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Roland Krause - Publications

Affiliations: 
Computational Molecular Biology Max-Planck-Institute for Molecular Genetics, Berlin, Berlin, Germany 
Website:
http://www.molgen.mpg.de/~krause/

18 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Helbig I, Lopez-Hernandez T, Shor O, Galer P, Ganesan S, Pendziwiat M, Rademacher A, Ellis CA, Hümpfer N, Schwarz N, Seiffert S, Peeden J, Shen J, Štěrbová K, Hammer TB, ... ... Krause R, et al. A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy. American Journal of Human Genetics. PMID 31104773 DOI: 10.1016/J.Ajhg.2019.04.001  0.34
2018 Jabbari K, Bobbili DR, Lal D, Reinthaler EM, Schubert J, Wolking S, Sinha V, Motameny S, Thiele H, Kawalia A, Altmüller J, Toliat MR, Kraaij R, van Rooij J, Uitterlinden AG, ... ... Krause R, et al. Rare gene deletions in genetic generalized and Rolandic epilepsies. Plos One. 13: e0202022. PMID 30148849 DOI: 10.1371/Journal.Pone.0202022  0.354
2018 Bobbili DR, Lal D, May P, Reinthaler EM, Jabbari K, Thiele H, Nothnagel M, Jurkowski W, Feucht M, Nürnberg P, Lerche H, Zimprich F, Krause R, Neubauer BA, Reinthaler EM, ... ... Krause R, et al. Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. European Journal of Human Genetics : Ejhg. PMID 29358611 DOI: 10.1038/S41431-017-0034-X  0.321
2017 Niturad CE, Lev D, Kalscheuer VM, Charzewska A, Schubert J, Lerman-Sagie T, Kroes HY, Oegema R, Traverso M, Specchio N, Lassota M, Chelly J, Bennett-Back O, Carmi N, Koffler-Brill T, ... ... Krause R, et al. Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features. Brain : a Journal of Neurology. PMID 29053855 DOI: 10.1093/Brain/Awx236  0.311
2017 Keck M, Androsova G, Gualtieri F, Walker A, von Rüden EL, Russmann V, Deeg CA, Hauck SM, Krause R, Potschka H. A systems level analysis of epileptogenesis-associated proteome alterations. Neurobiology of Disease. PMID 28576708 DOI: 10.1016/J.Nbd.2017.05.017  0.335
2016 Köhler S, Vasilevsky NA, Engelstad M, Foster E, McMurry J, Aymé S, Baynam G, Bello SM, Boerkoel CF, Boycott KM, Brudno M, Buske OJ, Chinnery PF, Cipriani V, Connell LE, ... ... Krause R, et al. The Human Phenotype Ontology in 2017. Nucleic Acids Research. PMID 27899602 DOI: 10.1093/Nar/Gkw1039  0.31
2016 Lal D, Reinthaler EM, Dejanovic B, May P, Thiele H, Lehesjoki AE, Schwarz G, Riesch E, Ikram MA, Duijn CM, Uitterlinden AG, Hofman A, Steinböck H, Gruber-Sedlmayr U, Neophytou B, ... ... Krause R, et al. Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes. Plos One. 11: e0150426. PMID 26990884 DOI: 10.1371/Journal.Pone.0150426  0.303
2015 Lal D, Steinbrücker S, Schubert J, Sander T, Becker F, Weber Y, Lerche H, Thiele H, Krause R, Lehesjoki AE, Nürnberg P, Palotie A, Neubauer BA, Muhle H, Stephani U, et al. Investigation of GRIN2A in common epilepsy phenotypes. Epilepsy Research. 115: 95-9. PMID 26220384 DOI: 10.1016/J.Eplepsyres.2015.05.010  0.3
2011 Wiedenhoeft J, Krause R, Eulenstein O. The plexus model for the inference of ancestral multidomain proteins. Ieee/Acm Transactions On Computational Biology and Bioinformatics / Ieee, Acm. 8: 890-901. PMID 21282868 DOI: 10.1109/Tcbb.2011.22  0.347
2008 Tegha-Dunghu J, Neumann B, Reber S, Krause R, Erfle H, Walter T, Held M, Rogers P, Hupfeld K, Ruppert T, Ellenberg J, Gruss OJ. EML3 is a nuclear microtubule-binding protein required for the correct alignment of chromosomes in metaphase. Journal of Cell Science. 121: 1718-26. PMID 18445686 DOI: 10.1242/Jcs.019174  0.329
2007 Rungsarityotin W, Krause R, Schödl A, Schliep A. Identifying protein complexes directly from high-throughput TAP data with Markov random fields. Bmc Bioinformatics. 8: 482. PMID 18093306 DOI: 10.1186/1471-2105-8-482  0.353
2007 Hooper SD, Boué S, Krause R, Jensen LJ, Mason CE, Ghanim M, White KP, Furlong EE, Bork P. Identification of tightly regulated groups of genes during Drosophila melanogaster embryogenesis. Molecular Systems Biology. 3: 72. PMID 17224916 DOI: 10.1038/Msb4100112  0.442
2006 Gavin AC, Aloy P, Grandi P, Krause R, Boesche M, Marzioch M, Rau C, Jensen LJ, Bastuck S, Dümpelfeld B, Edelmann A, Heurtier MA, Hoffman V, Hoefert C, Klein K, et al. Proteome survey reveals modularity of the yeast cell machinery. Nature. 440: 631-6. PMID 16429126 DOI: 10.1038/Nature04532  0.506
2004 Krause R, von Mering C, Bork P, Dandekar T. Shared components of protein complexes--versatile building blocks or biochemical artefacts? Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 26: 1333-43. PMID 15551274 DOI: 10.1002/Bies.20141  0.488
2004 Gagneur J, Krause R, Bouwmeester T, Casari G. Modular decomposition of protein-protein interaction networks. Genome Biology. 5: R57. PMID 15287979 DOI: 10.1186/Gb-2004-5-8-R57  0.336
2003 Krause R, von Mering C, Bork P. A comprehensive set of protein complexes in yeast: mining large scale protein-protein interaction screens. Bioinformatics (Oxford, England). 19: 1901-8. PMID 14555622 DOI: 10.1093/Bioinformatics/Btg344  0.495
2002 von Mering C, Krause R, Snel B, Cornell M, Oliver SG, Fields S, Bork P. Comparative assessment of large-scale data sets of protein-protein interactions. Nature. 417: 399-403. PMID 12000970 DOI: 10.1038/Nature750  0.482
2002 Gavin AC, Bösche M, Krause R, Grandi P, Marzioch M, Bauer A, Schultz J, Rick JM, Michon AM, Cruciat CM, Remor M, Höfert C, Schelder M, Brajenovic M, Ruffner H, et al. Functional organization of the yeast proteome by systematic analysis of protein complexes. Nature. 415: 141-7. PMID 11805826 DOI: 10.1038/415141A  0.505
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