Costin Leu
Costin Leu
Research staff at the Cleveland Clinic
Verified email at
Cited by
Cited by
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
15q13. 3 microdeletions increase risk of idiopathic generalized epilepsy
I Helbig, HC Mefford, AJ Sharp, M Guipponi, M Fichera, A Franke, ...
Nature genetics 41 (2), 160-162, 2009
Recurrent microdeletions at 15q11. 2 and 16p13. 11 predispose to idiopathic generalized epilepsies
CGF de Kovel, H Trucks, I Helbig, HC Mefford, C Baker, C Leu, C Kluck, ...
Brain 133 (1), 23-32, 2010
Familial and sporadic 15q13. 3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance
LM Dibbens, S Mullen, I Helbig, HC Mefford, MA Bayly, S Bellows, C Leu, ...
Human molecular genetics 18 (19), 3626-3631, 2009
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
D Kasperavičiūtė, CB Catarino, M Matarin, C Leu, J Novy, A Tostevin, ...
Brain 136 (10), 3140-3150, 2013
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16. 1, 2q22. 3 and 17q21. 32
Epicure Consortium, EMINet Consortium, M Steffens, C Leu, AK Ruppert, ...
Human molecular genetics 21 (24), 5359-5372, 2012
Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies
TILAE Consortium
The Lancet. Neurology 13 (9), 893, 2014
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy
P Striano, YG Weber, MR Toliat, J Schubert, C Leu, R Chaimana, ...
Neurology 78 (8), 557-562, 2012
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ...
The American Journal of Human Genetics 105 (2), 267-282, 2019
CHD2 variants are a risk factor for photosensitivity in epilepsy
EC Galizia, CT Myers, C Leu, CGF De Kovel, T Afrikanova, ...
Brain 138 (5), 1198-1208, 2015
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
TILAE Consortium
Nature communications 9, 2018
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy
D Lal, H Trucks, RS Mřller, H Hjalgrim, BPC Koeleman, CGF de Kovel, ...
Epilepsia 54 (2), 265-271, 2013
Dysfunction of NaV1. 4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study
R Männikkö, L Wong, DJ Tester, MG Thor, R Sud, DM Kullmann, ...
The Lancet 391 (10129), 1483-1492, 2018
Pitfalls in genetic testing: the story of missed SCN1A mutations
T Djémié, S Weckhuysen, S von Spiczak, GL Carvill, J Jaehn, ...
Molecular genetics & genomic medicine 4 (4), 457-464, 2016
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study
P May, S Girard, M Harrer, DR Bobbili, J Schubert, S Wolking, F Becker, ...
The Lancet Neurology 17 (8), 699-708, 2018
Carbamazepine‐and oxcarbazepine‐induced hyponatremia in people with epilepsy
B Berghuis, J van der Palen, GJ de Haan, D Lindhout, BPC Koeleman, ...
Epilepsia 58 (7), 1227-1233, 2017
Whole-genome linkage scan for epilepsy-related photosensitivity: a mega-analysis
CGF De Kovel, D Pinto, U Tauer, S Lorenz, H Muhle, C Leu, BA Neubauer, ...
Epilepsy research 89 (2-3), 286-294, 2010
Genome-wide polygenic burden of rare deleterious variants in sudden unexpected death in epilepsy
C Leu, S Balestrini, B Maher, L Hernández-Hernández, P Gormley, ...
EBioMedicine 2 (9), 1063-1070, 2015
Genome‐wide linkage meta‐analysis identifies susceptibility loci at 2q34 and 13q31. 3 for genetic generalized epilepsies
Epicure Consortium, C Leu, CGF de Kovel, F Zara, P Striano, M Pezzella, ...
Epilepsia 53 (2), 308-318, 2012
Diagnostic implications of genetic copy number variation in epilepsy plus
A Coppola, E Cellini, H Stamberger, E Saarentaus, V Cetica, D Lal, ...
Epilepsia 60 (4), 689-706, 2019
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