Carsten Drepper

Distribution of transcripts of the GFOD gene family members gfod1 and gfod2 in the zebrafish central nervous system.

Authors:

Carina G Lechermeier Andrea D'Orazio Marcel Romanos Christina Lillesaar Carsten Drepper

Gene Expr Patterns 2020 06 18;36:119111. Epub 2020 Mar 18.

Child and Adolescent Psychiatry, Center of Mental Health, University Hospital of Würzburg, Würzburg, Germany. Electronic address:

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June 2020

Anxiety risk SNPs on chromosome 2 modulate arousal in children in a fear generalization paradigm.

Authors:

Julia Reinhard Carsten Drepper Heike Weber Miriam A Schiele Katharina Kneer Anna Mittermeier Lillien Frey Andreas Reif Paul Pauli Katharina Domschke Jürgen Deckert Marcel Romanos

Eur Child Adolesc Psychiatry 2020 Sep 21;29(9):1301-1310. Epub 2019 Dec 21.

Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Center of Mental Health, University Hospital of Würzburg, Würzburg, Germany.

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September 2020

Transcript Analysis of Zebrafish GLUT3 Genes, and , Define Overlapping as Well as Distinct Expression Domains in the Zebrafish () Central Nervous System.

Authors:

Carina G Lechermeier Frederic Zimmer Teresa M Lüffe Klaus-Peter Lesch Marcel Romanos Christina Lillesaar Carsten Drepper

Front Mol Neurosci 2019 27;12:199. Epub 2019 Aug 27.

Child and Adolescent Psychiatry, Center of Mental Health, University Hospital of Würzburg, Würzburg, Germany.

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August 2019

Transcranial sonography in psychiatry as a potential tool in diagnosis and research.

Authors:

Carsten Drepper Julia Geißler Giuseppe Pastura Rezzak Yilmaz Daniela Berg Marcel Romanos Manfred Gerlach

World J Biol Psychiatry 2018 10 30;19(7):484-496. Epub 2017 Oct 30.

a Center of Mental Health, Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy , University Hospital of Würzburg , Würzburg , Germany.

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October 2018

C9ORF72 interaction with cofilin modulates actin dynamics in motor neurons.

Authors:

Rajeeve Sivadasan Daniel Hornburg Carsten Drepper Nicolas Frank Sibylle Jablonka Anna Hansel Xenia Lojewski Jared Sterneckert Andreas Hermann Pamela J Shaw Paul G Ince Matthias Mann Felix Meissner Michael Sendtner

Nat Neurosci 2016 12 10;19(12):1610-1618. Epub 2016 Oct 10.

Institute of Clinical Neurobiology, University Hospital of Wuerzburg, Wuerzburg, Germany.

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December 2016

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.

Authors:

