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Co-authors
(34)
Heike Olbrich
2
Rolf Marschalek
2
Andreas von Deimling
2
Peter Lichter
2
Olaf Witt
2
Journals
(3)
Neurogenetics
1
KLIN PADIAT
1
ACTA NEUROPATHOL
1
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(14)
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Authors
Huriye Cin
Huriye Cin,German Cancer Research Center,Neuroscience,Genetics & Genealogy,Family Medicine
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Huriye Cin
German Cancer Research Center
Publications:
3
|
Citations:
11
Fields:
Neuroscience
,
Genetics & Genealogy
,
Family Medicine
View FAQ about top research areas and Fields of study
Collaborated with
34 co-authors
from 2008 to 2011
|
Cited by
78 authors
Cumulative
Annual
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Publications
(3)
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RefWorks
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Oncogenic FAM131B–BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma
(
Citations: 2
)
Huriye Cin
,
Claus Meyer
,
Ricarda Herr
,
Wibke G. Janzarik
,
Sally Lambert
,
David T. W. Jones
,
Karine Jacob
,
Axel Benner
,
Hendrik Witt
,
Marc Remke
,
Sebastian Bender
,
Fabian Falkenstein
http://academic.research.microsoft.com/io.ashx?type=5&id=48392153&selfId1=27468020&selfId2=0&maxNumber=12&query=
Journal:
Acta Neuropathologica - ACTA NEUROPATHOL
, vol. 121, no. 6, pp. 763-774, 2011
Tandem duplications of 7q34 and 3q25 in pilocytic astrocytoma result in RAF fusion genes
H Cin
,
C Meyer
,
H Witt
,
M Remke
,
W Janzarik
,
T Nu Van Anh
,
H Olbrich
,
A von Deimling
,
A Kulozik
,
R Marschalek
,
O Witt
,
H Omran
http://academic.research.microsoft.com/io.ashx?type=5&id=29000447&selfId1=27468020&selfId2=0&maxNumber=12&query=
Journal:
Klinische Padiatrie - KLIN PADIAT
, vol. 222, no. 03, 2010
Identification and characterisation of a large Senataxin ( SETX ) gene duplication in ataxia with ocular apraxia type 2 (AOA2)
(
Citations: 9
)
Larissa Arning
,
Ludger Schöls
,
Huriye Cin
,
Manfred Souquet
,
Jörg T. Epplen
,
Dagmar Timmann
Journal:
Neurogenetics
, vol. 9, no. 4, pp. 295-299, 2008
Sort by:
Citations
(11 times by 11 publications)
RNA processing pathways in amyotrophic lateral sclerosis
(
Citations: 4
)
Marka van Blitterswijk
,
John E. Landers
Journal:
Neurogenetics
, vol. 11, no. 3, pp. 275-290, 2010
Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxin
(
Citations: 2
)
Giovanni Airoldi
,
Andrea Guidarelli
,
Orazio Cantoni
,
Chris Panzeri
,
Chiara Vantaggiato
,
Sara Bonato
,
Maria Grazia D’Angelo
,
Sestina Falcone
,
Clara De Palma
,
Alessandra Tonelli
,
Claudia Crimella
,
Sara Bondioni
http://academic.research.microsoft.com/io.ashx?type=5&id=34384167&selfId1=27468020&selfId2=0&maxNumber=12&query=
Journal:
Neurogenetics
, vol. 11, no. 1, pp. 91-100, 2010
DNA repair deficiency and neurological disease
(
Citations: 18
)
Peter J. McKinnon
Journal:
Nature Reviews Neuroscience - NAT REV NEUROSCI
, vol. 10, no. 2, pp. 100-112, 2009
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients
(
Citations: 12
)
M. Anheim
,
B. Monga
,
M. Fleury
,
P. Charles
,
C. Barbot
,
M. Salih
,
J. P. Delaunoy
,
M. Fritsch
,
L. Arning
,
M. Synofzik
,
L. Schols
,
J. Sequeiros
http://academic.research.microsoft.com/io.ashx?type=5&id=37638110&selfId1=27468020&selfId2=0&maxNumber=12&query=
Journal:
Brain
, vol. 132, no. 10, pp. 2688-2698, 2009
Sensorimotor neuronopathy in ataxia with oculomotor apraxia type 2
(
Citations: 3
)
José Gazulla
,
Isabel Benavente
,
Isabel Pérez López-Fraile
,
Pedro Modrego
,
Michel Koenig
Journal:
Muscle & Nerve - MUSCLE NERVE
, vol. 40, no. 3, pp. 481-485, 2009
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