Risultati della ricerca - Martin Begemann

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  1. 1
    Concise Review: Roles of Polycomb Group Proteins in Development and Disease: A Stem Cell Perspective

    Concise Review: Roles of Polycomb Group Proteins in Development and Disease: A Stem Cell Perspective di Vinagolu K. Rajasekhar, Martin Begemann

    Pubblicazione 2007
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  2. 2
    Erythropoietin as candidate for supportive treatment of severe COVID-19

    Erythropoietin as candidate for supportive treatment of severe COVID-19 di Hannelore Ehrenreich, Karin Weißenborn, Martin Begemann, Markus Busch, Eduard Vieta, Kamilla Woznica Miskowiak

    Pubblicazione 2020
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  3. 3
    Autism beyond diagnostic categories: characterization of autistic phenotypes in schizophrenia

    Autism beyond diagnostic categories: characterization of autistic phenotypes in schizophrenia di Anne Kästner, Martin Begemann, Tanja Maria Michel, SARAH EVERTS, Beata Stepniak, Christiane Bach, Luise Poustka, Joachim Becker, Tobias Banaschewski, M. Dose, Hannelore Ehrenreich

    Pubblicazione 2015
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  4. 4
    Recombinant human erythropoietin delays loss of gray matter in chronic schizophrenia

    Recombinant human erythropoietin delays loss of gray matter in chronic schizophrenia di Torsten Wüstenberg, Martin Begemann, Claudia Bartels, Olaf Gefeller, Sabina Stawicki, Dunja Hinze‐Selch, Alexander Mohr, Peter Falkai, J. Aldenhoff, Michael Knauth, Klaus-Armin Nave, Hannelore Ehrenreich

    Pubblicazione 2010
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  5. 5
    Amino Acid Variation in HLA Class II Proteins Is a Major Determinant of Humoral Response to Common Viruses

    Amino Acid Variation in HLA Class II Proteins Is a Major Determinant of Humoral Response to Common Viruses di Christian Hammer, Martin Begemann, Paul J. McLaren, István Bartha, Angelika Michel, Beate Klose, Corinna Schmitt, Tim Waterboer, Michael Pawlita, Thomas F. Schulz, Hannelore Ehrenreich, Jacques Fellay

    Pubblicazione 2015
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  6. 6
    Factors predisposing to humoral autoimmunity against brain-antigens in health and disease: Analysis of 49 autoantibodies in over 7000 subjects

    Factors predisposing to humoral autoimmunity against brain-antigens in health and disease: Analysis of 49 autoantibodies in over 7000 subjects di Vinícius Daguano Gastaldi, Justus B. H. Wilke, Cosima A Weidinger, Carolin Walter, Nadine Barnkothe, Bianca Teegen, Felix Luessi, W. Stöcker, Fred Lühder, Martin Begemann, Frauke Zipp, Klaus‐Armin Nave, Hannelore Ehrenreich

    Pubblicazione 2022
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  7. 7
    Genome-wide association study results for educational attainment aid in identifying genetic heterogeneity of schizophrenia

    Genome-wide association study results for educational attainment aid in identifying genetic heterogeneity of schizophrenia di V. Bansal, Marina Mitjans, Casper A.P. Burik, Richard Karlsson Linnér, Aysu Okbay, Cornelius A. Rietveld, Martin Begemann, Stefan Bonn, Stephan Ripke, Ronald de Vlaming, Michel G. Nivard, Hannelore Ehrenreich, Philipp Koellinger

    Pubblicazione 2018
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  8. 8
    A myelin gene causative of a catatonia‐depression syndrome upon aging

    A myelin gene causative of a catatonia‐depression syndrome upon aging di Nora Hagemeyer, Sandra Goebbels, Sergi Papiol, Anne Kästner, Sabine Hofer, Martin Begemann, Ulrike C. Gerwig, Susann Boretius, Georg L. Wieser, Anja Ronnenberg, A. A. Gurvich, Stephan Heckers, Jens Frahm, Klaus‐Armin Nave, Hannelore Ehrenreich

    Pubblicazione 2012
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  9. 9
    A single gene defect causing claustrophobia

    A single gene defect causing claustrophobia di Ahmed El-Kordi, Anne Kästner, Sabrina Grube, Matthias Klugmann, Martin Begemann, Swetlana Sperling, Kurt Hammerschmidt, Christian Hammer, Beata Stepniak, Julia Patzig, Patricia de Monasterio‐Schrader, Nicola Strenzke, G. Flügge, Hauke Werner, Robert Pawlak, KA Nave, Hannelore Ehrenreich

