Torthaí cuardaigh - Wittig, Michael

CNVineta: a data mining tool for large case–control copy number variation datasets de réir Wittig, Michael, Helbig, Ingo, Schreiber, Stefan, Franke, Andre

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Fitness consequences of polymorphic inversions in the zebra finch genome de réir Knief, Ulrich, Hemmrich-Stanisak, Georg, Wittig, Michael, Franke, Andre, Griffith, Simon C., Kempenaers, Bart, Forstmeier, Wolfgang

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The age related markers lipofuscin and apoptosis show different genetic architecture by QTL mapping in short-lived Nothobranchius fish de réir Ng'oma, Enoch, Reichwald, Kathrin, Dorn, Alexander, Wittig, Michael, Balschun, Tobias, Franke, Andre, Platzer, Matthias, Cellerino, Allesandro

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Efficacy assessment of SNP sets for genome-wide disease association studies de réir Wollstein, Andreas, Herrmann, Alexander, Wittig, Michael, Nothnagel, Michael, Franke, Andre, Nürnberg, Peter, Schreiber, Stefan, Krawczak, Michael, Hampe, Jochen

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Acute physical exercise improves shifting in adolescents at school: evidence for a dopaminergic contribution de réir Berse, Timo, Rolfes, Kathrin, Barenberg, Jonathan, Dutke, Stephan, Kuhlenbäumer, Gregor, Völker, Klaus, Winter, Bernward, Wittig, Michael, Knecht, Stefan

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A post-GWAS analysis of predicted regulatory variants and tuberculosis susceptibility de réir Uren, Caitlin, Henn, Brenna M., Franke, Andre, Wittig, Michael, van Helden, Paul D., Hoal, Eileen G., Möller, Marlo

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A tissue-specific landscape of sense/antisense transcription in the mouse intestine de réir Klostermeier, Ulrich C, Barann, Matthias, Wittig, Michael, Häsler, Robert, Franke, Andre, Gavrilova, Olga, Kreck, Benjamin, Sina, Christian, Schilhabel, Markus B, Schreiber, Stefan, Rosenstiel, Philip

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Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci de réir Saadati, Hamid Reza, Wittig, Michael, Helbig, Ingo, Häsler, Robert, Anderson, Carl A., Mathew, Christopher G., Kupcinskas, Limas, Parkes, Miles, Karlsen, Tom Hemming, Rosenstiel, Philip, Schreiber, Stefan, Franke, Andre

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High-throughput method for the hybridisation-based targeted enrichment of long genomic fragments for PacBio third-generation sequencing de réir Steiert, Tim Alexander, Fuß, Janina, Juzenas, Simonas, Wittig, Michael, Hoeppner, Marc Patrick, Vollstedt, Melanie, Varkalaite, Greta, ElAbd, Hesham, Brockmann, Christian, Görg, Siegfried, Gassner, Christoph, Forster, Michael, Franke, Andre

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Development of a high-resolution NGS-based HLA-typing and analysis pipeline de réir Wittig, Michael, Anmarkrud, Jarl A., Kässens, Jan C., Koch, Simon, Forster, Michael, Ellinghaus, Eva, Hov, Johannes R., Sauer, Sascha, Schimmler, Manfred, Ziemann, Malte, Görg, Siegfried, Jacob, Frank, Karlsen, Tom H., Franke, Andre

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Complement Receptor 1 (CR1, CD35) Polymorphisms and Soluble CR1: A Proposed Anti-inflammatory Role to Quench the Fire of “Fogo Selvagem” Pemphigus Foliaceus de réir Oliveira, Luana Caroline, Kretzschmar, Gabriela Canalli, dos Santos, Andressa Cristina Moraes, Camargo, Carolina Maciel, Nisihara, Renato Mitsunori, Farias, Ticiana Della Justina, Franke, Andre, Wittig, Michael, Schmidt, Enno, Busch, Hauke, Petzl-Erler, Maria Luiza, Boldt, Angelica Beate Winter

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From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software de réir Forster, Michael, Forster, Peter, Elsharawy, Abdou, Hemmrich, Georg, Kreck, Benjamin, Wittig, Michael, Thomsen, Ingo, Stade, Björn, Barann, Matthias, Ellinghaus, David, Petersen, Britt-Sabina, May, Sandra, Melum, Espen, Schilhabel, Markus B., Keller, Andreas, Schreiber, Stefan, Rosenstiel, Philip, Franke, Andre

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Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome de réir Helbig, Ingo, Barcia, Giulia, Pendziwiat, Manuela, Ganesan, Shiva, Mueller, Stefanie H., Helbig, Katherine L., Vaidiswaran, Priya, Xian, Julie, Galer, Peter D., Afawi, Zaid, Specchio, Nicola, Kluger, Gerhard, Kuhlenbäumer, Gregor, Appenzeller, Silke, Wittig, Michael, Kramer, Uri, van Baalen, Andreas, Nabbout, Rima

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Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance de réir Dibbens, Leanne M., Mullen, Saul, Helbig, Ingo, Mefford, Heather C., Bayly, Marta A., Bellows, Susannah, Leu, Costin, Trucks, Holger, Obermeier, Tanja, Wittig, Michael, Franke, Andre, Caglayan, Hande, Yapici, Zuhal, Sander, Thomas, Eichler, Evan E., Scheffer, Ingrid E., Mulley, John C., Berkovic, Samuel F.

