Roland Krause
Roland Krause
University of Luxembourg, Luxembourg Centre for Systems Biomedicine
Verified email at - Homepage
Cited by
Cited by
Functional organization of the yeast proteome by systematic analysis of protein complexes
AC Gavin, M Bösche, R Krause, P Grandi, M Marzioch, A Bauer, J Schultz, ...
Nature 415 (6868), 141-147, 2002
Proteome survey reveals modularity of the yeast cell machinery
AC Gavin, P Aloy, P Grandi, R Krause, M Boesche, M Marzioch, C Rau, ...
Nature 440 (7084), 631-636, 2006
Comparative assessment of large-scale data sets of protein–protein interactions
C Von Mering, R Krause, B Snel, M Cornell, SG Oliver, S Fields, P Bork
Nature 417 (6887), 399-403, 2002
The human phenotype ontology in 2021
S Köhler, M Gargano, N Matentzoglu, LC Carmody, D Lewis-Smith, ...
Nucleic acids research 49 (D1), D1207-D1217, 2021
The human phenotype ontology in 2017
S Köhler, NA Vasilevsky, M Engelstad, E Foster, J McMurry, S Aymé, ...
Nucleic acids research 45 (D1), D865-D876, 2017
De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies
EKC EuroEPINOMICS-RES Consortium, Epilepsy Phenome/Genome Project
AJHG 95 (4), 360-370, 2014
The phenotypic spectrum of SCN8A encephalopathy
J Larsen, GL Carvill, E Gardella, G Kluger, G Schmiedel, N Barisic, ...
Neurology 84 (5), 480-489, 2015
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
De novo mutations in HCN1 cause early infantile epileptic encephalopathy
KBP Nava C, Dalle C, Rastetter A, Striano P, de Kovel, ...
Nature Genetics, 2014
Biomarkers of postoperative delirium and cognitive dysfunction
A Fournier, R Krause, G Winterer, R Schneider
Frontiers in aging neuroscience 7, 112, 2015
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
Nature communications 9 (1), 5269, 2018
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
Mutation in the transcriptional regulator PhoP contributes to avirulence of Mycobacterium tuberculosis H37Ra strain
JS Lee, R Krause, J Schreiber, HJ Mollenkopf, J Kowall, R Stein, BY Jeon, ...
Cell host & microbe 3 (2), 97-103, 2008
Modular decomposition of protein-protein interaction networks
J Gagneur, R Krause, T Bouwmeester, G Casari
Genome biology 5, 1-12, 2004
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
Identification of tightly regulated groups of genes during Drosophila melanogaster embryogenesis
SD Hooper, S Boué, R Krause, LJ Jensen, CE Mason, M Ghanim, ...
Molecular systems biology 3 (1), 72, 2007
CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures
RH Thomas, LM Zhang, GL Carvill, JS Archer, SB Heavin, ...
Neurology 84 (9), 951-958, 2015
A recurrent missense variant in AP2M1 impairs clathrin-mediated endocytosis and causes developmental and epileptic encephalopathy
I Helbig, T Lopez-Hernandez, O Shor, P Galer, S Ganesan, M Pendziwiat, ...
The American Journal of Human Genetics 104 (6), 1060-1072, 2019
70S-scanning initiation is a novel and frequent initiation mode of ribosomal translation in bacteria
H Yamamoto, D Wittek, R Gupta, B Qin, T Ueda, R Krause, K Yamamoto, ...
Proceedings of the National Academy of Sciences 113 (9), E1180-E1189, 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
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