Two Common Loss-of-Function Mutations within the Filaggrin Gene Predispose for Early Onset of Atopic Dermatitis von Stemmler, Susanne, Parwez, Qumar, Petrasch-Parwez, Elisabeth, Epplen, Joerg T., Hoffjan, Sabine

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Analysis of polymorphisms in RIG-I-like receptor genes in German multiple sclerosis patients von Varzari, Alexander, Bruch, Kathrin, Deyneko, Igor V, Chan, Andrew, Epplen, Joerg T, Hoffjan, Sabine

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Novel Nonsense Mutation in SLC39A13 Initially Presenting as Myopathy: Case Report and Review of the Literature von Dusanic, Maja, Dekomien, Gabriele, Lücke, Thomas, Vorgerd, Matthias, Weis, Joachim, Epplen, Joerg T., Köhler, Cornelia, Hoffjan, Sabine

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Molecular Genetics of Sex Identification, Breed Ancestry and Polydactyly in the Norwegian Lundehund Breed von Kropatsch, Regina, Melis, Claudia, Stronen, Astrid V, Jensen, Henrik, Epplen, Joerg T

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Lifespan, lifetime reproductive performance and paternity loss of within-pair and extra-pair offspring in the coal tit Periparus ater von Schmoll, Tim, Schurr, Frank M, Winkel, Wolfgang, Epplen, Joerg T, Lubjuhn, Thomas

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mtDNA nt13708A variant increases the risk of multiple sclerosis von Yu, Xinhua, Koczan, Dirk, Sulonen, Anna-Maija, Akkad, Denis A, Kroner, Antje, Comabella, Manuel, Costa, Gianna, Corongiu, Daniela, Goertsches, Robert, Camina-Tato, Montserrat, Thiesen, Hans-Juergen, Nyland, Harald I, Mørk, Sverre J, Montalban, Xavier, Rieckmann, Peter, Marrosu, Maria G, Myhr, Kjell-Morten, Epplen, Joerg T, Saarela, Janna, Ibrahim, Saleh M

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Autosomal dominant hereditary spastic paraplegia: novel mutations in the REEP1 gene (SPG31) von Schlang, Katharina J, Arning, Larissa, Epplen, Joerg T, Stemmler, Susanne

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The 14-bp deletion polymorphism in the HLA-G gene displays significant differences between ulcerative colitis and Crohn's disease and is associated with ileocecal resection in Croh... von Glas, Jürgen, Török, Helga-Paula, Tonenchi, Laurian, Wetzke, Martin, Beynon, Vanessa, Teshome, Molla Y., Cotofana, Sebastian, Schiemann, Uwe, Griga, Thomas, Klein, Wolfram, Epplen, Joerg T., Folwaczny, Christian, Folwaczny, Matthias, Mussack, Thomas, Weiss, Elisabeth H.

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Variation in the COL29A1 gene in German patients with atopic dermatitis, asthma and chronic obstructive pulmonary disease von HARAZIN, Monika, PARWEZ, Qumar, PETRASCH-PARWEZ, Elisabeth, EPPLEN, Joerg T., ARINIR, Umut, HOFFJAN, Sabine, STEMMLER, Susanne

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Association between a cannabinoid receptor gene ( CNR1) polymorphism and cannabinoid-induced alterations of the auditory event-related P300 potential von Stadelmann, Andreas M., Juckel, Georg, Arning, Larissa, Gallinat, Jürgen, Epplen, Jörg T., Roser, Patrik

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MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis von LILL, Christina M, SCHJEIDE, Brit-Maren M, BROER, Linda, SCHILLING, Marcel, AKKAD, Denis A, AKTAS, Orhan, ALLOZA, Iraide, ANTIGÜEDAD, Alfredo, ARROYO, Rafa, BLASCHKE, Paul, BUTTMANN, Mathias, CHAN, Andrew, GRAETZ, Christiane, COMPSTON, Alastair, COURNU-REBEIX, Isabelle, DÖRNER, Thomas, EPPLEN, Joerg T, FERNANDEZ, Oscar, CERDES, Lisa-Ann, GUILLOT-NOËL, Léna, HARTUNG, Hans-Peter, HOFFJAN, Sabine, IZQUIERDO, Guillermo, BAN, Maria, KEMPPINEN, Anu, KRONER, Antje, KUBISCH, Christian, KÜMPFEL, Tania, LI, Shu-Chen, LINDENBERGER, Ulman, LOHSE, Peter, LUBETZKI, Catherine, LUESSI, Felix, MALHOTRA, Sunny, ALCINA, Antonio, MESCHERIAKOVA, Julia, MONTALBAN, Xavier, PAPEIX, Caroline, PAREDES, Lidia F, RIECKMANN, Peter, STEINHAGEN-THIESSEN, Elisabeth, WINKELMANN, Alexander, ZETTL, Uwe K, HINTZEN, Rogier, VANDENBROECK, Koen, ORTIZ, Miguel A, STEWART, Graeme, FONTAINE, Bertrand, COMABELLA, Manuel, URCELAY, Elena, MATESANZ, Fuencisla, SAWCER, Stephen, BERTRAM, Lars, ZIPP, Frauke, PEREZ, Jennifer, DAMOTTE, Vincent, BOOTH, David, DE LAPUENTE, Aitzkoa Lopez

