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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
177 auth.
W. van Rheenen,
A. Shatunov,
Annelot M. Dekker,
R. Mclaughlin,
F. Diekstra,
S. Pulit,
Rick A. A. van der Spek,
U. Võsa,
S. de Jong,
M. Robinson,
Jian Yang,
I. Fogh,
P. T. V. van Doormaal,
Gijs H. P. Tazelaar,
M. Koppers,
...
A. Blokhuis,
W. Sproviero,
Ashley R. Jones,
K. Kenna,
K. V. van Eijk,
O. Harschnitz,
Raymond D. Schellevis,
W. Brands,
J. Medić,
A. Menelaou,
A. Vajda,
N. Ticozzi,
Kuang Lin,
B. Rogelj,
Katarina Vrabec,
M. Ravnik-Glavač,
B. Koritnik,
J. Zidar,
L. Leonardis,
L. D. Grošelj,
S. Millecamps,
F. Salachas,
V. Meininger,
M. de Carvalho,
S. Pinto,
J. Mora,
R. Rojas‐García,
M. Polak,
S. Chandran,
Shuna Colville,
R. Swingler,
K. Morrison,
P. Shaw,
J. Hardy,
R. Orrell,
A. Pittman,
K. Sidle,
P. Fratta,
A. Malaspina,
S. Topp,
S. Petri,
S. Abdulla,
C. Drepper,
M. Sendtner,
T. Meyer,
R. Ophoff,
K. Staats,
M. Wiedau-Pazos,
C. lomen-Hoerth,
V. V. Van Deerlin,
J. Trojanowski,
L. Elman,
L. McCluskey,
A. Başak,
Ceren Tunca,
Hamid Hamzeiy,
Y. Parman,
T. Meitinger,
P. Lichtner,
Milena Radivojkov-Blagojević,
C. Andres,
Cindy Maurel,
G. Bensimon,
B. Landwehrmeyer,
A. Brice,
C. Payan,
Safa Saker-Delye,
A. Dürr,
N. Wood,
L. Tittmann,
W. Lieb,
A. Franke,
M. Rietschel,
S. Cichon,
M. Nöthen,
P. Amouyel,
C. Tzourio,
J. Dartigues,
A. Uitterlinden,
F. Rivadeneira,
K. Estrada,
A. Hofman,
C. Curtis,
H. Blauw,
A. J. van der Kooi,
M. de Visser,
A. Goris,
Markus Weber,
C. Shaw,
Bradley N. Smith,
O. Pansarasa,
Cristina Cereda,
R. del Bo,
G. Comi,
S. D'alfonso,
C. Bertolin,
G. Soraru',
L. Mazzini,
V. Pensato,
C. Gellera,
C. Tiloca,
A. Ratti,
A. Calvo,
C. Moglia,
M. Brunetti,
S. Arcuti,
R. Capozzo,
C. Zecca,
C. Lunetta,
S. Penco,
N. Riva,
A. Padovani,
M. Filosto,
B. Muller,
Robbert Jan Stuit,
I. Blair,
Katharine Y. Zhang,
E. McCann,
J. Fifita,
G. Nicholson,
D. Rowe,
R. Pamphlett,
M. Kiernan,
J. Grosskreutz,
O. Witte,
T. Ringer,
T. Prell,
B. Stubendorff,
I. Kurth,
C. Hübner,
P. Leigh,
F. Casale,
A. Chiò,
E. Beghi,
E. Pupillo,
R. Tortelli,
G. Logroscino,
J. Powell,
A. Ludolph,
Jochen H Weishaupt,
W. Robberecht,
P. van Damme,
L. Franke,
T. Pers,
Robert H. Brown,
J. Glass,
J. Landers,
O. Hardiman,
P. Andersen,
P. Corcia,
P. Vourc'h,
V. Silani,
N. Wray,
P. Visscher,
P. D. de Bakker,
M. V. van Es,
R. Pasterkamp,
C. Lewis,
G. Breen,
A. Al-Chalabi,
L. H. van den Berg,
J. Veldink
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8 |
2016 |
8
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Haploinsufficiency leads to neurodegeneration in C9ORF72 ALS/FTD human induced motor neurons
43 auth.
Yingxiao Shi,
Shaoyu Lin,
K. Staats,
Yichen Li,
Wen-Hsuan Chang,
Shu-Ting Hung,
Eric Hendricks,
Gabriel R. Linares,
Yaoming Wang,
Esther Y. Son,
Xinmei Wen,
Kassandra Kisler,
Brent Wilkinson,
Louise Menendez,
Tohru Sugawara,
...
