H Järvinen

发表

LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

L. Aaltonen, K. Aittomäki, I. Tomlinson, 2005, Journal of Medical Genetics.

The C/C−13910 genotype of adult-type hypolactasia is associated with an increased risk of colorectal cancer in the Finnish population

I Tomlinson, L. Aaltonen, R. Houlston, 2005, Gut.

Hereditary Nonpolyposis Colorectal Cancer Patients Replication Errors in Benign and Malignant Tumors from

H T Lynch, K. Kinzler, B. Vogelstein, 2006 .

Gene expression signatures for colorectal cancer microsatellite status and HNPCC

T. Ørntoft, L. Aaltonen, D. Arango, 2005, British Journal of Cancer.

No evidence for dual role of loss of heterozygosity in hereditary non-polyposis colorectal cancer

L. Aaltonen, J. Mecklin, H. Järvinen, 2007, Oncogene.

Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease.

L. Aaltonen, R. Chadwick, A. de la Chapelle, 1998, The New England journal of medicine.

Genetic mapping of a locus predisposing to human colorectal cancer.

J. Weber, B. Vogelstein, L. Aaltonen, 1993, Science.

Serrated carcinomas form a subclass of colorectal cancer with distinct molecular basis

L. Aaltonen, D. Arango, S. Vanharanta, 2007, Oncogene.

Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes.

W F Bodmer, P Rozen, L. Aaltonen, 2001, American journal of human genetics.