Stefan Herms
Stefan Herms
IT-Support & Bioinformatics
Verified email at uni-bonn.de
TitleCited byYear
Biological insights from 108 schizophrenia-associated genetic loci
S Ripke, BM Neale, A Corvin, JTR Walters, KH Farh, PA Holmans, P Lee, ...
Nature 511 (7510), 421, 2014
36032014
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984, 2013
10342013
A mega-analysis of genome-wide association studies for major depressive disorder
S Ripke, NR Wray, CM Lewis, SP Hamilton, MM Weissman, G Breen, ...
Molecular psychiatry 18 (4), 497, 2013
8622013
Investigating neural primacy in Major Depressive Disorder: multivariate Granger causality analysis of resting-state fMRI time-series data
JP Hamilton, G Chen, ME Thomason, ME Schwartz, IH Gotlib
Molecular psychiatry 16 (7), 763, 2011
497*2011
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
NR Wray, S Ripke, M Mattheisen, M Trzaskowski, EM Byrne, A Abdellaoui, ...
Nature genetics 50 (5), 668, 2018
4922018
Direct conversion of fibroblasts into stably expandable neural stem cells
M Thier, P Wörsdörfer, YB Lakes, R Gorris, S Herms, T Opitz, D Seiferling, ...
Cell stem cell 10 (4), 473-479, 2012
4652012
“Too good to be true!”. The effectiveness of CSR history in countering negative publicity
J Vanhamme, B Grobben
Journal of Business Ethics 85 (2), 273, 2009
4642009
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24
S Birnbaum, KU Ludwig, H Reutter, S Herms, M Steffens, M Rubini, ...
Nature genetics 41 (4), 473, 2009
3842009
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
3792014
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), eaap8757, 2018
3682018
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate
E Mangold, KU Ludwig, S Birnbaum, C Baluardo, M Ferrian, S Herms, ...
Nature genetics 42 (1), 24, 2010
3592010
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
3192015
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, 2013
2752013
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373, 2017
2652017
Small molecules enable highly efficient neuronal conversion of human fibroblasts
J Ladewig, J Mertens, J Kesavan, J Doerr, D Poppe, F Glaue, S Herms, ...
Nature methods 9 (6), 575, 2012
2592012
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder
S Cichon, TW Mühleisen, FA Degenhardt, M Mattheisen, X Miró, ...
The American Journal of Human Genetics 88 (3), 372-381, 2011
2562011
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis
JZ Liu, JR Hov, T Folseraas, E Ellinghaus, SM Rushbrook, NT Doncheva, ...
Nature genetics 45 (6), 670, 2013
2542013
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci
KU Ludwig, E Mangold, S Herms, S Nowak, H Reutter, A Paul, J Becker, ...
Nature genetics 44 (9), 968, 2012
2472012
Genome-wide association study reveals two new risk loci for bipolar disorder
TW Mühleisen, M Leber, TG Schulze, J Strohmaier, F Degenhardt, ...
Nature communications 5, 3339, 2014
2462014
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ...
Nature genetics 49 (1), 27, 2017
2422017
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