检索结果 - Mühleisen, Thomas W

Integration of transcriptomic and cytoarchitectonic data implicates a role for MAOA and TAC1 in the limbic-cortical network 由 Bludau, Sebastian, Mühleisen, Thomas W., Eickhoff, Simon B., Hawrylycz, Michael J., Cichon, Sven, Amunts, Katrin

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Identification of Phonology-Related Genes and Functional Characterization of Broca’s and Wernicke’s Regions in Language and Learning Disorders 由 Unger, Nina, Heim, Stefan, Hilger, Dominique I., Bludau, Sebastian, Pieperhoff, Peter, Cichon, Sven, Amunts, Katrin, Mühleisen, Thomas W.

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Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study 由 Pechlivanis, Sonali, Mühleisen, Thomas W, Möhlenkamp, Stefan, Schadendorf, Dirk, Erbel, Raimund, Jöckel, Karl-Heinz, Hoffmann, Per, Nöthen, Markus M, Scherag, André, Moebus, Susanne

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Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults 由 Bittner, Nora, Jockwitz, Christiane, Mühleisen, Thomas W., Hoffstaedter, Felix, Eickhoff, Simon B., Moebus, Susanne, Bayen, Ute J., Cichon, Sven, Zilles, Karl, Amunts, Katrin, Caspers, Svenja

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A GWAS top hit for circulating leptin is associated with weight gain but not with leptin protein levels in lithium-augmented patients with major depression 由 Bopp, Sandra K, Heilbronner, Urs, Schlattmann, Peter, Buspavanich, Pichit J, Lang, Undine E, Heinz, Andreas, Schulze, Thomas G, Adli, Mazda, Mühleisen, Thomas W, Ricken, Roland

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Hippocampal Function in Healthy Carriers of the CLU Alzheimer's Disease Risk Variant 由 Erk, Susanne, Meyer-Lindenberg, Andreas, Opitz von Boberfeld, Carola, Esslinger, Christine, Schnell, Knut, Kirsch, Peter, Mattheisen, Manuel, Mühleisen, Thomas W., Cichon, Sven, Witt, Stephanie H., Rietschel, Marcella, Nöthen, Markus M., Walter, Henrik

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Reduced Cortical Thickness is Associated with the Glutamatergic Regulatory Gene Risk Variant DAOA Arg30Lys in Schizophrenia 由 Schultz, C Christoph, Nenadic, Igor, Koch, Kathrin, Wagner, Gerd, Roebel, Martin, Schachtzabel, Claudia, Mühleisen, Thomas W, Nöthen, Markus M, Cichon, Sven, Deufel, Thomas, Kiehntopf, Michael, Rietschel, Marcella, Reichenbach, Jürgen R, Sauer, Heinrich, Schlösser, Ralf G M

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A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry 由 Strohmaier, Jana, Frank, Josef, Wendland, Jens R., Schumacher, Johannes, Jamra, Rami Abou, Treutlein, Jens, Nieratschker, Vanessa, Breuer, René, Mattheisen, Manuel, Herms, Stefan, Mühleisen, Thomas W., Maier, Wolfgang, Nöthen, Markus M., Cichon, Sven, Rietschel, Marcella, Schulze, Thomas G.

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ZNF804A and Cortical Structure in Schizophrenia: In Vivo and Postmortem Studies 由 Schultz, Carl Christoph, Nenadic, Igor, Riley, Brien, Vladimirov, Vladimir I., Wagner, Gerd, Koch, Kathrin, Schachtzabel, Claudia, Mühleisen, Thomas W., Basmanav, Buket, Nöthen, Markus M., Deufel, Thomas, Kiehntopf, Michael, Rietschel, Marcella, Reichenbach, Jürgen R., Cichon, Sven, Schlösser, Ralf G. M., Sauer, Heinrich

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The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations 由 Schumacher, Johannes, Laje, Gonzalo, Jamra, Rami Abou, Becker, Tim, Mühleisen, Thomas W., Vasilescu, Catalina, Mattheisen, Manuel, Herms, Stefan, Hoffmann, Per, Hillmer, Axel M., Georgi, Alexander, Herold, Christine, Schulze, Thomas G., Propping, Peter, Rietschel, Marcella, McMahon, Francis J., Nöthen, Markus M., Cichon, Sven

