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Genetic testing for cancer predispositionENG, Charis; HAMPEL, Heather; DE LA CHAPELLE, Albert et al.Annual review of medicine. 2001, Vol 52, pp 371-400, issn 0066-4219Article

Lynch Syndrome Screening Strategies Among Newly Diagnosed Endometrial Cancer PatientsRESNICK, Kimberly; STRAUGHN, J. Michael; BACKES, Floor et al.Obstetrics and gynecology (New York. 1953). 2009, Vol 114, Num 3, pp 530-536, issn 0029-7844, 7 p.Article

Screening for lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patientsHAMPEL, Heather; FRANKEL, Wendy; PRIOR, Thomas W et al.Cancer research (Baltimore). 2006, Vol 66, Num 15, pp 7810-7817, issn 0008-5472, 8 p.Article

Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic studyBUCHANAN, Daniel D; SWEET, Kevin; ROBERTS, Aedan et al.International journal of colorectal disease (Print). 2010, Vol 25, Num 6, pp 703-712, issn 0179-1958, 10 p.Article

Risks of Lynch Syndrome Cancers for MSH6 Mutation CarriersBAGLIETTO, Laura; LINDOR, Noralane M; TENESA, Albert et al.Journal of the National Cancer Institute. 2010, Vol 102, Num 3, pp 193-201, issn 0027-8874, 9 p.Article

American founder mutation for lynch syndrome : Prevalence estimates and implicationsLYNCH, Henry T; DE LA CHAPELLE, Albert; FU, Yun-Xin et al.Cancer. 2006, Vol 106, Num 2, pp 448-452, issn 0008-543X, 5 p.Article

Improved survival with an intact DNA mismatch repair system in endometrial cancerCOHN, David E; FRANKEL, Wendy L; RESNICK, Kimberly E et al.Obstetrics and gynecology (New York. 1953). 2006, Vol 108, Num 5, pp 1208-1215, issn 0029-7844, 8 p.Article

Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of cowden and Bannayan-Riley-Ruvalcaba syndromesZHOU, Xiao-Ping; WOODFORD-RICHENS, Kelly; BODMER, Walter F et al.American journal of human genetics. 2001, Vol 69, Num 4, pp 704-711, issn 0002-9297Article

Allele-specific expression of TGFBR1 in colon cancer patientsTOMSIC, Jerneja; GUDA, Kishore; LIYANARACHCHI, Sandya et al.Carcinogenesis (New York. Print). 2010, Vol 31, Num 10, pp 1800-1804, issn 0143-3334, 5 p.Article

Feasibility of Screening for Lynch Syndrome Among Patients With Colorectal CancerHAMPEL, Heather; FRANKEL, Wendy L; PANESCU, Jenny et al.Journal of clinical oncology. 2008, Vol 26, Num 35, pp 5783-5788, issn 0732-183X, 6 p.Article

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 pathwayZHOU, Xiao-Ping; WAITE, Kristin A; MATLOFF, Ellen et al.American journal of human genetics. 2003, Vol 73, Num 2, pp 404-411, issn 0002-9297, 8 p.Article

Allele separation facilitates interpretation of potential splicing alterations and genomic rearrangementsNAKAGAWA, Hidewaki; HAI YAN; LOCKMAN, Janet et al.Cancer research (Baltimore). 2002, Vol 62, Num 16, pp 4579-4582, issn 0008-5472Article

Epigenetic PTEN silencing in malignant melanomas without PTEN mutationZHOU, Xiao-Ping; GIMM, Oliver; HAMPEL, Heather et al.The American journal of pathology. 2000, Vol 157, Num 4, pp 1123-1128, issn 0002-9440Article

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Somatic acquisition and signaling of TGFBR1*6A in cancerPASCHE, Boris; KNOBLOCH, Thomas J; PRIOR, Thomas W et al.JAMA, the journal of the American Medical Association. 2005, Vol 294, Num 13, pp 1634-1646, issn 0098-7484, 13 p.Article

A founder mutation of the MSH2 gene and Hereditary nonpolyposis colorectal cancer in the United StatesLYNCH, Henry T; CORONEL, Stephanie M; WAGNER, Anja et al.JAMA, the journal of the American Medical Association. 2004, Vol 291, Num 6, pp 718-724, issn 0098-7484, 7 p.Article

Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromesZHOU, Xiao-Ping; HAMPEL, Heather; THIELE, Hannelore et al.Lancet (British edition). 2001, Vol 358, Num 9277, pp 210-211, issn 0140-6736Article

Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinomaCHADWICK, Robert B; PYATT, Robert E; NIEMANN, Theodore H et al.Journal of medical genetics. 2001, Vol 38, Num 7, pp 461-466, issn 0022-2593Article

An American founder mutation in MLH1TOMSIC, Jerneja; LIYANARACHCHI, Sandya; VIEL, Alessandra et al.International journal of cancer (Print). 2012, Vol 130, Num 9, pp 2088-2095, issn 0020-7136, 8 p.Article

Identification of Lynch Syndrome Among Patients With Colorectal CancerMOREIRA, Leticia; BALAGUER, Francesc; HAILE, Robert et al.JAMA, the journal of the American Medical Association. 2012, Vol 308, Num 15, pp 1555-1565, issn 0098-7484, 11 p.Article

Germline Allele-Specific Expression of TGFBR1 Confers an Increased Risk of Colorectal CancerVALLE, Laura; SERENA-ACEDO, Tarsicio; PASCHE, Boris et al.Science (Washington, D.C.). 2008, Vol 321, Num 5894, pp 1361-1365, issn 0036-8075, 5 p.Article

Origins and Prevalence of the American Founder Mutation of MSH2CLENDENNING, Mark; BAZE, Mark E; GONG, Gordon et al.Cancer research (Baltimore). 2008, Vol 68, Num 7, pp 2145-2153, issn 0008-5472, 9 p.Article

The Frequency of Muir-Torre Syndrome Among Lynch Syndrome FamiliesSOUTH, Christopher D; HAMPEL, Heather; CORNERAS, Ilene et al.Journal of the National Cancer Institute. 2008, Vol 100, Num 4, pp 277-281, issn 0027-8874, 5 p.Article

Histologic features distinguish microsatellite-high from microsatellite-low and microsatellite-stable colorectal carcinomas, but do not differentiate germline mutations from methylation of the MLH1 promoterYEARSLEY, Martha; HAMPEL, Heather; LEHMAN, Amy et al.Human pathology. 2006, Vol 37, Num 7, pp 831-838, issn 0046-8177, 8 p.Article