Terkko Navigator / Aaltonen, L(auri) A.*

Lack of an association between gallstone disease and bilirubin levels with risk of colorectal cancer: a Mendelian randomisation analysis.

Prognostic Value of Immune Environment Analysis in Small Bowel Adenocarcinomas with Verified Mutational Landscape and Predisposing Conditions.

Colibactin DNA-damage signature indicates mutational impact in colorectal cancer.

Pan-cancer analysis of whole genomes.

Mutational processes of distinct POLE exonuclease domain mutants drive an enrichment of a specific TP53 mutation in colorectal cancer.

Modifiable pathways for colorectal cancer: a mendelian randomisation analysis.

Candidate Predisposition Variants in Kaposi Sarcoma as Detected by Whole-Genome Sequencing.

Genetic and epigenetic characterization of growth hormone - secreting pituitary tumors.

Retrotransposon insertions can initiate colorectal cancer and are associated with poor survival.

Association analyses identify 31 new risk loci for colorectal cancer susceptibility.

Exome and immune cell score analyses reveal great variation within synchronous primary colorectal cancers.

Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans.

Discovery of potential causative mutations in human coding and noncoding genome with the interactive software BasePlayer.

Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stability.

Contribution of allelic imbalance to colorectal cancer.

Comprehensive evaluation of coding region point mutations in microsatellite-unstable colorectal cancer.

Candidate susceptibility variants in angioimmunoblastic T-cell lymphoma.

Germline mutations in young non-smoking women with lung adenocarcinoma.

Exome-wide somatic mutation characterization of small bowel adenocarcinoma.

Oncogenic exon 2 mutations in Mediator subunit MED12 disrupt allosteric activation of Cyclin C-CDK8/19.

Detection of subclonal L1 transductions in colorectal cancer by long-distance inverse-PCR and Nanopore sequencing.

Global metabolomic profiling of uterine leiomyomas.

Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci.

Germline MSH6 Mutation in a Patient With Two Independent Primary Glioblastomas.

Pro-inflammatory fatty acid profile and colorectal cancer risk: A Mendelian randomisation analysis.

Comprehensive evaluation of protein coding mononucleotide microsatellites in microsatellite-unstable colorectal cancer.

Multiple clinical characteristics separate MED12-mutation-positive and -negative uterine leiomyomas.

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera.

Multiple components of PKA and TGF-β pathways are mutated in pseudomyxoma peritonei.

Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer.

Candidate susceptibility variants for esophageal squamous cell carcinoma.

Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.

Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer.

MED12 mutations and FH inactivation are mutually exclusive in uterine leiomyomas.

Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.

Integrated data analysis reveals uterine leiomyoma subtypes with distinct driver pathways and biomarkers.

Whole-Genome Sequencing of Growth Hormone (GH) - secreting Pituitary Adenomas.

CTCF/cohesin-binding sites are frequently mutated in cancer.

Clonally related uterine leiomyomas are common and display branched tumor evolution.

3'-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity.

Systematic search for rare variants in Finnish early-onset colorectal cancer patients.

Identification of homozygous deletion in ACAN and other candidate variants in familial classical Hodgkin lymphoma by exome sequencing.

Exome sequencing reveals three novel candidate predisposition genes for diffuse gastric cancer.

Whole genome sequencing identifies STAT4 as a putative susceptibility gene in classic Kaposi sarcoma.

Genomic profile of pseudomyxoma peritonei analyzed using next-generation sequencing and immunohistochemistry.

New Target Genes in Endometrial Tumors Show a Role for the Estrogen-Receptor Pathway in Microsatellite Unstable Cancers.

High Frequency of RPL22 Mutations in Microsatellite-Unstable Colorectal and Endometrial Tumours.

Identification of 33 candidate oncogenes by screening for base-specific mutations.

MED12 mutation frequency in unselected sporadic uterine leiomyomas.

Genomics of uterine leiomyomas: insights from high-throughput sequencing.