檢索結果 - Nazanin Mirza‐Schreiber

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  1. 1
    Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus

    Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus 由 Herbert Schulz, Ann‐Kathrin Ruppert, Stefan Herms, Christiane Wolf, Nazanin Mirza‐Schreiber, Oliver Stegle, Darina Czamara, Andreas J. Forstner, Sugirthan Sivalingam, Susanne Schoch, Susanne Moebus, Benno Pütz, Axel M. Hillmer, Nadine Fricker, Hartmut Vatter, Bertram Müller‐Myhsok, Markus M. Nöthen, Albert J. Becker, Per Hoffmann, Thomas Sander, Sven Cichon

    出版 2017
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  2. 2
    Episignature analysis of moderate effects and mosaics

    Episignature analysis of moderate effects and mosaics 由 Konrad Oexle, Michael Zech, Lara G. Stühn, Sandy Siegert, Theresa Brunet, Wolfgang M. Schmidt, Matias Wagner, Axel Schmidt, Hartmut Engels, Erik Tilch, Olivier Monestier, Anne Destrèe, Britta Hanker, Sylvia Boesch, Robert Jech, Riccardo Berutti, Frank J. Kaiser, Bernhard Haslinger, Tobias B. Haack, Barbara Garavaglia, Peter Krawitz, Juliane Winkelmann, Nazanin Mirza‐Schreiber

    出版 2023
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  3. 3
    Blood DNA methylation provides an accurate biomarker of <i>KMT2B</i>-related dystonia and predicts onset

    Blood DNA methylation provides an accurate biomarker of <i>KMT2B</i>-related dystonia and predicts onset 由 Nazanin Mirza‐Schreiber, Michael Zech, Rory Wilson, Theresa Brunet, Matias Wagner, Robert Jech, Sylvia Boesch, Matěj Škorvánek, Ján Necpál, David Weise, Sandrina Weber, Brit Mollenhauer, Claudia Trenkwalder, Esther M. Maier, Ingo Borggraefe, Katharina Vill, Annette Hackenberg, Veronika Pilshofer, Urania Kotzaeridou, Eva Maria Christina Schwaibold, Julia Hoefele, Mélanie Waldenberger, Christian Gieger, Annette Peters, Thomas Meitinger, Barbara Schormair, Juliane Winkelmann, Konrad Oexle

    出版 2021
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  4. 4
    Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

    Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia 由 Alessandro Gialluisi, Till F. M. Andlauer, Nazanin Mirza‐Schreiber, Kristina Moll, Jessica Becker, Per Hoffmann, Kerstin U. Ludwig, Darina Czamara, Beaté St Pourcain, William M. Brandler, Ferenc Honbolygó, Dénes Tóth, Valéria Csépe, Guillaume Huguet, Andrew P. Morris, Jacqueline Hulslander, Erik G. Willcutt, John C. DeFries, Richard K. Olson, Shelley D. Smith, Bruce F. Pennington, Anniek Vaessen, Urs Maurer, Heikki Lyytinen, Myriam Peyrard‐Janvid, Paavo H. T. Leppänen, Daniel Brandeis, Milene Bonte, John Stein, Joel B. Talcott, Fabien Fauchereau, Arndt Wilcke, Clyde Francks, Thomas Bourgeron, Anthony P. Monaco, Franck Ramus, Karin Landerl, Juha Kere, Thomas Scerri, Silvia Paracchini, Simon E. Fisher, Johannes Schumacher, Markus M. Nöthen, Bertram Müller‐Myhsok, Gerd Schulte‐Körne

    出版 2019
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  5. 5
    Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

    Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia 由 Alessandro Gialluisi, Till F. M. Andlauer, Nazanin Mirza‐Schreiber, Kristina Moll, Jessica Becker, Per Hoffmann, Kerstin U. Ludwig, Darina Czamara, Beaté St Pourcain, Ferenc Honbolygó, Dénes Tóth, Valéria Csépe, Guillaume Huguet, Yves Chaix, Stéphanie Iannuzzi, Jean‐François Démonet, Andrew P. Morris, Jacqueline Hulslander, Erik G. Willcutt, John C. DeFries, Richard K. Olson, Shelley D. Smith, Bruce F. Pennington, Anniek Vaessen, Urs Maurer, Heikki Lyytinen, Myriam Peyrard‐Janvid, Paavo H. T. Leppänen, Daniel Brandeis, Milene Bonte, John Stein, Joel B. Talcott, Fabien Fauchereau, Arndt Wilcke, Holger Kirsten, Bent Müller, Clyde Francks, Thomas Bourgeron, Anthony P. Monaco, Franck Ramus, Karin Landerl, Juha Kere, Thomas Scerri, Silvia Paracchini, Simon E. Fisher, Johannes Schumacher, Markus M. Nöthen, Bertram Müller‐Myhsok, Gerd Schulte‐Körne

    出版 2020
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  6. 6
    Genetic architecture of subcortical brain structures in 38,851 individuals

    Genetic architecture of subcortical brain structures in 38,851 individuals 由 Claudia L. Satizábal, Hieab H.H. Adams, Derrek P. Hibar, Charles C. White, Maria J. Knol, Jason L. Stein, Markus Scholz, Muralidharan Sargurupremraj, Neda Jahanshad, Gennady V. Roshchupkin, Albert V. Smith, Joshua C. Bis, Xueqiu Jian, Michelle Luciano, Edith Hofer, Alexander Teumer, Sven J. van der Lee, Jingyun Yang, Lisa R. Yanek, Tom V. Lee, Shuo Li, Yanhui Hu, Jia Yu Koh, John D. Eicher, Sylvane Desrivières, Alejandro Arias Vásquez, Ganesh Chauhan, Lavinia Athanasiu, Miguel E. Rentería, Sung Eun Kim, David Hoehn, Nicola J. Armstrong, Qiang Chen, Avram J. Holmes, Anouk den Braber, Iwona Kłoszewska, Micael Andersson, Thomas Espeseth, O. Grimm, Lucija Abramovic, Saud Alhusaini, Yuri Milaneschi, Martina Papmeyer, Tomas Axelsson, Stefan Ehrlich, Roberto Roiz‐Santiáñez, Bernd Kraemer, Asta K. Håberg, Hannah Jones, G. Bruce Pike, Dan J. Stein, Allison Stevens, Janita Bralten, Meike W. Vernooij, Tamara B. Harris, Irina Filippi, A. Veronica Witte, Tulio Guadalupe, Katharina Wittfeld, Thomas H. Mosley, James T. Becker, Nhat Trung Doan, Saskia P. Hagenaars, Yasaman Saba, Gabriel Cuéllar-Partida, Najaf Amin, Saima Hilal, Kwangsik Nho, Nazanin Mirza‐Schreiber, Konstantinos Arfanakis, Diane M. Becker, David Ames, Aaron L. Goldman, Phil Hyu Lee, Dorret I. Boomsma, Simon Lovestone, Sudheer Giddaluru, Stéphanie Le Hellard, Manuel Mattheisen, Marc M. Bohlken, Dalia Kasperavičiūtė, Lianne Schmaal, Stephen M. Lawrie, Ingrid Agartz, Esther Walton, Diana Tordesillas‐Gutiérrez, Gareth E. Davies, Jean Shin, Jonathan Ipser, Louis Vinke, Martine Hoogman, Tianye Jia, Ralph Burkhardt, Marieke Klein, Fabrice Crivello, Deborah Janowitz, Owen Carmichael, Unn K. Haukvik, Benjamin S. Aribisala, Helena Schmidt

    出版 2019
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  7. 7
    Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

    Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people 由 Else Eising, Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw, Carol A. Wang, Dongnhu T. Truong, Andrea G. Allegrini, Chin Yang Shapland, Gu Zhu, Karen G. Wigg, Margot Gerritse, Barbara Molz, Gökberk Alagöz, Alessandro Gialluisi, Filippo Abbondanza, Kaili Rimfeld, Marjolein van Donkelaar, Zhijie Liao, Philip R. Jansen, Till F. M. Andlauer, Timothy C. Bates, Manon Bernard, Kirsten Blokland, Milene Bonte, Anders D. Børglum, Thomas Bourgeron, Daniel Brandeis, Fabiola Ceroni, Valéria Csépe, Philip S. Dale, Peter F. de Jong, John C. DeFries, Jean‐François Démonet, Ditte Demontis, Yu Feng, Scott D. Gordon, Sharon Guger, Marianna E. Hayiou‐Thomas, Juan Hernández, Jouke‐Jan Hottenga, Charles Hulme, Juha Kere, Elizabeth N. Kerr, Tanner Koomar, Karin Landerl, Gabriel Leonard, Maureen W. Lovett, Heikki Lyytinen, Nicholas G. Martin, Angela Martinelli, Urs Maurer, Jacob J. Michaelson, Kristina Moll, Anthony P. Monaco, Angela Morgan, Markus M. Nöthen, Zdenka Pausová, Craig E. Pennell, Bruce F. Pennington, Kaitlyn M. Price, Veera M. Rajagopal, Franck Ramus, Louis Richer, Nuala H. Simpson, Shelley D. Smith, Maggie Snowling, John Stein, Lisa J. Strug, Joel B. Talcott, Henning Tiemeier, Marc P. van der Schroeff, Ellen Verhoef, Kate E. Watkins, Margaret Wilkinson, Margaret J. Wright, Cathy L. Barr, Dorret I. Boomsma, Manuel Carreiras, Marie-Christine Franken, Jeffrey R. Gruen, Michelle Luciano, Bertram Müller‐Myhsok, Dianne F. Newbury, Richard K. Olson, Silvia Paracchini, Tomáš Paus, Robert Plomin, Sheena Reilly, Gerd Schulte‐Körne, J. Bruce Tomblin, Elsje van Bergen, Andrew J. O. Whitehouse, Erik G. Willcutt, Beaté St Pourcain, Clyde Francks, Simon E. Fisher

    出版 2022
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  8. 8
    Discovery of 42 genome-wide significant loci associated with dyslexia

    Discovery of 42 genome-wide significant loci associated with dyslexia 由 Catherine Doust, Pierre Fontanillas, Else Eising, Scott D. Gordon, Zhengjun Wang, Gökberk Alagöz, Barbara Molz, Stella Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Daniella Coker, Gabriel Cuéllar-Partida, Devika Dhamija, Sayantan Das, Sarah L. Elson, Teresa Filshtein, Kipper Fletez‐Brant, Will Freyman, Pooja Gandhi, Karl Heilbron, Barry Hicks, David A. Hinds, Ethan M. Jewett, Yunxuan Jiang, Katelyn Kukar, Keng‐Han Lin, Maya Lowe, Jey C. McCreight, Matthew H. McIntyre, Steven J. Micheletti, Meghan E. Moreno, Joanna L. Mountain, Priyanka Nandakumar, Elizabeth S. Noblin, Jared O’Connell, Aaron A. Petrakovitz, G. David Poznik, Morgan Schumacher, Anjali J. Shastri, Janie F. Shelton, Jingchunzi Shi, Suyash Shringarpure, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Alejandro Hernandez, Corinna Wong, Christophe Toukam Tchakouté, Filippo Abbondanza, Andrea G. Allegrini, Till F. M. Andlauer, Cathy L. Barr, Manon Bernard, Kirsten Blokland, Milene Bonte, Dorret I. Boomsma, Thomas Bourgeron, Daniel Brandeis, Manuel Carreiras, Fabiola Ceroni, Valéria Csépe, Philip S. Dale, Peter F. de Jong, Jean‐François Démonet, Eveline L. de Zeeuw, Yu Feng, Marie-Christine Franken, Margot Gerritse, Alessandro Gialluisi, Sharon Guger, Marianna E. Hayiou‐Thomas, Juan Hernández, Jouke‐Jan Hottenga, Charles Hulme, Philip R. Jansen, Juha Kere, Elizabeth N. Kerr, Tanner Koomar, Karin Landerl, Gabriel Leonard, Zhijie Liao, Maureen W. Lovett, Heikki Lyytinen, Angela Martinelli, Urs Maurer, Jacob J. Michaelson, Nazanin Mirza‐Schreiber, Kristina Moll, Angela Morgan, Bertram Müller‐Myhsok, Dianne F. Newbury, Markus M. Nöthen, Tomáš Paus