Wouter van Rheenen Aleksey Shatunov Annelot M Dekker Russell L McLaughlin Frank P Diekstra Sara L Pulit Rick A A van der Spek Urmo Võsa Simone de Jong Matthew R Robinson Jian Yang Isabella Fogh Perry Tc van Doormaal Gijs H P Tazelaar Max Koppers Anna M Blokhuis William Sproviero Ashley R Jones Kevin P Kenna Kristel R van Eijk Oliver Harschnitz Raymond D Schellevis William J Brands Jelena Medic Androniki Menelaou Alice Vajda Nicola Ticozzi Kuang Lin Boris Rogelj Katarina Vrabec Metka Ravnik-Glavač Blaž Koritnik Janez Zidar Lea Leonardis Leja Dolenc Grošelj Stéphanie Millecamps François Salachas Vincent Meininger Mamede de Carvalho Susana Pinto Jesus S Mora Ricardo Rojas-García Meraida Polak Siddharthan Chandran Shuna Colville Robert Swingler Karen E Morrison Pamela J Shaw John Hardy Richard W Orrell Alan Pittman Katie Sidle Pietro Fratta Andrea Malaspina Simon Topp Susanne Petri Susanne Abdulla Carsten Drepper Michael Sendtner Thomas Meyer Roel A Ophoff Kim A Staats Martina Wiedau-Pazos Catherine Lomen-Hoerth Vivianna M Van Deerlin John Q Trojanowski Lauren Elman Leo McCluskey A Nazli Basak Ceren Tunca Hamid Hamzeiy Yesim Parman Thomas Meitinger Peter Lichtner Milena Radivojkov-Blagojevic Christian R Andres Cindy Maurel Gilbert Bensimon Bernhard Landwehrmeyer Alexis Brice Christine A M Payan Safaa Saker-Delye Alexandra Dürr Nicholas W Wood Lukas Tittmann Wolfgang Lieb Andre Franke Marcella Rietschel Sven Cichon Markus M Nöthen Philippe Amouyel Christophe Tzourio Jean-François Dartigues Andre G Uitterlinden Fernando Rivadeneira Karol Estrada Albert Hofman Charles Curtis Hylke M Blauw Anneke J van der Kooi Marianne de Visser An Goris Markus Weber Christopher E Shaw Bradley N Smith Orietta Pansarasa Cristina Cereda Roberto Del Bo Giacomo P Comi Sandra D'Alfonso Cinzia Bertolin Gianni Sorarù Letizia Mazzini Viviana Pensato Cinzia Gellera Cinzia Tiloca Antonia Ratti Andrea Calvo Cristina Moglia Maura Brunetti Simona Arcuti Rosa Capozzo Chiara Zecca Christian Lunetta Silvana Penco Nilo Riva Alessandro Padovani Massimiliano Filosto Bernard Muller Robbert Jan Stuit Ian Blair Katharine Zhang Emily P McCann Jennifer A Fifita Garth A Nicholson Dominic B Rowe Roger Pamphlett Matthew C Kiernan Julian Grosskreutz Otto W Witte Thomas Ringer Tino Prell Beatrice Stubendorff Ingo Kurth Christian A Hübner P Nigel Leigh Federico Casale Adriano Chio Ettore Beghi Elisabetta Pupillo Rosanna Tortelli Giancarlo Logroscino John Powell Albert C Ludolph Jochen H Weishaupt Wim Robberecht Philip Van Damme Lude Franke Tune H Pers Robert H Brown Jonathan D Glass John E Landers Orla Hardiman Peter M Andersen Philippe Corcia Patrick Vourc'h Vincenzo Silani Naomi R Wray Peter M Visscher Paul I W de Bakker Michael A van Es R Jeroen Pasterkamp Cathryn M Lewis Gerome Breen Ammar Al-Chalabi Leonard H van den Berg Jan H Veldink

Nat Genet 2016 09 25;48(9):1043-8. Epub 2016 Jul 25.

Department of Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands.

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September 2016

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis.

Authors:

Kevin P Kenna Perry T C van Doormaal Annelot M Dekker Nicola Ticozzi Brendan J Kenna Frank P Diekstra Wouter van Rheenen Kristel R van Eijk Ashley R Jones Pamela Keagle Aleksey Shatunov William Sproviero Bradley N Smith Michael A van Es Simon D Topp Aoife Kenna Jack W Miller Claudia Fallini Cinzia Tiloca Russell L McLaughlin Caroline Vance Claire Troakes Claudia Colombrita Gabriele Mora Andrea Calvo Federico Verde Safa Al-Sarraj Andrew King Daniela Calini Jacqueline de Belleroche Frank Baas Anneke J van der Kooi Marianne de Visser Anneloor L M A Ten Asbroek Peter C Sapp Diane McKenna-Yasek Meraida Polak Seneshaw Asress José Luis Muñoz-Blanco Tim M Strom Thomas Meitinger Karen E Morrison Giuseppe Lauria Kelly L Williams P Nigel Leigh Garth A Nicholson Ian P Blair Claire S Leblond Patrick A Dion Guy A Rouleau Hardev Pall Pamela J Shaw Martin R Turner Kevin Talbot Franco Taroni Kevin B Boylan Marka Van Blitterswijk Rosa Rademakers Jesús Esteban-Pérez Alberto García-Redondo Phillip Van Damme Wim Robberecht Adriano Chio Cinzia Gellera Carsten Drepper Michael Sendtner Antonia Ratti Jonathan D Glass Jesús S Mora Nazli A Basak Orla Hardiman Albert C Ludolph Peter M Andersen Jochen H Weishaupt Robert H Brown Ammar Al-Chalabi Vincenzo Silani Christopher E Shaw Leonard H van den Berg Jan H Veldink John E Landers

Nat Genet 2016 09 25;48(9):1037-42. Epub 2016 Jul 25.

