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

No evidence of EMAST in whole genome sequencing data from 248 colorectal cancers

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

Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

Sex differences in oncogenic mutational processes

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

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

Retraction: A TARBP2 mutation in human cancer impairs microRNA processing and DICER1 function

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