Max Koppers

Max Koppers

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Max Koppers

Max Koppers

Publications by authors named "Max Koppers"

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18Publications

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Late Endosomes Act as mRNA Translation Platforms and Sustain Mitochondria in Axons.

Cell 2019 01 3;176(1-2):56-72.e15. Epub 2019 Jan 3.

Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, UK. Electronic address:

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http://dx.doi.org/10.1016/j.cell.2018.11.030DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333918PMC
January 2019

Molecular control of local translation in axon development and maintenance.

Curr Opin Neurobiol 2018 08 14;51:86-94. Epub 2018 Mar 14.

Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, UK. Electronic address:

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http://dx.doi.org/10.1016/j.conb.2018.02.025DOI Listing
August 2018

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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http://dx.doi.org/10.1038/ng.3622DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556360PMC
September 2016

Full ablation of C9orf72 in mice causes immune system-related pathology and neoplastic events but no motor neuron defects.

Acta Neuropathol 2016 07 20;132(1):145-7. Epub 2016 May 20.

Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, Universiteitsweg 100, 3584 CG, Utrecht, The Netherlands.

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http://dx.doi.org/10.1007/s00401-016-1581-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911370PMC
July 2016

ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN.

Hum Mol Genet 2013 Sep 15;22(18):3690-704. Epub 2013 May 15.

Department of Neuroscience and Pharmacology, Rudolf Magnus Institute of Neuroscience, University Medical Centre Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1093/hmg/ddt222DOI Listing
September 2013

Protein aggregation in amyotrophic lateral sclerosis.

Acta Neuropathol 2013 Jun 15;125(6):777-94. Epub 2013 May 15.

Department of Neuroscience and Pharmacology, Rudolf Magnus Institute of Neuroscience, University Medical Center, Utrecht, The Netherlands.

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http://dx.doi.org/10.1007/s00401-013-1125-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661910PMC
June 2013

Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3.

Neurobiol Aging 2013 May 8;34(5):1518.e5-7. Epub 2012 Nov 8.

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

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.09.018DOI Listing
May 2013

VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient.

Neurobiol Aging 2012 Dec 9;33(12):2950.e1-4. Epub 2012 Aug 9.

Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, The Netherlands.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.07.004DOI Listing
December 2012

CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis.

Neurobiol Aging 2012 Aug 15;33(8):1852.e1-3. Epub 2012 Apr 15.

Department of Neurology, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.03.007DOI Listing
August 2012

VCP mutations in familial and sporadic amyotrophic lateral sclerosis.

Neurobiol Aging 2012 Apr 10;33(4):837.e7-13. Epub 2011 Nov 10.

Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1016/j.neurobiolaging.2011.10.006DOI Listing
April 2012

UNC13A is a modifier of survival in amyotrophic lateral sclerosis.

Neurobiol Aging 2012 Mar 25;33(3):630.e3-8. Epub 2011 Nov 25.

Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, 3584 CX, Utrecht, The Netherlands.

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http://dx.doi.org/10.1016/j.neurobiolaging.2011.10.029DOI Listing
March 2012