Enhanced insight into the autoimmune component of glaucoma: IgG autoantibody accumulation and pro-inflammatory conditions in human glaucomatous retina von Gramlich, Oliver W, Beck, Sabine, von Thun Und Hohenstein-Blaul, Nadine, Boehm, Nils, Ziegler, Anika, Vetter, Jan M, Pfeiffer, Norbert, Grus, Franz H

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Personalized medicine using DNA biomarkers: a review von Ziegler, Andreas, Koch, Armin, Krockenberger, Katja, Großhennig, Anika

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Depletion and activation of microglia impact metabolic connectivity of the mouse brain von Gnörich, Johannes, Reifschneider, Anika, Wind, Karin, Zatcepin, Artem, Kunte, Sebastian T, Beumers, Philipp, Bartos, Laura M, Wiedemann, Thomas, Grosch, Maximilian, Xiang, Xianyuan, Fard, Maryam K, Ruch, Francois, Werner, Georg, Koehler, Mara, Slemann, Luna, Hummel, Selina, Briel, Nils, Blume, Tanja, Shi, Yuan, Biechele, Gloria, Beyer, Leonie, Eckenweber, Florian, Scheifele, Maximilian, Bartenstein, Peter, Albert, Nathalie L, Herms, Jochen, Tahirovic, Sabina, Haass, Christian, Capell, Anja, Ziegler, Sibylle, Brendel, Matthias

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TSPO imaging using the novel PET ligand [18F]GE-180: quantification approaches in patients with multiple sclerosis von Vomacka, Lena, Albert, Nathalie Lisa, Lindner, Simon, Unterrainer, Marcus, Mahler, Christoph, Brendel, Matthias, Ermoschkin, Larissa, Gosewisch, Astrid, Brunegraf, Anika, Buckley, Christopher, Kümpfel, Tania, Rupprecht, Rainer, Ziegler, Sibylle, Kerschensteiner, Martin, Bartenstein, Peter, Böning, Guido

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Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease von Germain, Cécile, Luc, Gérald, Großhennig, Anika, Ruidavets, Jean-Bernard, Preuss, Michael, Morrison, Caroline, Schreiber, Stefan, Stark, Klaus, van der Harst, Pim, Trégouët, David-Alexandre, Cambien, Francois, Munteanu, Alexandru, Thompson, John R, Neureuther, Katharina, Rubin, Diana, Perret, Claire, Tiret, Laurence, Ball, Stephen G, Schäfer, Arne, Meisinger, Christa, Hall, Alistair S, Bugert, Peter, Braund, Peter S, Schunkert, Heribert, Linsel-Nitschke, Patrick, Evans, Alun, Wichmann, H-Erich, Meitinger, Thomas, Wright, Ben J, König, Inke R, Schrezenmeir, Jürgen, Ouwehand, Willem, Erdmann, Jeanette, Arveiler, Dominique, El Mokhtari, Nour E, Ziegler, Andreas, Balmforth, Anthony J, Hengstenberg, Christian, DeSuremain, Maylis, Samani, Nilesh J

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Lifespan effects of mitochondrial mutations von Hirose, Misa, Schilf, Paul, Gupta, Yask, Wright, Marvin N., Jöhren, Olaf, Wagner, Anika E., Sina, Christian, Ziegler, Andreas, Ristow, Michael, Ibrahim, Saleh M.

