Elisabeth Stögmann
Elisabeth Stögmann
Associate Professor of Neurology at the Medical University of Vienna
Verified email at - Homepage
Cited by
Cited by
Biological insights from 108 schizophrenia-associated genetic loci
C Pantelis, GN Papadimitriou, S Papiol, E Parkhomenko, MT Pato, ...
Nature 511 (7510), 421-427, 2014
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
Modeling linkage disequilibrium increases accuracy of polygenic risk scores
BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ...
The american journal of human genetics 97 (4), 576-592, 2015
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases
A Gusev, SH Lee, G Trynka, H Finucane, BJ Vilhjálmsson, H Xu, C Zang, ...
The American Journal of Human Genetics 95 (5), 535-552, 2014
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ...
Cell 173 (7), 1705-1715. e16, 2018
Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy
F Zimprich, R Sunder-Plassmann, E Stogmann, A Gleiss, A Dal-Bianco, ...
Neurology 63 (6), 1087-1089, 2004
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept
B Franke, JL Stein, S Ripke, V Anttila, DP Hibar, KJE Van Hulzen, ...
Nature neuroscience 19 (3), 420-431, 2016
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
A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy
E Stögmann, A Zimprich, C Baumgartner, S Aull‐Watschinger, V Höllt, ...
Annals of Neurology: Official Journal of the American Neurological …, 2002
Sex differences in Alzheimer's disease
R Schmidt, E Kienbacher, T Benke, P Dal-Bianco, M Delazer, G Ladurner, ...
Neuropsychiatrie: Klinik, Diagnostik, Therapie und Rehabilitation: Organ der …, 2008
Clinical seizure lateralization in frontal lobe epilepsy
SB Bonelli, S Lurger, F Zimprich, E Stogmann, E Assem‐Hilger, ...
Epilepsia 48 (3), 517-523, 2007
Estimation of genetic correlation via linkage disequilibrium score regression and genomic restricted maximum likelihood
G Ni, G Moser, S Ripke, BM Neale, A Corvin, JTR Walters, KH Farh, ...
The American Journal of Human Genetics 102 (6), 1185-1194, 2018
Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations
E Stogmann, P Lichtner, C Baumgartner, S Bonelli, E Assem-Hilger, ...
Neurology 67 (11), 2029-2031, 2006
A novel mutation in the VCP gene (G157R) in a German family with inclusion‐body myopathy with Paget disease of bone and frontotemporal dementia
A Djamshidian, J Schaefer, D Haubenberger, E Stogmann, F Zimprich, ...
Muscle & Nerve: Official Journal of the American Association of …, 2009
A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures
K Schlachter, U Gruber-Sedlmayr, E Stogmann, M Lausecker, C Hotzy, ...
Neurology 72 (11), 974-978, 2009
A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy
F Zimprich, E Stogmann, S Bonelli, C Baumgartner, JC Mueller, ...
Epilepsia 49 (6), 1108-1109, 2008
Sequence analysis of the complete SLITRK1 gene in Austrian patients with Tourette's disorder
A Zimprich, K Hatala, F Riederer, E Stogmann, HN Aschauer, ...
Psychiatric Genetics 18 (6), 308-309, 2008
Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2
E Stogmann, E Reinthaler, S ElTawil, MA El Etribi, M Hemeda, ...
Brain 136 (4), 1155-1160, 2013
Electromagnetic tomography for brain imaging: From virtual to human brain
S Semenov, B Seiser, E Stoegmann, E Auff
2014 IEEE Conference on Antenna Measurements & Applications (CAMA), 1-4, 2014
Central serotonin 1A receptor binding in temporal lobe epilepsy: a [carbonyl-11C] WAY-100635 PET study
E Assem-Hilger, R Lanzenberger, M Savli, W Wadsak, M Mitterhauser, ...
Epilepsy & Behavior 19 (3), 467-473, 2010
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