CNVineta: a data mining tool for large case–control copy number variation datasets

Bằng Wittig, Michael, Helbig, Ingo, Schreiber, Stefan, Franke, Andre
Được phát hành 2010

Fitness consequences of polymorphic inversions in the zebra finch genome

Bằng Knief, Ulrich, Hemmrich-Stanisak, Georg, Wittig, Michael, Franke, Andre, Griffith, Simon C., Kempenaers, Bart, Forstmeier, Wolfgang
Xuất bản năm Genome Biol (2016)

The age related markers lipofuscin and apoptosis show different genetic architecture by QTL mapping in short-lived Nothobranchius fish

Bằng Ng'oma, Enoch, Reichwald, Kathrin, Dorn, Alexander, Wittig, Michael, Balschun, Tobias, Franke, Andre, Platzer, Matthias, Cellerino, Allesandro
Được phát hành 2014

Efficacy assessment of SNP sets for genome-wide disease association studies

Bằng Wollstein, Andreas, Herrmann, Alexander, Wittig, Michael, Nothnagel, Michael, Franke, Andre, Nürnberg, Peter, Schreiber, Stefan, Krawczak, Michael, Hampe, Jochen
Được phát hành 2007

Acute physical exercise improves shifting in adolescents at school: evidence for a dopaminergic contribution

Bằng Berse, Timo, Rolfes, Kathrin, Barenberg, Jonathan, Dutke, Stephan, Kuhlenbäumer, Gregor, Völker, Klaus, Winter, Bernward, Wittig, Michael, Knecht, Stefan
Xuất bản năm Front Behav Neurosci (2015)

A post-GWAS analysis of predicted regulatory variants and tuberculosis susceptibility

Bằng Uren, Caitlin, Henn, Brenna M., Franke, Andre, Wittig, Michael, van Helden, Paul D., Hoal, Eileen G., Möller, Marlo
Xuất bản năm PLoS One (2017)

A tissue-specific landscape of sense/antisense transcription in the mouse intestine

Bằng Klostermeier, Ulrich C, Barann, Matthias, Wittig, Michael, Häsler, Robert, Franke, Andre, Gavrilova, Olga, Kreck, Benjamin, Sina, Christian, Schilhabel, Markus B, Schreiber, Stefan, Rosenstiel, Philip
Được phát hành 2011

Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci

Bằng 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
Xuất bản năm BMC Med Genet (2016)

Development of a high-resolution NGS-based HLA-typing and analysis pipeline

Bằng 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
Xuất bản năm Nucleic Acids Res (2015)

Complement Receptor 1 (CR1, CD35) Polymorphisms and Soluble CR1: A Proposed Anti-inflammatory Role to Quench the Fire of “Fogo Selvagem” Pemphigus Foliaceus

Bằng 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
Xuất bản năm Front Immunol (2019)

From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software

Bằng 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
Được phát hành 2013

Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome

Bằng 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
Xuất bản năm Ann Clin Transl Neurol (2020)

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

Bằng 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.
Được phát hành 2009

Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans

Bằng 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
Xuất bản năm Nat Commun (2018)

Systematic Association Mapping Identifies NELL1 as a Novel IBD Disease Gene

Bằng 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
Được phát hành 2007

Construction and benchmarking of a multi-ethnic reference panel for the imputation of HLA class I and II alleles

Bằng Degenhardt, Frauke, Wendorff, Mareike, Wittig, Michael, Ellinghaus, Eva, Datta, Lisa W, Schembri, John, Ng, Siew C, Rosati, Elisa, Hübenthal, Matthias, Ellinghaus, David, Jung, Eun Suk, Lieb, Wolfgang, Abedian, Shifteh, Malekzadeh, Reza, Cheon, Jae Hee, Ellul, Pierre, Sood, Ajit, Midha, Vandana, Thelma, B K, Wong, Sunny H, Schreiber, Stefan, Yamazaki, Keiko, Kubo, Michiaki, Boucher, Gabrielle, Rioux, John D, Lenz, Tobias L, Brant, Steven R, Franke, Andre
Xuất bản năm Hum Mol Genet (2019)

