Cancer immune control needs senescence induction by interferon-dependent cell cycle regulator pathways in tumours von Brenner, Ellen, Schörg, Barbara F., Ahmetlić, Fatima, Wieder, Thomas, Hilke, Franz Joachim, Simon, Nadine, Schroeder, Christopher, Demidov, German, Riedel, Tanja, Fehrenbacher, Birgit, Schaller, Martin, Forschner, Andrea, Eigentler, Thomas, Niessner, Heike, Sinnberg, Tobias, Böhm, Katharina S., Hömberg, Nadine, Braumüller, Heidi, Dauch, Daniel, Zwirner, Stefan, Zender, Lars, Sonanini, Dominik, Geishauser, Albert, Bauer, Jürgen, Eichner, Martin, Jarick, Katja J., Beilhack, Andreas, Biskup, Saskia, Döcker, Dennis, Schadendorf, Dirk, Quintanilla-Martinez, Leticia, Pichler, Bernd J., Kneilling, Manfred, Mocikat, Ralph, Röcken, Martin

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An Integrated Transcriptomics and Genomics Approach Detects an X/Autosome Translocation in a Female with Duchenne Muscular Dystrophy von Segarra-Casas, Alba, Yépez, Vicente A, Demidov, German, Laurie, Steven, Esteve-Codina, Anna, Gagneur, Julien, Parkhurst, Yolande, Muni-Lofra, Robert, Harris, Elizabeth, Marini-Bettolo, Chiara, Straub, Volker, Töpf, Ana

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A statistical approach to detection of copy number variations in PCR-enriched targeted sequencing data von Demidov, German, Simakova, Tamara, Vnuchkova, Julia, Bragin, Anton

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Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation von Susak, Hana, Serra-Saurina, Laura, Demidov, German, Rabionet, Raquel, Domenech, Laura, Bosio, Mattia, Muyas, Francesc, Estivill, Xavier, Escaramis, Georgia, Ossowski, Stephan

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Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank von Fawcett, Katherine A, Demidov, German, Shrine, Nick, Paynton, Megan L, Ossowski, Stephan, Sayers, Ian, Wain, Louise V, Hollox, Edward J

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Genomes in clinical care von Riess, Olaf, Sturm, Marc, Menden, Benita, Liebmann, Alexandra, Demidov, German, Witt, Dennis, Casadei, Nicolas, Admard, Jakob, Schütz, Leon, Ossowski, Stephan, Taylor, Stacie, Schaffer, Sven, Schroeder, Christopher, Dufke, Andreas, Haack, Tobias

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Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing data von Demidov, German, Park, Joohyun, Armeanu‐Ebinger, Sorin, Roggia, Cristiana, Faust, Ulrike, Cordts, Isabell, Blandfort, Maria, Haack, Tobias B., Schroeder, Christopher, Ossowski, Stephan

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Enhanced epigenetic profiling of classical human monocytes reveals a specific signature of healthy aging in the DNA methylome von Shchukina, Irina, Bagaitkar, Juhi, Shpynov, Oleg, Loginicheva, Ekaterina, Porter, Sofia, Mogilenko, Denis A., Wolin, Erica, Collins, Patrick, Demidov, German, Artomov, Mykyta, Zaitsev, Konstantin, Sidorov, Sviatoslav, Camell, Christina, Bambouskova, Monika, Arthur, Laura, Swain, Amanda, Panteleeva, Alexandra, Dievskii, Aleksei, Kurbatsky, Evgeny, Tsurinov, Petr, Chernyatchik, Roman, Dixit, Vishwa Deep, Jovanovic, Marko, Stewart, Sheila A., Daly, Mark J., Dmitriev, Sergey, Oltz, Eugene M., Artyomov, Maxim N.