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Regional desynchronization of microglial activity is associated with cognitive decline in Alzheimer's disease von Zatcepin, Artem, Gnörich, Johannes, Rauchmann, Boris-Stephan, Bartos, Laura M, Wagner, Stephan, Franzmeier, Nicolai, Malpetti, Maura, Xiang, Xianyuan, Shi, Yuan, Parhizkar, Samira, Grosch, Maximilian, Wind-Mark, Karin, Kunte, Sebastian T, Beyer, Leonie, Meyer, Carolin, Brösamle, Desirée, Wendeln, Ann-Christin, Osei-Sarpong, Collins, Heindl, Steffanie, Liesz, Arthur, Stoecklein, Sophia, Biechele, Gloria, Finze, Anika, Eckenweber, Florian, Lindner, Simon, Rominger, Axel, Bartenstein, Peter, Willem, Michael, Tahirovic, Sabina, Herms, Jochen, Buerger, Katharina, Simons, Mikael, Haass, Christian, Rupprecht, Rainer, Riemenschneider, Markus J, Albert, Nathalie L, Beyer, Marc, Neher, Jonas J, Paeger, Lars, Levin, Johannes, Höglinger, Günter U, Perneczky, Robert, Ziegler, Sibylle I, Brendel, Matthias

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Patient-specific image-based bone marrow dosimetry in Lu-177-[DOTA0,Tyr3]-Octreotate and Lu-177-DKFZ-PSMA-617 therapy: investigation of a new hybrid image approach von Gosewisch, Astrid, Delker, Andreas, Tattenberg, Sebastian, Ilhan, Harun, Todica, Andrei, Brosch, Julia, Vomacka, Lena, Brunegraf, Anika, Gildehaus, Franz Josef, Ziegler, Sibylle, Bartenstein, Peter, Böning, Guido

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New susceptibility locus for coronary artery disease on chromosome 3q22.3 von Perret, Claire, Blankenberg, Stefan, Stark, Klaus, Braund, Peter S, Rubin, Diana, Deloukas, Panos, Ball, Stephen G, Schäfer, Arne, Thompson, John R, Voight, Benjamin F, Zeller, Tanja, Schunkert, Heribert, Ouwehand, Willem H, Merlini, Piera Angelica, Schrezenmeir, Jürgen, Linsel-Nitschke, Patrick, Bernardinelli, Luisa, Elosua, Roberto, Wright, Ben, Peyvandi, Flora, Schillert, Arne, Meisinger, Christa, Hengstenberg, Christian, Samani, Nilesh J, Salomaa, Veikko, Peltonen, Leena, Melander, Olle, Schreiber, Stefan, Trégouët, David-Alexandre, Mokhtari, Nour Eddine El, Schwarz, Daniel F, Balmforth, Anthony J, Kathiresan, Sekar, Wagner, Arnika K, Siscovick, David S, Schwartz, Stephen M, Bugert, Peter, Ardissino, Diego, König, Inke R, Aherrahrou, Zouhair, Wild, Philipp, Erdmann, Jeanette, Baumert, Jens, Renner, Wilfried, Bruse, Petra, Klüter, Harald, Altshuler, David, März, Winfried, Wichmann, H-Erich, Ziegler, Andreas, Fischer, Marcus, Hall, Alistair S, Cambien, Francois, Meitinger, Thomas, Großhennig, Anika, Tiret, Laurence, O'Donnell, Christopher J, Peters, Annette

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Macrocephaly and developmental delay caused by missense variants in RAB5C von Koop, Klaas, Yuan, Weimin, Tessadori, Federico, Rodriguez-Polanco, Wilmer R, Grubbs, Jeremy, Zhang, Bo, Osmond, Matt, Graham, Gail, Sawyer, Sarah, Conboy, Erin, Vetrini, Francesco, Treat, Kayla, Płoski, Rafal, Pienkowski, Victor Murcia, Kłosowska, Anna, Fieg, Elizabeth, Krier, Joel, Mallebranche, Coralie, Alban, Ziegler, Aldinger, Kimberly A, Ritter, Deborah, Macnamara, Ellen, Sullivan, Bonnie, Herriges, John, Alaimo, Joseph T, Helbig, Catherine, Ellis, Colin A, Eyk, Clare, Gecz, Jozef, Farrugia, Daniel, Osei-Owusu, Ikeoluwa, Adès, Lesley, Boogaard, Marie-Jose, Fuchs, Sabine, Bakker, Jeroen, Duran, Karen, Dawson, Zachary D, Lindsey, Anika, Huang, Huiyan, Baldridge, Dustin, Silverman, Gary A, Grant, Barth D, Raizen, David, Network, Undiagnosed Diseases, Haaften, Gijs, Pak, Stephen C, Rehmann, Holger, Schedl, Tim, van Hasselt, Peter

