Roland Krause
Roland Krause
Luxembourg Centre for Systems Biomedicine
Verified email at uni.lu
TitleCited byYear
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
55192002
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, 2006
27002006
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
26402002
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
4282017
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
282*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
1552015
Modular decomposition of protein-protein interaction networks
J Gagneur, R Krause, T Bouwmeester, G Casari
Genome biology 5 (8), R57, 2004
1522004
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
1512008
De novo mutations in HCN1 cause early infantile epileptic encephalopathy
KBP Nava C, Dalle C, Rastetter A, Striano P, de Kovel, ...
Nature Genetics, 2014
1462014
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
1412015
Biomarkers of postoperative delirium and cognitive dysfunction
G Androsova, R Krause, G Winterer, R Schneider
Frontiers in aging neuroscience 7, 112, 2015
1032015
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), 2007
892007
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
732015
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
582004
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
572016
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
542016
A comprehensive set of protein complexes in yeast: mining large scale protein–protein interaction screens
R Krause, C von Mering, P Bork
Bioinformatics 19 (15), 1901-1908, 2003
482003
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
462008
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
432015
Microblogging the ISMB: a new approach to conference reporting
N Saunders, P Beltrão, L Jensen, D Jurczak, R Krause, M Kuhn, S Wu
PLoS Computational Biology 5 (1), 2009
372009
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Articles 1–20