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Bethany Van Guelpen

Researcher at Umeå University

Publications -  139
Citations -  5017

Bethany Van Guelpen is an academic researcher from Umeå University. The author has contributed to research in topics: Colorectal cancer & Cancer. The author has an hindex of 31, co-authored 104 publications receiving 3742 citations. Previous affiliations of Bethany Van Guelpen include University of Virginia.

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Body Size and Risk of Colon and Rectal Cancer in the European Prospective Investigation Into Cancer and Nutrition (EPIC)

TL;DR: In this paper, the authors used multivariable adjusted Cox proportional hazards models to examine the association between anthropometric measures and risks of colon and rectal cancer among 368 277 men and women who were free of cancer at baseline from nine countries of the European Prospective Investigation Into Cancer and Nutrition.
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Discovery of common and rare genetic risk variants for colorectal cancer

Jeroen R. Huyghe, +224 more
- 01 Jan 2019 - 
TL;DR: Genome-wide association analyses based on whole-genome sequencing and imputation identify 40 new risk variants for colorectal cancer, including a strongly protective low-frequency variant at CHD1 and loci implicating signaling and immune function in disease etiology.
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Lifetime and baseline alcohol intake and risk of colon and rectal cancers in the European prospective investigation into cancer and nutrition (EPIC).

TL;DR: In this large European cohort, both lifetime and baseline alcohol consumption increase colon and rectum cancer risk, with more apparent risk increases for alcohol intakes greater than 30 g/day.
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Colorectal cancer prognosis depends on T-cell infiltration and molecular characteristics of the tumor

TL;DR: Patients whose tumors are highly infiltrated by T cells have a beneficial prognosis, regardless of MSI, whereas the role of CIMP status in this context is less clear.
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The Role of the CpG Island Methylator Phenotype in Colorectal Cancer Prognosis Depends on Microsatellite Instability Screening Status

TL;DR: A poor prognosis is found in CIMP-low patients regardless of MSI screening status, and in CimP-high patients with MSS, although not consistently statistically significant.