Výsledky vyhledávání - Franziska Degenhardt

Upřesnit hledání
  1. 1
    MicroRNAs as the cause of schizophrenia in 22q11.2 deletion carriers, and possible implications for idiopathic disease: a mini-review

    MicroRNAs as the cause of schizophrenia in 22q11.2 deletion carriers, and possible implications for idiopathic disease: a mini-review Autor Andreas J. Forstner, Franziska Degenhardt, Gerhard Schratt, Markus M. Nöthen

    Vydáno 2013
    Získat plný text Získat plný text
    Revisão
    Přidat do oblíbených
    Uloženo v:
  2. 2
    Maternal heterozygous NLRP7 variant results in recurrent reproductive failure and imprinting disturbances in the offspring

    Maternal heterozygous NLRP7 variant results in recurrent reproductive failure and imprinting disturbances in the offspring Autor Lukas Soellner, Matthias Begemann, Franziska Degenhardt, Annegret Geipel, Thomas Eggermann, Elisabeth Mangold

    Vydáno 2017
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  3. 3
    Polygenic risk has an impact on the structural plasticity of hippocampal subfields during aerobic exercise combined with cognitive remediation in multi-episode schizophrenia

    Polygenic risk has an impact on the structural plasticity of hippocampal subfields during aerobic exercise combined with cognitive remediation in multi-episode schizophrenia Autor Sergi Papiol, David Popovic, Daniel Keeser, A. Hasan, Neil Thomas, Franziska Degenhardt, Moritz J. Rossner, Heike Bickeböller, Andrea Schmitt, Peter Falkai, Berend Malchow

    Vydáno 2017
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  4. 4
    Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients

    Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients Autor Josef Frank, Maren Lang, Stephanie H. Witt, Jana Strohmaier, Dan Rujescu, Sven Cichon, Franziska Degenhardt, Markus M. Nöthen, David Collier, Stephan Ripke, Dieter Naber, Marcella Rietschel

    Vydáno 2014
    Získat plný text Získat plný text
    Carta
    Přidat do oblíbených
    Uloženo v:
  5. 5
    Identification and functional characterization of rare SHANK2 variants in schizophrenia

    Identification and functional characterization of rare SHANK2 variants in schizophrenia Autor Slavil Peykov, Simone Berkel, Michael Schoen, Kerstin Weiß, Franziska Degenhardt, Jana Strohmaier, B Weiss, Christian Proepper, Gerhard Schratt, Markus M. Nöthen, Tobias M. Boeckers, Marcella Rietschel, Gudrun Rappold

    Vydáno 2015
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  6. 6
    Phosphatase inhibitor-1-deficient mice are protected from catecholamine-induced arrhythmias and myocardial hypertrophy

    Phosphatase inhibitor-1-deficient mice are protected from catecholamine-induced arrhythmias and myocardial hypertrophy Autor Ali El‐Armouche, Katrin Wittköpper, Franziska Degenhardt, Florian Weinberger, Michael Didié, Ivan Melnychenko, Michael Grimm, Micha Peeck, Wolfram H. Zimmermann, Bernhard Unsöld, Gerd Hasenfuß, Dobromir Dobrev, Thomas Eschenhagen

    Vydáno 2008
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  7. 7
    Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population

    Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population Autor Jessica Martin, Fabian Streit, Jens Treutlein, Maren Lang, Josef Frank, Andreas J. Forstner, Franziska Degenhardt, Stephanie H. Witt, Thomas G. Schulze, Sven Cichon, Markus M. Nöthen, Marcella Rietschel, Jana Strohmaier

    Vydáno 2017
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  8. 8
    Polygenic burden associated to oligodendrocyte precursor cells and radial glia influences the hippocampal volume changes induced by aerobic exercise in schizophrenia patients

    Polygenic burden associated to oligodendrocyte precursor cells and radial glia influences the hippocampal volume changes induced by aerobic exercise in schizophrenia patients Autor Sergi Papiol, Daniel Keeser, Alkomiet Hasan, Neil Thomas, Florian Raabe, Franziska Degenhardt, Moritz J. Rossner, Heike Bickeböller, Ludovico Cantuti‐Castelvetri, Mikael Simons, Thomas Wobrock, Andrea Schmitt, Berend Malchow, Peter Falkai

