Search Results - "Haile, Robert"
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Racial and Ethnic Disparities in Cancer Survival: The Contribution of Tumor, Sociodemographic, Institutional, and Neighborhood Characteristics
Published in Journal of clinical oncology (01-01-2018)“…Purpose Racial/ethnic disparities in cancer survival in the United States are well documented, but the underlying causes are not well understood. We quantified…”
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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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3
“Cancer Center Catchment Area Assessment”—Letter
Published in Cancer epidemiology, biomarkers & prevention (01-07-2022)Get full text
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4
Environmental epigenetics: prospects for studying epigenetic mediation of exposure–response relationships
Published in Human genetics (01-10-2012)“…Changes in epigenetic marks such as DNA methylation and histone acetylation are associated with a broad range of disease traits, including cancer, asthma,…”
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Potential impact of family history–based screening guidelines on the detection of early‐onset colorectal cancer
Published in Cancer (01-07-2020)“…Background Initiating screening at an earlier age based on cancer family history is one of the primary recommended strategies for the prevention and detection…”
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A cancer care desert: living in between the urban and rural and the case for defining semirural regions
Published in Frontiers in oncology (22-05-2023)Get full text
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7
Impaired Immune Health in Survivors of Diffuse Large B-Cell Lymphoma
Published in Journal of clinical oncology (20-05-2020)“…Therapeutic advances for diffuse large B-cell lymphoma (DLBCL) have led to an increasing number of survivors. Both DLBCL and its treatments perturb the immune…”
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Adolescent and young adult oncology patients: Disparities in access to specialized cancer centers
Published in Cancer (01-07-2017)“…BACKGROUND Adolescents and young adults (AYAs) ages 15 to 39 years with cancer continue to experience disparate survival outcomes compared with their younger…”
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Risk factors by molecular subtypes of breast cancer across a population-based study of women 56 years or younger
Published in Breast cancer research and treatment (01-11-2011)“…Differences in incidence, prognosis, and treatment response suggest gene expression patterns may discern breast cancer subtypes with unique risk factor…”
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Cigarette Smoking and Colorectal Cancer Risk by Molecularly Defined Subtypes
Published in JNCI : Journal of the National Cancer Institute (21-07-2010)“…Background Cigarette smoking is an established risk factor for colorectal cancer. Because colorectal carcinogenesis is a heterogeneous process, we investigated…”
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Risk of extracolonic cancers for people with biallelic and monoallelic mutations in MUTYH
Published in International journal of cancer (01-10-2016)“…Germline mutations in the DNA base excision repair gene MUTYH are known to increase a carrier's risk of colorectal cancer. However, the risks of other…”
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12
Continued Increase in Melanoma Incidence across all Socioeconomic Status Groups in California, 1998–2012
Published in Journal of investigative dermatology (01-11-2017)“…Melanoma incidence has been increasing in light-skinned populations worldwide, but the reasons for the increase have been controversial. Our prior assessment…”
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Risk of Colorectal Cancer for Carriers of Mutations in MUTYH , With and Without a Family History of Cancer
Published in Gastroenterology (New York, N.Y. 1943) (01-05-2014)“…We studied 2332 individuals with monoallelic mutations in MUTYH among 9504 relatives of 264 colorectal cancer (CRC) cases with a MUTYH mutation. We estimated…”
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14
Worldwide Practice Patterns in Lynch Syndrome Diagnosis and Management, Based on Data From the International Mismatch Repair Consortium
Published in Clinical gastroenterology and hepatology (01-12-2018)“…Families with a history of Lynch syndrome often do not adhere to guidelines for genetic testing and screening. We investigated practice patterns related to…”
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Cancer Risks for MLH1 and MSH2 Mutation Carriers
Published in Human mutation (01-03-2013)“…ABSTRACT We studied 17,576 members of 166 MLH1 and 224 MSH2 mutation‐carrying families from the Colon Cancer Family Registry. Average cumulative risks of…”
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Risk of Asynchronous Contralateral Breast Cancer in Noncarriers of BRCA1 and BRCA2 Mutations With a Family History of Breast Cancer: A Report From the Women's Environmental Cancer and Radiation Epidemiology Study
Published in Journal of clinical oncology (01-02-2013)“…To fully characterize the risk of contralateral breast cancer (CBC) in patients with breast cancer with a family history who test negative for BRCA1 and BRCA2…”
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Risk of Metachronous Colon Cancer Following Surgery for Rectal Cancer in Mismatch Repair Gene Mutation Carriers
Published in Annals of surgical oncology (01-06-2013)“…Background Despite regular surveillance colonoscopy, the metachronous colorectal cancer risk for mismatch repair (MMR) gene mutation carriers after segmental…”
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Melanoma awareness and prevention among latinx and non‐latinx white adults in urban and rural California: A qualitative exploration
Published in Cancer medicine (Malden, MA) (01-03-2023)“…Background Melanoma mortality rates in the US are highest among older men, individuals of lower socioeconomic status (SES), and people of color. To better…”
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Folic acid supplementation and risk of colorectal neoplasia during long-term follow-up of a randomized clinical trial
Published in The American journal of clinical nutrition (01-10-2019)“…The Aspirin/Folate Polyp Prevention Study previously found folic acid increased risk of advanced and multiple colorectal adenomas during a surveillance…”
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Population-Based Study of the Risk of Second Primary Contralateral Breast Cancer Associated With Carrying a Mutation in BRCA1 or BRCA2
Published in Journal of clinical oncology (10-05-2010)“…Women with breast cancer diagnosed early in life comprise a substantial portion of those tested for BRCA1/BRCA2 mutations; however, little information is…”
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