Integration of transcriptomic and cytoarchitectonic data implicates a role for MAOA and TAC1 in the limbic-cortical network

Yazar: Bludau, Sebastian, Mühleisen, Thomas W., Eickhoff, Simon B., Hawrylycz, Michael J., Cichon, Sven, Amunts, Katrin
Yayımlandı Brain Struct Funct (2018)

Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study

Yazar: Pechlivanis, Sonali, Mühleisen, Thomas W, Möhlenkamp, Stefan, Schadendorf, Dirk, Erbel, Raimund, Jöckel, Karl-Heinz, Hoffmann, Per, Nöthen, Markus M, Scherag, André, Moebus, Susanne
Baskı/Yayın Bilgisi 2013

Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults

Yazar: 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
Yayımlandı Nat Commun (2019)

Hippocampal Function in Healthy Carriers of the CLU Alzheimer's Disease Risk Variant

Yazar: 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
Yayımlandı J Neurosci (2011)

Reduced Cortical Thickness is Associated with the Glutamatergic Regulatory Gene Risk Variant DAOA Arg30Lys in Schizophrenia

Yazar: 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
Baskı/Yayın Bilgisi 2011

Genome-wide significant association between a ‘negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1

Yazar: Meier, S, Mattheisen, M, Vassos, E, Strohmaier, J, Treutlein, J, Josef, F, Breuer, R, Degenhardt, F, Mühleisen, T W, Müller-Myhsok, B, Steffens, M, Schmael, C, McMahon, F J, Nöthen, M M, Cichon, S, Schulze, T G, Rietschel, M
Baskı/Yayın Bilgisi 2012

A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry

Yazar: 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.
Baskı/Yayın Bilgisi 2010

Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study

Yazar: Hammer, C, Cichon, S, Mühleisen, T W, Haenisch, B, Degenhardt, F, Mattheisen, M, Breuer, R, Witt, S H, Strohmaier, J, Oruc, L, Rivas, F, Babadjanova, G, Grigoroiu-Serbanescu, M, Hauser, J, Röth, R, Rappold, G, Rietschel, M, Nöthen, M M, Niesler, B
Baskı/Yayın Bilgisi 2012

ZNF804A and Cortical Structure in Schizophrenia: In Vivo and Postmortem Studies

Yazar: 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
Baskı/Yayın Bilgisi 2014

The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

Yazar: 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
Baskı/Yayın Bilgisi 2009

Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains

Yazar: Erk, S, Mohnke, S, Ripke, S, Lett, T A, Veer, I M, Wackerhagen, C, Grimm, O, Romanczuk-Seiferth, N, Degenhardt, F, Tost, H, Mattheisen, M, Mühleisen, T W, Charlet, K, Skarabis, N, Kiefer, F, Cichon, S, Witt, S H, Nöthen, M M, Rietschel, M, Heinz, A, Meyer-Lindenberg, A, Walter, H
Yayımlandı Transl Psychiatry (2017)

Effects of BDNF Val(66)Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans

Yazar: Schweiger, J. I., Bilek, E., Schäfer, A., Braun, U., Moessnang, C., Harneit, A., Post, P., Otto, K., Romanczuk-Seiferth, N., Erk, S., Wackerhagen, C., Mattheisen, M., Mühleisen, T. W., Cichon, S., Nöthen, M. M., Frank, J., Witt, S. H., Rietschel, M., Heinz, A., Walter, H., Meyer-Lindenberg, A., Tost, H.
Yayımlandı Neuropsychopharmacology (2018)

Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1

Yazar: 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
Baskı/Yayın Bilgisi 2010

Epistatic interaction of genetic depression risk variants in the human subgenual cingulate cortex during memory encoding

Yazar: Schott, B H, Assmann, A, Schmierer, P, Soch, J, Erk, S, Garbusow, M, Mohnke, S, Pöhland, L, Romanczuk-Seiferth, N, Barman, A, Wüstenberg, T, Haddad, L, Grimm, O, Witt, S, Richter, S, Klein, M, Schütze, H, Mühleisen, T W, Cichon, S, Rietschel, M, Noethen, M M, Tost, H, Gundelfinger, E D, Düzel, E, Heinz, A, Meyer-Lindenberg, A, Seidenbecher, C I, Walter, H
Baskı/Yayın Bilgisi 2014

Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia

Yazar: 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
Baskı/Yayın Bilgisi 2014

Studying variability in human brain aging in a population-based German cohort—rationale and design of 1000BRAINS

Yazar: 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
Baskı/Yayın Bilgisi 2014

Common variation at 10p12.31 near MLLT10 influences meningioma risk

Yazar: 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
Yayımlandı Nat Genet (2011)

The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A

Yazar: Vijayakrishnan, Jayaram, Henrion, Marc, Moorman, Anthony V., Fiege, Bettina, Kumar, Rajiv, Inacio da Silva Filho, Miguel, Holroyd, Amy, Koehler, Rolf, Thomsen, Hauke, Irving, Julie A., Allan, James M., Lightfoot, Tracy, Roman, Eve, Kinsey, Sally E., Sheridan, Eamonn, Thompson, Pamela D., Hoffmann, Per, Nöthen, Markus M., Mühleisen, Thomas W., Eisele, Lewin, Bartram, Claus R., Schrappe, Martin, Greaves, Mel, Hemminki, Kari, Harrison, Christine J., Stanulla, Martin, Houlston, Richard S.
Yayımlandı Sci Rep (2015)

Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk

Yazar: 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
Yayımlandı Nat Genet (2011)

Genetic factors influencing a neurobiological substrate for psychiatric disorders

Yazar: 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
Yayımlandı Transl Psychiatry (2021)