| 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 | 1604 | 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 | 1514 | 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 | 1053 | 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 | 831 | 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 | 698 | 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 | 649 | 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 | 617 | 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 | 605 | 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 | 601 | 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 | 595 | 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 | 534 | 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 | 522 | 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 | 511 | 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 | 486 | 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 | 480 | 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 | 457 | 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 | 456 | 2019 |
| Clinical relevance of microsatellite instability in colorectal cancer A De La Chapelle, H Hampel Journal of Clinical Oncology 28 (20), 3380-3387, 2010 | 405 | 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 | 399 | 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 | 398 | 2014 |
Albert de la ChapelleProfessor, Ohio State UniversityVerified email at osumc.edu