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The functional BDNF Val66Met polymorphism affects functions of pre-attentive visual sensory memory processes von Beste, Christian, Schneider, Daniel, Epplen, Jörg T., Arning, Larissa

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Large males dominate: ecology, social organization, and mating system of wild cavies, the ancestors of the guinea pig von Asher, Matthias, Lippmann, Tanja, Epplen, Jörg T, Kraus, Cornelia, Trillmich, Fritz, Sachser, Norbert

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On the Wegener granulomatosis associated region on chromosome 6p21.3 von Szyld, Paweł, Jagiello, Peter, Csernok, Elena, Gross, Wolfgang L, Epplen, Joerg T

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Genome-wide significant association with seven novel multiple sclerosis risk loci von Lill, Christina M, Luessi, Felix, Alcina, Antonio, Sokolova, Ekaterina A, Ugidos, Nerea, de la Hera, Belén, Guillot-Noël, Léna, Malhotra, Sunny, Reinthaler, Eva, Schjeide, Brit-Maren M, Mescheriakova, Julia Y, Mashychev, Andriy, Wohlers, Inken, Akkad, Denis A, Aktas, Orhan, Alloza, Iraide, Antigüedad, Alfredo, Arroyo, Rafa, Astobiza, Ianire, Blaschke, Paul, Boyko, Alexei N, Buttmann, Mathias, Chan, Andrew, Dörner, Thomas, Epplen, Joerg T, Favorova, Olga O, Fedetz, Maria, Fernández, Oscar, García-Martínez, Angel, Gerdes, Lisa-Ann, Graetz, Christiane, Hartung, Hans-Peter, Hoffjan, Sabine, Izquierdo, Guillermo, Korobko, Denis S, Kroner, Antje, Kubisch, Christian, Kümpfel, Tania, Leyva, Laura, Lohse, Peter, Malkova, Nadezhda A, Montalban, Xavier, Popova, Ekaterina V, Rieckmann, Peter, Rozhdestvenskii, Alexei S, Schmied, Christiane, Smagina, Inna V, Tsareva, Ekaterina Y, Winkelmann, Alexander, Zettl, Uwe K, Binder, Harald, Cournu-Rebeix, Isabelle, Hintzen, Rogier, Zimprich, Alexander, Comabella, Manuel, Fontaine, Bertrand, Urcelay, Elena, Vandenbroeck, Koen, Filipenko, Maxim, Matesanz, Fuencisla, Zipp, Frauke, Bertram, Lars

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When control fails: Influence of the prefrontal but not striatal dopaminergic system on behavioural flexibility in a change detection task von Schulz, Stefanie, Arning, Larissa, Pinnow, Marlies, Wascher, Edmund, Epplen, Jörg T., Beste, Christian

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Differential effects of ADORA2A gene variations in pre-attentive visual sensory memory subprocesses von Beste, Christian, Stock, Ann-Kathrin, Ness, Vanessa, Epplen, Jörg T, Arning, Larissa

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Association of variation in the LAMA3 gene, encoding the alpha-chain of laminin 5, with atopic dermatitis in a German case-control cohort von Stemmler, Susanne, Parwez, Qumar, Petrasch-Parwez, Elisabeth, Epplen, Joerg T, Hoffjan, Sabine

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N-methyl-d-aspartate receptor 2B subunit (GRIN2B) gene variation is associated with alerting, but not with orienting and conflicting in the Attention Network Test von Schulz, Stefanie, Arning, Larissa, Pinnow, Marlies, Epplen, Jörg T., Beste, Christian

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The SEM6A6 Locus Is Not Associated With Granulomatosis With Polyangiitis or Other Forms of Antineutrophil Cytoplasmic Antibody–Associated Vasculitides in Europeans: Comment on the... von Wieczorek, Stefan, Holle, Julia U., Cohen Tervaert, Jan Willem, Harper, Lorraine, Moosig, Frank, Gross, Wolfgang L., Epplen, Joerg T.

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