The Role of Osteopontin (OPN/SPP1) Haplotypes in the Susceptibility to Crohn's Disease

by Glas, Jürgen, Seiderer, Julia, Bayrle, Corinna, Wetzke, Martin, Fries, Christoph, Tillack, Cornelia, Olszak, Torsten, Beigel, Florian, Steib, Christian, Friedrich, Matthias, Diegelmann, Julia, Czamara, Darina, Brand, Stephan
Published 2011

The endocrine stress response is linked to one specific locus on chromosome 3 in a mouse model based on extremes in trait anxiety

by Gonik, Mariya, Frank, Elisabeth, Keßler, Melanie S, Czamara, Darina, Bunck, Mirjam, Yen, Yi-Chun, Pütz, Benno, Holsboer, Florian, Bettecken, Thomas, Landgraf, Rainer, Müller-Myhsok, Bertram, Touma, Chadi, Czibere, Ludwig
Published 2012

Intestinal DMBT1 Expression Is Modulated by Crohn’s Disease-Associated IL23R Variants and by a DMBT1 Variant Which Influences Binding of the Transcription Factors CREB1 and ATF-2

by Diegelmann, Julia, Czamara, Darina, Le Bras, Emmanuelle, Zimmermann, Eva, Olszak, Torsten, Bedynek, Andrea, Göke, Burkhard, Franke, Andre, Glas, Jürgen, Brand, Stephan
Published 2013

CEACAM6 Gene Variants in Inflammatory Bowel Disease

by Glas, Jürgen, Seiderer, Julia, Fries, Christoph, Tillack, Cornelia, Pfennig, Simone, Weidinger, Maria, Beigel, Florian, Olszak, Torsten, Lass, Ulrich, Göke, Burkhard, Ochsenkühn, Thomas, Wolf, Christiane, Lohse, Peter, Müller-Myhsok, Bertram, Diegelmann, Julia, Czamara, Darina, Brand, Stephan
Published 2011

Analysis of IL12B Gene Variants in Inflammatory Bowel Disease

by Glas, Jürgen, Seiderer, Julia, Wagner, Johanna, Olszak, Torsten, Fries, Christoph, Tillack, Cornelia, Friedrich, Matthias, Beigel, Florian, Stallhofer, Johannes, Steib, Christian, Wetzke, Martin, Göke, Burkhard, Ochsenkühn, Thomas, Diegelmann, Julia, Czamara, Darina, Brand, Stephan
Published 2012

PTPN2 Gene Variants Are Associated with Susceptibility to Both Crohn's Disease and Ulcerative Colitis Supporting a Common Genetic Disease Background

by Glas, Jürgen, Wagner, Johanna, Seiderer, Julia, Olszak, Torsten, Wetzke, Martin, Beigel, Florian, Tillack, Cornelia, Stallhofer, Johannes, Friedrich, Matthias, Steib, Christian, Göke, Burkhard, Ochsenkühn, Thomas, Karbalai, Nazanin, Diegelmann, Julia, Czamara, Darina, Brand, Stephan
Published 2012

PTGER4 Expression-Modulating Polymorphisms in the 5p13.1 Region Predispose to Crohn's Disease and Affect NF-κB and XBP1 Binding Sites

by Glas, Jürgen, Seiderer, Julia, Czamara, Darina, Pasciuto, Giulia, Diegelmann, Julia, Wetzke, Martin, Olszak, Torsten, Wolf, Christiane, Müller-Myhsok, Bertram, Balschun, Tobias, Achkar, Jean-Paul, Kamboh, M. Ilyas, Franke, Andre, Duerr, Richard H., Brand, Stephan
Published 2012

IRGM Variants and Susceptibility to Inflammatory Bowel Disease in the German Population

by Glas, Jürgen, Seiderer, Julia, Bues, Stephanie, Stallhofer, Johannes, Fries, Christoph, Olszak, Torsten, Tsekeri, Eleni, Wetzke, Martin, Beigel, Florian, Steib, Christian, Friedrich, Matthias, Göke, Burkhard, Diegelmann, Julia, Czamara, Darina, Brand, Stephan
Published 2013

Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach

by Hennings, Johannes M., Kohli, Martin A., Czamara, Darina, Giese, Maria, Eckert, Anne, Wolf, Christiane, Heck, Angela, Domschke, Katharina, Arolt, Volker, Baune, Bernhard T., Horstmann, Sonja, Brückl, Tanja, Klengel, Torsten, Menke, Andreas, Müller-Myhsok, Bertram, Ising, Marcus, Uhr, Manfred, Lucae, Susanne
Published 2013

Children with ADHD Symptoms Have a Higher Risk for Reading, Spelling and Math Difficulties in the GINIplus and LISAplus Cohort Studies

by Czamara, Darina, Tiesler, Carla M. T., Kohlböck, Gabriele, Berdel, Dietrich, Hoffmann, Barbara, Bauer, Carl-Peter, Koletzko, Sibylle, Schaaf, Beate, Lehmann, Irina, Herbarth, Olf, von Berg, Andrea, Müller-Myhsok, Bertram, Schulte-Körne, Gerd, Heinrich, Joachim
Published 2013

Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice

by Brenndörfer, Julia, Altmann, André, Widner-Andrä, Regina, Pütz, Benno, Czamara, Darina, Tilch, Erik, Kam-Thong, Tony, Weber, Peter, Rex-Haffner, Monika, Bettecken, Thomas, Bultmann, Andrea, Müller-Myhsok, Bertram, Binder, Elisabeth E., Landgraf, Rainer, Czibere, Ludwig
Published 2015

MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease

by Schormair, Barbara, Plag, Jens, Kaffe, Maria, Groß, Nadine, Czamara, Darina, Samtleben, Walter, Lichtner, Peter, Ströhle, Andreas, Stefanidis, Ioannis, Vainas, Andreas, Dardiotis, Efthimios, Sakkas, George K, Gieger, Christian, Müller-Myhsok, Bertram, Meitinger, Thomas, Heemann, Uwe, Hadjigeorgiou, Georgios M, Oexle, Konrad, Winkelmann, Juliane
Published 2011

Rare Variants in PLXNA4 and Parkinson’s Disease

by Schulte, Eva C., Stahl, Immanuel, Czamara, Darina, Ellwanger, Daniel C., Eck, Sebastian, Graf, Elisabeth, Mollenhauer, Brit, Zimprich, Alexander, Lichtner, Peter, Haubenberger, Dietrich, Pirker, Walter, Brücke, Thomas, Bereznai, Benjamin, Molnar, Maria J., Peters, Annette, Gieger, Christian, Müller-Myhsok, Bertram, Trenkwalder, Claudia, Winkelmann, Juliane
Published 2013

Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders

by Arloth, Janine, Bogdan, Ryan, Weber, Peter, Frishman, Goar, Menke, Andreas, Wagner, Klaus V., Balsevich, Georgia, Schmidt, Mathias V., Karbalai, Nazanin, Czamara, Darina, Altmann, Andre, Trümbach, Dietrich, Wurst, Wolfgang, Mehta, Divya, Uhr, Manfred, Klengel, Torsten, Erhardt, Angelika, Carey, Caitlin E., Conley, Emily Drabant, Ruepp, Andreas, Müller-Myhsok, Bertram, Hariri, Ahmad R., Binder, Elisabeth B.
Published 2015

A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder

by Hung, Chi-Fa, Breen, Gerome, Czamara, Darina, Corre, Tanguy, Wolf, Christiane, Kloiber, Stefan, Bergmann, Sven, Craddock, Nick, Gill, Michael, Holsboer, Florian, Jones, Lisa, Jones, Ian, Korszun, Ania, Kutalik, Zoltan, Lucae, Susanne, Maier, Wolfgang, Mors, Ole, Owen, Michael J, Rice, John, Rietschel, Marcella, Uher, Rudolf, Vollenweider, Peter, Waeber, Gerard, Craig, Ian W, Farmer, Anne E, Lewis, Cathryn M, Müller-Myhsok, Bertram, Preisig, Martin, McGuffin, Peter, Rivera, Margarita
Published 2015

Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma

by Becker, Jessica, May, Andrea, Gerges, Christian, Anders, Mario, Veits, Lothar, Weise, Katharina, Czamara, Darina, Lyros, Orestis, Manner, Hendrik, Terheggen, Grischa, Venerito, Marino, Noder, Tania, Mayershofer, Rupert, Hofer, Jan-Hinnerk, Karch, Hans-Werner, Ahlbrand, Constantin J, Arras, Michael, Hofer, Sebastian, Mangold, Elisabeth, Heilmann-Heimbach, Stefanie, Heinrichs, Sophie K M, Hess, Timo, Kiesslich, Ralf, Izbicki, Jakob R, Hölscher, Arnulf H, Bollschweiler, Elfriede, Malfertheiner, Peter, Lang, Hauke, Moehler, Markus, Lorenz, Dietmar, Müller-Myhsok, Bertram, Ott, Katja, Schmidt, Thomas, Whiteman, David C, Vaughan, Thomas L, Nöthen, Markus M, Hackelsberger, Andreas, Schumacher, Brigitte, Pech, Oliver, Vashist, Yogesh, Vieth, Michael, Weismüller, Josef, Neuhaus, Horst, Rösch, Thomas, Ell, Christian, Gockel, Ines, Schumacher, Johannes
Published 2015

Correction: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1

by Winkelmann, Juliane, Czamara, Darina, Schormair, Barbara, Knauf, Franziska, Schulte, Eva C., Trenkwalder, Claudia, Dauvilliers, Yves, Polo, Olli, Högl, Birgit, Berger, Klaus, Fuhs, Andrea, Gross, Nadine, Stiasny-Kolster, Karin, Oertel, Wolfgang, Bachmann, Cornelius G., Paulus, Walter, Xiong, Lan, Montplaisir, Jacques, Rouleau, Guy A., Fietze, Ingo, Vávrová, Jana, Kemlink, David, Sonka, Karel, Nevsimalova, Sona, Lin, Siong-Chi, Wszolek, Zbigniew, Vilariño-Güell, Carles, Farrer, Matthew J., Gschliesser, Viola, Frauscher, Birgit, Falkenstetter, Tina, Poewe, Werner, Allen, Richard P., Earley, Christopher J., Ondo, William G., Le, Wei-Dong, Spieler, Derek, Kaffe, Maria, Zimprich, Alexander, Kettunen, Johannes, Perola, Markus, Silander, Kaisa, Cournu-Rebeix, Isabelle, Francavilla, Marcella, Fontenille, Claire, Fontaine, Bertrand, Vodicka, Pavel, Prokisch, Holger, Lichtner, Peter, Peppard, Paul, Faraco, Juliette, Mignot, Emmanuel, Gieger, Christian, Illig, Thomas, Wichmann, H.-Erich, Müller-Myhsok, Bertram, Meitinger, Thomas
Published 2011

Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1

by Winkelmann, Juliane, Czamara, Darina, Schormair, Barbara, Knauf, Franziska, Schulte, Eva C., Trenkwalder, Claudia, Dauvilliers, Yves, Polo, Olli, Högl, Birgit, Berger, Klaus, Fuhs, Andrea, Gross, Nadine, Stiasny-Kolster, Karin, Oertel, Wolfgang, Bachmann, Cornelius G., Paulus, Walter, Xiong, Lan, Montplaisir, Jacques, Rouleau, Guy A., Fietze, Ingo, Vávrová, Jana, Kemlink, David, Sonka, Karel, Nevsimalova, Sona, Lin, Siong-Chi, Wszolek, Zbigniew, Vilariño-Güell, Carles, Farrer, Matthew J., Gschliesser, Viola, Frauscher, Birgit, Falkenstetter, Tina, Poewe, Werner, Allen, Richard P., Earley, Christopher J., Ondo, William G., Le, Wei-Dong, Spieler, Derek, Kaffe, Maria, Zimprich, Alexander, Kettunen, Johannes, Perola, Markus, Silander, Kaisa, Cournu-Rebeix, Isabelle, Francavilla, Marcella, Fontenille, Claire, Fontaine, Bertrand, Vodicka, Pavel, Prokisch, Holger, Lichtner, Peter, Peppard, Paul, Faraco, Juliette, Mignot, Emmanuel, Gieger, Christian, Illig, Thomas, Wichmann, H.-Erich, Müller-Myhsok, Bertram, Meitinger, Thomas
Published 2011

