Journal Articles
Neuhausen S; Gilewski T; Norton L; Tran T; McGuire P; Swensen J; Hampel H; Borgen P; Brown K; Skolnick M; Shattuck-Eidens D; Jhanwar S; Goldgar D; Offit K. "Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer.." Nature Genetics. Vol. 13, no. 1. (May 1996.): 126
Offit K; Gilewski T; McGuire P; Schluger A; Hampel H; Brown K; Swensen J; Neuhausen S; Skolnick M; Norton L; Goldgar D. "Germline BRCA1 185delAG mutations in Jewish women with breast cancer.." Lancet. Vol. 347, no. 9016. (June 1996.): 1643
Laken SJ; Petersen GM; Gruber SB; Oddoux C; Ostrer H; Giardiello FM; Hamilton SR; Hampel H; Markowitz A; Klimstra D; Jhanwar S; Winawer S; Offit K; Luce MC; Kinzler KW; Vogelstein B. "Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.." Nature Genetics. Vol. 17, no. 1. (September 1997.): 79
Shattuck-Eidens D; Oliphant A; McClure M; McBride C; Gupte J; Rubano T; Pruss D; Tavtigian SV; Teng DH; Adey N; Staebell M; Gumpper K; Lundstrom R; Hulick M; Kelly M; Holmen J; Lingenfelter B; Manley S; Fujimura F; Luce M; Ward B; Cannon-Albright L; Steele L; Offit K; Thomas A. "BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.." JAMA: The Journal Of The American Medical Association. Vol. 278, no. 15. (October 1997.): 1242
Frank TS; Manley SA; Olopade OI; Cummings S; Garber JE; Bernhardt B; Antman K; Russo D; Wood ME; Mullineau L; Isaacs C; Peshkin B; Buys S; Venne V; Rowley PT; Loader S; Offit K; Robson M; Hampel H; Brener D; Winer EP; Clark S; Weber B; Strong LC; Thomas A. "Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk.." Journal Of Clinical Oncology: Official Journal Of The American Society Of Clinical Oncology. Vol. 16, no. 7. (July 1998.): 2417
Hampel H. "Cancer risk assessment and genetic testing: Coming of age in the community setting." Oncology Issues: journal of the Association of Community Cancer Centers. Vol. 14, no. 4. (January 1999.): 14-15
Westman J; Hampel H; Bradley T. "Efficacy of a touchscreen computer based family cancer history questionnaire and subsequent cancer risk assessment.." Journal Of Medical Genetics. Vol. 37, no. 5. (May 2000.): 354
Zhou XP; Gimm O; Hampel H; Niemann T; Walker MJ; Eng C. "Epigenetic PTEN silencing in malignant melanomas without PTEN mutation.." The American Journal Of Pathology. Vol. 157, no. 4. (October 2000.): 1123
Hampel H; Allen CM; Chernausek SD; Prior TW; Eng C. "De novo RET mutation positive Multiple Endocrine Neoplasia Type 2B and hereditary nonpolyposis colorectal cancer syndrome occurring in the same family: parent-of-origin and mismatch repair." Journal of Endocrine Genetics. Vol. 3, no. 1. (January 2000.): 143-147
Hampel H; Peltomaki P. "Hereditary colorectal cancer: risk assessment and management.." Clinical Genetics. Vol. 58, no. 2. (August 2000.): 89
Zhou XP; Marsh DJ; Hampel H; Mulliken JB; Gimm O; Eng C. "Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis.." Human Molecular Genetics. Vol. 9, no. 5. (March 2000.): 765
Zhou X; Hampel H; Thiele H; Gorlin RJ; Hennekam RC; Parisi M; Winter RM; Eng C. "Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes.." Lancet. Vol. 358, no. 9277. (July 2001.): 210
Pilarski RT; Hampel H; Eng C. "PTEN Hamartoma Tumor Syndrome (PHTS)." GeneReviews: Genetic Disease Online Reviews at GeneTests-GeneClinics [Database Online]. (November 2001)
Zhou XP; Woodford-Richens K; Lehtonen R; Kurose K; Aldred M; Hampel H; Launonen V; Virta S; Pilarski R; Salovaara R; Bodmer WF; Conrad BA; Dunlop M; Hodgson SV; Iwama T; Järvinen H; Kellokumpu I; Kim JC; Leggett B; Markie D; Mecklin JP; Neale K; Phillips R; Piris J; Rozen P; Houlston RS; Aaltonen LA; Tomlinson IP; Eng C. "Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes.." American Journal Of Human Genetics. Vol. 69, no. 4. (October 2001.): 704
Huang Y; Prasad M; Lemon WJ; Hampel H; Wright FA; Kornacker K; LiVolsi V; Frankel W; Kloos RT; Eng C; Pellegata NS; de la Chapelle A. "Gene expression in papillary thyroid carcinoma reveals highly consistent profiles.." Proceedings Of The National Academy Of Sciences Of The United States Of America. Vol. 98, no. 26. (December 2001.): 15044
Eng C; Hampel H; de la Chapelle A. "Genetic testing for cancer predisposition.." Annual Review Of Medicine. Vol. 52, (January 2001.): 371
Chadwick RB; Pyatt RE; Niemann TH; Richards SK; Johnson CK; Stevens MW; Meek JE; Hampel H; Prior TW; de la Chapelle A. "Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinoma.." Journal Of Medical Genetics. Vol. 38, no. 7. (July 2001.): 461
Hampel H.. Journal of Genetic Counseling. (January 2002.)