Phillip E. Woolwine,
Mickey M Huang,
Michael J. Cowan,
Brandon B Ge,
N. Koutsodendris,
Kaitlin P Sandor,
Jacob Komberg,
V. Vangoor,
Ketharini Senthilkumar,
Valerie Hennes,
Carina Seah,
Amy R. Nelson,
Tze-Yuan Cheng,
S. J. Lee,
Paul R. August,
Jason A. Chen,
N. Wisniewski,
V. Hanson-Smith,
T. G. Belgard,
Alice Zhang,
M. Coba,
C. Grunseich,
Michael E. Ward,
L. H. van den Berg,
R. Pasterkamp,
D. Trotti,
B. Zlokovic,
J. Ichida
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8 |
2018 |
8
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EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans
23 auth.
A. V. Hoecke,
Lies Schoonaert,
R. Lemmens,
M. Timmers,
K. Staats,
A. Laird,
Elke Peeters,
T. Philips,
A. Goris,
B. Dubois,
...
P. Andersen,
A. Al-Chalabi,
V. Thijs,
A. Turnley,
P. V. Vught,
J. Veldink,
O. Hardiman,
L. Bosch,
P. Gonzalez-Perez,
P. Damme,
Robert H. Brown,
L. H. Berg,
W. Robberecht
|
8 |
2012 |
8
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|
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Oligodendrocyte dysfunction in the pathogenesis of amyotrophic lateral sclerosis.
12 auth.
T. Philips,
A. Bento-Abreu,
Annelies Nonneman,
W. Haeck,
K. Staats,
Veerle Geelen,
...
N. Hersmus,
B. Küsters,
L. Van Den Bosch,
P. van Damme,
W. Richardson,
W. Robberecht
|
7 |
2013 |
7
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The microRNA-29 Family Dictates the Balance Between Homeostatic and Pathological Glucose Handling in Diabetes and Obesity
16 auth.
J. Dooley,
Josselyn E Garcia-Perez,
J. Sreenivasan,
Susan M. Schlenner,
R. Vangoitsenhoven,
Aikaterini S. Papadopoulou,
L. Tian,
Susann Schonefeldt,
L. Serneels,
C. Deroose,
...
K. Staats,
B. Van der Schueren,
B. de Strooper,
O. McGuinness,
C. Mathieu,
A. Liston
|
7 |
2015 |
7
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|
🐜
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Elongator subunit 3 (ELP3) modifies ALS through tRNA modification
23 auth.
A. Bento-Abreu,
Gunilla Jager,
B. Swinnen,
L. Rué,
S. Hendrickx,
Ashley Jones,
K. Staats,
Ines Taes,
Caroline Eykens,
Annelies Nonneman,
...
Rik Nuyts,
M. Timmers,
L. Silva,
A. Chariot,
L. Nguyen,
J. Ravits,
R. Lemmens,
D. Cabooter,
L. Van Den Bosch,
P. van Damme,
A. Al-Chalabi,
Anders S. Bystrom,
W. Robberecht
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6 |
2018 |
6
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|
🦁
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Rapamycin increases survival in ALS mice lacking mature lymphocytes
9 auth.
K. Staats,
Sara Hernández,
S. Schönefeldt,
A. Bento-Abreu,
J. Dooley,
P. van Damme,
...
A. Liston,
W. Robberecht,
L. Van Den Bosch
|
6 |
2013 |
6
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|
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ADAR2 mislocalization and widespread RNA editing aberrations in C9orf72-mediated ALS/FTD
18 auth.
Stephen Moore,
Eric B. Alsop,
Ileana Lorenzini,
Alexander Starr,
Benjamin E. Rabichow,
E. Mendez,
Jennifer L. Levy,
Camelia Burciu,
Rebecca A. Reiman,
Jeannie Chew,
...
Veronique V. Belzil,
D. Dickson,
J. Robertson,
K. Staats,
J. Ichida,
L. Petrucelli,
K. Keuren-Jensen,
R. Sattler
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5 |
2019 |
5
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|
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Olmsted syndrome: exploration of the immunological phenotype
19 auth.
D. Danso-Abeam,
Jianguo Zhang,
J. Dooley,
K. Staats,
L. Van Eyck,
Thomas van Brussel,
Shari Zaman,
E. Hauben,
M. Van de Velde,
M. Morren,
...
M. Renard,
C. van Geet,
H. Schaballie,
D. Lambrechts,
Jinsheng Tao,
Dean Franckaert,
S. Humblet-Baron,
I. Meyts,
A. Liston
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5 |
2013 |
5
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Astrocytes in amyotrophic lateral sclerosis: direct effects on motor neuron survival
K. Staats,
L. Bosch
|
5 |
2009 |
5
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