Center-Authored Papers
Filters: Author is Winship, Ingrid [Clear All Filters]
Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers? European journal of cancer (Oxford, England : 1990). 49(7):1578-87. Abstract
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2013.
Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers.. Obstetrics and gynecology. 117(4):899-905. Abstract
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2011.
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.. Gastroenterology. 135(2):419-28. Abstract
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2008.
Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study.. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 30(9):958-64. Abstract
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2012.
Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22.. PloS one. 7(5):e38175. Abstract
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2012.
Family History of Colorectal Cancer in BRAF p.V600E mutated Colorectal Cancer Cases.. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. Abstract
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2013.
Genome-wide association study identifies multiple risk loci for renal cell carcinoma.. Nature communications. 8:15724. Abstract
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2017.
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2011.
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.. Journal of medical genetics. Abstract
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2016.
Risk of Metachronous Colon Cancer Following Surgery for Rectal Cancer in Mismatch Repair Gene Mutation Carriers.. Annals of surgical oncology. 20(6):1829-1836. Abstract
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2013.
Risks of colorectal and other cancers after endometrial cancer for women with lynch syndrome.. Journal of the National Cancer Institute. 105(4):274-9. Abstract
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2013.
Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome.. Journal of the National Cancer Institute. 104(18):1363-72. Abstract
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2012. Doing Business with Arnold Library
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