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New euchromatic variant dup(11)(p15.3p15.1) transmitted through two generations defined by low coverage whole genome sequencing von Singer, Sylke, Gazou, Anastasia, Sturm, Marc, Demidov, German, Mazzola, Pascale, Riess, Olaf, Ossowski, Stephan, Dufke, Andreas

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MDM2, MDM4 and EGFR Amplifications and Hyperprogression in Metastatic Acral and Mucosal Melanoma von Forschner, Andrea, Hilke, Franz-Joachim, Bonzheim, Irina, Gschwind, Axel, Demidov, German, Amaral, Teresa, Ossowski, Stephan, Riess, Olaf, Schroeder, Christopher, Martus, Peter, Klumpp, Bernhard, Gonzalez-Menendez, Irene, Garbe, Claus, Niessner, Heike, Sinnberg, Tobias

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Circulating cell-free DNA: A potential biomarker to differentiate inflammation and infection during radiochemotherapy von Zwirner, Kerstin, Hilke, Franz J., Demidov, German, Ossowski, Stephan, Gani, Cihan, Rieß, Olaf, Zips, Daniel, Welz, Stefan, Schroeder, Christopher

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Methods for detection of germline and somatic copy-number variants in next generation sequencing data von Demidov, German

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INTERPRETATION OF RELIGIOUS PHENOMENA IN RUSSIAN PHILOSOPHY IN THE BEGINNING OF 20TH CENTURY AS A RESPONSE TO THE MODERNITY CHALLENGES von Demidov, German V.

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Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma Patients von Hilke, Franz J., Sinnberg, Tobias, Gschwind, Axel, Niessner, Heike, Demidov, German, Amaral, Teresa, Ossowski, Stephan, Bonzheim, Irina, Roecken, Martin, Riess, Olaf, Garbe, Claus, Schroeder, Christopher, Forschner, Andrea

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Detection and Characterization of a De Novo Alu Retrotransposition Event Causing NKX2‐1‐Related Disorder von Magrinelli, Francesca, Rocca, Clarissa, Simone, Roberto, Zenezini Chiozzi, Riccardo, Jaunmuktane, Zane, Mencacci, Niccolò E., Tinazzi, Michele, Jayawant, Sandeep, Nemeth, Andrea H., Demidov, German, Houlden, Henry, Bhatia, Kailash P.

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Allele balance bias identifies systematic genotyping errors and false disease associations von Muyas, Francesc, Bosio, Mattia, Puig, Anna, Susak, Hana, Domènech, Laura, Escaramis, Georgia, Zapata, Luis, Demidov, German, Estivill, Xavier, Rabionet, Raquel, Ossowski, Stephan

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Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation von Susak, Hana, Serra-Saurina, Laura, Demidov, German, Rabionet Janssen, Raquel, Domènech, Laura, Bosio, Mattia, Muyas, Francesc, Estivill, Xavier, 1955, Escaramís Babiano, Geòrgia, Ossowski, Stephan

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Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation von Sušak, Hana, 1985, Serra Saurina, Laura, Demidov, German, 1990, Rabionet, Raquel, Domènech Salgado, Laura, 1989, Bosio, Mattia, Muyas Remolar, Francesc, 1992, Estivill, Xavier, 1955, Escaramís, Geòrgia, Ossowski, Stephan

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A statistical approach to detection of copy number variations in PCR-enriched targeted sequencing data von Demidov, German, 1990, Simakova, Tamara, Vnuchkova, Julia, Bragin, Anton

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Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases von Estévez-Arias, Berta, Matalonga, Leslie, Yubero, Delia, Polavarapu, Kiran, Codina, Anna, Ortez, Carlos, Carrera-García, Laura, Expósito-Escudero, Jesica, Jou, Cristina, Meyer, Stefanie, Kilicarslan, Ozge Aksel, Aleman, Alberto, Thompson, Rachel, Luknárová, Rebeka, Esteve-Codina, Anna, Gut, Marta, Laurie, Steven, Demidov, German, Yépez, Vicente A, Beltran, Sergi, Gagneur, Julien, Topf, Ana, Lochmüller, Hanns, Nascimento, Andres, Hoenicka, Janet, Palau, Francesc, Natera-de Benito, Daniel

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