    出版 2022
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  9. 9
    Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949)

    Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949) 由 Gail Davies, Nicola J. Armstrong, Joshua C. Bis, Jan Bressler, Vincent Chouraki, Sudheer Giddaluru, Edith Hofer, Carla A. Ibrahim‐Verbaas, Mirna Kirin, Jari Lahti, S J van der Lee, Stéphanie Le Hellard, Tsan Liu, Riccardo E. Marioni, Christopher Oldmeadow, Iris Postmus, Albert V. Smith, Jennifer A. Smith, Anbupalam Thalamuthu, Russell Thomson, Véronique Vitart, Jiao Wang, Lei Yu, Lina Zgaga, Wei Zhao, Ruth Boxall, Sarah E. Harris, W. David Hill, David C. Liewald, Michelle Luciano, Hieab H.H. Adams, David Ames, Najaf Amin, Philippe Amouyel, Amelia A. Assareh, Rhoda Au, James T. Becker, Alexa Beiser, Claudine Berr, Lars Bertram, Eric Boerwinkle, B. M. Buckley, Harry Campbell, Janie Corley, Philip L. De Jager, Carole Dufouil, Johan G. Eriksson, Thomas Espeseth, Jessica D. Faul, Ian Ford, Generation Scotland, Rebecca F. Gottesman, M E Griswold, Vilmundur Guðnason, Tamara B. Harris, G. Heiss, A Hofman, E.G. Holliday, Jennifer E. Huffman, Sharon L. R. Kardia, Nicole A. Kochan, D S Knopman, John B. Kwok, Jean‐Charles Lambert, Teresa Lee, G. Li, Shu Li, M Loitfelder, O L Lopez, Astri J. Lundervold, Annamari Lundqvist, Karen A. Mather, Nazanin Mirza‐Schreiber, Lars Nyberg, Ben A. Oostra, Aarno Palotie, Goran Papenberg, Alison Pattie, Katja Petrovic, Ozren Polašek, Bruce M. Psaty, Paul Redmond, Simone Reppermund, Jerome I. Rotter, Helena Schmidt, Maaike Schuur, P W Schofield, Rodney J. Scott, V M Steen, David J. Stott, John C. van Swieten, Kent D. Taylor, Julian N. Trollor, Stella Trompet, André G. Uitterlinden, Galit Weinstein, Elisabeth Widén, B. Gwen Windham, J. Wouter Jukema, A F Wright

    出版 2015
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    Revisão
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  10. 10
    Novel genetic loci underlying human intracranial volume identified through genome-wide association

    Novel genetic loci underlying human intracranial volume identified through genome-wide association 由 Hieab H.H. Adams, Derrek P. Hibar, Vincent Chouraki, Jason L. Stein, Paul Nyquist, Miguel E. Rentería, Stella Trompet, Alejandro Arias Vásquez, Sudha Seshadri, Sylvane Desrivières, Ashley Beecham, Neda Jahanshad, Katharina Wittfeld, Sven J. van der Lee, Lucija Abramovic, Saud Alhusaini, Najaf Amin, Micael Andersson, Konstantinos Arfanakis, Benjamin S. Aribisala, Nicola J. Armstrong, Lavinia Athanasiu, Tomas Axelsson, Alexa Beiser, Manon Bernard, Joshua C. Bis, Laura M. E. Blanken, Susan H. Blanton, Marc M. Bohlken, Marco P. Boks, Janita Bralten, Adam M. Brickman, Owen Carmichael, M. Mallar Chakravarty, Ganesh Chauhan, Qiang Chen, Christopher R. K. Ching, Gabriel Cuéllar-Partida, Anouk den Braber, Nhat Trung Doan, Stefan Ehrlich, Irina Filippi, Tian Ge, Sudheer Giddaluru, Aaron L. Goldman, Rebecca F. Gottesman, Corina U. Greven, O. Grimm, Michael Griswold, Tulio Guadalupe, Johanna Haß, Unn K. Haukvik, Saima Hilal, Edith Hofer, David Hoehn, Avram J. Holmes, Martine Hoogman, Deborah Janowitz, Tianye Jia, Dalia Kasperavičiūtė, Sung Eun Kim, Marieke Klein, Bernd Kraemer, Phil H. Lee, Jiemin Liao, David C. Liewald, Lorna M. Lopez, Michelle Luciano, Christine Macare, André F. Marquand, Mar Matarín, Karen A. Mather, Manuel Mattheisen, Bernard Mazoyer, David R. McKay, Rebekah McWhirter, Yuri Milaneschi, Nazanin Mirza‐Schreiber, Ryan L. Muetzel, Susana Muñoz Maniega, Kwangsik Nho, Allison C. Nugent, Loes M. Olde Loohuis, Jaap Oosterlaan, Martina Papmeyer, Irene Pappa, Lukas Pirpamer, Sara Pudas, Benno Pütz, Kumar B. Rajan, Adaikalavan Ramasamy, Jennifer S. Richards, Shannon L. Risacher, Roberto Roiz‐Santiáñez, Nanda Rommelse, Emma J. Rose, Natalie A. Royle, Tatjana Rundek, Philipp G. Sämann, Claudia L. Satizábal

