Center-Authored Papers

Filters: Author is Hampel, Heather  [Clear All Filters]
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Senter L, Clendenning M, Sotamaa K, Hampel H, Green J, Potter JD, Lindblom A, Lagerstedt K, Thibodeau SN, Lindor NM et al..  2008.  The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.. Gastroenterology. 135(2):419-28. Abstract
Provenzale D, Jasperson K, Ahnen DJ, Aslanian H, Bray T, Cannon JA, David DS, Early DS, Erwin D, Ford JM et al..  2015.  Colorectal Cancer Screening, Version 1.2015.. Journal of the National Comprehensive Cancer Network : JNCCN. 13(8):959-68. Abstract
Burt RW, Cannon JA, David DS, Early DS, Ford JM, Giardiello FM, Halverson AL, Hamilton SR, Hampel H, Ismail MK et al..  2013.  Colorectal cancer screening.. Journal of the National Comprehensive Cancer Network : JNCCN. 11(12):1538-75. Abstract
Kastrinos F, Ojha RP, Leenen C, Alvero C, Mercado RC, Balmaña J, Valenzuela I, Balaguer F, Green R, Lindor NM et al..  2016.  Comparison of Prediction Models for Lynch Syndrome Among Individuals With Colorectal Cancer.. Journal of the National Cancer Institute. 108(2) Abstract
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Huyghe JR, Bien SA, Harrison TA, Kang HM, Chen S, Schmit SL, Conti DV, Qu C, Jeon J, Edlund CK et al..  2018.  Discovery of common and rare genetic risk variants for colorectal cancer.. Nature genetics. Abstract
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Cohen SA, Turner EH, Beightol MB, Jacobson A, Gooley TA, Salipante SJ, Haraldsdottir S, Smith C, Scroggins S, Tait JF et al..  2016.  Frequent PIK3CA Mutations in Colorectal and Endometrial Tumors with 2 or More Somatic Mutations in Mismatch Repair Genes.. Gastroenterology. Abstract
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Provenzale D, Gupta S, Ahnen DJ, Bray T, Cannon JA, Cooper G, David DS, Early DS, Erwin D, Ford JM et al..  2016.  Genetic/Familial High-Risk Assessment: Colorectal Version 1.2016, NCCN Clinical Practice Guidelines in Oncology.. Journal of the National Comprehensive Cancer Network : JNCCN. 14(8):1010-30. Abstract
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Moreira L, Balaguer F, Lindor N, de la Chapelle A, Hampel H, Aaltonen LA, Hopper JL, Le Marchand L, Gallinger S, Newcomb PA et al..  2012.  Identification of Lynch syndrome among patients with colorectal cancer.. JAMA : the journal of the American Medical Association. 308(15):1555-65. Abstract
Jones KA, Kim PD, Patel BB, Kelsen SG, Braverman A, Swinton DJ, Gafken PR, Jones LA, Lane WS, Neveu JM et al..  2013.  Immunodepletion plasma proteomics by tripleTOF 5600 and Orbitrap elite/LTQ-Orbitrap Velos/Q exactive mass spectrometers.. Journal of proteome research. 12(10):4351-65. Abstract
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Guindalini RSC, Win AK, Gulden C, Lindor NM, Newcomb PA, Haile RW, Raymond V, Stoffel E, Hall M, Llor X et al..  2015.  Mutation spectrum and risk of colorectal cancer in African American families with Lynch Syndrome.. Gastroenterology. 149(6):1446-1453. Abstract
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Goodenberger MKL, Thomas BC, Riegert-Johnson D, Boland RC, Plon SE, Clendenning M, Win AK, Senter L, Lipkin SM, Stadler ZK et al..  2016.  PMS2 monoallelic mutation carriers: the known unknown.. Genetics in medicine : official journal of the American College of Medical Genetics. 18(1):13-19. Abstract
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Baglietto L, Lindor NM, Dowty JG, White DM, Wagner A, Gomez Garcia EB, Vriends AHJT, Cartwright NR, Barnetson RA, Farrington SM et al..  2010.  Risks of Lynch syndrome cancers for MSH6 mutation carriers.. Journal of the National Cancer Institute. 102(3):193-201. Abstract