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Validity and Prognostic Value of a Polygenic Risk Score for Parkinson’s Disease de réir Koch, Sebastian, Laabs, Björn-Hergen, Kasten, Meike, Vollstedt, Eva-Juliane, Becktepe, Jos, Brüggemann, Norbert, Franke, Andre, Krämer, Ulrike M., Kuhlenbäumer, Gregor, Lieb, Wolfgang, Mollenhauer, Brit, Neis, Miriam, Trenkwalder, Claudia, Schäffer, Eva, Usnich, Tatiana, Wittig, Michael, Klein, Christine, König, Inke R., Lohmann, Katja, Krawczak, Michael, Caliebe, Amke

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Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans de réir Krause-Kyora, Ben, Nutsua, Marcel, Boehme, Lisa, Pierini, Federica, Pedersen, Dorthe Dangvard, Kornell, Sabin-Christin, Drichel, Dmitriy, Bonazzi, Marion, Möbus, Lena, Tarp, Peter, Susat, Julian, Bosse, Esther, Willburger, Beatrix, Schmidt, Alexander H., Sauter, Jürgen, Franke, Andre, Wittig, Michael, Caliebe, Amke, Nothnagel, Michael, Schreiber, Stefan, Boldsen, Jesper L., Lenz, Tobias L., Nebel, Almut

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Systematic Association Mapping Identifies NELL1 as a Novel IBD Disease Gene de réir Franke, Andre, Hampe, Jochen, Rosenstiel, Philip, Becker, Christian, Wagner, Florian, Häsler, Robert, Little, Randall D., Huse, Klaus, Ruether, Andreas, Balschun, Tobias, Wittig, Michael, ElSharawy, Abdou, Mayr, Gabriele, Albrecht, Mario, Prescott, Natalie J., Onnie, Clive M., Fournier, Hélène, Keith, Tim, Radelof, Uwe, Platzer, Matthias, Mathew, Christopher G., Stoll, Monika, Krawczak, Michael, Nürnberg, Peter, Schreiber, Stefan

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Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine mapping in the MHC and genome wide de réir Stuart, Philip E., Tsoi, Lam C., Nair, Rajan P., Ghosh, Manju, Kabra, Madhulika, Shaiq, Pakeeza A., Raja, Ghazala K., Qamar, Raheel, Thelma, B.K., Patrick, Matthew T., Parihar, Anita, Singh, Sonam, Khandpur, Sujay, Kumar, Uma, Wittig, Michael, Degenhardt, Frauke, Tejasvi, Trilokraj, Voorhees, John J., Weidinger, Stephan, Franke, Andre, Abecasis, Goncalo R., Sharma, Vinod K., Elder, James T.

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Genetic Associations and Differential mRNA Expression Levels of Host Genes Suggest a Viral Trigger for Endemic Pemphigus Foliaceus de réir Hoch, Valéria Bumiller-Bini, Kohler, Ana Flávia, Augusto, Danillo G., Lobo-Alves, Sara Cristina, Malheiros, Danielle, Cipolla, Gabriel Adelman, Boldt, Angelica Beate Winter, Braun-Prado, Karin, Wittig, Michael, Franke, Andre, Pföhler, Claudia, Worm, Margitta, van Beek, Nina, Goebeler, Matthias, Sárdy, Miklós, Ibrahim, Saleh, Busch, Hauke, Schmidt, Enno, Hundt, Jennifer Elisabeth, de Araujo-Souza, Patrícia Savio, Petzl-Erler, Maria Luiza

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UBTF::ATXN7L3 gene fusion defines novel B cell precursor ALL subtype with CDX2 expression and need for intensified treatment de réir Bastian, Lorenz, Hartmann, Alina M., Beder, Thomas, Hänzelmann, Sonja, Kässens, Jan, Bultmann, Miriam, Hoeppner, Marc P., Franzenburg, Sören, Wittig, Michael, Franke, Andre, Nagel, Inga, Spielmann, Malte, Reimer, Niklas, Busch, Hauke, Schwartz, Stefan, Steffen, Björn, Viardot, Andreas, Döhner, Konstanze, Kondakci, Mustafa, Wulf, Gerald, Wendelin, Knut, Renzelmann, Andrea, Kiani, Alexander, Trautmann, Heiko, Neumann, Martin, Gökbuget, Nicola, Brüggemann, Monika, Baldus, Claudia D.

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