Publikationen von 0000-0003-2603-1502
(ORCID: 0000-0003-2603-1502)

Schlicht, Kristina, Nyczka, Piotr, Caliebe, Amke, Freitag-Wolf, Sandra, Claringbould, Annique, Franke, Lude, Võsa, Urmo, Kardia, Sharon L. R., Smith, Jennifer A. , Zhao, Wei, Gieger, Christian, Peters, Annette, Prokisch, Holger, Strauch, Konstantin, Baurecht, Hansjörg, Weidinger, Stephan, Rosenstiel, Philip , Hütt, Marc-Thorsten, Knecht, Carolin, Szymczak, Silke und Krawczak, Michael (2019) The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus. Human Genetics 138 (4), S. 375-388. Volltext nicht vorhanden.

Schupp, Jonas Christian , Freitag-Wolf, Sandra, Bargagli, Elena, Mihailović-Vučinić, Violeta, Rottoli, Paola, Grubanovic, Aleksandar, Müller, Annegret, Jochens, Arne, Tittmann, Lukas, Schnerch, Jasmin, Olivieri, Carmela, Fischer, Annegret, Jovanovic, Dragana, Filipovic, Snežana, Videnovic-Ivanovic, Jelica, Bresser, Paul, Jonkers, René, O'Reilly, Kate, Ho, Ling-Pei, Gaede, Karoline I., Zabel, Peter, Dubaniewicz, Anna , Marshall, Ben, Kieszko, Robert, Milanowski, Janusz, Günther, Andreas, Weihrich, Anette, Petrek, Martin, Kolek, Vitezslav, Keane, Michael P., O'Beirne, Sarah , Donnelly, Seamas , Haraldsdottir, Sigridur Olina, Jorundsdottir, Kristin B., Costabel, Ulrich, Bonella, Francesco , Wallaert, Benoît, Grah, Christian, Peroš-Golubičić, Tatjana, Luisetti, Mauritio, Kadija, Zamir, Pabst, Stefan, Grohé, Christian, Strausz, János, Vašáková, Martina, Sterclova, Martina, Millar, Ann, Homolka, Jiří, Slováková, Alena, Kendrick, Yvonne, Crawshaw, Anjali, Wuyts, Wim, Spencer, Lisa, Pfeifer, Michael, Valeyre, Dominique, Poletti, Venerino , Wirtz, Hubertus, Prasse, Antje, Schreiber, Stefan, Krawczak, Michael und Müller-Quernheim, Joachim (2018) Phenotypes of organ involvement in sarcoidosis. European Respiratory Journal 51 (1), S. 1700991. Volltext nicht vorhanden.

Grassmann, Felix , Friedrich, Ulrike, Fauser, Sascha, Schick, Tina, Milenkovic, Andrea, Schulz, Heidi L., von Strachwitz, Claudia N., Bettecken, Thomas, Lichtner, Peter, Meitinger, Thomas , Arend, Nicole, Wolf, Armin, Haritoglou, Christos, Rudolph, Guenther, Chakravarthy, Usha , Silvestri, Giuliana, McKay, Gareth J. , Freitag-Wolf, Sandra, Krawczak, Michael , Smith, R. Theodore, Merriam, John C., Merriam, Joanna E., Allikmets, Rando, Heid, Iris M. und Weber, Bernhard H. F. (2015) A Candidate Gene Association Study Identifies DAPL1 as a Female-Specific Susceptibility Locus for Age-Related Macular Degeneration (AMD). NeuroMolecular Medicine 17 (2), S. 111-120.

Ahrens, Markus, Ammerpohl, Ole, von Schönfels, Witigo, Kolarova, Julia, Bens, Susanne, Itzel, Timo, Teufel, Andreas, Herrmann, Alexander, Brosch, Mario , Hinrichsen, Holger, Erhart, Wiebke, Egberts, Jan, Sipos, Bence, Schreiber, Stefan , Häsler, Robert, Stickel, Felix, Becker, Thomas, Krawczak, Michael , Röcken, Christoph, Siebert, Reiner, Schafmayer, Clemens und Hampe, Jochen (2013) DNA Methylation Analysis in Nonalcoholic Fatty Liver Disease Suggests Distinct Disease-Specific and Remodeling Signatures after Bariatric Surgery. Cell Metabolism 18 (2), S. 296-302. Volltext nicht vorhanden.

Stickel, Felix, Buch, Stephan, Lau, Katharina, zu Schwabedissen, Henriette Meyer, Berg, Thomas , Ridinger, Monika, Rietschel, Marcella, Schafmayer, Clemens, Braun, Felix, Hinrichsen, Holger, Günther, Rainer, Arlt, Alexander , Seeger, Marcus, Müller, Sebastian, Seitz, Helmut Karl, Soyka, Michael, Lerch, Markus , Lammert, Frank, Sarrazin, Christoph, Kubitz, Ralf, Häussinger, Dieter, Hellerbrand, Claus, Bröring, Dieter, Schreiber, Stefan , Kiefer, Falk, Spanagel, Rainer, Mann, Karl, Datz, Christian, Krawczak, Michael , Wodarz, Norbert, Völzke, Henry und Hampe, Jochen (2011) Genetic variation in the PNPLA3 gene is associated with alcoholic liver injury in caucasians. Hepatology 53 (1), S. 86-95. Volltext nicht vorhanden.

Del Greco M., F., Pattaro, C., Luchner, A., Pichler, I. , Winkler, T., Hicks, A. A. , Fuchsberger, C. , Franke, A. , Melville, S. A., Peters, A. , Wichmann, H. E., Schreiber, S. , Heid, I. M., Krawczak, M. , Minelli, C., Wiedermann, C. J. und Pramstaller, P. P. (2011) Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. Human Molecular Genetics 20 (8), S. 1660-1671. Volltext nicht vorhanden.

Pattaro, Cristian, De Grandi, Alessandro, Vitart, Veronique, Hayward, Caroline , Franke, Andre , Aulchenko, Yurii S , Johansson, Asa , Wild, Sarah H, Melville, Scott A, Isaacs, Aaron, Polasek, Ozren , Ellinghaus, David, Kolcic, Ivana , Nöthlings, Ute, Zgaga, Lina , Zemunik, Tatijana, Gnewuch, Carsten, Schreiber, Stefan , Campbell, Susan, Hastie, Nick, Boban, Mladen , Meitinger, Thomas , Oostra, Ben A, Riegler, Peter, Minelli, Cosetta, Wright, Alan F, Campbell, Harry, van Duijn, Cornelia M, Gyllensten, Ulf, Wilson, James F , Krawczak, Michael , Rudan, Igor und Pramstaller, Peter P (2010) A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2with serum creatinine level. BMC Medical Genetics 11 (1). Volltext nicht vorhanden.

Fritsche, L. G. , Freitag-Wolf, S., Bettecken, T., Meitinger, T. , Keilhauer, C. N., Krawczak, Michael und Weber, Bernhard H. F. (2009) Age-related macular degeneration and functional promoter and coding variants of the apolipoprotein E gene. Human Mutation 30, S. 1048-1053. Volltext nicht vorhanden.