Zobrazeno 1 - 10
of 117
pro vyhledávání: '"Breuer, René"'
Autor:
Nieratschker, Vanessa, Lahtinen, Jenni, Meier, Sandra, Strohmaier, Jana, Frank, Josef, Heinrich, Angela, Breuer, René, Witt, Stephanie H., Nöthen, Markus M., Rietschel, Marcella, Hovatta, Iiris
Publikováno v:
In Schizophrenia Research September 2013 149(1-3):116-120
Autor:
Nieratschker, Vanessa, Frank, Josef, Mühleisen, Thomas W., Strohmaier, Jana, Wendland, Jens R., Schumacher, Johannes, Treutlein, Jens, Breuer, René, Jamra, Rami Abou, Mattheisen, Manuel, Herms, Stefan, Schmäl, Christine, Maier, Wolfgang, Nöthen, Markus M., Cichon, Sven, Rietschel, Marcella, Schulze, Thomas G.
Publikováno v:
In Schizophrenia Research September 2010 122(1-3):24-30
Autor:
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.
Publikováno v:
In Schizophrenia Research May 2010 118(1-3):98-105
Autor:
Treutlein, Jens, Mühleisen, Thomas W., Frank, Josef, Mattheisen, Manuel, Herms, Stefan, Ludwig, Kerstin U., Treutlein, Tsendsesmee, Schmael, Christine, Strohmaier, Jana, Böβhenz, Katja Veronika, Breuer, René, Paul, Torsten, Witt, Stephanie H., Schulze, Thomas G., Schlösser, Ralf G.M., Nenadic, Igor, Sauer, Heinrich, Becker, Tim, Maier, Wolfgang, Cichon, Sven, Nöthen, Markus M., Rietschel, Marcella
Publikováno v:
In Schizophrenia Research 2009 111(1):123-130
Autor:
Chang, Hong, Li, Lingyi, Peng, Tao, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean Pierre, Henry, Chantal, Rietschel, Marcella, Backlund, Lena, Frisén, Louise, Lavebratt, Catharina, Schalling, Martin, Ösby, Urban, Mühleisen, Thomas W., Leber, Markus, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Hofmann, Andrea, Breuer, René, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, André, Witt, Stephanie H., Streit, Fabian, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Wright, Adam, Fullerton, Janice M., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Becker, Tim, Schumacher, Johannes, Propping, Peter, Xiao, Xiao, Li, Ming
Publikováno v:
Chang, H, Li, L, Peng, T, Grigoroiu-Serbanescu, M, Bergen, S E, Landén, M, Hultman, C M, Forstner, A J, Strohmaier, J, Hecker, J, Schulze, T G, Müller-Myhsok, B, Reif, A, Mitchell, P B, Martin, N G, Cichon, S, Nöthen, M M, Jamain, S, Leboyer, M, Bellivier, F, Etain, B, Kahn, J P, Henry, C, Rietschel, M, Backlund, L, Frisén, L, Lavebratt, C, Schalling, M, Ösby, U, Mühleisen, T W, Leber, M, Degenhardt, F, Treutlein, J, Mattheisen, M, Hofmann, A, Breuer, R, Meier, S, Herms, S, Hoffmann, P, Lacour, A, Witt, S H, Streit, F, Lucae, S, Maier, W, Schwarz, M, Vedder, H, Kammerer-Ciernioch, J, Pfennig, A, Bauer, M, Hautzinger, M, Wright, A, Fullerton, J M, Schofield, P R, Montgomery, G W, Medland, S E, Gordon, S D, Becker, T, Schumacher, J, Propping, P, Xiao, X & Li, M 2017, ' Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1 ', Molecular Neurobiology, vol. 54, no. 7, pp. 5166-5176 . https://doi.org/10.1007/s12035-016-0041-x
MOLECULAR NEUROBIOLOGY
Molecular Neurobiology
Molecular Neurobiology, Humana Press, 2017, 54 (7), pp.5166-5176. ⟨10.1007/s12035-016-0041-x⟩
MOLECULAR NEUROBIOLOGY
Molecular Neurobiology
Molecular Neurobiology, Humana Press, 2017, 54 (7), pp.5166-5176. ⟨10.1007/s12035-016-0041-x⟩
