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    <title>PuSH - HMGU Publikationen</title>
    <link>https://push-zb.helmholtz-munich.de</link>
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    PuSH - Publikationen-Server des Helmholtz Zentrums München
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    <language>de-de</language>

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      <title><![CDATA[Krey-Grauert, I.* ; Ferro, I.F. &amp; Wagner, M. Antisense oligonucleotide therapies for monogenic disorders. Med. Genet. 37, 179-187 (2025)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75249&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75249&amp;la=de</guid>
      <pubDate>Tue, 29 Jul 2025 00:00:00 +0000</pubDate>
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      <title><![CDATA[Florian, K.* et al. Quality assurance within the context of genome diagnostics (a german perspective). Med. Genet. 35, 91-104 (2023)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68504&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68504&amp;la=de</guid>
      <pubDate>Fri, 08 Dec 2023 00:00:00 +0000</pubDate>
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    <item>
      <title><![CDATA[Wahida, A. &amp; Buschhorn, L.* Liquid biopsies and those three little words: Finding the perfect match for the MTB. Med. Genet. 35, 269-273 (2023)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=69084&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=69084&amp;la=de</guid>
      <pubDate>Wed, 10 Jan 2024 00:00:00 +0000</pubDate>
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    <item>
      <title><![CDATA[Sanin, V.* et al. Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: Design of the VRONI study. Med. Genet. 34, 41-51 (2022)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65043&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65043&amp;la=de</guid>
      <pubDate>Wed, 29 Jun 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Prokisch, H. Molecular diagnostics of Mendelian disorders via combined DNA and RNA sequencing. Med. Genet. 31, 191-197 (2019)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56852&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56852&amp;la=de</guid>
      <pubDate>Tue, 24 Sep 2019 00:00:00 +0000</pubDate>
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      <title><![CDATA[Prokisch, H. ; Sperl, W.* ; Meitinger, T. &amp; Mayr, J.A.* Mitochondriopathien – neue Trends in Diagnostik und Therapie. Med. Genet. 27, 282-287 (2015)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46825&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46825&amp;la=de</guid>
      <pubDate>Thu, 24 Sep 2015 00:00:00 +0000</pubDate>
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      <title><![CDATA[Bettecken, T.* et al. Next Generation Sequencing in der diagnostischen Praxis. Med. Genet. 26, 21-27 (2014)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42778&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42778&amp;la=de</guid>
      <pubDate>Tue, 18 Nov 2014 00:00:00 +0000</pubDate>
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      <title><![CDATA[Rogowski, W.H. Public and Professional Policy Committee der ESHG: Aktivitäten zur Priorisierung genetischer Tests. Med. Genet. 26, 48 (2014)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=32060&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=32060&amp;la=de</guid>
      <pubDate>Mon, 01 Sep 2014 00:00:00 +0000</pubDate>
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      <title><![CDATA[Prokisch, H. ; Oexle, K.* &amp; Meitinger, T. Exomdiagnostik verändert die Sicht auf Mitochondriopathien. Med. Genet. 24, 183-186 (2012)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=10712&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=10712&amp;la=de</guid>
      <pubDate>Thu, 01 Nov 2012 00:00:00 +0000</pubDate>
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      <title><![CDATA[Heid, I.M. ; Winkler, T.W.* ; Grassmann, F.* &amp; Weber, B.H.F.* Wie groß sind die kleinen genetischen Risiken? Med. Genet. 23, 377-384 (2011)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6912&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6912&amp;la=de</guid>
      <pubDate>Sat, 31 Dec 2011 00:00:00 +0000</pubDate>
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    <item>
      <title><![CDATA[Kronenberg, F.* &amp; Heid, I.M. Genetik intermediärer Phänotypen. Med. Genet. 19, 304-308 (2007)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2379&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2379&amp;la=de</guid>
      <pubDate>Sat, 04 Aug 2007 00:00:00 +0000</pubDate>
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    <item>
      <title><![CDATA[Bickeböller, H. Parametrische und modellfreie Kopplungsanalysen. Med. Genet. 12, 400-402 (2000)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=21643&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=21643&amp;la=de</guid>
      <pubDate>Sun, 31 Dec 2000 00:00:00 +0000</pubDate>
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    <item>
      <title><![CDATA[Golla, A. Familienbasierte Assoziationsstudien. Med. Genet. 12, 419-422 (2000)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=21642&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=21642&amp;la=de</guid>
      <pubDate>Sun, 31 Dec 2000 00:00:00 +0000</pubDate>
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    <item>
      <title><![CDATA[Wjst, M. Checklisten zu Design, Durchführung und Datenanalyse in der molekularen Epidemiologie. Med. Genet. 12, 416-418 (2000)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=21634&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=21634&amp;la=de</guid>
      <pubDate>Sun, 31 Dec 2000 00:00:00 +0000</pubDate>
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    <item>
      <title><![CDATA[Wjst, M. Gene für Asthma. Med. Genet. 12, 443-447 (2000)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=21641&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=21641&amp;la=de</guid>
      <pubDate>Sun, 31 Dec 2000 00:00:00 +0000</pubDate>
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