    Vydáno 2019
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  9. 9
    Association of a Reproducible Epigenetic Risk Profile for Schizophrenia With Brain Methylation and Function

    Association of a Reproducible Epigenetic Risk Profile for Schizophrenia With Brain Methylation and Function Autor Junfang Chen, Zhenxiang Zang, Urs Braun, Kristina Schwarz, Anais Harneit, Thomas Kremer, Ren Ma, Janina I. Schweiger, Carolin Moessnang, Lena S. Geiger, Han Cao, Franziska Degenhardt, Markus M. Nöthen, Heike Tost, Andreas Meyer‐Lindenberg, Emanuel Schwarz

    Vydáno 2020
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  10. 10
    Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study

    Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study Autor Christian Hammer, Sven Cichon, Thomas W. Mühleisen, Britta Haenisch, Franziska Degenhardt, Manuel Mattheisen, René Breuer, Stephanie H. Witt, Jana Strohmaier, L Oruc, Fernando Silva, Gulja Babadjanova, Maria Grigoroiu‐Serbânescu, Joanna Hauser, Ralph Röth, Gudrun Rappold, Marcella Rietschel, Markus M. Nöthen, Beate Niesler

    Vydáno 2012
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  11. 11
    Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease

    Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease Autor Florian Uellendahl-Werth, Carlo Maj, Oleg Borisov, Simonas Juzėnas, Eike Matthias Wacker, Isabella Friis Jørgensen, Tim Alexander Steiert, Saptarshi Bej, Peter Krawitz, Per Hoffmann, Christoph Schramm, Olaf Wolkenhauer, Karina Banasik, Søren Brunak, Stefan Schreiber, Tom H. Karlsen, Franziska Degenhardt, Markus M. Nöthen, André Franke, Trine Folseraas, David Ellinghaus

    Vydáno 2022
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  12. 12
    Systematic Integration of Brain eQTL and GWAS Identifies<i>ZNF323</i>as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function

    Systematic Integration of Brain eQTL and GWAS Identifies<i>ZNF323</i>as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pu... Autor Xiong‐Jian Luo, Manuel Mattheisen, Ming Li, Liang Huang, Marcella Rietschel, Anders D. Børglum, Thomas D. Als, Edwin J. van den Oord, Karolina A. Åberg, Ole Mors, Preben Bo Mortensen, Zhenwu Luo, Franziska Degenhardt, Sven Cichon, Thomas G. Schulze, Markus M. Nöthen, Bing Su, Zhongming Zhao, Lin Gan, Yong‐Gang Yao

    Vydáno 2015
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  13. 13
    Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness

    Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness Autor F.F. Brockschmidt, Stefanie Heilmann‐Heimbach, Justine A. Ellis, Sibylle Eigelshoven, S. Hanneken, Christine Herold, Susanne Moebus, Margrieta A Alblas, Bärbel Lippke, Nadine Kluck, Lutz Priebe, Franziska Degenhardt, Rami Abou Jamra, Christian Meesters, Karl‐Heinz Jöckel, Raimund Erbel, Stephen Harrap, Johannes Schumacher, Holger Fröhlich, Roland Kruse, Axel M. Hillmer, Tim Becker, Markus M. Nöthen

    Vydáno 2011
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  14. 14
    High loading of polygenic risk in cases with chronic schizophrenia

    High loading of polygenic risk in cases with chronic schizophrenia Autor Sandra Meier, Esben Agerbo, Robert Maier, Carsten Bøcker Pedersen, Maren Lang, Jakob Grove, Mads V. Hollegaard, Ditte Demontis, Betina B. Trabjerg, Carsten Hjorthøj, Stephan Ripke, Franziska Degenhardt, Markus M. Nöthen, Dan Rujescu, Wolfgang Maier, Thomas Werge, Ole Mors, David M. Hougaard, Anders D. Børglum, Naomi R. Wray, Marcella Rietschel, Merete Nordentoft, Preben Bo Mortensen, Manuel Mattheisen

    Vydáno 2015
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  15. 15
    Genome‐wide CNV analysis in 221 unrelated patients and targeted high‐throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis

