismatch repair genes and ) account for some familial aggregation of colorectal…”
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DNA methylation‐based biological aging and cancer risk and survival: Pooled analysis of seven prospective studies
Published in International journal of cancer (15-04-2018)“…The association between aging and cancer is complex. Recent studies have developed measures of biological aging based on DNA methylation and called them “age…”
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Familial aggregation of esophageal cancer
Published in Chinese medical journal (05-04-2023)“…The study has several strengths including its large sample size of 33,008 participants with a high proportion of family history (15.2% having an affected…”
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Residential surrounding greenness and DNA methylation: An epigenome-wide association study
Published in Environment international (01-09-2021)“…[Display omitted] •Greenspace was associated with DNA methylation of multiple human genome loci.•Those loci are mapped to many genes related to many human…”
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Mammographic Density Phenotypes and Risk of Breast Cancer: A Meta-analysis
Published in JNCI : Journal of the National Cancer Institute (10-05-2014)“…Fibroglandular breast tissue appears dense on mammogram, whereas fat appears nondense. It is unclear whether absolute or percentage dense area more strongly…”
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Wildfire-related PM2.5 and DNA methylation: An Australian twin and family study
Published in Environment international (01-01-2023)“…[Display omitted] •Wildfire PM2.5 was associated with DNA methylation of many human genome loci.•Those loci were mapped to 47 genes related to many human…”
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Ability of known colorectal cancer susceptibility SNPs to predict colorectal cancer risk: A cohort study within the UK Biobank
Published in PloS one (15-09-2021)“…Colorectal cancer risk stratification is crucial to improve screening and risk-reducing recommendations, and consequently do better than a one-size-fits-all…”
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A streamlined model for use in clinical breast cancer risk assessment maintains predictive power and is further improved with inclusion of a polygenic risk score
Published in PloS one (22-01-2021)“…Five-year absolute breast cancer risk prediction models are required to comply with national guidelines regarding risk reduction regimens. Models including the…”
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Polygenic risk scores for cardiovascular diseases and type 2 diabetes
Published in PloS one (02-12-2022)“…Polygenic risk scores (PRSs) are a promising approach to accurately predict an individual's risk of developing disease. The area under the receiver operating…”
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13
Heritable DNA methylation marks associated with susceptibility to breast cancer
Published in Nature communications (28-02-2018)“…Mendelian-like inheritance of germline DNA methylation in cancer susceptibility genes has been previously reported. We aimed to scan the genome for heritable…”
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Epigenetic supersimilarity of monozygotic twin pairs
Published in Genome Biology (09-01-2018)“…Monozygotic twins have long been studied to estimate heritability and explore epigenetic influences on phenotypic variation. The phenotypic and epigenetic…”
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Colorectal and Other Cancer Risks for Carriers and Noncarriers From Families With a DNA Mismatch Repair Gene Mutation: A Prospective Cohort Study
Published in Journal of clinical oncology (20-03-2012)“…To determine whether cancer risks for carriers and noncarriers from families with a mismatch repair (MMR) gene mutation are increased above the risks of the…”
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16
Identification of IL6R and chromosome 11q13.5 as risk loci for asthma
Published in The Lancet (British edition) (10-09-2011)“…Summary Background We aimed to identify novel genetic variants affecting asthma risk, since these might provide novel insights into molecular mechanisms…”
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Epigenome-wide association study of short-term temperature fluctuations based on within-sibship analyses in Australian females
Published in Environment international (01-01-2023)“…•This is the first study to assess the epigenetic impact of short-term temperature fluctuations.•Significant changes in methylation levels in 14…”
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Blood DNA methylation score predicts breast cancer risk: applying OPERA in molecular, environmental, genetic and analytic epidemiology
Published in Molecular oncology (01-01-2022)“…In this issue, Kresovich and colleagues have published a hallmark paper in Molecular, Environmental, Genetic and Analytic Epidemiology. By applying artificial…”
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Tamoxifen and Risk of Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
Published in Journal of clinical oncology (01-09-2013)“…To determine whether adjuvant tamoxifen treatment for breast cancer (BC) is associated with reduced contralateral breast cancer (CBC) risk for BRCA1 and/or…”
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The Clinical Phenotype of Lynch Syndrome Due to Germ-Line PMS2 Mutations
Published in Gastroenterology (New York, N.Y. 1943) (01-08-2008)“…Background & Aims: Although the clinical phenotype of Lynch syndrome (also known as hereditary nonpolyposis colorectal cancer) has been well described, little…”
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