All papers authored by Costin Leu
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2020
Arthur Stefanski 
,
Yamile Calle‐López ,
Costin Leu ,
Eduardo Pérez‐Palma,
Elia Pestana‐Knight,
Dennis Lal
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,
Yamile Calle‐López ,
Costin Leu ,
Eduardo Pérez‐Palma,
Elia Pestana‐Knight,
Dennis Lal
Download from onlinelibrary.wiley.com
2019
Lisa-Marie Niestroj ,
Patrick May ,
Mykyta Artomov ,
Katja Kobow ,
Roland Coras,
Eduardo Pérez-Palma,
Janine Altmüller ,
Holger Thiele,
Peter Nürnberg,
Costin Leu ,
Aarno Palotie,
Mark J. Daly ,
Karl Martin Klein,
Rudi Beschorner ,
Yvonne G. Weber
and 2 other authors
,
Patrick May ,
Mykyta Artomov ,
Katja Kobow ,
Roland Coras,
Eduardo Pérez-Palma,
Janine Altmüller ,
Holger Thiele,
Peter Nürnberg,
Costin Leu ,
Aarno Palotie,
Mark J. Daly ,
Karl Martin Klein,
Rudi Beschorner ,
Yvonne G. Weber
and 2 other authors
Assessment of genetic variant burden in epilepsy-associated brain lesions
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2016
Tania Djémié,
Sarah Weckhuysen,
Sarah von Spiczak,
Carolien G. de Kovel,
Carla Marini,
Jacinta M. McMahon,
Davide Mei,
Rikke S. Møller,
Hiltrud Muhle,
Candace T. Myers,
Caroline Nava,
Jose M. Serratosa,
Sanjay M. Sisodiya,
Ulrich Stephani,
Pasquale Striano
and 32 other authors
Pitfalls in genetic testing: the story of missed SCN1A mutations
Download from doi.org
2015
Natasha E. Schoeler,
Costin Leu ,
Jon White,
Vincent Plagnol ,
Sian Ellard,
Mar Matarin,
Gary Yellen,
Elizabeth A. Thiele,
Mark Mackay,
Jacinta M. McMahon,
Ingrid E. Scheffer,
Josemir W. Sander,
J. Helen Cross,
Sanjay M. Sisodiya
,
Jon White,
Vincent Plagnol ,
Sian Ellard,
Mar Matarin,
Gary Yellen,
Elizabeth A. Thiele,
Mark Mackay,
Jacinta M. McMahon,
Ingrid E. Scheffer,
Josemir W. Sander,
J. Helen Cross,
Sanjay M. Sisodiya
Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsy
Download from www.ncbi.nlm.nih.gov
Carolien G. F. de Kovel,
Holger Thiele,
Pierangelo Veggiotti,
P. Veggotti,
Candace T. Myers,
Galizia Ec,
Teresa G. Martins,
Manuela Pendziwiat,
Thomas Sander,
Ann-Kathrin Ruppert,
Møller Rs,
Rikke S. Møller,
Julian Schubert,
Peter Nürnberg,
Aarno Palotie
and 55 other authors
CHD2 variants are a risk factor for photosensitivity in epilepsy
Download from www.ncbi.nlm.nih.gov
2013
Dalia Kasperaviciute,
Claudia B. Catarino,
Mar Matarin,
Costin Leu ,
Jan Novy,
Anna Tostevin,
The Uk Brain Expression Consortium,
Barbara Leal,
Ellen V. S. Hessel,
Kerstin Hallmann,
Michael S. Hildebrand,
Hans-Henrik M. Dahl,
Mina Ryten,
Saud Alhusaini,
Daniah Trabzuni
and 59 other authors
Download from doi.org
,
Jan Novy,
Anna Tostevin,
The Uk Brain Expression Consortium,
Barbara Leal,
Ellen V. S. Hessel,
Kerstin Hallmann,
Michael S. Hildebrand,
Hans-Henrik M. Dahl,
Mina Ryten,
Saud Alhusaini,
Daniah Trabzuni
and 59 other authors
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2012
P. Striano,
M. R. Toliat,
Yvonne G. Weber,
Julian Schubert,
A. Polvi,
R. Chaimana,
A. Robbiano,
F. Zara,
S. Baulac,
J. M. Serratosa,
R. Guerrero,
