Microsatellite instabilityDE LA CHAPELLE, Albert.The New England journal of medicine. 2003, Vol 349, Num 3, pp 209-210, issn 0028-4793, 2 p.Article

Inherited human diseases: Victories challenges, disappointmentsDE LA CHAPELLE, Albert.American journal of human genetics. 2003, Vol 72, Num 2, pp 236-240, issn 0002-9297, 5 p.Conference Paper

Clinical Relevance of Microsatellite Instability in Colorectal CancerDE LA CHAPELLE, Albert; HAMPEL, Heather.Journal of clinical oncology. 2010, Vol 28, Num 20, pp 3380-3387, issn 0732-183X, 8 p.Article

MicroRNAs in Thyroid CancerDE LA CHAPELLE, Albert; JAZDZEWSKI, Krystian.The Journal of clinical endocrinology and metabolism. 2011, Vol 96, Num 11, pp 3326-3336, issn 0021-972X, 11 p.Article

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

Hereditary colorectal cancerLYNCH, Henry T; DE LA CHAPELLE, Albert.The New England journal of medicine. 2003, Vol 348, Num 10, pp 919-932, issn 0028-4793, 14 p.Article

Israël, son serviteur (lk 1,54) = Israel, his servant (Lk 1 : 54)CHAPELLE, Albert.Nouvelle revue théologique. 2003, Vol 125, Num 2, pp 177-186, issn 0029-4845, 10 p.Article

Le clonage d'êtres humains = The cloning of human beingsCHAPELLE, Albert.Nouvelle revue théologique. 2001, Vol 123, Num 1, pp 27-45, issn 0029-4845Article

Le péché, offense de Dieu, et l'immutabilité divineCHAPELLE, Albert.Nouvelle revue théologique. 2009, Vol 131, Num 1, pp 87-99, issn 0029-4845, 13 p.Article

Mystiques et mystère chez le P. J. Maréchal = Mystics and Mystery in J. MaréchalCHAPELLE, Albert.Nouvelle revue théologique. 2000, Vol 122, Num 4, pp 547-554, issn 0029-4845Article

Hypermethylation, but not LOH, is associated with the low expression of MT1G and CRABP1 in papillary thyroid carcinomaHUANG, Ying; DE LA CHAPELLE, Albert; PELLEGATA, Natalia S et al.International journal of cancer. 2003, Vol 104, Num 6, pp 735-744, issn 0020-7136, 10 p.Article

Molecular profiling of chronic lymphocytic leukaemia : genetics meets epigenetics to identify predisposing genesPLASS, Christoph; BYRD, John C; RAVAL, Aparna et al.British journal of haematology. 2007, Vol 139, Num 5, pp 744-752, issn 0007-1048, 9 p.Article

Identification of a novel noncoding RNA gene, NAMA, that is downregulated in papillary thyroid carcinoma with BRAF mutation and associated with growth arrestYOON, Heejei; HUILING HE; NAGY, Rebecca et al.International journal of cancer. 2007, Vol 121, Num 4, pp 767-775, issn 0020-7136, 9 p.Article

Role of cancer-associated stromal fibroblasts in metastatic colon cancer to the liver and their expression profilesNAKAGAWA, Hidewaki; LIYANARACHCHI, Sandya; DAVULURI, Ramana V et al.Oncogene (Basingstoke). 2004, Vol 23, Num 44, pp 7366-7377, issn 0950-9232, 12 p.Article

Age-related hypermethylation of the 5' region of MLH1 in normal colonic mucosa is associated with microsatellite-unstable colorectal cancer development¹NAKAGAWA, Hidewaki; NUOVO, Gerard J; ZERVOS, Emmanuel E et al.Cancer research (Baltimore). 2001, Vol 61, Num 19, pp 6991-6995, issn 0008-5472Article

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

Homozygous AMN mutation in hereditary selective intestinal malabsorption of vitamin B12 in JordanAL-ALAMI, Jamil R; TANNER, Stephan M; TAYEH, Marwan K et al.Saudi medical journal. 2005, Vol 26, Num 7, pp 1061-1064, issn 0379-5284, 4 p.Article

p53 Codon 72 and MDM2 SNP309 polymorphisms and age of colorectal cancer onset in Lynch syndromeSOTAMAA, Kaisa; LIYANARACHCHI, Sandya; MECKLIN, Jukka-Pekka et al.Clinical cancer research. 2005, Vol 11, Num 19, pp 6840-6844, issn 1078-0432, 5 p., 1Article

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

A Susceptibility Locus for Papillary Thyroid Carcinoma on Chromosome 8q24HUILING HE; NAGY, Rebecca; LIYANARACHCHI, Sandya et al.Cancer research (Chicago, Ill.). 2009, Vol 69, Num 2, pp 625-631, issn 0008-5472, 7 p.Article

Is the disruption of an N-myristoyltransferase (NMT2) associated with hypoplastic testes?QUINTERO-RIVERA, Fabiola; LEACH, Natalia T; DE LA CHAPELLE, Albert et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 15, pp 1796-1798, issn 1552-4825, 3 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

miR-3151 interplays with its host gene BAALC and independently affects outcome of patients with cytogenetically normal acute myeloid leukemiaEISFELD, Ann-Kathrin; MARCUCCI, Guido; MENDLER, Jason H et al.Blood. 2012, Vol 120, Num 2, pp 249-258, issn 0006-4971, 10 p.Article

Differential gene expression in patients genetically predisposed to pancreatic cancerZERVOS, Emmanuel E; TANNER, Stephan M; OSBORNE, Dana A et al.The Journal of surgical research. 2006, Vol 135, Num 2, pp 317-322, issn 0022-4804, 6 p.Article