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Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1 由 McMahon, Francis J., Akula, Nirmala, Schulze, Thomas G., Muglia, Pierandrea, Tozzi, Federica, Detera-Wadleigh, Sevilla D., Steele, C.J.M., Breuer, René, Strohmaier, Jana, Wendland, Jens R., Mattheisen, Manuel, Mühleisen, Thomas W., Maier, Wolfgang, Nöthen, Markus M., Cichon, Sven, Farmer, Anne, Vincent, John B., Holsboer, Florian, Preisig, Martin, Rietschel, Marcella

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Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia 由 Juraeva, Dilafruz, Haenisch, Britta, Zapatka, Marc, Frank, Josef, Witt, Stephanie H., Mühleisen, Thomas W., Treutlein, Jens, Strohmaier, Jana, Meier, Sandra, Degenhardt, Franziska, Giegling, Ina, Ripke, Stephan, Leber, Markus, Lange, Christoph, Schulze, Thomas G., Mössner, Rainald, Nenadic, Igor, Sauer, Heinrich, Rujescu, Dan, Maier, Wolfgang, Børglum, Anders, Ophoff, Roel, Cichon, Sven, Nöthen, Markus M., Rietschel, Marcella, Mattheisen, Manuel, Brors, Benedikt

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Studying variability in human brain aging in a population-based German cohort—rationale and design of 1000BRAINS 由 Caspers, Svenja, Moebus, Susanne, Lux, Silke, Pundt, Noreen, Schütz, Holger, Mühleisen, Thomas W., Gras, Vincent, Eickhoff, Simon B., Romanzetti, Sandro, Stöcker, Tony, Stirnberg, Rüdiger, Kirlangic, Mehmet E., Minnerop, Martina, Pieperhoff, Peter, Mödder, Ulrich, Das, Samir, Evans, Alan C., Jöckel, Karl-Heinz, Erbel, Raimund, Cichon, Sven, Nöthen, Markus M., Sturma, Dieter, Bauer, Andreas, Jon Shah, N., Zilles, Karl, Amunts, Katrin

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Common variation at 10p12.31 near MLLT10 influences meningioma risk 由 Dobbins, Sara E, Broderick, Peter, Melin, Beatrice, Feychting, Maria, Johansen, Christoffer, Andersson, Ulrika, Brännström, Thomas, Schramm, Johannes, Olver, Bianca, Lloyd, Amy, Ma, Yussanne P, Hosking, Fay J, Lönn, Stefan, Ahlbom, Anders, Henriksson, Roger, Schoemaker, Minouk J, Hepworth, Sarah J, Hoffmann, Per, Mühleisen, Thomas W, Nöthen, Markus M, Moebus, Susanne, Eisele, Lewin, Kosteljanetz, Michael, Muir, Kenneth, Swerdlow, Anthony, Simon, Matthias, Houlston, Richard S

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Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk 由 Broderick, Peter, Chubb, Daniel, Johnson, David C, Weinhold, Niels, Försti, Asta, Lloyd, Amy, Olver, Bianca, Ma, Yussanne, Dobbins, Sara E, Walker, Brian A, Davies, Faith E, Gregory, Walter A, Childs, J. Anthony, Ross, Fiona M, Jackson, Graham H, Neben, Kai, Jauch, Anna, Hoffmann, Per, Mühleisen, Thomas W, Nöthen, Markus M, Moebus, Susanne, Tomlinson, Ian P, Goldschmidt, Hartmut, Hemminki, Kari, Morgan, Gareth J, Houlston, Richard S