Costin Leu ,
E. LeGuern,
P. Nurnberg,
A.-E. Lehesjoki
and 4 other authors
,
E. LeGuern,
P. Nurnberg,
A.-E. Lehesjoki
and 4 other authors
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy
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Consortium Epicure,
C. G. F. de Kovel,
G.-J. de Haan,
S. von Spiczak,
M. Steffens,
EMINet Consortium,
Ruppert Ak,
A.-K. Ruppert,
F. Zara,
P. Striano,
A. Robbiano,
P. Tinuper,
G. Capovilla,
Costin Leu ,
C. G. De Kovel
and 106 other authors
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,
C. G. De Kovel
and 106 other authors
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2010
Michael Steffens,
Thomas Sander,
Markus M. Nöthen,
Thomas F. Wienker,
Tim Becker,
Rolf Fimmers,
Christine Herold,
Daniela A. Holler,
Stefan Herms,
Sven Cichon,
Bastian Bohn,
Thomas Gerstner,
Costin Leu ,
Michael Griebel,
Max P. Baur
Download from www.researchgate.net
,
Michael Griebel,
Max P. Baur
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C. G. F. de Kovel ,
D. Pinto,
U. Tauer,
S. Lorenz,
H. Muhle,
Costin Leu ,
B. A. Neubauer,
A. Hempelmann,
P. M. C. Callenbach,
I. E. Scheffer,
S. F. Berkovic,
G. Rudolf,
P. Striano,
A. Siren,
B. Baykan
and 6 other authors
,
D. Pinto,
U. Tauer,
S. Lorenz,
H. Muhle,
Costin Leu ,
B. A. Neubauer,
A. Hempelmann,
P. M. C. Callenbach,
I. E. Scheffer,
S. F. Berkovic,
G. Rudolf,
P. Striano,
A. Siren,
B. Baykan
and 6 other authors
Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis
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2009
Carolien G. F. de Kovel ,
P. de Jonghe,
Holger Trucks,
Heather C. Mefford,
Ingo Helbig,
Hiltrud Muhle,
Carl Baker,
Sarah von Spiczak,
Philipp Ostertag,
Costin Leu ,
Christian Kluck,
Dorothée Kasteleijn-Nolst Trenite,
Tanja Obermeier,
Michael Steffens,
Rikke S. Møller
and 33 other authors
,
P. de Jonghe,
Holger Trucks,
Heather C. Mefford,
Ingo Helbig,
Hiltrud Muhle,
Carl Baker,
Sarah von Spiczak,
Philipp Ostertag,
Costin Leu ,
Christian Kluck,
Dorothée Kasteleijn-Nolst Trenite,
Tanja Obermeier,
Michael Steffens,
Rikke S. Møller
and 33 other authors
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
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S. von Spiczak,
F. Zara,
C. G. F. de Kovel,
Z. Yapici,
Leanne M. Dibbens,
Saul Mullen,
Heather C. Mefford,
Holger Trucks,
Tanja Obermeier,
Michael Wittig,
P. De Jonghe,
Zuhal Yapici,
H. Hjalgrim,
Thomas Sander,
J. M. Madsen
and 59 other authors
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Ingo Helbig,
Heather C. Mefford,
Andrew J. Sharp,
Michel Guipponi,
Marco Fichera,
Andre Franke,
Hiltrud Muhle,
Carolien de Kovel ,
Carl Baker,
Sarah von Spiczak,
Katherine L. Kron,
Ines Steinich,
Verena Gaus,
Costin Leu ,
Bettina Schmitz
and 29 other authors
,
Carl Baker,
Sarah von Spiczak,
Katherine L. Kron,
Ines Steinich,
Verena Gaus,
Costin Leu ,
Bettina Schmitz
and 29 other authors
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
Download from www.ncbi.nlm.nih.govMissing publications? Search for publications with a matching author name.