HLA haplotypes in primary sclerosing cholangitis patients of admixed and non-European ancestry

Bằng Henriksen, Eva Kristine Klemsdal, Viken, Marte K., Wittig, Michael, Holm, Kristian, Folseraas, Trine, Mucha, Sören, Melum, Espen, Hov, Johannes R., Lazaridis, Konstantinos N., Juran, Brian D., Chazouillères, Olivier, Färkkilä, Martti, Gotthardt, Daniel Nils, Invernizzi, Pietro, Carbone, Marco, Hirschfield, Gideon M., Rushbrook, Simon M., Goode, Elizabeth, Ponsioen, Cyriel Y., Weersma, Rinse K., Eksteen, Bertus, Yimam, Kidist K., Gordon, Stuart C., Goldberg, David, Yu, Lei, Bowlus, Christopher L., Franke, Andre, Lie, Benedicte A., Karlsen, Tom H.
Xuất bản năm HLA (2017)

Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA1*05:05 and -DRB1*07:01, in Germans

Bằng Schwarm, Christian, Gola, Damian, Holtsche, Maike M., Dieterich, Anabelle, Bhandari, Anita, Freitag, Miriam, Nürnberg, Peter, Toliat, Mohammad, Lieb, Wolfgang, Wittig, Michael, Franke, André, Worm, Margitta, Sticherling, Michael, Ehrchen, Jan, Günther, Claudia, Gläser, Regine, Peitsch, Wiebke K., Sárdy, Miklós, Eming, Rüdiger, Hertl, Michael, Benoit, Sandrine, Goebeler, Matthias, Pföhler, Claudia, Kunz, Manfred, Kreuter, Alexander, van Beek, Nina, Erdmann, Jeanette, Busch, Hauke, Zillikens, Detlef, Sadik, Christian D., Hirose, Misa, König, Inke R., Schmidt, Enno, Ibrahim, Saleh M.
Xuất bản năm Orphanet J Rare Dis (2021)

Identifying genetic modifiers of age-associated penetrance in X-linked dystonia-parkinsonism

Bằng Laabs, Björn-Hergen, Klein, Christine, Pozojevic, Jelena, Domingo, Aloysius, Brüggemann, Norbert, Grütz, Karen, Rosales, Raymond L., Jamora, Roland Dominic, Saranza, Gerard, Diesta, Cid Czarina E., Wittig, Michael, Schaake, Susen, Dulovic-Mahlow, Marija, Quismundo, Jana, Otto, Pia, Acuna, Patrick, Go, Criscely, Sharma, Nutan, Multhaupt-Buell, Trisha, Müller, Ulrich, Hanssen, Henrike, Kilpert, Fabian, Franke, Andre, Rolfs, Arndt, Bauer, Peter, Dobričić, Valerija, Lohmann, Katja, Ozelius, Laurie J., Kaiser, Frank J., König, Inke R., Westenberger, Ana
Xuất bản năm Nat Commun (2021)

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

Bằng Helbig, Ingo, Mefford, Heather C, Sharp, Andrew J, Guipponi, Michel, Fichera, Marco, Franke, Andre, Muhle, Hiltrud, de Kovel, Carolien, Baker, Carl, von Spiczak, Sarah, Kron, Katherine L, Steinich, Ines, Kleefuβ-Lie, Ailing A, Leu, Costin, Gaus, Verena, Schmitz, Bettina, Klein, Karl M, Reif, Philipp S, Rosenow, Felix, Weber, Yvonne, Lerche, Holger, Zimprich, Fritz, Urak, Lydia, Fuchs, Karoline, Feucht, Martha, Genton, Pierre, Thomas, Pierre, Visscher, Frank, de Haan, Gerrit-Jan, Møller, Rikke S, Hjalgrim, Helle, Luciano, Daniela, Wittig, Michael, Nothnagel, Michael, Elger, Christian E, Nürnberg, Peter, Romano, Corrado, Malafosse, Alain, Koeleman, Bobby P C, Lindhout, Dick, Stephani, Ulrich, Schreiber, Stefan, Eichler, Evan E, Sander, Thomas
Được phát hành 2009