Our publications listed in the Puplication Repository of the Max Planck Society (PuRe)

Journal Article (128)

41.
Journal Article
Wierling, C. K.; Kessler, T.; Ogilvie, L. A.; Lange, B.; Yaspo, M.-L.; Lehrach, H.: Network and systems biology: essential steps in virtualising drug discovery and development. Drug Discovery Today: Technology 15, pp. 33 - 40 (2015)
42.
Journal Article
George, J.; Lim, J. S.; Jang, S. J.; Cun, Y.; Ozretic, L.; Kong, G.; Leenders, F.; Lu, X.; Fernandez-Cuesta, L.; Bosco, G. et al.; Müller, C.; Dahmen, I.; Jahchan, N. S.; Park, K. S.; Yang, D.; Karnezis, A. N.; Vaka, D.; Torres, A.; Wang, M. S.; Korbel, J. O.; Menon, R.; Chun, S. M.; Kim, D.; Wilkerson, M.; Hayes, N.; Engelmann, D.; Putzer, B.; Bos, M.; Michels, S.; Vlasic, I.; Seidel, D.; Pinther, B.; Schaub, P.; Becker, C.; Altmuller, J.; Yokota, J.; Kohno, T.; Iwakawa, R.; Tsuta, K.; Noguchi, M.; Muley, T.; Hoffmann, H.; Schnabel, P. A.; Petersen, I.; Chen, Y.; Soltermann, A.; Tischler, V.; Choi, C. M.; Kim, Y. H.; Massion, P. P.; Zou, Y.; Jovanovic, D.; Kontic, M.; Wright, G. M.; Russell, P. A.; Solomon, B.; Koch, I.; Lindner, M.; Muscarella, L. A.; la Torre, A.; Field, J. K.; Jakopovic, M.; Knezevic, J.; Castanos-Velez, E.; Roz, L.; Pastorino, U.; Brustugun, O. T.; Lund-Iversen, M.; Thunnissen, E.; Köhler, J.; Schuler, M.; Botling, J.; Sandelin, M.; Sanchez-Cespedes, M.; Salvesen, H. B.; Achter, V.; Lang, U.; Bogus, M.; Schneider, P. M.; Zander, T.; Ansen, S.; Hallek, M.; Wolf, J.; Vingron, M.; Yatabe, Y.; Travis, W. D.; Nurnberg, P.; Reinhardt, C.; Perner, S.; Heukamp, L.; Büttner, R.; Haas, S. A.; Brambilla, E.; Peifer, M.; Sage, J.; Thomas, R. K.: Comprehensive genomic profiles of small cell lung cancer. Nature 524 (7563), pp. 47 - 53 (2015)
43.
Journal Article
Kumar, R.; Corbett, M. A.; van Bon, B. W.; Woenig, J. A.; Weir, L.; Douglas, E.; Friend, K. L.; Gardner, A.; Shaw, M.; Jolly, L. A. et al.; Tan, C.; Hunter, M. F.; Hackett, A.; Field, M.; Palmer, E. E.; Leffler, M.; Rogers, C.; Boyle, J.; Bienek, M.; Jensen, C.; Van Buggenhout, G.; Van Esch, H.; Hoffmann, K.; Raynaud, M.; Zhao, H.; Reed, R.; Hu, H.; Haas, S. A.; Haan, E.; Kalscheuer, V. M.; Gecz, J.: THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability. The American Journal of Human Genetics 97 (2), pp. 302 - 310 (2015)
44.