Foulkes WD; Thiffault I; Gruber SB; Horwitz M; Hamel N; Lee C; Shia J; Markowitz A; Figer A; Friedman E; Farber D; Greenwood CM; Bonner JD; Nafa K; Walsh T; Marcus V; Tomsho L; Gebert J; Macrae FA; Gaff CL; Paillerets BB; Gregersen PK; Weitzel JN; Gordon PH; MacNamara E; King MC; Hampel H; De La Chapelle A; Boyd J; Offit K; Rennert G; Chong G; Ellis NA. "The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.." American Journal Of Human Genetics. Vol. 71, no. 6. (December 2002.): 1395
Nakagawa H; Yan H; Lockman J; Hampel H; Kinzler KW; Vogelstein B; De La Chapelle A. "Allele separation facilitates interpretation of potential splicing alterations and genomic rearrangements.." Cancer Research. Vol. 62, no. 16. (August 2002.): 4579
Humar B; Toro T; Graziano F; Müller H; Dobbie Z; Kwang-Yang H; Eng C; Hampel H; Gilbert D; Winship I; Parry S; Ward R; Findlay M; Christian A; Tucker M; Tucker K; Merriman T; Guilford P. "Novel germline CDH1 mutations in hereditary diffuse gastric cancer families.." Human Mutation. Vol. 19, no. 5. (May 2002.): 518
Zhou XP; Hampel H; Roggenbuck J; Saba N; Prior TW; Eng C. "A 39-bp deletion polymorphism in PTEN in African American individuals: implications for molecular diagnostic testing.." The Journal Of Molecular Diagnostics: JMD. Vol. 4, no. 2. (May 2002.): 114
Bennett RL; Hampel HL; Mandell JB; Marks JH. "Genetic counselors: translating genomic science into clinical practice.." The Journal Of Clinical Investigation. Vol. 112, no. 9. (November 2003.): 1274
Zhou XP; Waite KA; Pilarski R; Hampel H; Fernandez MJ; Bos C; Dasouki M; Feldman GL; Greenberg LA; Ivanovich J; Matloff E; Patterson A; Pierpont ME; Russo D; Nassif NT; Eng C. "Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway.." American Journal Of Human Genetics. Vol. 73, no. 2. (August 2003.): 404
Pyatt RE; Nakagawa H; Hampel H; Sedra M; Fuchik MB; Comeras I; de la Chapelle A; Prior TW. "Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2.." Clinical Genetics. Vol. 63, no. 3. (March 2003.): 215
Offit K; Bertagnolli MM; Bombard AT; Come S; Eng C; Garber JE; Joffe S; Greene MH; Tucker MA; Gruber SB; Guillem JG; Robson M; Halberg FE; Hampel H; Olopade OI; Rieger PT; Rodriquez-Bigas MG; Tomlinson G; Watson MS; Weber BL; Weitzel J; Wiesner GL. "American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility." Journal Of Clinical Oncology: Official Journal Of The American Society Of Clinical Oncology. Vol. 21, no. 12. (June 2003.): 2397-2406
McGarrity TJ; Wagner Baker MJ; Ruggiero FM; Thiboutot DM; Hampel H; Zhou XP; Eng C. "GI polyposis and glycogenic acanthosis of the esophagus associated with PTEN mutation positive Cowden syndrome in the absence of cutaneous manifestations.." The American Journal Of Gastroenterology. Vol. 98, no. 6. (June 2003.): 1429
King MC; Marks JH; Mandell JB. "Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2.." Science (New York, N.Y.). Vol. 302, no. 5645. (October 2003.): 643
Nakagawa H; Hampel H; de la Chapelle A. "Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques.." Human Mutation. Vol. 22, no. 3. (September 2003.): 258
Kariola R; Hampel H; Frankel WL; Raevaara TE; de la Chapelle A; Nyström-Lahti M. "MSH6 missense mutations are often associated with no or low cancer susceptibility.." British Journal Of Cancer. Vol. 91, no. 7. (October 2004.): 1287
Nakagawa H; Lockman JC; Frankel WL; Hampel H; Steenblock K; Burgart LJ; Thibodeau SN; de la Chapelle A. "Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation.." Cancer Research. Vol. 64, no. 14. (July 2004.): 4721