    Pubblicazione 2013
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  10. 10
    A CAG repeat polymorphism of <i>KCNN3</i> predicts SK3 channel function and cognitive performance in schizophrenia

    A CAG repeat polymorphism of <i>KCNN3</i> predicts SK3 channel function and cognitive performance in schizophrenia di Sabrina Grube, Martin Fungisai Gerchen, Bartosz Adamcio, Luis A. Pardo, Sabine Martin, Dörthe Malzahn, Sergi Papiol, Martin Begemann, Katja Ribbe, Heidi Friedrichs, Konstantin Radyushkin, Michael Müller, Fritz Benseler, J. Riggert, Peter Falkai, Heike Bickeböller, Klaus‐Armin Nave, Nils Brose, Walter Stühmer, Hannelore Ehrenreich

    Pubblicazione 2011
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  11. 11
    Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes

    Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes di Beata Stepniak, Anne Kästner, Giulia Poggi, Marina Mitjans, Martin Begemann, Annette M. Hartmann, Sandra Van der Auwera, Farahnaz Sananbenesi, Dilja Krueger‐Burg, Gabriela Matuszko, Cornelia Brosi, Georg Homuth, Henry Völzke, Fritz Benseler, Claudia Bagni, Utz Fischer, Alexander Dityatev, Hans J. Grabe, Dan Rujescu, André Fischer, Hannelore Ehrenreich

    Pubblicazione 2015
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  12. 12
    Microglia ablation alleviates myelin-associated catatonic signs in mice

    Microglia ablation alleviates myelin-associated catatonic signs in mice di Hana Jáňová, Sahab Arinrad, Evan A. Balmuth, Marina Mitjans, Johannes Hertel, Mohamad Habes, Robert A. Bittner, Hong Pan, Sandra Goebbels, Martin Begemann, Ulrike C. Gerwig, Sönke Langner, Hauke Werner, Sarah Kittel‐Schneider, Georg Homuth, Christos Davatzikos, Henry Völzke, Brian L. West, Andreas Reif, Hans J. Grabe, Susann Boretius, Hannelore Ehrenreich, Klaus‐Armin Nave

    Pubblicazione 2017
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  13. 13
    Convergence of placenta biology and genetic risk for schizophrenia

    Convergence of placenta biology and genetic risk for schizophrenia di Gianluca Ursini, Giovanna Punzi, Qiang Chen, Stefano Marenco, Joshua F. Robinson, Annamaria Porcelli, Emily G. Hamilton, Marina Mitjans, Giancarlo Maddalena, Martin Begemann, Jan Seidel, Hidenaga Yanamori, Andrew E. Jaffe, Karen F. Berman, Michael Egan, Richard E. Straub, Carlo Colantuoni, Giuseppe Blasi, Ryota Hashimoto, Dan Rujescu, Hannelore Ehrenreich, Alessandro Bertolino, Daniel R. Weinberger

    Pubblicazione 2018
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  14. 14
    Uncoupling the widespread occurrence of anti-NMDAR1 autoantibodies from neuropsychiatric disease in a novel autoimmune model

    Uncoupling the widespread occurrence of anti-NMDAR1 autoantibodies from neuropsychiatric disease in a novel autoimmune model di Hong Pan, Bárbara Oliveira, Gesine Saher, Ekrem Dere, Daniel Tapken, Marina Mitjans, Jan Seidel, Janina Wesolowski, Debia Wakhloo, Christina Klein-Schmidt, Anja Ronnenberg, Kerstin Schwabe, Ralf H. Trippe, Kerstin Mätz‐Rensing, Stefan A. Berghoff, Yazeed Al-Krinawe, Henrik Martens, Martin Begemann, W. Stöcker, Franz‐Josef Kaup, Reinhard Mischke, Susann Boretius, Klaus‐Armin Nave, Joachim K. Krauss, Michael Hollmann, Fred Lühder, Hannelore Ehrenreich

    Pubblicazione 2018
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  15. 15
    Modification of Cognitive Performance in Schizophrenia by Complexin 2 Gene Polymorphisms

