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TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
21 auth.
J. Sreedharan,
I. Blair,
V. Tripathi,
Xun Hu,
C. Vance,
B. Rogelj,
S. Ackerley,
S. Ackerley,
J. Durnall,
K. Williams,
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E. Buratti,
F. Baralle,
J. Belleroche,
J. Mitchell,
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A. Al-Chalabi,
C. Miller,
C. Miller,
G. Nicholson,
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C. Shaw
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11 |
2008 |
11
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Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
24 auth.
C. Vance,
B. Rogelj,
T. Hortobágyi,
K. D. Vos,
A. Nishimura,
J. Sreedharan,
Xun Hu,
Bradley N. Smith,
D. Ruddy,
Paul Wright,
...
J. Ganesalingam,
K. Williams,
V. Tripathi,
Safa Al-Saraj,
A. Al-Chalabi,
P. Leigh,
I. Blair,
G. Nicholson,
G. Nicholson,
J. Belleroche,
J. Gallo,
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11 |
2009 |
11
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Fronto-striatal cognitive deficits at different stages of Parkinson's disease.
8 auth.
A. Owen,
M. James,
P. Leigh,
B. Summers,
C. Marsden,
N. Quinn,
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K. Lange,
T. Robbins
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9 |
1992 |
9
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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,
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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,
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J. Hardy,
R. Orrell,
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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,
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M. de Visser,
A. Goris,
Markus Weber,
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Bradley N. Smith,
O. Pansarasa,
Cristina Cereda,
R. del Bo,
G. Comi,
S. D'alfonso,
C. Bertolin,
G. Soraru',
L. Mazzini,
V. Pensato,
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C. Zecca,
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2016 |
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Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
62 auth.
M. A. Es,
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C. Saris,
H. Blauw,
P. V. Vught,
A. Birve,
Robin Lemmens,
R. Lemmens,
H. J. Schelhaas,
E. Groen,
M. Huisman,
A. Kooi,
M. Visser,
C. Dahlberg,
K. Estrada,
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F. Rivadeneira,
A. Hofman,
M. Zwarts,
P. V. Doormaal,
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P. Muglia,
B. Tomik,
A. Słowik,
A. Uitterlinden,
C. Hendrich,
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A. Ludolph,
J. Glass,
S. Purcell,
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8 |
2009 |
8
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A proposed staging system for amyotrophic lateral sclerosis
13 auth.
J. Roche,
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R. Rojas‐García,
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C. Shaw,
A. Al-Chalabi
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8 |
2012 |
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An estimate of amyotrophic lateral sclerosis heritability using twin data
7 auth.
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F. Rijsdijk
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8 |
2010 |
8
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Reorganization of cortical blood flow and transcranial magnetic stimulation maps in human subjects after upper limb amputation.
8 auth.
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8 |
1994 |
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Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration
35 auth.
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K. Miśkiewicz,
Wendy J. Broom,
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P. V. Vught,
J. Landers,
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B. Neale,
M. R. Turner,
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R. Ophoff,
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Cortical function in amyotrophic lateral sclerosis. A positron emission tomography study.
7 auth.
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1993 |
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8 auth.
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Richard S. J. Frackowiak,
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8 |
1993 |
8
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Functional magnetic resonance imaging of verbal fluency and confrontation naming using compressed image acquisition to permit overt responses
8 auth.
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L. Goldstein,
A. Simmons,
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P. Leigh
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8 |
2003 |
8
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Natural history and clinical features of the flail arm and flail leg ALS variants
12 auth.
L. Wijesekera,
S. Mathers,
P. Talman,
C. Galtrey,
Michael H. Parkinson,
J. Ganesalingam,
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Mary‐Ann Ampong,
C. Ellis,
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A. Al-Chalabi,
P. Leigh
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2009 |
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