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Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia
40 auth.
A. Freischmidt,
T. Wieland,
Benjamin Richter,
W. Ruf,
V. Schaeffer,
Kathrin Müller,
Nicolai Marroquin,
Frida Nordin,
A. Hübers,
P. Weydt,
S. Pinto,
R. Press,
S. Millecamps,
N. Molko,
E. Bernard,
...
C. Desnuelle,
M. Soriani,
J. Dorst,
E. Graf,
U. Nordström,
Marisa S. Feiler,
Stefan Putz,
T. Boeckers,
T. Meyer,
A. Winkler,
J. Winkelman,
M. Carvalho,
D. Thal,
M. Otto,
T. Brännström,
A. Volk,
P. Kursula,
K. Danzer,
P. Lichtner,
I. Dikič,
T. Meitinger,
A. Ludolph,
T. Strom,
P. Andersen,
Jochen H Weishaupt
|
9 |
2015 |
9
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|
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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
192 auth.
W. V. Rheenen,
Rick A. A. van der Spek,
Mark K. Bakker,
J. Vugt,
P. Hop,
R. Zwamborn,
N. D. Klein,
H. Westra,
O. Bakker,
Patrick Deelen,
Gemma L Shireby,
E. Hannon,
M. Moisse,
D. Baird,
Restuadi Restuadi,
...
E. Dolzhenko,
Annelot M. Dekker,
Klara Gawor,
H. Westeneng,
Gijs H. P. Tazelaar,
K. V. van Eijk,
M. Kooyman,
Ross P. Byrne,
Mark A. Doherty,
M. Heverin,
Ahmad Al Khleifat,
A. Iacoangeli,
A. Shatunov,
N. Ticozzi,
Johnathan Cooper-Knock,
Bradley N. Smith,
M. Gromicho,
S. Chandran,
S. Pal,
K. Morrison,
P. Shaw,
J. Hardy,
R. Orrell,
M. Sendtner,
Thomas Meyer,
Nazlı A Başak,
A. J. van der Kooi,
A. Ratti,
I. Fogh,
C. Gellera,
Giuseppe Lauria Pinter,
S. Corti,
Cristina Cereda,
D. Sproviero,
S. D'alfonso,
G. Soraru',
G. Siciliano,
M. Filosto,
A. Padovani,
A. Chiò,
A. Calvo,
C. Moglia,
M. Brunetti,
A. Canosa,
M. Grassano,
E. Beghi,
E. Pupillo,
G. Logroscino,
B. Nefussy,
Alma Osmanovic,
Angelica Nordin,
Y. Lerner,
Michal Zabari,
M. Gotkine,
R. Baloh,
S. Bell,
P. Vourc'h,
P. Corcia,
P. Couratier,
S. Millecamps,
V. Meininger,
F. Salachas,
J. M. Pardina,
A. Assialioui,
R. Rojas‐García,
P. Dion,
J. Ross,
A. Ludolph,
Jochen H Weishaupt,
David Brenner,
A. Freischmidt,
G. Bensimon,
A. Brice,
A. Dürr,
C. Payan,
Safa Saker-Delye,
N. Wood,
S. Topp,
R. Rademakers,
L. Tittmann,
W. Lieb,
A. Franke,
S. Ripke,
A. Braun,
J. Kraft,
D. Whiteman,
C. Olsen,
A. Uitterlinden,
A. Hofman,
M. Rietschel,
S. Cichon,
M. Nöthen,
P. Amouyel,
B. Traynor,
A. Singleton,
Miguel Mitne Neto,
Ruben J. Cauchi,
R. Ophoff,
M. Wiedau-Pazos,
C. lomen-Hoerth,
V. V. Van Deerlin,
J. Grosskreutz,
A. Rödiger,
N. Gaur,
Alexander Jörk,
Tabea Barthel,
Erik Theele,
B. Ilse,
B. Stubendorff,
O. Witte,
R. Steinbach,
C. Hübner,
C. Graff,
L. Brylev,
V. Fominykh,
V. Demeshonok,
A. Ataulina,
B. Rogelj,
B. Koritnik,
J. Zidar,
M. Ravnik-Glavač,
D. Glavač,
Z. Stevic,
V. Drory,
M. Povedano,
I. Blair,
M. Kiernan,
Beben Benyamin,
R. Henderson,
S. Furlong,
S. Mathers,
P. Mccombe,
M. Needham,
S. Ngo,
G. Nicholson,
R. Pamphlett,
D. Rowe,
F. Steyn,
K. Williams,
K. Mather,
P. Sachdev,
A. Henders,
L. Wallace,
M. Carvalho,
S. Pinto,
S. Petri,
Markus Weber,
G. Rouleau,
V. Silani,
C. Curtis,
G. Breen,
J. Glass,
Robert H. Brown,
J. Landers,
C. Shaw,
P. Andersen,
E. Groen,
M. A. Es,
R. Pasterkamp,
Dongsheng Fan,
F. Garton,
A. McRae,
G. Davey Smith,
T. Gaunt,
M. Eberle,
J. Mill,
R. Mclaughlin,
O. Hardiman,
K. Kenna,
N. Wray,
E. Tsai,
H. Runz,
L. Franke,
A. Al-Chalabi,
P. Damme,
L. H. van den Berg,
J. Veldink
|
8 |
2021 |
8
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|
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TDP-43 is intercellularly transmitted across axon terminals
12 auth.