    Modification of Cognitive Performance in Schizophrenia by Complexin 2 Gene Polymorphisms di Martin Begemann, Sabrina Grube, Sergi Papiol, Dörthe Malzahn, Henning Krampe, Katja Ribbe, Heidi Friedrichs, Konstantin Radyushkin, Ahmed El-Kordi, Fritz Benseler, Kathrin Hannke, Swetlana Sperling, Dayana Schwerdtfeger, Ivonne Thanhäuser, Martin Fungisai Gerchen, Mohammad Ghorbani, Stefan Gutwinski, Constanze Hilmes, Richard Leppert, Anja Ronnenberg, Julia F. Sowislo, Sabina Stawicki, Maren Stödtke, Christoph Johannes Szuszies, Kerstin Reim, J. Riggert, Fritz Eckstein, Peter Falkai, Heike Bickeböller, Klaus‐Armin Nave, Nils Brose, Hannelore Ehrenreich

    Pubblicazione 2010
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  16. 16
    The cross-sectional GRAS sample: A comprehensive phenotypical data collection of schizophrenic patients

    The cross-sectional GRAS sample: A comprehensive phenotypical data collection of schizophrenic patients di Katja Ribbe, Heidi Friedrichs, Martin Begemann, Sabrina Grube, Sergi Papiol, Anne Kästner, Martin Fungisai Gerchen, Verena Ackermann, Asieh Tarami, Annika Treitz, Marlene Flögel, Lothar Adler, Josef B. Aldenhoff, Marianne Becker-Emner, Thomas Becker, Adelheid Czernik, M. Dose, Here Folkerts, Roland Freese, Rolf W. Günther, Sabine C. Herpertz, Dirk Hesse, Gunther Kruse, Heinrich Kunze, Michael Franz, Frank Löhrer, Wolfgang Maier, Andreas Mielke, Rüdiger Müller‐Isberner, Cornelia Oestereich, Frank-Gerald Pajonk, Thomas Pollmächer, Udo Schneider, H Schwarz, Birgit Kröner‐Herwig, Ursula Havemann‐Reinecke, Jens Frahm, Walter Stühmer, Peter Falkai, Nils Brose, Klaus‐Armin Nave, Hannelore Ehrenreich

    Pubblicazione 2010
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  17. 17
    Biological insights from 108 schizophrenia-associated genetic loci

    Biological insights from 108 schizophrenia-associated genetic loci di Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Ina Giegling, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, В. Е. Голимбет, Srihari Gopal, Jacob Gratten, Lieuwe de Haan, Christian Hammer, Marian L. Hamshere, Mark Hansen, Thomas Hansen, Vahram Haroutunian, Annette M. Hartmann, Frans Henskens, Stefan Herms, Joel N. Hirschhorn, Per Hoffmann, Andrea Hofman, Mads V. Hollegaard, David M. Hougaard, Masashi Ikeda, Inge Joa

    Pubblicazione 2014
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  18. 18
    Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

    Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases di Alexander Gusev, Sang Lee, Gosia Trynka, Hilary K. Finucane, Bjarni J. Vilhjálmsson, Han Xu, Chongzhi Zang, Stephan Ripke, Brendan Bulik‐Sullivan, Eli A. Stahl, Anna K. Kähler, Christina M. Hultman, Shaun Purcell, Steven A. McCarroll, Mark J. Daly, Bogdan Paşaniuc, Patrick F. Sullivan, Benjamin M. Neale, Naomi R. Wray, Soumya Raychaudhuri, Alkes L. Price, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Anders D. Børglum, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael H. Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva

    Pubblicazione 2014
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  19. 19
    Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood

    Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood di Guiyan Ni, G. Möser, Naomi R. Wray, Sang Lee, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Ina Giegling, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, В. Е. Голимбет, Srihari Gopal, Jacob Gratten, Lieuwe de Haan, Christian Hammer, Marian L. Hamshere, Thomas Hansen, Thomas Hansen, Vahram Haroutunian, Annette M. Hartmann, Frans A. Henskens, Stefan Herms, Joel N. Hirschhorn, Per Hoffmann, Andrea Hofman

    Pubblicazione 2018
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  20. 20
    A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

    A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts di Guiyan Ni, Jian Zeng, Joana Revez, Ying Wang, Zhili Zheng, Tian Ge, Restuadi Restuadi, Jacqueline Kiewa, Dale R. Nyholt, Jonathan R. I. Coleman, Jordan W. Smoller, Jian Yang, Peter M. Visscher, Naomi R. Wray, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberley D. Chambert, Raymond C. K. Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Ina Giegling, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, В. Е. Голимбет, Srihari Gopal, Jacob Gratten, Lieuwe de Haan, Christian Hammer, Marian L. Hamshere

    Pubblicazione 2021
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