Journal Article
Snijders Blok, L.; Madsen, E.; Juusola, J.; Gilissen, C.; Baralle, D.; Reijnders, M. R.; Venselaar, H.; Helsmoortel, C.; Cho, M. T.; Hoischen, A. et al.; Vissers, L. E.; Koemans, T. S.; Wissink-Lindhout, W.; Eichler, E. E.; Romano, C.; Van Esch, H.; Stumpel, C.; Vreeburg, M.; Smeets, E.; Oberndorff, K.; van Bon, B. W.; Shaw, M.; Gecz, J.; Haan, E.; Bienek, M.; Jensen, C.; Loeys, B. L.; Van Dijck, A.; Innes, A. M.; Racher, H.; Vermeer, S.; Di Donato, N.; Rump, A.; Tatton-Brown, K.; Parker, M. J.; Henderson, A.; Lynch, S. A.; Fryer, A.; Ross, A.; Vasudevan, P.; Kini, U.; Newbury-Ecob, R.; Chandler, K.; Male, A.; Study, D. D. D.; Dijkstra, S.; Schieving, J.; Giltay, J.; van Gassen, K. L.; Schuurs-Hoeijmakers, J.; Tan, P. L.; Pediaditakis, I.; Haas, S. A.; Retterer, K.; Reed, P.; Monaghan, K. G.; Haverfield, E.; Natowicz, M.; Myers, A.; Kruer, M. C.; Stein, Q.; Strauss, K. A.; Brigatti, K. W.; Keating, K.; Burton, B. K.; Kim, K. H.; Charrow, J.; Norman, J.; Foster-Barber, A.; Kline, A. D.; Kimball, A.; Zackai, E.; Harr, M.; Fox, J.; McLaughlin, J.; Lindstrom, K.; Haude, K. M.; van Roozendaal, K.; Brunner, H.; Chung, W. K.; Kooy, R. F.; Pfundt, R.; Kalscheuer, V. M.; Mehta, S. G.; Katsanis, N.; Kleefstra, T.: Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling. The American Journal of Human Genetics 97 (2), pp. 343 - 352 (2015)
45.
Journal Article
Kang, J.; Lienhard, M.; Pastor, W. A.; Chawla, A.; Novotny, M.; Tsagaratou, A.; Lasken, R. S.; Thompson, E. C.; Surani, M. A.; Koralov, S. B. et al.; Kalantry, S.; Chavez, L.; Rao, A.: Simultaneous deletion of the methylcytosine oxidases Tet1 and Tet3 increases transcriptome variability in early embryogenesis. Proceedings of the National Academy of Sciences of the United States of America 112 (31), pp. E4236 - E4245 (2015)
46.
Journal Article
Flöttmann, R.; Knaus, A.; Zemojtel, T.; Robinson, P. N.; Mundlos, S.; Horn, D.; Spielmann, M.: FGFR2 mutation in a patient without typical features of Pfeiffer syndrome--The emerging role of combined NGS and phenotype based strategies. European Journal of Medical Genetics 58 (8), pp. 376 - 380 (2015)
47.
Journal Article
Glémin, S.; Arndt, P. F.; Messer, P. W.; Petrov, D.; Galtier, N.; Duret, L.: Quantification of GC-biased gene conversion in the human genome. Genome Research 25 (8), pp. 1215 - 1228 (2015)
48.
Journal Article
Lelieveld, S. H.; Spielmann, M.; Mundlos, S.; Veltman, J. A.; Gilissen, C.: Comparison of Exome and Genome Sequencing Technologies for the Complete Capture of Protein-Coding Regions. Human Mutations 36 (8), pp. 815 - 822 (2015)
49.
Journal Article
Pek, J.; Chalmers, R. P.; Kok, B. E.; Losardo, D.: Visualizing confidence bands for semiparametrically estimated nonlinear relations among latent variables. Journal of Educational and Behavioral Statistics 40 (4), pp. 402 - 423 (2015)
50.
Journal Article
Shehata, S. N.; Deak, M.; Morrice, N. A.; Ohta, E.; Hunter, R. W.; Kalscheuer, V. M.; Sakamoto, K.: Cyclin Y phosphorylation- and 14-3-3-binding-dependent activation of PCTAIRE-1/CDK16. Biochemical Journal 469 (3), pp. 409 - 420 (2015)
51.
