Biological insights from 108 schizophrenia-associated genetic loci C Pantelis, GN Papadimitriou, S Papiol, E Parkhomenko, MT Pato, ... Nature 511 (7510), 421-427, 2014 | 7394 | 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 | 1370 | 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 | 1310 | 2015 |
Mapping genomic loci implicates genes and synaptic biology in schizophrenia V Trubetskoy, AF Pardiñas, T Qi, G Panagiotaropoulou, S Awasthi, ... Nature 604 (7906), 502-508, 2022 | 1157 | 2022 |
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 | 649 | 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 | 508 | 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 | 247 | 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 | 238 | 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 | 194 | 2013 |
Complement genes contribute sex-biased vulnerability in diverse disorders N Kamitaki, A Sekar, RE Handsaker, H De Rivera, K Tooley, DL Morris, ... Nature 582 (7813), 577-581, 2020 | 180 | 2020 |
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 | 143 | 2018 |
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 | 139 | 2002 |
A comparison of ten polygenic score methods for psychiatric disorders applied across multiple cohorts G Ni, J Zeng, JA Revez, Y Wang, Z Zheng, T Ge, R Restuadi, J Kiewa, ... Biological psychiatry 90 (9), 611-620, 2021 | 131 | 2021 |
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 | 114 | 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 | 109 | 2007 |
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 | 86 | 2006 |
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 | 82 | 2013 |
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 | 79 | 2009 |
Sex-dependent shared and nonshared genetic architecture across mood and psychotic disorders GAM Blokland, J Grove, CY Chen, C Cotsapas, S Tobet, R Handa, ... Biological psychiatry 91 (1), 102-117, 2022 | 78 | 2022 |
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 | 75 | 2009 |