Lynch HT; Coronel SM; Okimoto R; Hampel H; Sweet K; Lynch JF; Barrows A; Wijnen J; van der Klift H; Franken P; Wagner A; Fodde R; de la Chapelle A. "A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States.." JAMA: The Journal Of The American Medical Association. Vol. 291, no. 6. (February 2004.): 718
Hampel H; Sweet K; Westman JA; Offit K; Eng C. "Referral for cancer genetics consultation: a review and compilation of risk assessment criteria.." Journal Of Medical Genetics. Vol. 41, no. 2. (February 2004.): 81
Pasche B; Knobloch TJ; Bian Y; Liu J; Phukan S; Rosman D; Kaklamani V; Baddi L; Siddiqui FS; Frankel W; Prior TW; Schuller DE; Agrawal A; Lang J; Dolan ME; Vokes EE; Lane WS; Huang CC; Caldes T; Di Cristofano A; Hampel H; Nilsson I; von Heijne G; Fodde R; Murty VV; de la Chapelle A; Weghorst CM. "Somatic acquisition and signaling of TGFBR1*6A in cancer.." JAMA: The Journal Of The American Medical Association. Vol. 294, no. 13. (October 2005.): 1634
Raevaara TE; Korhonen MK; Lohi H; Hampel H; Lynch E; Lönnqvist KE; Holinski-Feder E; Sutter C; McKinnon W; Duraisamy S; Gerdes AM; Peltomäki P; Kohonen-Ccorish M; Mangold E; Macrae F; Greenblatt M; de la Chapelle A; Nyström M. "Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1.." Gastroenterology. Vol. 129, no. 2. (August 2005.): 537
Hampel H; Frankel WL; Martin E; Arnold M; Khanduja K; Kuebler P; Nakagawa H; Sotamaa K; Prior TW; Westman J; Panescu J; Fix D; Lockman J; Comeras I; de la Chapelle A. "Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).." The New England Journal Of Medicine. Vol. 352, no. 18. (May 2005.): 1851
Hampel H; Stephens JA; Pukkala E; Sankila R; Aaltonen LA; Mecklin JP; de la Chapelle A. "Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset.." Gastroenterology. Vol. 129, no. 2. (August 2005.): 415
Clendenning M; Hampel H; LaJeunesse J; Lindblom A; Lockman J; Nilbert M; Senter L; Sotamaa K; de la Chapelle A. "Long-range PCR facilitates the identification of PMS2-specific mutations.." Human Mutation. Vol. 27, no. 5. (May 2006.): 490
Lynch HT; de la Chapelle A; Hampel H; Wagner A; Fodde R; Lynch JF; Okimoto R; Clark MB; Coronel S; Trowonou A; Fu YX; Haynatzki GR; Gong G. "American founder mutation for Lynch syndrome. Prevalence estimates and implications.." Cancer. Vol. 106, no. 2. (January 2006.): 448
Agnese DM; Hampel H; Farrar WB. "Utilization of genetic counseling services by surgical oncologists: education a must.." Clinical Genetics. Vol. 70, no. 6. (December 2006.): 524
Cohn DE; Frankel WL; Resnick KE; Zanagnolo VL; Copeland LJ; Hampel H; Kelbick N; Morrison CD; Fowler JM. "Improved survival with an intact DNA mismatch repair system in endometrial cancer.." Obstetrics And Gynecology. Vol. 108, no. 5. (November 2006.): 1208
Hampel H; Frankel W; Panescu J; Lockman J; Sotamaa K; Fix D; Comeras I; La Jeunesse J; Nakagawa H; Westman JA; Prior TW; Clendenning M; Penzone P; Lombardi J; Dunn P; Cohn DE; Copeland L; Eaton L; Fowler J; Lewandowski G; Vaccarello L; Bell J; Reid G; de la Chapelle A. "Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.." Cancer Research. Vol. 66, no. 15. (August 2006.): 7810
Yearsley M; Hampel H; Lehman A; Nakagawa H; de la Chapelle A; Frankel WL. "Histologic features distinguish microsatellite-high from microsatellite-low and microsatellite-stable colorectal carcinomas, but do not differentiate germline mutations from methylation of the MLH1 promoter.." Human Pathology. Vol. 37, no. 7. (July 2006.): 831