Department of Neurology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.

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September 2016

Developmental exposure to acetaminophen does not induce hyperactivity in zebrafish larvae.

Authors:

Isabel Reuter Sabine Knaup Marcel Romanos Klaus-Peter Lesch Carsten Drepper Christina Lillesaar

J Neural Transm (Vienna) 2016 08 26;123(8):841-8. Epub 2016 Apr 26.

Department of Physiological Chemistry, Biocenter, Am Hubland, University of Würzburg, 97074, Würzburg, Germany.

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August 2016

Dysregulated IGFBP5 expression causes axon degeneration and motoneuron loss in diabetic neuropathy.

Authors:

Christian M Simon Stefanie Rauskolb Jennifer M Gunnersen Bettina Holtmann Carsten Drepper Benjamin Dombert Massimiliano Braga Stefan Wiese Sibylle Jablonka Dirk Pühringer Jürgen Zielasek Andreas Hoeflich Vincenzo Silani Eckhard Wolf Susanne Kneitz Claudia Sommer Klaus V Toyka Michael Sendtner

Acta Neuropathol 2015 Sep 30;130(3):373-87. Epub 2015 May 30.

Institute for Clinical Neurobiology, University of Würzburg, Versbacher-Str. 5, 97078, Würzburg, Germany.

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September 2015

Deep proteomic evaluation of primary and cell line motoneuron disease models delineates major differences in neuronal characteristics.

Authors:

Daniel Hornburg Carsten Drepper Falk Butter Felix Meissner Michael Sendtner Matthias Mann

Mol Cell Proteomics 2014 Dec 5;13(12):3410-20. Epub 2014 Sep 5.

From the ‡Max Planck Institute of Biochemistry, Martinsried, 82152, Germany;

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December 2014

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis.

Nat Neurosci 2014 May 30;17(5):664-666. Epub 2014 Mar 30.

Neuromuscular Diseases Research Unit, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, 35 Convent Drive, Bethesda, MD 20892, USA.

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May 2014

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.

Authors:

Elisa Majounie Alan E Renton Kin Mok Elise G P Dopper Adrian Waite Sara Rollinson Adriano Chiò Gabriella Restagno Nayia Nicolaou Javier Simon-Sanchez John C van Swieten Yevgeniya Abramzon Janel O Johnson Michael Sendtner Roger Pamphlett Richard W Orrell Simon Mead Katie C Sidle Henry Houlden Jonathan D Rohrer Karen E Morrison Hardev Pall Kevin Talbot Olaf Ansorge Dena G Hernandez Sampath Arepalli Mario Sabatelli Gabriele Mora Massimo Corbo Fabio Giannini Andrea Calvo Elisabet Englund Giuseppe Borghero Gian Luca Floris Anne M Remes Hannu Laaksovirta Leo McCluskey John Q Trojanowski Vivianna M Van Deerlin Gerard D Schellenberg Michael A Nalls Vivian E Drory Chin-Song Lu Tu-Hsueh Yeh Hiroyuki Ishiura Yuji Takahashi Shoji Tsuji Isabelle Le Ber Alexis Brice Carsten Drepper Nigel Williams Janine Kirby Pamela Shaw John Hardy Pentti J Tienari Peter Heutink Huw R Morris Stuart Pickering-Brown Bryan J Traynor

Lancet Neurol 2012 Apr 9;11(4):323-30. Epub 2012 Mar 9.

Molecular Genetics Unit, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.

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April 2012

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.

Brain 2012 Mar;135(Pt 3):784-93

Department of Neuroscience, University of Turin and Azienda Ospedale Università San Giovanni Battista of Turin, I-10126 Turin, Italy.

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March 2012

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.

