Riku Katainen
Helsinki, Finland
Last Updated: 09/26/2026
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Found 44 publications
Large-scale analysis of chromosomal aberrations in uterine leiomyoma.
Journal: American journal of obstetrics and gynecology
Published: June 13, 2025
Activation of FGFR genes by genetic and epigenetic alterations in uterine leiomyomas.
Journal: BJC reports
Published: September 04, 2024
Lynch syndrome-associated and sporadic microsatellite unstable colorectal cancers: different patterns of clonal evolution yield highly similar tumours.
Journal: Human molecular genetics
Published: April 08, 2024
Genome-wide somatic mutation analysis of sinonasal adenocarcinoma with and without wood dust exposure.
Journal: Genes and environment : the official journal of the Japanese Environmental Mutagen Society
Published: January 26, 2024
Previously reported CCDC26 risk variant and novel germline variants in GALNT13, AR, and MYO10 associated with familial glioma in Finland.
Journal: Scientific reports
Published: December 21, 2023
APOBEC mutagenesis is a common process in normal human small intestine.
Journal: Nature genetics
Published: May 08, 2022
Next-generation sequencing in a large pedigree segregating visceral artery aneurysms suggests potential role of COL4A1/COL4A2 in disease etiology.
Journal: Vascular
Published: July 20, 2021
Exome sequencing reveals candidate mutations implicated in sinonasal carcinoma and malignant transformation of sinonasal inverted papilloma.
Journal: Oral oncology
Published: June 24, 2021
WNT2 activation through proximal germline deletion predisposes to small intestinal neuroendocrine tumors and intestinal adenocarcinomas.
Journal: Human molecular genetics
Published: April 23, 2021
Last Updated: 09/26/2026