Lauri J. Sipila
Helsinki, Finland
Last Updated: 09/26/2026
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Found 11 publications
Cancer incidence following non-neoplastic medical conditions: a prospective population-based cohort study.
Journal: Acta oncologica (Stockholm, Sweden)
Published: May 17, 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
Detection of a major Lynch Syndrome-causing MLH1 founder variant in a large-scale genotyped cohort.
Journal: Familial cancer
Published: January 19, 2024
Sex-specific familial aggregation of cancers in Finland.
Journal: Scientific reports
Published: June 20, 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
WNT2 activation through proximal germline deletion predisposes to small intestinal neuroendocrine tumors and intestinal adenocarcinomas.
Journal: Human molecular genetics
Published: April 23, 2021
Parity associates with chromosomal damage in uterine leiomyomas.
Journal: Nature communications
Published: January 27, 2020
Candidate Predisposition Variants in Kaposi Sarcoma as Detected by Whole-Genome Sequencing.
Journal: Open forum infectious diseases
Published: May 23, 2019
Candidate susceptibility variants in angioimmunoblastic T-cell lymphoma.
Journal: Familial cancer
Published: August 12, 2018
Germline mutations in young non-smoking women with lung adenocarcinoma.
Journal: Lung cancer (Amsterdam, Netherlands)
Published: December 19, 2017
Potential role of a navigator gene NAV3 in colorectal cancer.
Journal: British journal of cancer
Published: December 17, 2011
Showing 1-11 of 11
Last Updated: 09/26/2026