Roland Krause
Roland Krause
Luxembourg Centre for Systems Biomedicine
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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 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, UBS 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
Modular decomposition of protein-protein interaction networks
J Gagneur, R Krause, T Bouwmeester, G Casari
Genome biology 5 (8), 1-12, 2004
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
Biomarkers of postoperative delirium and cognitive dysfunction
G Androsova, R Krause, G Winterer, R Schneider
Frontiers in aging neuroscience 7, 112, 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 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
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
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
Crowdsourced estimation of cognitive decline and resilience in Alzheimer's disease
G Allen, N Amoroso, V Balagurusamy, C Bare, D Beaton, R Bellotti, ...
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
TILAE Consortium
Nature communications 9, 2018
Shared components of protein complexes—versatile building blocks or biochemical artefacts?
R Krause, C von Mering, P Bork, T Dandekar
Bioessays 26 (12), 1333-1343, 2004
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
EML3 is a nuclear microtubule-binding protein required for the correct alignment of chromosomes in metaphase
J Tegha-Dunghu, B Neumann, S Reber, R Krause, H Erfle, T Walter, ...
Journal of cell science 121 (10), 1718-1726, 2008
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