Ollila S; Sarantaus L; Kariola R; Chan P; Hampel H; Holinski-Feder E; Macrae F; Kohonen-Corish M; Gerdes AM; Peltomäki P; Mangold E; de la Chapelle A; Greenblatt M; Nyström M. "Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein.." Gastroenterology. Vol. 131, no. 5. (November 2006.): 1408
Chen H; Taylor NP; Sotamaa KM; Mutch DG; Powell MA; Schmidt AP; Feng S; Hampel HL; de la Chapelle A; Goodfellow PJ. "Evidence for heritable predisposition to epigenetic silencing of MLH1.." International Journal Of Cancer. Journal International Du Cancer. Vol. 120, no. 8. (April 2007.): 1684
Hampel H; Panescu J; Lockman J; Sotamaa K; Fix D; Comeras I; LaJeunesse J; Nakagawa H; Westman JA; Prior TW; Clendenning M; de la Chapelle A; Frankel W; Penzone P; Cohn DE; Copeland L; Eaton L; Fowler J; Lombardi J; Dunn P; Bell J; Reid G; Lewandowski G; Vaccarello L. "Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients.." Cancer Research. Vol. 67, no. 19. (October 2007.): 9603
Valle L; Serena-Acedo T; Liyanarachchi S; Hampel H; Comeras I; Li Z; Zeng Q; Zhang HT; Pennison MJ; Sadim M; Pasche B; Tanner SM; de la Chapelle A. "Germline allele-specific expression of TGFBR1 confers an increased risk of colorectal cancer.." Science (New York, N.Y.). Vol. 321, no. 5894. (September 2008.): 1361
Clendenning M; Senter L; Hampel H; Robinson KL; Sun S; Buchanan D; Walsh MD; Nilbert M; Green J; Potter J; Lindblom A; de la Chapelle A. "A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome.." Journal Of Medical Genetics. Vol. 45, no. 6. (June 2008.): 340
Cohn DE; Pavelka JC; Frankel WL; Morrison CD; Hampel H; Copeland LJ; Fowler JM. "Correlation between patient weight and defects in DNA mismatch repair: is this the link between an increased risk of previous cancer in thinner women with endometrial cancer?." International Journal Of Gynecological Cancer: Official Journal Of The International Gynecological Cancer Society. Vol. 18, no. 1. (January 2008.): 136
Dai Z; Papp AC; Wang D; Hampel H; Sadee W. "Genotyping panel for assessing response to cancer chemotherapy.." BMC Medical Genomics. Vol. 1, (January 2008.): 24
McClain MR; Palomaki GE; Hampel H; Westman JA; Haddow JE. "Screen positive rates among six family history screening protocols for breast/ovarian cancer in four cohorts of women.." Familial Cancer. Vol. 7, no. 4. (January 2008.): 341
South CD; Hampel H; Comeras I; Westman JA; Frankel WL; de la Chapelle A. "The frequency of Muir-Torre syndrome among Lynch syndrome families.." Journal Of The National Cancer Institute. Vol. 100, no. 4. (February 2008.): 277
Clendenning M; Baze ME; Sun S; Walsh K; Liyanarachchi S; Fix D; Schunemann V; Comeras I; Deacon M; Lynch JF; Gong G; Thomas BC; Thibodeau SN; Lynch HT; Hampel H; de la Chapelle A. "Origins and prevalence of the American Founder Mutation of MSH2.." Cancer Research. Vol. 68, no. 7. (April 2008.): 2145
Senter L; Clendenning M; Sotamaa K; Hampel H; Green J; Potter JD; Lindblom A; Lagerstedt K; Thibodeau SN; Lindor NM; Young J; Winship I; Dowty JG; White DM; Hopper JL; Baglietto L; Jenkins MA; de la Chapelle A. "The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.." Gastroenterology. Vol. 135, no. 2. (August 2008.): 419