    出版 2016
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  11. 11
    The genetic architecture of the human cerebral cortex

    The genetic architecture of the human cerebral cortex 由 Katrina L. Grasby, Neda Jahanshad, Jodie N. Painter, Lucía Colodro‐Conde, Janita Bralten, Derrek P. Hibar, Penelope A. Lind, Fabrizio Pizzagalli, Christopher R. K. Ching, Mary McMahon, Natalia Shatokhina, Leo Zsembik, Ingrid Agartz, Saud Alhusaini, Marcio Almeida, Dag Alnæs, Inge K. Amlien, Micael Andersson, Tyler Ard, Nicola J. Armstrong, Allison E. Ashley‐Koch, Joshua Atkins, Manon Bernard, Rachel M. Brouwer, Elizabeth E.L. Buimer, Robin Bülow, Christian Bürger, Dara M. Cannon, M. Mallar Chakravarty, Qiang Chen, Joshua W. Cheung, Baptiste Couvy‐Duchesne, Anders M. Dale, Shareefa Dalvie, Tânia Kawasaki de Araujo, Greig I. de Zubicaray, Sonja M. C. de Zwarte, Anouk den Braber, Nhat Trung Doan, Katharina Dohm, Stefan Ehrlich, Hannah-Ruth Engelbrecht, Susanne Erk, Chun Chieh Fan, Iryna O. Fedko, Sonya Foley, Judith M. Ford, Masaki Fukunaga, Melanie E. Garrett, Tian Ge, Sudheer Giddaluru, Aaron L. Goldman, Melissa J. Green, Nynke A. Groenewold, Dominik Grotegerd, Tiril P. Gurholt, Boris A. Gutman, Narelle K. Hansell, Mathew A. Harris, Marc Harrison, Courtney C. Haswell, Michael A. Hauser, Stefan Herms, Dirk J. Heslenfeld, New Fei Ho, David Hoehn, Per Hoffmann, Laurena Holleran, Martine Hoogman, Jouke‐Jan Hottenga, Masashi Ikeda, Deborah Janowitz, Iris E. Jansen, Tianye Jia, Christiane Jockwitz, Ryota Kanai, Sherif Karama, Dalia Kasperavičiūtė, Tobias Kaufmann, Sinéad Kelly, Masataka Kikuchi, Marieke Klein, Michael Knapp, Annchen R. Knodt, Bernd Krämer, Max Lam, T. Lancaster, Phil H. Lee, Tristram A. Lett, Lindsay B. Lewis, Íscia Lopes‐Cendes, Michelle Luciano, Fabìo Macciardi, André F. Marquand, Samuel R. Mathias, Tracy R. Melzer, Yuri Milaneschi, Nazanin Mirza‐Schreiber, José C.V. Moreira, Thomas W. Mühleisen

    出版 2018
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