Authors:

Alan E Renton Elisa Majounie Adrian Waite Javier Simón-Sánchez Sara Rollinson J Raphael Gibbs Jennifer C Schymick Hannu Laaksovirta John C van Swieten Liisa Myllykangas Hannu Kalimo Anders Paetau Yevgeniya Abramzon Anne M Remes Alice Kaganovich Sonja W Scholz Jamie Duckworth Jinhui Ding Daniel W Harmer Dena G Hernandez Janel O Johnson Kin Mok Mina Ryten Danyah Trabzuni Rita J Guerreiro Richard W Orrell James Neal Alex Murray Justin Pearson Iris E Jansen David Sondervan Harro Seelaar Derek Blake Kate Young Nicola Halliwell Janis Bennion Callister Greg Toulson Anna Richardson Alex Gerhard Julie Snowden David Mann David Neary Michael A Nalls Terhi Peuralinna Lilja Jansson Veli-Matti Isoviita Anna-Lotta Kaivorinne Maarit Hölttä-Vuori Elina Ikonen Raimo Sulkava Michael Benatar Joanne Wuu Adriano Chiò Gabriella Restagno Giuseppe Borghero Mario Sabatelli David Heckerman Ekaterina Rogaeva Lorne Zinman Jeffrey D Rothstein Michael Sendtner Carsten Drepper Evan E Eichler Can Alkan Ziedulla Abdullaev Svetlana D Pack Amalia Dutra Evgenia Pak John Hardy Andrew Singleton Nigel M Williams Peter Heutink Stuart Pickering-Brown Huw R Morris Pentti J Tienari Bryan J Traynor

Neuron 2011 Oct 21;72(2):257-68. Epub 2011 Sep 21.

Neuromuscular Diseases Research Unit, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD 20892, USA.

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October 2011

A new postal code for dendritic mRNA transport in neurons.

Authors:

Carsten Drepper Michael Sendtner

EMBO Rep 2011 Jul 1;12(7):614-6. Epub 2011 Jul 1.

Institute for Clinical Neurobiology in Würzburg, Germany.

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July 2011

PTEN depletion rescues axonal growth defect and improves survival in SMN-deficient motor neurons.

Authors:

Ke Ning Carsten Drepper Chiara F Valori Mansoor Ahsan Matthew Wyles Adrian Higginbottom Thomas Herrmann Pamela Shaw Mimoun Azzouz Michael Sendtner

Hum Mol Genet 2010 Aug 4;19(16):3159-68. Epub 2010 Jun 4.

Academic Neurology Unit, Department of Neuroscience, School of Medicine and Biomedical Sciences, University of Sheffield, Sheffield S10 2RX, UK.

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August 2010

Isolation and enrichment of embryonic mouse motoneurons from the lumbar spinal cord of individual mouse embryos.

Authors:

Stefan Wiese Thomas Herrmann Carsten Drepper Sibylle Jablonka Natalia Funk Alice Klausmeyer Mary-Louise Rogers Robert Rush Michael Sendtner

Nat Protoc 2010 Jan 17;5(1):31-8. Epub 2009 Dec 17.

Institute for Clinical Neurobiology, Wuerzburg, Germany.

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January 2010

C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany.

Authors:

Carsten Drepper Thomas Herrmann Carsten Wessig Marcus Beck Michael Sendtner

Neurobiol Aging 2011 Mar 16;32(3):548.e1-4. Epub 2009 Dec 16.

Institute for Clinical Neurobiology, Zinklesweg 10, University of Wuerzburg, D-97078 Wuerzburg, Germany.

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March 2011

A functional screen implicates microRNA-138-dependent regulation of the depalmitoylation enzyme APT1 in dendritic spine morphogenesis.

Nat Cell Biol 2009 Jun 24;11(6):705-16. Epub 2009 May 24.

Interdisziplinäres Zentrum für Neurowissenschaften, SFB488 Junior Group, Universität Heidelberg, and Institut für Neuroanatomie, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 345, 69120 Heidelberg, Germany.

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June 2009

Mutation of Vps54 causes motor neuron disease and defective spermiogenesis in the wobbler mouse.

Authors:

Thomas Schmitt-John Carsten Drepper Anke Mussmann Phillip Hahn Melanie Kuhlmann Cora Thiel Martin Hafner Andreas Lengeling Peter Heimann Julie M Jones Miriam H Meisler Harald Jockusch

Nat Genet 2005 Nov 23;37(11):1213-5. Epub 2005 Oct 23.

Developmental Biology and Molecular Pathology, Bielefeld University, Germany.

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November 2005

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