| 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 | 6146 | 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 | 3119 | 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 | 3011 | 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 | 740 | 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 | 624 | 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 | 440* | 2014 |
| The human phenotype ontology in 2017 S Kohler, NA Vasilevsky, M Engelstad, E Foster, J McMurry, S Ayme, ... | 350 | 2017 |
| The phenotypic spectrum of SCN8A encephalopathy J Larsen, GL Carvill, E Gardella, G Kluger, G Schmiedel, N Barisic, ... Neurology 84 (5), 480-489, 2015 | 294 | 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 | 286 | 2015 |
| Biomarkers of postoperative delirium and cognitive dysfunction A Fournier, R Krause, G Winterer, R Schneider Frontiers in aging neuroscience 7, 112, 2015 | 247 | 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 | 246 | 2019 |
| Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies Nature communications 9 (1), 5269, 2018 | 246 | 2018 |
| De novo mutations in HCN1 cause early infantile epileptic encephalopathy KBP Nava C, Dalle C, Rastetter A, Striano P, de Kovel, ... Nature Genetics, 2014 | 246 | 2014 |
| 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 | 193 | 2008 |
| Modular decomposition of protein-protein interaction networks J Gagneur, R Krause, T Bouwmeester, G Casari Genome biology 5, 1-12, 2004 | 180 | 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 | 145 | 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 | 101 | 2007 |
| 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 | 100 | 2019 |
| 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 | 100 | 2015 |
| 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 | 97 | 2016 |
Peer BorkDirector of EMBL HeidelbergVerified email at embl.de
