Glucocorticoid receptor variants in childhood attention-deficit/hyperactivity disorder and comorbid psychiatric disorders von Schote, Andrea B, Bonenberger, Martina, Pálmason, Haukur, Seitz, Christiane, Meyer, Jobst, Freitag, Christine M

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Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant von Pálmason, Haukur, Moser, Dirk, Sigmund, Jessica, Vogler, Christian, Hänig, Susann, Schneider, Anna, Seitz, Christiane, Marcus, Alexander, Meyer, Jobst, Freitag, Christine M.

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Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder von Elia, Josephine, Glessner, Joseph T, Wang, Kai, Takahashi, Nagahide, Shtir, Corina J, Hadley, Dexter, Sleiman, Patrick M A, Zhang, Haitao, Kim, Cecilia E, Robison, Reid, Lyon, Gholson J, Flory, James H, Bradfield, Jonathan P, Imielinski, Marcin, Hou, Cuiping, Frackelton, Edward C, Chiavacci, Rosetta M, Sakurai, Takeshi, Rabin, Cara, Middleton, Frank A, Thomas, Kelly A, Garris, Maria, Mentch, Frank, Freitag, Christine M, Steinhausen, Hans-Christoph, Todorov, Alexandre A, Reif, Andreas, Rothenberger, Aribert, Franke, Barbara, Mick, Eric O, Roeyers, Herbert, Buitelaar, Jan, Lesch, Klaus-Peter, Banaschewski, Tobias, Ebstein, Richard P, Mulas, Fernando, Oades, Robert D, Sergeant, Joseph, Sonuga-Barke, Edmund, Renner, Tobias J, Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Walitza, Susanne, Meyer, Jobst, Pálmason, Haukur, Seitz, Christiane, Loo, Sandra K, Smalley, Susan L, Biederman, Joseph, Kent, Lindsey, Asherson, Philip, Anney, Richard J L, Gaynor, J William, Shaw, Philip, Devoto, Marcella, White, Peter S, Grant, Struan F A, Buxbaum, Joseph D, Rapoport, Judith L, Williams, Nigel M, Nelson, Stanley F, Faraone, Stephen V, Hakonarson, Hakon

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Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3 von Williams, Nigel M., Franke, Barbara, Mick, Eric, Anney, Richard J.L., Freitag, Christine M., Gill, Michael, Thapar, Anita, O'Donovan, Michael C., Owen, Michael J., Holmans, Peter, Kent, Lindsey, Middleton, Frank, Zhang-James, Yanli, Liu, Lu, Meyer, Jobst, Nguyen, Thuy Trang, Romanos, Jasmin, Romanos, Marcel, Seitz, Christiane, Renner, Tobias J., Walitza, Susanne, Warnke, Andreas, Palmason, Haukur, Buitelaar, Jan, Rommelse, Nanda, Vasquez, Alejandro Arias, Hawi, Ziarih, Langley, Kate, Sergeant, Joseph, Steinhausen, Hans-Christoph, Roeyers, Herbert, Biederman, Joseph, Zaharieva, Irina, Hakonarson, Hakon, Elia, Josephine, Lionel, Anath C., Crosbie, Jennifer, Marshall, Christian R., Schachar, Russell, Scherer, Stephen W., Todorov, Alexandre, Smalley, Susan L., Loo, Sandra, Nelson, Stanley, Shtir, Corina, Asherson, Philip, Reif, Andreas, Lesch, Klaus-Peter, Faraone, Stephen V.

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Group A streptococcal disease in paediatric inpatients: a European perspective von Boeddha, Navin P., Atkins, Lucy, de Groot, Ronald, Driessen, Gertjan, Hazelzet, Jan, Zenz, Werner, Carrol, Enitan D., Anderson, Suzanne T., Martinon-Torres, Federico, Agyeman, Philipp K. A., Galassini, Rachel, Herberg, Jethro, Levin, Michael, Schlapbach, Luregn J., Emonts, Marieke

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Impact of autism-associated genetic variants in interaction with environmental factors on ADHD comorbidities: an exploratory pilot study von Waltes, Regina, Freitag, Christine M., Herlt, Timo, Lempp, Thomas, Seitz, Christiane, Palmason, Haukur, Meyer, Jobst, Chiocchetti, Andreas G.

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Cortisol awakening response in healthy children and children with ADHD: Impact of comorbid disorders and psychosocial risk factors von Freitag, Christine M, Hänig, Susann, Palmason, Haukur, Meyer, Jobst, Wüst, Stefan, Seitz, Christiane

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Biological and psychosocial environmental risk factors influence symptom severity and psychiatric comorbidity in children with ADHD von Freitag, Christine M., Hänig, Susann, Schneider, Anna, Seitz, Christiane, Palmason, Haukur, Retz, Wolfgang, Meyer, Jobst

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Psychiatric gene discoveries shape evidence on ADHD’s biology von Thapar, A, Martin, J, Mick, E, Arias Vásquez, A, Langley, K, Scherer, S W, Schachar, R, Crosbie, J, Williams, N, Franke, B, Elia, J, Glessner, J, Hakonarson, H, Owen, M J, Faraone, S V, O'Donovan, M C, Holmans, P

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Correction to: Group A streptococcal disease in paediatric inpatients: a European perspective von Boeddha, Navin P., Atkins, Lucy, de Groot, Ronald, Driessen, Gertjan, Hazelzet, Jan, Zenz, Werner, Carrol, Enitan D., Anderson, Suzanne T., Martinon-Torres, Federico, Agyeman, Philipp K. A., Galassini, Rachel, Herberg, Jethro, Levin, Michael, Schlapbach, Luregn J., Emonts, Marieke

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Empirically Determined, Psychopathological Subtypes in Children With ADHD von Zenglein, Yvonne, Schwenck, Christina, Westerwald, Eva, Schmidt, Catharina, Beuth, Sonja, Meyer, Jobst, Palmason, Haukur, Seitz, Christiane, Hänig, Susann, Freitag, Christine M.

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Risk factors of autistic symptoms in children with ADHD von Kröger, Anne, Hänig, Susann, Seitz, Christiane, Palmason, Haukur, Meyer, Jobst, Freitag, Christine M.

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Haplotype co-segregation with attention deficit-hyperactivity disorder in unrelated german multi-generation families von Lin, Michelle K., Freitag, Christine M., Schote, Andrea B., Pálmason, Haukur, Seitz, Christiane, Renner, Tobias J., Romanos, Marcel, Walitza, Susanne, Jacob, Christian P., Reif, Andreas, Warnke, Andreas, Cantor, Rita M., Lesch, Klaus-Peter, Meyer, Jobst

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Haplotype co-segregation with attention deficit-hyperactivity disorder in unrelated German multi-generation families von Lin, Michelle K, Freitag, Christine M, Schote, Andrea B, Pálmason, Haukur, Seitz, Christiane, Renner, Tobias J, Romanos, Marcel, Walitza, Susanne, Jacob, Christian P, Reif, Andreas, Warnke, Andreas, Cantor, Rita M, Lesch, Klaus-Peter, Meyer, Jobst

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Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3 von Williams, Nigel M, Franke, Barbara, Mick, Eric, Anney, Richard J.L, Freitag, Christine M, Gill, Michael, Thapar, Anita, O'Donovan, Michael C, Owen, Michael J, Holmans, Peter, Kent, Lindsey, Middleton, Frank, Zhang-James, Yanli, Liu, Lu, Meyer, Jobst, Nguyen, Thuy Trang, Romanos, Jasmin, Romanos, Marcel, Seitz, Christiane, Renner, Tobias J, Walitza, Susanne, Warnke, Andreas, Palmason, Haukur, Buitelaar, Jan, Rommelse, Nanda, Vasquez, Alejandro Arias, Hawi, Ziarih, Langley, Kate, Sergeant, Joseph, Steinhausen, Hans-Christoph, Roeyers, Herbert, Biederman, Joseph, Zaharieva, Irina, Hakonarson, Hakon, Elia, Josephine, Lionel, Anath C, Crosbie, Jennifer, Marshall, Christian R, Schachar, Russell, Scherer, Stephen W, Todorov, Alexandre, Smalley, Susan L, Loo, Sandra, Nelson, Stanley, Shtir, Corina, Asherson, Philip, Reif, Andreas, Lesch, Klaus-Peter, Faraone, Stephen V

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A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD von Jain, Mahim, Vélez, Jorge I, Acosta, Maria T, Palacio, Louis Guillermo, Balog, Joan, Roessler, Erich, Pineda, David, Londoño, Ana C, Palacio, Juan Davis, Arbelaez, Andres, Lopera, Francisco, Elia, Josephine, Hakonarson, Hakon, Seitz, Christiane, Freitag, Christine M, Palmason, Haukur, Meyer, Jobst, Romanos, Marcel, Walitza, Susanne, Hemminger, Uwe, Warnke, Andreas, Romanos, Jasmin, Renner, Tobias, Jacob, Christian, Lesch, Klaus-Peter, Swanson, James, Castellanos, Francisco Xavier, Bailey-Wilson, Joan E, Arcos-Burgos, Mauricio, Muenke, Maximilian

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Henry Moore – Natur und Figur von Lischka‐Seitz, Christiane

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Henry Moore - Natur und Figur von Lischka-Seitz, Christiane

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4G/5G promoter polymorphism in the plasminogen-activator-inhibitor-1 gene in children with systemic meningococcaemia von GEISHOFER, Gotho, BINDER, Alexander, ZENZ, Werner, MÜLLER, Martin, ZÖHRER, Bettina, RESCH, Bernhard, MÜLLER, Wilhelm, FABER, Jörg, FINN, Adam, ENDLER, Georg, MANNHALTER, Christine

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Monoclonal antibodies for the detection of desialylation of erythrocyte membranes during haemolytic disease and haemolytic uraemic syndrome caused by the in vivo action of microbia... von Seitz, R C, Poschmann, A, Hellwege, H H

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