Hampel H; Frankel WL; Martin E; Arnold M; Khanduja K; Kuebler P; Clendenning M; Sotamaa K; Prior T; Westman JA; Panescu J; Fix D; Lockman J; LaJeunesse J; Comeras I; de la Chapelle A. "Feasibility of screening for Lynch syndrome among patients with colorectal cancer.." Journal Of Clinical Oncology: Official Journal Of The American Society Of Clinical Oncology. Vol. 26, no. 35. (December 2008.): 5783
Hampel H, Frankel W, de la Chapelle A. "A Reply to LH Jensen et al and S. Jahn et al.." Journal of Clinical Oncology. Vol. 27, no. 34. (January 2009.): E225-E225
Hampel H. "Genetic testing for hereditary colorectal cancer.." Surgical Oncology Clinics Of North America. Vol. 18, no. 4. (October 2009.): 687
Palomaki GE; McClain MR; Melillo S; Hampel HL; Thibodeau SN. "EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome.." Genetics In Medicine: Official Journal Of The American College Of Medical Genetics. Vol. 11, no. 1. (January 2009.): 42
Resnick KE; Hampel H; Fishel R; Cohn DE. "Current and emerging trends in Lynch syndrome identification in women with endometrial cancer.." Gynecologic Oncology. Vol. 114, no. 1. (July 2009.): 128
Hampel H; Grubs RE; Walton CS; Nguyen E; Breidenbach DH; Nettles S; Callanan N; Corliss M; Fox S; Hiraki S; Ku L; Neufeld-Kaiser W; Riley B; Taylor J; Weik L. "Genetic counseling practice analysis.." Journal Of Genetic Counseling. Vol. 18, no. 3. (June 2009.): 205
Backes FJ; Leon ME; Ivanov I; Suarez A; Frankel WL; Hampel H; Fowler JM; Copeland LJ; O'Malley DM; Cohn DE. "Prospective evaluation of DNA mismatch repair protein expression in primary endometrial cancer.." Gynecologic Oncology. Vol. 114, no. 3. (September 2009.): 486
Resnick K; Straughn JM Jr; Backes F; Hampel H; Matthews KS; Cohn DE. "Lynch syndrome screening strategies among newly diagnosed endometrial cancer patients.." Obstetrics And Gynecology. Vol. 114, no. 3. (September 2009.): 530
de la Chapelle A; Palomaki G; Hampel H. "Identifying Lynch syndrome.." International Journal Of Cancer. Journal International Du Cancer. Vol. 125, no. 6. (September 2009.): 1492
Hampel H. "Recontacting patients who have tested negative for BRCA1 and BRCA2 mutations: how, who and why?." Journal Of Genetic Counseling. Vol. 18, no. 6. (December 2009.): 527
South,Christopher,D; Yearsley,Martha; Martin,Edward; Arnold,Mark; Frankel,Wendy; Hampel,Heather. "Immunohistochemistry staining for the mismatch repair proteins in the clinical care of patients with colorectal cancer." GENETICS IN MEDICINE. Vol. 11, no. 11. (November 2009.): 812-817
Backes,Floor,J; Hampel,Heather; Backes,Katherine,A; Vaccarello,Luis; Lewandowski,George; Bell,Jeffrey,A; Reid,Gary,C; Copeland,Larry,J; Fowler,Jeffrey,M; Cohn,David,E. "Are prediction models for Lynch syndrome valid for probands with endometrial cancer?." Familial Cancer. Vol. 8, no. 4. (December 2009.): 483-487
Buchanan,Daniel,D; Sweet,Kevin; Drini,Musa; Jenkins,Mark,A; Win,Aung,Ko; Gattas,Michael; Walsh,Michael,D; Clendenning,Mark; McKeone,Diane; Walters,Rhiannon; Roberts,Aedan; Young,Alasdair; Hampel,Heather; Hopper,John,L; Goldblatt,Jack; George,Jill; Suthers,Graeme,K; Phillips,Kerry; Young,Graeme,P; Chow,Elizabeth; Parry,Susan; Woodall,Sonja; Tucker,Kathy; Muir,Amanda; Field,Michael; Greening,Sian; Gallinger,Steven; Green,Jane; Woods,Michael,O; Spaetgens,Renee; De la Chapelle,Albert; Macrae,Finlay; Walker,Neal,I; Jass,Jeremy,R; Young,Joanne,P. "Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study." INTERNATIONAL JOURNAL OF COLORECTAL DISEASE. Vol. 25, no. 6. (June 2010.): 703-712
