Heather Hampel
Heather Hampel
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Cited by
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer)
H Hampel, WL Frankel, E Martin, M Arnold, K Khanduja, P Kuebler, ...
New England Journal of Medicine 352 (18), 1851-1860, 2005
ACG clinical guideline: genetic testing and management of hereditary gastrointestinal cancer syndromes
S Syngal, RE Brand, JM Church, FM Giardiello, HL Hampel, RW Burt
Official journal of the American College of Gastroenterology| ACG 110 (2 …, 2015
Feasibility of screening for Lynch syndrome among patients with colorectal cancer
H Hampel, WL Frankel, E Martin, M Arnold, K Khanduja, P Kuebler, ...
Journal of Clinical Oncology 26 (35), 5783-5788, 2008
Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC
SJ Laken, GM Petersen, SB Gruber, C Oddoux, H Ostrer, FM Giardiello, ...
Nature genetics 17 (1), 79-83, 1997
Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients
H Hampel, W Frankel, J Panescu, J Lockman, K Sotamaa, D Fix, ...
Cancer research 66 (15), 7810-7817, 2006
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations
L Senter, M Clendenning, K Sotamaa, H Hampel, J Green, JD Potter, ...
Gastroenterology 135 (2), 419-428. e1, 2008
Identification of Lynch syndrome among patients with colorectal cancer
L Moreira, F Balaguer, N Lindor, A De la Chapelle, H Hampel, ...
Jama 308 (15), 1555-1565, 2012
Prevalence and spectrum of germline cancer susceptibility gene mutations among patients with early-onset colorectal cancer
R Pearlman, WL Frankel, B Swanson, W Zhao, A Yilmaz, K Miller, ...
JAMA oncology 3 (4), 464-471, 2017
Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk.
TS Frank, SA Manley, OI Olopade, S Cummings, JE Garber, B Bernhardt, ...
Journal of Clinical Oncology 16 (7), 2417-2425, 1998
American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility
ME Robson, AR Bradbury, B Arun, SM Domchek, JM Ford, HL Hampel, ...
Journal of Clinical Oncology 33 (31), 3660-3667, 2015
EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome
GE Palomaki, MR McClain, S Melillo, HL Hampel, SN Thibodeau
Genetics in Medicine 11 (1), 42-65, 2009
Gene expression in papillary thyroid carcinoma reveals highly consistent profiles
Y Huang, M Prasad, WJ Lemon, H Hampel, FA Wright, K Kornacker, ...
Proceedings of the National Academy of Sciences 98 (26), 15044-15049, 2001
BRCA1 sequence analysis in women at high risk for susceptibility mutations: risk factor analysis and implications for genetic testing
D Shattuck-Eidens, A Oliphant, M McClure, C McBride, J Gupte, T Rubano, ...
Jama 278 (15), 1242-1250, 1997
Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset
H Hampel, JA Stephens, E Pukkala, R Sankila, LA Aaltonen, JP Mecklin, ...
Gastroenterology 129 (2), 415-421, 2005
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition …
H Hampel, RL Bennett, A Buchanan, R Pearlman, GL Wiesner
Genetics in Medicine 17 (1), 70-87, 2015
Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers
L Baglietto, NM Lindor, JG Dowty, DM White, A Wagner, ...
Journal of the national cancer institute 102 (3), 193-201, 2010
Discovery of common and rare genetic risk variants for colorectal cancer
JR Huyghe, SA Bien, TA Harrison, HM Kang, S Chen, SL Schmit, ...
Nature genetics 51 (1), 76-87, 2019
Clinical relevance of microsatellite instability in colorectal cancer
A De La Chapelle, H Hampel
Journal of Clinical Oncology 28 (20), 3380-3387, 2010
Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations
S Haraldsdottir, H Hampel, J Tomsic, WL Frankel, R Pearlman, ...
Gastroenterology 147 (6), 1308-1316. e1, 2014
Microsatellite instability detection by next generation sequencing
SJ Salipante, SM Scroggins, HL Hampel, EH Turner, CC Pritchard
Clinical chemistry 60 (9), 1192-1199, 2014
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