Journal Article
Stange, K.; Ott, C. E.; Schmidt-von Kegler, M.; Gillesen-Kaesbach, G.; Mundlos, S.; Dathe, K.; Seemann, P.: Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations? JOURNAL OF HUMAN GENETICS 60 (8), pp. 419 - 425 (2015)
52.
Journal Article
Chierchia, G.; Coricelli, G.: The impact of perceived similarity on tacit coordination: Propensity for matching and aversion to decoupling choices. Frontiers in Behavioral Neuroscience 9, 202 (2015)
53.
Journal Article
Flöttmann, R.; Wagner, J.; Kobus, K.; Curry, C. J.; Savarirayan, R.; Nishimura, G.; Yasui, N.; Spranger, J.; Van Esch, H.; Lyons, M. J. et al.; DuPont, B. R.; Dwivedi, A.; Klopocki, E.; Horn, D.; Mundlos, S.; Spielmann, M.: Microdeletions on 6p22.3 are associated with mesomelic dysplasia Savarirayan type. Journal of Medical Genetics 52 (7), pp. 476 - 483 (2015)
54.
Journal Article
Francioli, L. C.; Polak, P. P.; Koren, A.; Menelaou, A.; Chun, S.; Renkens, I.; Genome of the Netherlands, C.; van Duijn, C. M.; Swertz, M.; Wijmenga, C. et al.; van Ommen, G.; Slagboom, P. E.; Boomsma, D. I.; Ye, K.; Guryev, V.; Arndt, P. F.; Kloosterman, W. P.; de Bakker, P. I.; Sunyaev, S. R.: Genome-wide patterns and properties of de novo mutations in humans. Nature Genetics 47 (7), pp. 822 - 826 (2015)
55.
Journal Article
Kok, B. E.; Fredrickson, B. L.: Evidence for the upward spiral stands steady: A response to Heathers, Brown, Coyne, & Friedman. Psychological Science 26 (7), pp. 1144 - 1146 (2015)
56.
Journal Article
Lumma, A.-L.; Kok, B. E.; Singer, T.: Is meditation always relaxing?: Investigating heart rate, heart rate variability, experienced effort and likeability during training of three types of meditation. International Journal of Psychophysiology 97 (1), pp. 38 - 45 (2015)
57.
Journal Article
Pasqualini, L.; Bu, H.; Puhr, M.; Narisu, N.; Rainer, J.; Schlick, B.; Schäfer, G.; Angelova, M.; Trajanoski, Z.; Börno, S. T. et al.; Schweiger, M. R.; Fuchsberger, C.; Klocker, H.: miR-22 and miR-29a are members of the androgen receptor cistrome modulating LAMC1 and Mcl-1 in prostate cancer. Molecular Endocrinology 29 (7), pp. 1037 - 1054 (2015)
58.
Journal Article
Konishi, M.; McLaren, D. G.; Engen, H. G.; Smallwood, J.: Shaped by the past: The default mode network supports cognition that is independent of immediate perceptual input. PLoS One 10 (6), e0132209 (2015)
59.
Journal Article
Jolly, L. A.; Nguyen, L. S.; Domingo, D.; Sun, Y.; Barry, S.; Hancarova, M.; Plevova, P.; Vlckova, M.; Havlovicova, M.; Kalscheuer, V. M. et al.; Graziano, C.; Pippucci, T.; Bonora, E.; Sedlacek, Z.; Gecz, J.: HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain. Human Molecular Genetics 24 (12), pp. 3335 - 3347 (2015)
60.
Journal Article
Chaban, Y.; Lurz, R.; Brasilès, S.; Cornilleau, C.; Karreman, M.; Zinn-Justin, S.; Tavares, P.; Orlova, E. V.: Structural rearrangements in the phage head-to-tail interface during assembly and infection. Proceedings of the National Academy of Sciences of the United States of America 112 (22), pp. 7009 - 7014 (2015)
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