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Holger Lerche
Holger Lerche
Professor für Neurologie, Universität Tübingen
Verified email at uni-tuebingen.de
Title
Cited by
Cited by
Year
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13662018
Incidence and mechanisms of cardiorespiratory arrests in epilepsy monitoring units (MORTEMUS): a retrospective study
P Ryvlin, L Nashef, SD Lhatoo, LM Bateman, J Bird, A Bleasel, P Boon, ...
The Lancet Neurology 12 (10), 966-977, 2013
10252013
Histopathological findings in brain tissue obtained during epilepsy surgery
I Blumcke, R Spreafico, G Haaker, R Coras, K Kobow, CG Bien, M Pfäfflin, ...
New England Journal of Medicine 377 (17), 1648-1656, 2017
7472017
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
6762009
Efficient generation of neural stem cell-like cells from adult human bone marrow stromal cells
A Hermann, R Gastl, S Liebau, MO Popa, J Fiedler, BO Boehm, M Maisel, ...
Journal of cell science 117 (19), 4411-4422, 2004
6532004
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
M Wolff, KM Johannesen, UBS Hedrich, S Masnada, G Rubboli, ...
Brain 140 (5), 1316-1336, 2017
5132017
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
JR Lemke, D Lal, EM Reinthaler, I Steiner, M Nothnagel, M Alber, ...
Nature genetics 45 (9), 1067-1072, 2013
5042013
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
5012010
Randomized phase III study 306: adjunctive perampanel for refractory partial-onset seizures
GL Krauss, JM Serratosa, V Villanueva, M Endziniene, Z Hong, J French, ...
Neurology 78 (18), 1408-1415, 2012
4792012
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
K Haug, M Warnstedt, AK Alekov, T Sander, A Ramírez, B Poser, ...
Nature genetics 33 (4), 527-532, 2003
4602003
Targeted next generation sequencing as a diagnostic tool in epileptic disorders
JR Lemke, E Riesch, T Scheurenbrand, M Schubach, C Wilhelm, I Steiner, ...
Epilepsia 53 (8), 1387-1398, 2012
3942012
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak
YG Weber, A Storch, TV Wuttke, K Brockmann, J Kempfle, S Maljevic, ...
The Journal of clinical investigation 118 (6), 2157-2168, 2008
3902008
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1
A Suls, P Dedeken, K Goffin, H Van Esch, P Dupont, D Cassiman, ...
Brain 131 (7), 1831-1844, 2008
3812008
Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current
K Jurkat-Rott, N Mitrovic, C Hang, A Kouzmenkine, P Iaizzo, J Herzog, ...
Proceedings of the National Academy of Sciences 97 (17), 9549-9554, 2000
3292000
De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies
S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ...
The American Journal of Human Genetics 95 (4), 360-370, 2014
3172014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
M Muona, SF Berkovic, LM Dibbens, KL Oliver, S Maljevic, MA Bayly, ...
Nature genetics 47 (1), 39-46, 2015
3152015
The new anticonvulsant retigabine favors voltage-dependent opening of the Kv7. 2 (KCNQ2) channel by binding to its activation gate
TV Wuttke, G Seebohm, S Bail, S Maljevic, H Lerche
Molecular pharmacology 67 (4), 1009-1017, 2005
3122005
Early‐onset absence epilepsy caused by mutations in the glucose transporter GLUT1
A Suls, SA Mullen, YG Weber, K Verhaert, B Ceulemans, R Guerrini, ...
Annals of Neurology: Official Journal of the American Neurological …, 2009
3032009
The phenotypic spectrum of SCN8A encephalopathy
J Larsen, GL Carvill, E Gardella, G Kluger, G Schmiedel, N Barisic, ...
Neurology 84 (5), 480-489, 2015
2862015
De novo loss-or gain-of-function mutations in KCNA2 cause epileptic encephalopathy
S Syrbe, U Hedrich, E Riesch, T Djémié, S Müller, RS Møller, B Maher, ...
Nature genetics 47 (4), 393-399, 2015
2852015
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