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Co-authors
(104)
Leonard H. van den Berg
5
Jan Herman Veldink
5
Roel A. Ophoff
4
Michael A. van Es
4
Helenius Jurgen Schelhaas
4
Journals
(5)
HUM MOL GENET
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NAT GENET
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Authors
Ewout J. N. Groen
Ewout J. N. Groen,University Medical Center Utrecht,Neuroscience,Genetics & Genealogy,Molecular Biology
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Ewout J. N. Groen
University Medical Center Utrecht
Publications:
5
|
Citations:
40
Fields:
Neuroscience
,
Genetics & Genealogy
,
Molecular Biology
View FAQ about top research areas and Fields of study
Collaborated with
104 co-authors
from 2009 to 2011
|
Cited by
226 authors
Cumulative
Annual
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Publications
(5)
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RefWorks
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Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
M. A. van Es
,
H. J. Schelhaas
,
P. W. van Vught
,
N. Ticozzi
,
P. M. Andersen
,
E. J. Groen
,
C. Schulte
,
H. M. Blauw
,
M. Koppers
,
F. P. Diekstra
,
K. Fumoto
,
A. L. Leclerc
http://academic.research.microsoft.com/io.ashx?type=5&id=59744323&selfId1=27238345&selfId2=0&maxNumber=12&query=
Journal:
Annals of Neurology - ANN NEUROL
, pp. 964-973, 2011
FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands
(
Citations: 11
)
E. J. N. Groen
,
M. A. van Es
,
Vught van P. W. J
,
W. G. M. Spliet
,
J. van Engelen-Lee
,
M. de Visser
,
J. H. J. Wokke
,
H. J. Schelhaas
,
R. A. Ophoff
,
K. Fumoto
,
R. J. Pasterkamp
,
D. Dooijes
http://academic.research.microsoft.com/io.ashx?type=5&id=33972953&selfId1=27238345&selfId2=0&maxNumber=12&query=
Journal:
Archives of Neurology - ARCH NEUROL
, vol. 67, no. 2, pp. 224-30, 2010
A large genome scan for rare CNVs in amyotrophic lateral sclerosis
(
Citations: 2
)
H. M. Blauw
,
A. Al-Chalabi
,
P. M. Andersen
,
P. W. J. van Vught
,
F. P. Diekstra
,
M. A. van Es
,
C. G. J. Saris
,
E. J. N. Groen
,
W. van Rheenen
,
M. Koppers
,
R. van't Slot
,
E. Strengman
http://academic.research.microsoft.com/io.ashx?type=5&id=37624015&selfId1=27238345&selfId2=0&maxNumber=12&query=
Journal:
Human Molecular Genetics - HUM MOL GENET
, vol. 19, no. 17, pp. 4091-4099, 2010
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
(
Citations: 27
)
Michael A van Es
,
Jan H Veldink
,
Christiaan G J Saris
,
Hylke M Blauw
,
Paul W J van Vught
,
Anna Birve
,
Robin Lemmens
,
Helenius J Schelhaas
,
Ewout J N Groen
,
Mark H B Huisman
,
Anneke J van der Kooi
,
Marianne de Visser
http://academic.research.microsoft.com/io.ashx?type=5&id=37053791&selfId1=27238345&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, vol. 41, no. 10, pp. 1083-1087, 2009
VCP mutations in familial and sporadic amyotrophic lateral sclerosis
Max Koppers
,
Marka M. van Blitterswijk
,
Lotte Vlam
,
Paulina A. Rowicka
,
Paul W. J. van Vught
,
Ewout J. N. Groen
,
Wim G. M. Spliet
,
JooYeon Engelen-Lee
,
Helenius J. Schelhaas
,
Marianne de Visser
,
Anneke J. van der Kooi
,
W-Ludo van der Pol
http://academic.research.microsoft.com/io.ashx?type=5&id=49247503&selfId1=27238345&selfId2=0&maxNumber=12&query=
Journal:
Neurobiology of Aging - NEUROBIOL AGING
Sort by:
Citations
(40 times by 37 publications)
Brain Expression Genome-Wide Association Study (eGWAS) Identifies Human Disease-Associated Variants
Fanggeng Zou
,
High Seng Chai
,
Curtis S. Younkin
,
Mariet Allen
,
Julia Crook
,
V. Shane Pankratz
,
Minerva M. Carrasquillo
,
Christopher N. Rowley
,
Asha A. Nair
,
Sumit Middha
,
Sooraj Maharjan
,
Thuy Nguyen
http://academic.research.microsoft.com/io.ashx?type=5&id=57409926&selfId1=27238345&selfId2=0&maxNumber=12&query=
Journal:
PLOS Genetics - PLOS GENET
, vol. 8, no. 6, 2012
Distinct pathological subtypes of FTLD-FUS
(
Citations: 9
)
Ian R. A. Mackenzie
,
David G. Munoz
,
Hirofumi Kusaka
,
Osamu Yokota
,
Kenji Ishihara
,
Sigrun Roeber
,
Hans A. Kretzschmar
,
Nigel J. Cairns
,
Manuela Neumann
Journal:
Acta Neuropathologica - ACTA NEUROPATHOL
, vol. 121, no. 2, pp. 207-218, 2011
Research Advances in Amyotrophic Lateral Sclerosis, 2009 to 2010
(
Citations: 4
)
Rebecca Traub
,
Hiroshi Mitsumoto
,
Lewis P. Rowland
Journal:
Current Neurology and Neuroscience Reports - CURR NEUROL NEUROSCI REP
, vol. 11, no. 1, pp. 67-77, 2011
Modelling the Effects of Penetrance and Family Size on Rates of Sporadic and Familial Disease
(
Citations: 1
)
Ammar Al-Chalabi
,
Cathryn M. Lewis
Journal:
Human Heredity - HUM HERED
, vol. 71, pp. 281-288, 2011
A de novo missense mutation of the FUS gene in a “true” sporadic ALS case
(
Citations: 2
)
Adriano Chiò
,
Andrea Calvo
,
Cristina Moglia
,
Irene Ossola
,
Maura Brunetti
,
Luca Sbaiz
,
Shiao-lin Lai
,
Yevgeniya Abramzon
,
Bryan J. Traynor
,
Gabriella Restagno
Journal:
Neurobiology of Aging - NEUROBIOL AGING
, vol. 32, no. 3, pp. 553.e23-553.e26, 2011
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