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Lack of Association Between the MEF2A Gene and Myocardial Infarction von LIEB, Wolfgang, MAYER, Björn, WICHMANN, H.-Erich, MEITINGER, Thomas, KREUTZ, Reinhold, ZIEGLER, Andreas, SCHUNKERT, Heribert, ERDMANN, Jeanette, KÖNIG, Inke R, BORWITZKY, Iris, GOTZ, Anika, KAIN, Silke, HENGSTENBERG, Christian, LINSEL-NITSCHKE, Patrick, FISCHER, Marcus, DORING, Angela

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Feasibility of short imaging protocols for 18FPI-2620 tau-PET in progressive supranuclear palsy von Song, Mengmeng, Scheifele, Maximilian, Barthel, Henryk, van Eimeren, Thilo, Beyer, Leonie, Marek, Ken, Eckenweber, Florian, Palleis, Carla, Kaiser, Lena, Finze, Anika, Kern, Maike, Nitschmann, Alexander, Biechele, Gloria, Katzdobler, Sabrina, Bischof, Gèrard, Hammes, Jochen, Jessen, Frank, Saur, Dorothee, Schroeter, Matthias L, Rumpf, Jost-Julian, Rullmann, Michael, Schildan, Andreas, Patt, Marianne, Neumaier, Bernd, Stephens, Andrew W, Rauchmann, Boris-Stephan, Perneczky, Robert, Levin, Johannes, Classen, Joseph, Höglinger, Günter U, Bartenstein, Peter, Boening, Guido, Ziegler, Sibylle, Villemagne, Victor, Drzezga, Alexander, Seibyl, John, Sabri, Osama, Brendel, Matthias

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The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol von Samani, Nilesh J., Braund, Peter S., Erdmann, Jeanette, Götz, Anika, Tomaszewski, Maciej, Linsel-Nitschke, Patrick, Hajat, Cother, Mangino, Massimo, Hengstenberg, Christian, Stark, Klaus, Ziegler, Andreas, Caulfield, Mark, Burton, Paul R., Schunkert, Heribert, Tobin, Martin D.

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Plasma Carotenoid- and Retinol-Weighted Multi-SNP Scores and Risk of Breast Cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium von HENDRICKSON, Sara J, LINDSTRÖM, Sara, CLAVEL-CHAPELON, Françoise, FIGUEROA, Jonine D, GAPSTUR, Susan M, GARCIA-CLOSAS, Montserrat, GAUDET, Mia M, HAIMAN, Christopher A, HAZRA, Aditi, HENDERSON, Brian, HOOVER, Robert, HÜSING, Anika, HEATHER ELIASSEN, A, JOHANSSON, Mattias, KAAKS, Rudolf, KHAW, Kay-Tee, KOLONEL, Laurence N, LE MARCHAND, Loic, LISSOWSKA, Jolanta, LUND, Eiliv, MCCULLOUGH, Marjorie L, PEPLONSKA, Beata, RIBOLI, Elio, ROSNER, Bernard A, SACERDOTE, Carlotta, SANCHEZ, María-José, TJONNELAND, Anne, TRICHOPOULOS, Dimitrios, GILS, Carla H. Van, YEAGER, Meredith, KRAFT, Peter, HUNTER, David J, ZIEGLER, Regina G, WILLETT, Walter C, CHEN, Constance, BARRDAHL, Myrto, BRINTON, Louise, BURING, Julie, CANZIAN, Federico, CHANOCK, Stephen