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Genetic factors influencing a neurobiological substrate for psychiatric disorders 由 Andlauer, Till F. M., Mühleisen, Thomas W., Hoffstaedter, Felix, Teumer, Alexander, Wittfeld, Katharina, Teuber, Anja, Reinbold, Céline S., Grotegerd, Dominik, Bülow, Robin, Caspers, Svenja, Dannlowski, Udo, Herms, Stefan, Hoffmann, Per, Kircher, Tilo, Minnerup, Heike, Moebus, Susanne, Nenadić, Igor, Teismann, Henning, Völker, Uwe, Etkin, Amit, Berger, Klaus, Grabe, Hans J., Nöthen, Markus M., Amunts, Katrin, Eickhoff, Simon B., Sämann, Philipp G., Müller-Myhsok, Bertram, Cichon, Sven

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Common and Rare Variant Analysis in Early-Onset Bipolar Disorder Vulnerability 由 Jamain, Stéphane, Cichon, Sven, Etain, Bruno, Mühleisen, Thomas W., Georgi, Alexander, Zidane, Nora, Chevallier, Lucie, Deshommes, Jasmine, Nicolas, Aude, Henrion, Annabelle, Degenhardt, Franziska, Mattheisen, Manuel, Priebe, Lutz, Mathieu, Flavie, Kahn, Jean-Pierre, Henry, Chantal, Boland, Anne, Zelenika, Diana, Gut, Ivo, Heath, Simon, Lathrop, Mark, Maier, Wolfgang, Albus, Margot, Rietschel, Marcella, Schulze, Thomas G., McMahon, Francis J., Kelsoe, John R., Hamshere, Marian, Craddock, Nicholas, Nöthen, Markus M., Bellivier, Frank, Leboyer, Marion

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The CCND1 870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma 由 Weinhold, Niels, Johnson, David C, Chubb, Daniel, Chen, Bowang, Försti, Asta, Hosking, Fay J, Broderick, Peter, Ma, Yussanne P, Dobbins, Sara E, Hose, Dirk, Walker, Brian A, Davies, Faith E, Kaiser, Martin F, Li, Ni L, Gregory, Walter A, Jackson, Graham H, Witzens-Harig, Mathias, Neben, Kai, Hoffmann, Per, Nöthen, Markus M, Mühleisen, Thomas W, Eisele, Lewin, Ross, Fiona M, Jauch, Anna, Goldschmidt, Hartmut, Houlston, Richard S, Morgan, Gareth J, Hemminki, Kari

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DCLK1 Variants Are Associated across Schizophrenia and Attention Deficit/Hyperactivity Disorder 由 Håvik, Bjarte, Degenhardt, Franziska A., Johansson, Stefan, Fernandes, Carla P. D., Hinney, Anke, Scherag, André, Lybæk, Helle, Djurovic, Srdjan, Christoforou, Andrea, Ersland, Kari M., Giddaluru, Sudheer, O'Donovan, Michael C., Owen, Michael J., Craddock, Nick, Mühleisen, Thomas W., Mattheisen, Manuel, Schimmelmann, Benno G., Renner, Tobias, Warnke, Andreas, Herpertz-Dahlmann, Beate, Sinzig, Judith, Albayrak, Özgür, Rietschel, Marcella, Nöthen, Markus M., Bramham, Clive R., Werge, Thomas, Hebebrand, Johannes, Haavik, Jan, Andreassen, Ole A., Cichon, Sven, Steen, Vidar M., Le Hellard, Stéphanie

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Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk 由 Chubb, Daniel, Weinhold, Niels, Broderick, Peter, Chen, Bowang, Johnson, David C, Försti, Asta, Vijayakrishnan, Jayaram, Migliorini, Gabriele, Dobbins, Sara E, Holroyd, Amy, Hose, Dirk, Walker, Brian A, Davies, Faith E, Gregory, Walter A, Jackson, Graham H, Irving, Julie A, Pratt, Guy, Fegan, Chris, Fenton, James AL, Neben, Kai, Hoffmann, Per, Nöthen, Markus M, Mühleisen, Thomas W, Eisele, Lewin, Ross, Fiona M, Straka, Christian, Einsele, Hermann, Langer, Christian, Dörner, Elisabeth, Allan, James M, Jauch, Anna, Morgan, Gareth J, Hemminki, Kari, Houlston, Richard S, Goldschmidt, Hartmut

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