    Genome‐wide CNV analysis in 221 unrelated patients and targeted high‐throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis Autor Sukanya Horpaopan, Isabel Spier, Alexander M. Zink, Janine Altmüller, Stefanie Holzapfel, Andreas Laner, Stefanie Vogt, Siegfried Uhlhaas, Stefanie Heilmann‐Heimbach, Dietlinde Stienen, Sandra M. Pasternack, Kathleen Keppler, R. Adam, Katrin Kayser, Susanne Moebus, Markus Draaken, Franziska Degenhardt, Hartmut Engels, Andrea Hofmann, Markus M. Nöthen, Verena Steinke, Alberto Pérez-Bouza, Stefan Herms, Elke Holinski‐Feder, Holger Fröhlich, Hölger Thiele, Per Hoffmann, Stefan Aretz

    Vydáno 2014
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  16. 16
    Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia

    Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia Autor Dilafruz Juraeva, Britta Haenisch, Marc Zapatka, Josef Frank, Stephanie H. Witt, Thomas W. Mühleisen, Jens Treutlein, Jana Strohmaier, Sandra Meier, Franziska Degenhardt, Ina Giegling, Stephan Ripke, Markus Leber, Christoph Lange, Thomas G. Schulze, Rainald Mößner, Igor Nenadić, Heinrich Sauer, Dan Rujescu, Wolfgang Maier, Anders D. Børglum, Roel A. Ophoff, Sven Cichon, Markus M. Nöthen, Marcella Rietschel, Manuel Mattheisen, Benedikt Brors

    Vydáno 2014
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  17. 17
    Maternal variants in <i>NLRP</i> and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring

    Maternal variants in <i>NLRP</i> and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring Autor Matthias Begemann, Faisal I. Rezwan, Jasmin Beygo, Louise E Docherty, Julia Kolarova, Christopher Schroeder, Karin Buiting, Kamal Chokkalingam, Franziska Degenhardt, Emma Wakeling, Stephanie Kleinle, Daniela González Fassrainer, Barbara Oehl‐Jaschkowitz, Claire Turner, Michał Patalan, Maria Giżewska, Gerhard Binder, Cấn Thị Bích Ngọc, Vũ Chí Dũng, Sarju Mehta, Gareth Baynam, Julian Hamilton‐Shield, Sara Aljareh, Oluwakemi Lokulo‐Sodipe, Rachel Horton, Reiner Siebert, Miriam Elbracht, I. Karen Temple, Thomas Eggermann, Deborah Mackay

    Vydáno 2018
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  18. 18
    Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families

    Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families Autor José Guzmán‐Parra, Fabian Streit, Andreas J. Forstner, Jana Strohmaier, Maria José González, Susana Gil Flores, Francisco J. Cabaleiro Fabeiro, Francisco del Río Noriega, Fermín Pérez, Jesus Haro González, Guillermo Orozco Díaz, Yolanda de Diego‐Otero, Berta Moreno‐Küstner, Georg Auburger, Franziska Degenhardt, Stefanie Heilmann‐Heimbach, Stefan Herms, Per Hoffmann, Josef Frank, Jerome C. Foo, Lea Sirignano, Stephanie H. Witt, Sven Cichon, Fabio Rivas, Fermín Mayoral, Markus M. Nöthen, Till F. M. Andlauer, Marcella Rietschel

    Vydáno 2021
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  19. 19
    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 Autor 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

    Vydáno 2012
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  20. 20
    Review and Consensus on Pharmacogenomic Testing in Psychiatry

    Review and Consensus on Pharmacogenomic Testing in Psychiatry Autor Chad A. Bousman, Susanne Bengesser, Katherine J. Aitchison, Azmeraw T. Amare, H.N. Aschauer, Bernhard T. Baune, Bahareh Behroozi Asl, Jeffrey R. Bishop, Margit Burmeister, Boris Chaumette, Li-Shiun Chen, Zachary A. Cordner, Jürgen Deckert, Franziska Degenhardt, Lynn E. DeLisi, Lasse Folkersen, James L. Kennedy, Teri E. Klein, Joseph L. McClay, Francis J. McMahon, Richard Musil, Nancy L. Saccone, Katrin Sangkuhl, Robert Stowe, Ene‐Choo Tan, Arun K. Tiwari, Clement C. Zai, Gwyneth Zai, Jianping Zhang, Andrea Gaedigk, Daniel J. Müller

    Vydáno 2020
    Získat plný text Získat plný text
    Revisão
    Přidat do oblíbených
    Uloženo v:

Vyhledávací nástroje: