نتائج البحث - Jobst Meyer

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  1. 1
    Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations

    Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations حسب Jobst Meyer

    منشور في 1997
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  2. 2
    Elevated Social Stress Levels and Depressive Symptoms in Primary Hyperhidrosis

    Elevated Social Stress Levels and Depressive Symptoms in Primary Hyperhidrosis حسب Katharina M. Gross, Andrea B. Schote, Katja Kerstin Schneider, André Schulz, Jobst Meyer

    منشور في 2014
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  3. 3
    Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15

    Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15 حسب Gerald Stöber, Kathrin Saar, Franz Rüschendorf, Jobst Meyer, Gudrun Nürnberg, Susanne Jatzke, Ernst Franzek, André Reis, Klaus‐Peter Lesch, Thomas F. Wienker, H. Beckmann

    منشور في 2000
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  4. 4
    Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15

    Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15 حسب Gerald Stöber, Kathrin Saar, Franz Rüschendorf, Jobst Meyer, Gudrun Nürnberg, Susanne Jatzke, Ernst Franzek, André Reis, Klaus‐Peter Lesch, Thomas F. Wienker, H. Beckmann

    منشور في 2000
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  5. 5
    A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree

    A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree حسب Jobst Meyer, A Huberth, Guillermo J. Ortega, Yana V. Syagailo, Susanne Jatzke, Rainald Mößner, Tim M. Strom, Isabel Ulzheimer-Teuber, G. Stöber, Angelika Schmitt, Klaus‐Peter Lesch

    منشور في 2001
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  6. 6
    Association and linkage of allelic variants of the dopamine transporter gene in ADHD

    Association and linkage of allelic variants of the dopamine transporter gene in ADHD حسب Susann Friedel, Kathrin Saar, Sascha Sauer, Astrid Dempfle, Susanne Walitza, Tobias Renner, Marcel Romanos, Christine M. Freitag, Christiane Seitz, Haukur Pálmason, André Scherag, Christine Windemuth-Kieselbach, Benno G. Schimmelmann, C. Wewetzer, Jobst Meyer, Andreas Warnke, Klaus‐Peter Lesch, Richard Reinhardt, Beate Herpertz‐Dahlmann, Mark W. Linder, Anke Hinney, Helmut Remschmidt, H. Schäfer, Kerstin Konrad, Norbert Hübner, Johannes Hebebrand

    منشور في 2002
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  7. 7
    A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD

    A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD حسب Mahim Jain, Jorge I. Vélez, Maria T. Acosta, Luis Palacio, József Á. Balog, Erich Roessler, David Pineda, Ana C. Londoño, Juan David Palacio, A Arbelaez, Francisco Lopera, Josephine Elia, Hákon Hákonarson, Christiane Seitz, Christine M. Freitag, Haukur Pálmason, Jobst Meyer, Marcel Romanos, Susanne Walitza, U. Hemminger, Andreas Warnke, Jasmin Romanos, Tobias Renner, Christian Jacob, Klaus‐Peter Lesch, James M. Swanson, F. Xavier Castellanos, Joan E. Bailey‐Wilson, Mauricio Arcos‐Burgos, Maximilian Muenke

    منشور في 2011
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  8. 8
    Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder

    Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder حسب Benjamin M. Neale, Sarah E. Medland, Stephan Ripke, Richard Anney, Philip Asherson, Jan Buitelaar, Barbara Franke, Michael Gill, Lindsey Kent, Peter Holmans, Frank A. Middleton, Anita Thapar, Klaus‐Peter Lesch, Stephen V. Faraone, Mark J. Daly, Thuy Trang Nguyen, H. Schäfer, Hans‐Christoph Steinhausen, Andreas Reif, Tobias Renner, Marcel Romanos, Jasmin Romanos, Andreas Warnke, Susanne Walitza, Christine M. Freitag, Jobst Meyer, Haukur Pálmason, Aribert Rothenberger, Ziarih Hawi, Joseph A. Sergeant, Herbert Roeyers, Eric Mick, Joseph Biederman

    منشور في 2010
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  9. 9
    Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

    Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder حسب Ivonne Jarick, A-L Volckmar, Carolin Pütter, Sonali Pechlivanis, Thuy Trang Nguyen, Maria R. Dauvermann, Sebastian Beck, Özgür Albayrak, Susann Scherag, Susanne Gilsbach, Sven Cichon, Per Hoffmann, Franziska Degenhardt, Markus M. Nöthen, S. Schreiber, H-E Wichmann, KH Jöckel, Joachim Heinrich, Carla M. T. Tiesler, Stephen V. Faraone, Susanne Walitza, Judith Sinzig, Christine M. Freitag, Jobst Meyer, B Herpertz‐Dahlmann, Gerd Lehmkuhl, Tobias Renner, Andreas Warnke, Marcel Romanos, Klaus‐Peter Lesch, Andreas Reif, Benno G. Schimmelmann, Johannes Hebebrand, André Scherag, Anke Hinney

    منشور في 2012
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  10. 10
    High Loading of Polygenic Risk for ADHD in Children With Comorbid Aggression

    High Loading of Polygenic Risk for ADHD in Children With Comorbid Aggression حسب Marian L. Hamshere, K. Langley, Joanna Martin, Sharifah Shameem Agha, Evie Stergiakouli, Richard Anney, Jan K. Buitelaar, Stephen V. Faraone, Klaus‐Peter Lesch, Benjamin M. Neale, Barbara Franke, Edmund Sonuga‐Barke, Philip Asherson, Andrew Merwood, Jonna Kuntsi, Sarah E. Medland, Stephan Ripke, Hans‐Christoph Steinhausen, Christine M. Freitag, Andreas Reif, Tobias Renner, Marcel Romanos, Jasmin Romanos, Andreas Warnke, Jobst Meyer, Haukur Pálmason, Alejandro Arias Vásquez, Nanda Lambregts-Rommelse, Herbert Roeyers, Joseph Biederman, Alysa E. Doyle, Hákon Hákonarson, Aribert Rothenberger, Tobias Banaschewski, Robert D. Oades, James J. McGough, Lindsey Kent, Nigel Williams, Michael J. Owen, Peter Holmans, Michael O’Donovan, Anita Thapar

    منشور في 2013
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  11. 11
    Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3

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

    منشور في 2011
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  12. 12
    A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

    A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication حسب Mauricio Arcos‐Burgos, Mahim Jain, Maria T. Acosta, Sharon B. Shively, Horia Stanescu, David H. Wallis, Sabina Domené, Jorge I. Vélez, Jayaprakash D. Karkera, József Á. Balog, K Berg, Robert Kleta, William A. Gahl, Erich Roessler, Rui Long, J. Lie, David Pineda, Ana C. Londoño, Juan David Palacio, A Arbelaez, Francisco Lopera, Josephine Elia, Hákon Hákonarson, Stefan Johansson, P.M. Knappskog, Jan Haavik, Marta Ribasés, Bru Cormand, Mónica Bayés, Miguel Casas, Josep Antoni Ramos‐Quiroga, Amaia Hervás, Brion S. Maher, Stephen V. Faraone, Christiane Seitz, Christine M. Freitag, Haukur Pálmason, Jobst Meyer, Marcel Romanos, Susanne Walitza, U. Hemminger, Andreas Warnke, Jasmin Romanos, Tobias Renner, Christian Jacob, Klaus‐Peter Lesch, James M. Swanson, Alexander O. Vortmeyer, Joan E. Bailey‐Wilson, F. Xavier Castellanos, Maximilian Muenke

    منشور في 2010
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  13. 13
    Meta‐analysis of genome‐wide linkage scans of attention deficit hyperactivity disorder

    Meta‐analysis of genome‐wide linkage scans of attention deficit hyperactivity disorder حسب Kaixin Zhou, Astrid Dempfle, Mauricio Arcos‐Burgos, Steven C. Bakker, Tobias Banaschewski, Joseph Biederman, Jan Buitelaar, F. Xavier Castellanos, Alysa E. Doyle, Richard P. Ebstein, Jenny Ekholm, Paola Forabosco, Barbara Franke, Christine M. Freitag, Susann Friedel, Michael Gill, Johannes Hebebrand, Anke Hinney, Christian Jacob, Klaus‐Peter Lesch, Sandra K. Loo, Francisco Lopera, James T. McCracken, James J. McGough, Jobst Meyer, Eric Mick, Ana Miranda, Maximilian Muenke, Fernando Mulas, Stanley F. Nelson, Trang Nguyen, Robert D. Oades, Matthew N. Ogdie, Juan David Palacio, David Pineda, Andreas Reif, Tobias Renner, Herbert Roeyers, Marcel Romanos, Aribert Rothenberger, H. Schäfer, Joseph A. Sergeant, Richard J. Sinke, Susan L. Smalley, Edmund Sonuga‐Barke, Hans‐Christoph Steinhausen, Emma van der Meulen, Susanne Walitza, Andreas Warnke, Cathryn M. Lewis, Stephen V. Faraone, Philip Asherson

    منشور في 2008
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  14. 14
    Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder

    Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder حسب Benjamin M. Neale, Sarah E. Medland, Stephan Ripke, Philip Asherson, Barbara Franke, Klaus‐Peter Lesch, Stephen V. Faraone, Thuy Trang Nguyen, H. Schäfer, Peter Holmans, Mark J. Daly, Hans‐Christoph Steinhausen, Christine M. Freitag, Andreas Reif, Tobias Renner, Marcel Romanos, Jasmin Romanos, Susanne Walitza, Andreas Warnke, Jobst Meyer, Haukur Pálmason, Jan K. Buitelaar, Alejandro Arias Vásquez, Nanda Lambregts-Rommelse, Michael Gill, Richard Anney, Kate Langely, Michael O’Donovan, Nigel Williams, Michael J. Owen, Anita Thapar, Lindsey Kent, Joseph A. Sergeant, Herbert Roeyers, Eric Mick, Joseph Biederman, Alysa E. Doyle, Susan L. Smalley, Sandra K. Loo, Hákon Hákonarson, Josephine Elia, Alexandre A. Todorov, Ana Miranda, Fernando Mulas, Richard P. Ebstein, Aribert Rothenberger, Tobias Banaschewski, Robert D. Oades, Edmund Sonuga‐Barke, James J. McGough, Laura Nisenbaum, Frank A. Middleton, Xiaolan Hu, Stan F. Nelson

    منشور في 2010
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  15. 15
    Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

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

    منشور في 2011
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  16. 16
    Common variant at 16p11.2 conferring risk of psychosis

    Common variant at 16p11.2 conferring risk of psychosis حسب Stacy Steinberg, Simone de Jong, Manuel Mattheisen, Javier Costas, Ditte Demontis, Stéphane Jamain, Olli Pietiläinen, Kuang Lin, Sergi Papiol, Johanna Huttenlocher, Engilbert Sigurðsson, Evangelos Vassos, Ina Giegling, René Breuer, G. T. Fraser, Nicholas Walker, Ingrid Melle, Srdjan Djurovic, Ingrid Agartz, Annamari Tuulio‐Henriksson, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Line Olsen, Thomas Hansen, Andrés Ingason, Matti Pirinen, E Strengman, David M. Hougaard, Torben Ørntoft, Michael Didriksen, Mads V. Hollegaard, Merete Nordentoft, Л. И. Абрамова, В. Г. Каледа, Manuel Arrojo, Julio Sanjuán, Celso Arango, Bruno Étain, Frank Bellivier, A. Méary, Franck Schürhoff, Andreı̈ Szöke, Michele Ribolsi, Valentina Magni, Alberto Siracusano, Swetlana Sperling, Moritz J. Rossner, Claus Christiansen, Lambertus A. Kiemeney, Barbara Franke, Leonard H. van den Berg, Jan H. Veldink, Sarah Curran, Patrick Bolton, Martin Poot, Wouter Staal, Karola Rehnström, Helena Kilpinen, Christine M. Freitag, Jobst Meyer, Patrik K. E. Magnusson, Evald Sæmundsen, Igor Martsenkovsky, I Bikshaieva, I.I. Martsenkovska, O.S. Vashchenko, Marija Raleva, K Paketchieva, Branislav Stefanovski, Naser Durmishi, Milica Pejović-Milovančević, Dušica Lečić Toševski, Teimuraz Silagadze, N Naneishvili, Nina Mikeladze, Simon Surguladze, John B. Vincent, Anne Farmer, Philip B. Mitchell, A. Jordan Wright, Peter R. Schofield, Janice M. Fullerton, Grant W. Montgomery, Nicholas G. Martin, I. Alex Rubino, Ruud van Winkel, Günter Kenis, Marc D. Binder, János Réthelyi, István Bitter, Lars Terenius, Erik G. Jönsson, S C Bakker, Jim van Os, Assen Jablensky, Marion Leboyer, Elvira Bramon, John Powell, Robin Murray

    منشور في 2012
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