Genome-wide analysis (GWA) is an effective strategy to discover extreme effects surpassing genome-wide significant levels in studying complex disorders; however, when sample size is limited, the true effects may fail to achieve genome-wide significan
Autor:
Breuer, René, Mattheisen, Manuel, Frank, Josef, Krumm, Bertram, Treutlein, Jens, Kassem, Layla, Strohmaier, Jana, Herms, Stefan, Mühleisen, Thomas W., Degenhardt, Franziska, Cichon, Sven, Nöthen, Markus M., Karypis, George, Kelsoe, John, Greenwood, Tiffany, Nievergelt, Caroline, Shilling, Paul, Shekhtman, Tatyana, Edenberg, Howard, Craig, David, Szelinger, Szabolcs, Nurnberger, John, Gershon, Elliot, Alliey-Rodriguez, Ney, Zandi, Peter, Goes, Fernando, Schork, Nicholas, Smith, Erin, Koller, Daniel, Zhang, Peng, Badner, Judith, Berrettini, Wade, Bloss, Cinnamon, Byerley, William, Coryell, William, Foroud, Tatiana, Guo, Yirin, Hipolito, Maria, Keating, Brendan, Lawson, William, Liu, Chunyu, Mahon, Pamela, McInnis, Melvin, Murray, Sarah, Nwulia, Evaristus, Potash, James, Rice, John, Scheftner, William, Zöllner, Sebastian, McMahon, Francis J., Rietschel, Marcella, Schulze, Thomas G.
Publikováno v:
International Journal of Bipolar Disorders
International Journal of Bipolar Disorders 6(1), 24 (2018). doi:10.1186/s40345-018-0132-x
International Journal of Bipolar Disorders, Vol 6, Iss 1, Pp 1-10 (2018)
Breuer, R, Mattheisen, M, Frank, J, Krumm, B, Treutlein, J, Kassem, L, Strohmaier, J, Herms, S, Mühleisen, T W, Degenhardt, F, Cichon, S, Nöthen, M M, Karypis, G, Kelsoe, J, Greenwood, T, Nievergelt, C, Shilling, P, Shekhtman, T, Edenberg, H, Craig, D, Szelinger, S, Nurnberger, J, Gershon, E, Alliey-Rodriguez, N, Zandi, P, Goes, F, Schork, N, Smith, E, Koller, D, Zhang, P, Badner, J, Berrettini, W, Bloss, C, Byerley, W, Coryell, W, Foroud, T, Guo, Y, Hipolito, M, Keating, B, Lawson, W, Liu, C, Mahon, P, McInnis, M, Murray, S, Nwulia, E, Potash, J, Rice, J, Scheftner, W, Zöllner, S, McMahon, F J, Rietschel, M & Schulze, T G 2018, ' Detecting significant genotype–phenotype association rules in bipolar disorder : market research meets complex genetics ', International Journal of Bipolar Disorders, vol. 6, no. 1, 24 . https://doi.org/10.1186/s40345-018-0132-x
International Journal of Bipolar Disorders 6(1), 24 (2018). doi:10.1186/s40345-018-0132-x
International Journal of Bipolar Disorders, Vol 6, Iss 1, Pp 1-10 (2018)
Breuer, R, Mattheisen, M, Frank, J, Krumm, B, Treutlein, J, Kassem, L, Strohmaier, J, Herms, S, Mühleisen, T W, Degenhardt, F, Cichon, S, Nöthen, M M, Karypis, G, Kelsoe, J, Greenwood, T, Nievergelt, C, Shilling, P, Shekhtman, T, Edenberg, H, Craig, D, Szelinger, S, Nurnberger, J, Gershon, E, Alliey-Rodriguez, N, Zandi, P, Goes, F, Schork, N, Smith, E, Koller, D, Zhang, P, Badner, J, Berrettini, W, Bloss, C, Byerley, W, Coryell, W, Foroud, T, Guo, Y, Hipolito, M, Keating, B, Lawson, W, Liu, C, Mahon, P, McInnis, M, Murray, S, Nwulia, E, Potash, J, Rice, J, Scheftner, W, Zöllner, S, McMahon, F J, Rietschel, M & Schulze, T G 2018, ' Detecting significant genotype–phenotype association rules in bipolar disorder : market research meets complex genetics ', International Journal of Bipolar Disorders, vol. 6, no. 1, 24 . https://doi.org/10.1186/s40345-018-0132-x