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Feasibility of short imaging protocols for [18F]PI‐2620 tau‐PET in progressive supranuclear palsy von Song, Mengmeng, Scheifele, Maximilian, Barthel, Henryk, van Eimeren, Thilo, Beyer, Leonie, Marek, Ken, Eckenweber, Florian, Palleis, Carla, Finze, Anika, Kaiser, Lena, Kern, Maike, Nitschmann, Alexander, Biechele, Gloria, Katzdobler, Sabrina, Bischof, Gerard N, Hammes, Jochen, Jessen, Frank, Saur, Dorothee, Schroeter, Matthias L., Rumpf, Jost‐Julian, Rullmann, Michael, Schildan, Andreas, Patt, Marianne, Neumaier, Bernd, Stephens, Andrew W, Rauchmann, Boris‐Stephan, Perneczky, Robert, Levin, Johannes, Classen, Joseph, Höglinger, Günter, Bartenstein, Peter, Boening, Guido, Ziegler, Sibylle, Villemagne, Victor L L, Drzezga, Alexander, Seibyl, John P, Sabri, Osama, Brendel, Matthias

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Association of a functional polymorphism in the CYP4A11 gene with systolic blood pressure in survivors of myocardial infarction von Mayer, Björn, Lieb, Wolfgang, Götz, Anika, König, Inke R, Kauschen, Lena F, Linsel-Nitschke, Patrick, Pomarino, Andrea, Holmer, Stephan, Hengstenberg, Christian, Doering, Angela, Loewel, Hannelore, Hense, Hans-Werner, Ziegler, Andreas, Erdmann, Jeanette, Schunkert, Heribert

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Effekt Glückssache?: Zwei teststarke, präregistrierte Replikationsstudien zum Einfluss von Glück auf kognitive Leistung von Dickhäuser, Oliver, Heinze, Adrian, Hamm, Marie Luisa, Bales, Anika Sophie, Bellmann, Svenja Amelie, Böger, Daniela, Gagelmann, Lidia Katarzyna, Kuhlenkamp, Felix, Merger, Julia Kathleen, Viehweger, Hanna, Ziegler, Julian, Neuenstein, Anna von

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Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction von Lieb, Wolfgang, Zeller, Tanja, Mangino, Massimo, Götz, Anika, Braund, Peter, Wenzel, Juergen J., Horn, Christian, Proust, Carole, Linsel-Nitschke, Patrick, Amouyel, Philippe, Bruse, Petra, Arveiler, Dominique, König, Inke R., Ferrières, Jean, Ziegler, Andreas, Balmforth, Anthony J., Evans, Alun, Ducimetière, Pierre, Cambien, Francois, Hengstenberg, Christian, Stark, Klaus, Hall, Alistair S., Schunkert, Heribert, Blankenberg, Stefan, Samani, Nilesh J., Erdmann, Jeanette, Tiret, Laurence

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Abstract 3452: The Common Variant Rs9939609 In The FTO Gene Is Associated With Myocardial Infarction In Two Large German Populations (German Family MI Study And KORA-B) von Erdmann, Jeanette, Götz, Anika, Bruse, Petra, Medack, Anja, Lieb, Wolfgang, Fischer, Marcus, Baessler, Andrea, Stark, Klaus, Hengstenberg, Christian, Ziegler, Andreas, Schunkert, Heribert

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Correction: Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease—A Mendelian Randomisation Study... von Linsel-Nitschke, Patrick, Götz, Anika, Erdmann, Jeanette, Braenne, Ingrid, Braund, Peter, Hengstenberg, Christian, Stark, Klaus, Fischer, Marcus, Schreiber, Stefan, El Mokhtari, Nour Eddine, Schaefer, Arne, Schrezenmeir, Jürgen, Rubin, Diana, Hinney, Anke, Reinehr, Thomas, Roth, Christian, Ortlepp, Jan, Hanrath, Peter, Hall, Alistair S., Mangino, Massimo, Lieb, Wolfgang, Lamina, Claudia, Heid, Iris M., Doering, Angela, Gieger, Christian, Peters, Annette, Meitinger, Thomas, Wichmann, H.-Erich, König, Inke R., Ziegler, Andreas, Kronenberg, Florian, Samani, Nilesh J., Schunkert, Heribert

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