Baglietto,Laura; Lindor,Noralane,M; Dowty,James,G; White,Darren,M; Wagner,Anja; Garcia,Encarna,BGomez; Vriends,Annette,HJT; Cartwright,Nicola,R; Barnetson,Rebecca,A; Farrington,Susan,M; Tenesa,Albert; Hampel,Heather; Buchanan,Daniel; Arnold,Sven; Young,Joanne; Walsh,Michael,D; Jass,Jeremy; Macrae,Finlay; Antill,Yoland; Winship,Ingrid,M; Giles,Graham,G; Goldblatt,Jack; Parry,Susan; Suthers,Graeme; Leggett,Barbara; Butz,Malinda; Aronson,Melyssa; Poynter,Jenny,N; Baron,John,A; Le Marchand,Loic; Haile,Robert; Gallinger,Steve; Hopper,John,L; Potter,John; De la Chapelle,Albert; Vasen,Hans,F; Dunlop,Malcolm,G; Thibodeau,Stephen,N; Jenkins,Mark,A. "Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers." Journal Of The National Cancer Institute. Vol. 102, no. 3. (February 2010.): 193-201
Hampel,Heather. "Point: justification for Lynch syndrome screening among all patients with newly diagnosed colorectal cancer." JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK. Vol. 8, no. 5. (May 2010.): 597-601
Daly MB, Axilbund JE, Buys S, Crawford B, Farrell CD, Friedman S, Garger JE, Goorha S, Gruber SB, Hampel H, Kaklamani V, Kohlmann W, Kurian A, Litton J, Marcom PK, Nussbaum R, Offit K, Pal T, Pasche B, Pilarski R, Reiser G, Shannon KM, Smith JR, Swisher E, Weitzel JN. "Genetic/familial high-risk assessment: breast and ovarian.." Journal of the National Comprehensive Cancer Network. Vol. 8, no. 5. (May 2010.): 562-594
de la Chapelle,Albert; Hampel,Heather. "Clinical relevance of microsatellite instability in colorectal cancer." JOURNAL OF CLINICAL ONCOLOGY. Vol. 28, no. 20. (July 2010.): 3380-3387
Tomsic J, Guda K, Liyanarachchi S, Hampel H, Natale L, Markowitz SD, Tanner SM, de la Chapelle A.. "Allele-specific expression of TGFRBR1 in colon cancer patients.." Carcinogenesis. Vol. 31, no. 10. (August 2010.): 1800-1804
Mvundura,Mercy; Grosse,Scott,D; Hampel,Heather; Palomaki,Glenn,E. "The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer." GENETICS IN MEDICINE. Vol. 12, no. 2. (February 2010.): 93-104
Backes,Floor,J; Mitchell,Elizabeth; Hampel,Heather; Cohn,David,E. "Endometrial cancer patients and compliance with genetic counseling: Room for improvement." GYNECOLOGIC ONCOLOGY. Vol. 123, no. 3. (December 2011.): 532-536
Hampel H, de la Chapelle A. "The search for unaffected individuals with Lynch syndrome: Do the ends justify the means?." Cancer Prevention Research. Vol. 4, (January 2011.): 1-5
Stuenkel,Aaron,J; Campion,Maryann; Allain,Dawn; Hampel,Heather. "Transition to the clinical doctorate: attitudes of the genetic counseling training program directors in North America.." Journal of genetic counseling. Vol. 21, no. 1. (February 2012.): 136-149
Gerber,Madelyn,M; Hampel,Heather; Schulz,Nathan,P; Fernandez,Soledad; Wei,Lai; Zhou,Xiao-Ping; De la Chapelle,Albert; Toland,Amanda,Ewart. "Evaluation of Allele-Specific Somatic Changes of Genome-Wide Association Study Susceptibility Alleles in Human Colorectal Cancers." PLOS ONE. Vol. 7, no. 5. (May 2012.): e37672
Tomsic,Jerneja; Liyanarachchi,Sandya; Hampel,Heather; Morak,Monika; Thomas,Brittany,C; Raymond,Victoria,M; Chittenden,Anu; Schackert,Hans,K; Gruber,Stephen,B; Syngal,Sapna; Viel,Alessandra; Holinski-Feder,Elke; Thibodeau,Stephen,N; de la Chapelle,Albert. "An American founder mutation in MLH1." INTERNATIONAL JOURNAL OF CANCER. Vol. 130, no. 9. (May 2012.): 2088-2095
Hampel,Heather; De la Chapelle,Albert. "How do we approach the goal of identifying everybody with Lynch Syndrome?." Familial cancer. Vol. 12, no. 2. (June 2013.): 313-317