<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Peltomaki P | Seppälä Lab</title><link>https://www.seppalalab.org/author/peltomaki-p/</link><atom:link href="https://www.seppalalab.org/author/peltomaki-p/index.xml" rel="self" type="application/rss+xml"/><description>Peltomaki P</description><generator>Hugo Blox Builder (https://hugoblox.com)</generator><language>en</language><lastBuildDate>Thu, 01 Jan 2026 00:00:00 +0000</lastBuildDate><image><url>https://www.seppalalab.org/media/logo_hu_e3f0d28ad302f75b.png</url><title>Peltomaki P</title><link>https://www.seppalalab.org/author/peltomaki-p/</link></image><item><title>MLH1 Lynch Syndrome Colorectal Cancers Are Driven by Heterogeneous Wnt Pathway Gene Mutations</title><link>https://www.seppalalab.org/publication/hokkanen-2026-mlh1/</link><pubDate>Thu, 01 Jan 2026 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/hokkanen-2026-mlh1/</guid><description/></item><item><title>Genome-wide DNA methylation profiles of colorectal tumors in Lynch syndrome and familial adenomatous polyposis</title><link>https://www.seppalalab.org/publication/maki-nevala-2025-genome-wide/</link><pubDate>Wed, 01 Jan 2025 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/maki-nevala-2025-genome-wide/</guid><description/></item><item><title>Detection of a major Lynch Syndrome-causing MLH1 founder variant in a large-scale genotyped cohort</title><link>https://www.seppalalab.org/publication/sipila-2024-detection/</link><pubDate>Mon, 01 Jan 2024 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/sipila-2024-detection/</guid><description/></item><item><title>Lynch Syndrome Genetics and Clinical Implications</title><link>https://www.seppalalab.org/publication/peltomaki-2023-lynch/</link><pubDate>Sun, 01 Jan 2023 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/peltomaki-2023-lynch/</guid><description/></item><item><title>Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database</title><link>https://www.seppalalab.org/publication/dominguez-valentin-2023-mortality/</link><pubDate>Sun, 01 Jan 2023 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/dominguez-valentin-2023-mortality/</guid><description/></item><item><title>Tumor-independent Detection of Inherited Mismatch Repair Deficiency for the Diagnosis of Lynch Syndrome with High Specificity and Sensitivity</title><link>https://www.seppalalab.org/publication/kansikas-2023-tumor-independent/</link><pubDate>Sun, 01 Jan 2023 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/kansikas-2023-tumor-independent/</guid><description/></item><item><title>Body Weight, Physical Activity, and Risk of Cancer in Lynch Syndrome</title><link>https://www.seppalalab.org/publication/sievanen-2021-body/</link><pubDate>Fri, 01 Jan 2021 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/sievanen-2021-body/</guid><description/></item><item><title>Immunoprofiles and DNA Methylation of Inflammatory Marker Genes in Ulcerative Colitis-Associated Colorectal Tumorigenesis</title><link>https://www.seppalalab.org/publication/maki-nevala-2021-immunoprofiles/</link><pubDate>Fri, 01 Jan 2021 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/maki-nevala-2021-immunoprofiles/</guid><description/></item><item><title>No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study</title><link>https://www.seppalalab.org/publication/dominguez-valentin-2021-no/</link><pubDate>Fri, 01 Jan 2021 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/dominguez-valentin-2021-no/</guid><description/></item><item><title>Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome</title><link>https://www.seppalalab.org/publication/engel-2020-associations/</link><pubDate>Wed, 01 Jan 2020 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/engel-2020-associations/</guid><description/></item><item><title>Epidemiological, clinical and molecular characterization of Lynch-like syndrome: A population-based study</title><link>https://www.seppalalab.org/publication/porkka-2019-epidemiological/</link><pubDate>Tue, 01 Jan 2019 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/porkka-2019-epidemiological/</guid><description/></item></channel></rss>