Background Disentangling the etiology of common, complex diseases is a major challenge in genetic research. For bipolar disorder (BD), several genome-wide association studies (GWAS) have been performed. Similar to other complex disorders, major break
Autor:
Breuer, René, Mattheisen, Manuel, Frank, Josef, Krumm, Bertram, Treutlein, Jens, Kassem, Layla, Strohmaier, Jana, Herms, Stefan, Mühleisen, Thomas, Degenhardt, Franziska, Cichon, Sven, Nöthen, Markus, Karypis, George, Kelsoe, John, Greenwood, Tiffany, Nievergelt, Caroline, Shilling, Paul, Shekhtman, Tatyana, Edenberg, Howard, Craig, David, Szelinger, Szabolcs, Nurnberger, John, Gershon, Elliot, Ney Alliey-Rodriguez, Zandi, Peter, Goes, Fernando, Schork, Nicholas, Smith, Erin, Koller, Daniel, Zhang, Peng, Badner, Judith, Berrettini, Wade, Cinnamon Bloss, Byerley, William, Coryell, William, Foroud, Tatiana, Yirin Guo, Hipolito, Maria, Keating, Brendan, Lawson, William, Chunyu Liu, Mahon, Pamela, McInnis, Melvin, Murray, Sarah, Evaristus Nwulia, Potash, James, Rice, John, Scheftner, William, Zöllner, Sebastian, McMahon, Francis, Rietschel, Marcella, Schulze, Thomas
Additional file 4: Text S1. Supplementary notes on methods.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bce82891b194ac78b2473d9337e00e1
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Autor:
Mühleisen, Thomas W, Mattheisen, Manuel, Rivandeneira, Fernando, Hofman, Albert, Uitterlinden, André G, Moebus, Susanne, Gieger, Christian, Emeny, Rebecca, Ladwig, Karl-Heinz, Wichmann, H-Erich, Schwarz, Markus, Kammerer-Ciernioch, Jutta, Strohmaier, Jana, Schlösser, Ralf G M, Nenadic, Igor, Sauer, Heinrich, Mössner, Rainald, Maier, Wolfgang, Rujescu, Dan, Lange, Christoph, Ophoff, Roel A, Schulze, Thomas G, Rietschel, Marcella, Degenhardt, Franziska, Nöthen, Markus M, Priebe, Lutz, Schultz, C Christoph, Kahn, René S, Linszen, Don H, van Os, Jim, Wiersma, Durk, Bruggeman, Richard, Cahn, Wiepke, de Haan, Lieuwe, Krabbendam, Lydia, Myin-Germeys, Inez, Breuer, René, Wichmann, H -Erich, Breuer, Rene, Meier, Sandra, Hoffmann, Per, Cichon, Sven, Investigators, GROUP
Publikováno v:
Schizophrenia Research, 138(1), 69-73. Elsevier Science
Schizophrenia research, 138(1), 69-73. Elsevier
Schizophrenia research 138(1), 69-73 (2012). doi:10.1016/j.schres.2012.03.007
Schizophrenia Research, 138(1), 69-73. Elsevier
Schizophrenia research, 138(1), 69-73. Elsevier
Schizophrenia research 138(1), 69-73 (2012). doi:10.1016/j.schres.2012.03.007
Schizophrenia Research, 138(1), 69-73. Elsevier
A recent study found genome-wide significant association between common variation in the gene neurocan (NCAN, rs1064395) and bipolar disorder (BD). In view of accumulating evidence that BD and schizophrenia partly share genetic risk factors, we teste
Autor:
Arloth, Janine, Bogdan, Ryan, Altmann, Andre, Lawson, William B, Lewis, Glyn, MacIntyre, Donald, Maier, Wolfgang, Mattheisen, Manuel, McGrath, Patrick J, McIntosh, Andrew, McLean, Alan, Middeldorp, Christel M, Middleton, Lefkos, Trümbach, Dietrich, Montgomery, Grant M, Murphy, Shawn N, Nauck, Matthias, Nolen, Willem A, Nyholt, Dale R, O'Donovan, Michael, Oskarsson, Högni, Pedersen, Nancy, Scheftner, William A, Schulz, Andrea, Wurst, Wolfgang, Schulze, Thomas G, Shyn, Stanley I, Sigurdsson, Engilbert, Slager, Susan L, Smit, Johannes