Marisa S. Feiler,
B. Strobel,
A. Freischmidt,
Anika M. Helferich,
Julia Kappel,
Bryson M Brewer,
...
Deyu Li,
D. Thal,
P. Walther,
A. Ludolph,
K. Danzer,
Jochen H Weishaupt
|
8 |
2015 |
8
🐜
|
|
🐜
|
Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation
31 auth.
Marcel Naumann,
A. Pal,
A. Goswami,
Xenia Lojewski,
Julia Japtok,
A. Vehlow,
M. Naujock,
R. Günther,
Mengmeng Jin,
Nancy Stanslowsky,
P. Reinhardt,
J. Sterneckert,
Marie Frickenhaus,
F. Pan-Montojo,
E. Storkebaum,
...
I. Poser,
A. Freischmidt,
Jochen H Weishaupt,
K. Holzmann,
D. Troost,
A. Ludolph,
T. Boeckers,
S. Liebau,
S. Petri,
N. Cordes,
A. Hyman,
F. Wegner,
S. Grill,
J. Weis,
A. Storch,
A. Hermann
|
7 |
2018 |
7
🐜
|
|
🐜
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Hot-spot KIF5A mutations cause familial ALS
54 auth.
David Brenner,
Rüstem Yilmaz,
Kathrin Müller,
T. Grehl,
S. Petri,
T. Meyer,
J. Grosskreutz,
P. Weydt,
W. Ruf,
C. Neuwirth,
Markus Weber,
S. Pinto,
K. Claeys,
B. Schrank,
B. Jordan,
...
Antje Knehr,
Kornelia Günther,
A. Hübers,
D. Zeller,
C. Kubisch,
S. Jablonka,
M. Sendtner,
T. Klopstock,
M. de Carvalho,
A. Sperfeld,
G. Borck,
A. Volk,
J. Dorst,
J. Weis,
M. Otto,
Joachim Schuster,
K. Del Tredici,
H. Braak,
K. Danzer,
A. Freischmidt,
T. Meitinger,
T. Strom,
A. Ludolph,
P. Andersen,
Jochen H Weishaupt,
U. Weyen,
A. Hermann,
T. Hagenacker,
J. Koch,
P. Lingor,
B. Göricke,
S. Zierz,
P. Baum,
Joachim Wolf,
A. Winkler,
P. Young,
U. Bogdahn,
J. Prudlo,
J. Kassubek
|
7 |
2018 |
7
🐜
|
|
🐜
|
Age-dependent defects of alpha-synuclein oligomer uptake in microglia and monocytes
17 auth.
Corinna Bliederhaeuser,
Veselin Grozdanov,
Anna Speidel,
L. Zondler,
W. Ruf,
Hanna Bayer,
M. Kiechle,
Marisa S. Feiler,
A. Freischmidt,
David Brenner,
...
Anke Witting,
B. Hengerer,
M. Fändrich,
A. Ludolph,
Jochen H Weishaupt,
F. Gillardon,
K. Danzer
|
7 |
2016 |
7
🐜
|
|
🐜
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Extracellular vesicle sorting of α-Synuclein is regulated by sumoylation
28 auth.
Marcel Kunadt,
K. Eckermann,
Anne Stuendl,
J. Gong,
Belisa Russo,
Katrin Strauss,
S. Rai,
S. Kügler,
Lisandro J. Falomir Lockhart,
M. Schwalbe,
P. Krumova,
L. M. Oliveira,
M. Bähr,
W. Möbius,
J. Levin,
...
A. Giese,
N. Kruse,
B. Mollenhauer,
Ruth Geiss-Friedlander,
A. Ludolph,
A. Freischmidt,
Marisa S. Feiler,
K. Danzer,
M. Zweckstetter,
T. Jovin,
M. Simons,
Jochen H Weishaupt,
A. Schneider
|
7 |
2015 |
7
🐜
|
|
🦁
|
Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis
A. Freischmidt,
Kathrin Müller,
A. Ludolph,
Jochen H Weishaupt
|
7 |
2013 |
7
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|
|
🐜
|
Peripheral monocytes are functionally altered and invade the CNS in ALS patients
22 auth.
L. Zondler,
Kathrin Müller,
Samira Khalaji,
Corinna Bliederhäuser,
W. Ruf,
Veselin Grozdanov,
M. Thiemann,
Katrin Fundel-Clemes,
A. Freischmidt,
K. Holzmann,
...
B. Strobel,
P. Weydt,
Anke Witting,
D. Thal,
Anika M. Helferich,
B. Hengerer,
K. Gottschalk,
O. Hill,
M. Kluge,
A. Ludolph,
K. Danzer,
J. Weishaupt
|
7 |
2016 |
7
🐜
|
|
🦁
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Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriers.
17 auth.
A. Freischmidt,
Kathrin Müller,
L. Zondler,
P. Weydt,
A. Volk,
Anže Božič,
M. Walter,
M. Bonin,
B. Mayer,
C. V. von Arnim,
...
M. Otto,
C. Dieterich,
K. Holzmann,
P. Andersen,
A. Ludolph,
K. Danzer,
Jochen H Weishaupt
|
6 |
2014 |
6
🦁
|
|
🦁
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Serum microRNAs in sporadic amyotrophic lateral sclerosis
A. Freischmidt,
Kathrin Müller,
L. Zondler,
P. Weydt,
Jochen H Weishaupt
|
6 |
2015 |
6
🦁
|
