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Cancer Research|June 3, 2005
Mutations in two short noncoding mononucleotide repeats in most microsatellite-unstable colorectal cancersTuija Hienonen, Heli Sammalkorpi, Susa Enholm, et al.
Oncogene|April 11, 2003
Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excess of allelic imbalance in chromosome 20q in familial casesPäivi Laiho, Tuija Hienonen, Auli Karhu, et al.
Blood|May 13, 2011
Exome sequencing reveals germline NPAT mutation as a candidate risk factor for Hodgkin lymphomaSilva Saarinen, Mervi Aavikko, Kristiina Aittomäki, et al.
Science (New York, N.Y.)|August 27, 2011
MED12, the mediator complex subunit 12 gene, is mutated at high frequency in uterine leiomyomasNetta Mäkinen, Miika Mehine, Jaana Tolvanen, et al.
Cancer Research|January 9, 2003
EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancerShantie Jagmohan-Changur, Taija Poikonen, Susa Vilkki, et al.
Genes, Chromosomes & Cancer|April 18, 2009
Array comparative genomic hybridization identifies a distinct DNA copy number profile in renal cell cancer associated with hereditary leiomyomatosis and renal cell cancerTaru A Koski, Heli J Lehtonen, Kowan J Jee, et al.
Molecular Cancer Research : MCR|June 17, 2010
Mutations in the circadian gene CLOCK in colorectal cancerPia Alhopuro, Mikael Björklund, Heli Sammalkorpi, et al.
Familial Cancer|January 22, 2010
No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndromePia Vahteristo, Taru A Koski, Laura Näätsaari, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2007
Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutationsMarianthi Georgitsi, Anniina Raitila, Auli Karhu, et al.
The American Journal of Pathology|December 26, 2003
Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumorsRainer Lehtonen, Maija Kiuru, Sakari Vanharanta, et al.
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