<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Vasen H | Seppälä Lab</title><link>https://www.seppalalab.org/author/vasen-h/</link><atom:link href="https://www.seppalalab.org/author/vasen-h/index.xml" rel="self" type="application/rss+xml"/><description>Vasen H</description><generator>Hugo Blox Builder (https://hugoblox.com)</generator><language>en</language><lastBuildDate>Fri, 01 Jan 2021 00:00:00 +0000</lastBuildDate><image><url>https://www.seppalalab.org/media/logo_hu_e3f0d28ad302f75b.png</url><title>Vasen H</title><link>https://www.seppalalab.org/author/vasen-h/</link></image><item><title>Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report</title><link>https://www.seppalalab.org/publication/dominguez-valentin-2021-risk-reducing/</link><pubDate>Fri, 01 Jan 2021 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/dominguez-valentin-2021-risk-reducing/</guid><description/></item><item><title>The "unnatural" history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance</title><link>https://www.seppalalab.org/publication/ahadova-2021-the/</link><pubDate>Fri, 01 Jan 2021 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/ahadova-2021-the/</guid><description/></item><item><title>Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report</title><link>https://www.seppalalab.org/publication/seppala-2021-uptake/</link><pubDate>Fri, 01 Jan 2021 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/seppala-2021-uptake/</guid><description/></item><item><title>Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database</title><link>https://www.seppalalab.org/publication/dominguez-valentin-2020-cancer/</link><pubDate>Wed, 01 Jan 2020 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/dominguez-valentin-2020-cancer/</guid><description/></item><item><title>Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database</title><link>https://www.seppalalab.org/publication/dominguez-valentin-2020-correction/</link><pubDate>Wed, 01 Jan 2020 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/dominguez-valentin-2020-correction/</guid><description/></item><item><title>Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report</title><link>https://www.seppalalab.org/publication/seppala-2019-lack/</link><pubDate>Tue, 01 Jan 2019 00:00:00 +0000</pubDate><guid>https://www.seppalalab.org/publication/seppala-2019-lack/</guid><description/></item></channel></rss>