An epigenetic clock for gestational age at birth based on blood methylation data

by Knight, Anna K., Craig, Jeffrey M., Theda, Christiane, Bækvad-Hansen, Marie, Bybjerg-Grauholm, Jonas, Hansen, Christine S., Hollegaard, Mads V., Hougaard, David M., Mortensen, Preben B., Weinsheimer, Shantel M., Werge, Thomas M., Brennan, Patricia A., Cubells, Joseph F., Newport, D. Jeffrey, Stowe, Zachary N., Cheong, Jeanie L. Y., Dalach, Philippa, Doyle, Lex W., Loke, Yuk J., Baccarelli, Andrea A., Just, Allan C., Wright, Robert O., Téllez-Rojo, Mara M., Svensson, Katherine, Trevisi, Letizia, Kennedy, Elizabeth M., Binder, Elisabeth B., Iurato, Stella, Czamara, Darina, Räikkönen, Katri, Lahti, Jari M. T., Pesonen, Anu-Katriina, Kajantie, Eero, Villa, Pia M., Laivuori, Hannele, Hämäläinen, Esa, Park, Hea Jin, Bailey, Lynn B., Parets, Sasha E., Kilaru, Varun, Menon, Ramkumar, Horvath, Steve, Bush, Nicole R., LeWinn, Kaja Z., Tylavsky, Frances A., Conneely, Karen N., Smith, Alicia K.
Published 2016

Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation

by Andlauer, Till F. M., Buck, Dorothea, Antony, Gisela, Bayas, Antonios, Bechmann, Lukas, Berthele, Achim, Chan, Andrew, Gasperi, Christiane, Gold, Ralf, Graetz, Christiane, Haas, Jürgen, Hecker, Michael, Infante-Duarte, Carmen, Knop, Matthias, Kümpfel, Tania, Limmroth, Volker, Linker, Ralf A., Loleit, Verena, Luessi, Felix, Meuth, Sven G., Mühlau, Mark, Nischwitz, Sandra, Paul, Friedemann, Pütz, Michael, Ruck, Tobias, Salmen, Anke, Stangel, Martin, Stellmann, Jan-Patrick, Stürner, Klarissa H., Tackenberg, Björn, Then Bergh, Florian, Tumani, Hayrettin, Warnke, Clemens, Weber, Frank, Wiendl, Heinz, Wildemann, Brigitte, Zettl, Uwe K., Ziemann, Ulf, Zipp, Frauke, Arloth, Janine, Weber, Peter, Radivojkov-Blagojevic, Milena, Scheinhardt, Markus O., Dankowski, Theresa, Bettecken, Thomas, Lichtner, Peter, Czamara, Darina, Carrillo-Roa, Tania, Binder, Elisabeth B., Berger, Klaus, Bertram, Lars, Franke, Andre, Gieger, Christian, Herms, Stefan, Homuth, Georg, Ising, Marcus, Jöckel, Karl-Heinz, Kacprowski, Tim, Kloiber, Stefan, Laudes, Matthias, Lieb, Wolfgang, Lill, Christina M., Lucae, Susanne, Meitinger, Thomas, Moebus, Susanne, Müller-Nurasyid, Martina, Nöthen, Markus M., Petersmann, Astrid, Rawal, Rajesh, Schminke, Ulf, Strauch, Konstantin, Völzke, Henry, Waldenberger, Melanie, Wellmann, Jürgen, Porcu, Eleonora, Mulas, Antonella, Pitzalis, Maristella, Sidore, Carlo, Zara, Ilenia, Cucca, Francesco, Zoledziewska, Magdalena, Ziegler, Andreas, Hemmer, Bernhard, Müller-Myhsok, Bertram
Published 2016