H, Stefansson, Hreinn, Steffens, Michael, Thorgeirsson, Thorgeir, Tozzi, Federica, Treutlein, Jens, Mehta, Divya, Uhr, Manfred, van den Oord, Edwin J C G, Van Grootheest, Gerard, Völzke, Henry, Weilburg, Jeffrey B, Willemsen, Gonneke, Zitman, Frans G, Neale, Benjamin, Daly, Mark, Levinson, Douglas F, Sullivan, Patrick F, Klengel, Torsten, Erhardt, Angelika, Carey, Caitlin E, Conley, Emily Drabant, Consortium, Major Depressive Disorder Working Group of the Psychiatric Genomics, Weber, Peter, Ruepp, Andreas, Müller-Myhsok, Bertram, Hariri, Ahmad R, Binder, Elisabeth B, PGC, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Ripke, Stephan, Wray, Naomi R, Lewis, Cathryn M, Hamilton, Steven P, Weissman, Myrna M, Frishman, Goar, Breen, Gerome, Byrne, Enda M, Blackwood, Douglas H R, Boomsma, Dorret I, Cichon, Sven, Heath, Andrew C, Holsboer, Florian, Lucae, Susanne, Madden, Pamela A F, Martin, Nicholas G, Menke, Andreas, McGuffin, Peter, Muglia, Pierandrea, Noethen, Markus M, Penninx, Brenda P, Pergadia, Michele L, Potash, James B, Rietschel, Marcella, Lin, Danyu, Shi, Jianxin, Wagner, Klaus V, Steinberg, Stacy, Grabe, Hans J, Lichtenstein, Paul, Magnusson, Patrik, Perlis, Roy H, Preisig, Martin, Smoller, Jordan W, Stefansson, Kari, Uher, Rudolf, Kutalik, Zoltan, Balsevich, Georgia, Tansey, Katherine E, Teumer, Alexander, Viktorin, Alexander, Barnes, Michael R, Bettecken, Thomas, Breuer, René, Castro, Victor M, Churchill, Susanne E, Coryell, William H, Schmidt, Mathias V, Craddock, Nick, Craig, Ian W, Czamara, Darina, De Geus, Eco J, Degenhardt, Franziska, Farmer, Anne E, Fava, Maurizio, Frank, Josef, Gainer, Vivian S, Gallagher, Patience J, Karbalai, Nazanin, Gordon, Scott D, Goryachev, Sergey, Gross, Magdalena, Guipponi, Michel, Henders, Anjali K, Herms, Stefan, Hickie, Ian B, Hoefels, Susanne, Hoogendijk, Witte, Hottenga, Jouke Jan, Iosifescu, Dan V, Ising, Marcus, Jones, Ian, Jones, Lisa, Jung-Ying, Tzeng, Knowles, James A, Kohane, Isaac S, Kohli, Martin A, Korszun, Ania, Landen, Mikael
Publikováno v:
Arloth, J, Bogdan, R, Weber, P, Frishman, G, Menke, A, Wagner, K V, Balsevich, G, Schmidt, M V, Karbalai, N, Czamara, D, Altmann, A, Trümbach, D, Wurst, W, Mehta, D, Uhr, M, Klengel, T, Erhardt, A, Carey, C E, Drabant Conley, E, Boomsma, D I, Penninx, B W J H, de Geus, E J C, Hottenga, J J, Middeldorp, C M, Willemsen, G, Smit, J H, Ruepp, A, Müller-Myhsok, B, Hariri, A & Binder, E B 2015, ' Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders ', Neuron, vol. 86, pp. 1189-1202 . https://doi.org/10.1016/j.neuron.2015.05.034
Neuron 86, 1189-1202 (2015)
Neuron, 86, 1189-1202. Cell Press
Neuron
Neuron 86(5), 1189-1202 (2015). doi:10.1016/j.neuron.2015.05.034
NEURON
Neuron 86, 1189-1202 (2015)
Neuron, 86, 1189-1202. Cell Press
Neuron
Neuron 86(5), 1189-1202 (2015). doi:10.1016/j.neuron.2015.05.034
NEURON
Summary Depression risk is exacerbated by genetic factors and stress exposure; however, the biological mechanisms through which these factors interact to confer depression risk are poorly understood. One putative biological mechanism implicates varia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41f8e3dd82fe25b350acb65eab97194b
https://eprints.worc.ac.uk/5045/1/1-s2.0-S0896627315004730-main.pdf
https://eprints.worc.ac.uk/5045/1/1-s2.0-S0896627315004730-main.pdf