Max Planck Institute for Molecular Genetics

Max Planck Publications of Lastname Lab

The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.

Journal Article (128)

Journal Article

Kumar, R.; Corbett, M. A.; Van Bon, B. W.; Gardner, A.; Woenig, J. A.; Jolly, L. A.; Douglas, E.; Friend, K.; Tan, C.; Van Esch, H. et al.; Holvoet, M.; Raynaud, M.; Field, M.; Leffler, M.; Budny, B.; Wisniewska, M.; Badura-Stronka, M.; Latos-Bielenska, A.; Batanian, J.; Rosenfeld, J. A.; Basel-Vanagaite, L.; Jensen, C.; Bienek, M.; Froyen, G.; Ullmann, R.; Hu, H.; Love, M. I.; Haas, S. A.; Stankiewicz, P.; Cheung, S. W.; Baxendale, A.; Nicholl, J.; Thompson, E. M.; Haan, E.; Kalscheuer, V. M.; Gecz, J.: Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems. Human Molecular Genetics 24 (25), pp. 7171 - 7181 (2015)

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McCall, C.; Hildebrandt, L. K.; Bornemann, B.; Singer, T.: Physiophenomenology in retrospect: Memory reliably reflects physiological arousal during a prior threatening experience. Consciousness and Cognition 38, pp. 60 - 70 (2015)

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Yamamoto, H.; Collier, M.; Loerke, J.; Ismer, J.; Schmidt, A.; Hilal, T.; Sprink, T.; Yamamoto, K.; Mielke, T.; Bürger, J. et al.; Shaikh, T. R.; Dabrowski, M.; Hildebrand, P. W.; Scheerer, P.; Spahn, C. M. T.: Molecular architecture of the ribosome-bound Hepatitis C Virus internal ribosomal entry site RNA. EMBO Journal 34 (24), pp. 3042 - 3058 (2015)

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Wruck, W.; Kashofer, K.; Rehman, S.; Daskalaki, A.; Berg, D.; Gralka, E.; Jozefczuk, J.; Drews, K.; Pandey, V.; Regenbrecht, C. et al.; Wierling, C. K.; Turano, P.; Korf, U.; Zatloukal, K.; Lehrach, H.; Westerhoff, H. V.; Adjaye, J.: Multi-omic profiles of human non-alcoholic fatty liver disease tissue highlight heterogenic phenotypes. Scientific Data 2, 150068 (2015)

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O'Rawe, J. A.; Wu, Y.; Dorfel, M. J.; Rope, A. F.; Au, P. Y.; Parboosingh, J. S.; Moon, S.; Kousi, M.; Kosma, K.; Smith, C. S. et al.; Tzetis, M.; Schuette, J. L.; Hufnagel, R. B.; Prada, C. E.; Martinez, F.; Orellana, C.; Crain, J.; Caro-Llopis, A.; Oltra, S.; Monfort, S.; Jimenez-Barron, L. T.; Swensen, J.; Ellingwood, S.; Smith, R.; Fang, H.; Ospina, S.; Stegmann, S.; Den Hollander, N.; Mittelman, D.; Highnam, G.; Robison, R.; Yang, E.; Faivre, L.; Roubertie, A.; Riviere, J. B.; Monaghan, K. G.; Wang, K.; Davis, E. E.; Katsanis, N.; Kalscheuer, V. M.; Wang, E. H.; Metcalfe, K.; Kleefstra, T.; Innes, A. M.; Kitsiou-Tzeli, S.; Rosello, M.; Keegan, C. E.; Lyon, G. J.: TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations. The American Journal of Human Genetics 97 (6), pp. 922 - 932 (2015)

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Guy, M. P.; Shaw, M.; Weiner, C. L.; Hobson, L.; Stark, Z.; Rose, K.; Kalscheuer, V. M.; Gecz, J.; Phizicky, E. M.: Defects in tRNA Anticodon Loop 2'-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations in FTSJ1. Human Mutation 36 (12), pp. 1176 - 1187 (2015)

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Ropers, H. H.; Wienker, T. F.: Penetrance of pathogenic mutations in haploinsufficient genes for intellectual disability and related disorders. European Journal of Medical Genetics 58 (12), pp. 715 - 718 (2015)

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Steinbeis, N.; Engert, V.; Linz, R.; Singer, T.: The effects of stress and affiliation on social decision-making: Investigating the tend-and-befriend pattern. Psychoneuroendocrinology 62, pp. 138 - 148 (2015)

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Wisniewski, D.; Reverberi, C.; Tusche, A.; Haynes, J.-D.: The neural representation of voluntary task-set selection in dynamic environments. Cerebral Cortex 25 (12), pp. 4715 - 4726 (2015)

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Zanni, G.; Kalscheuer, V. M.; Friedrich, A.; Barresi, S.; Alfieri, P.; Di Capua, M.; Haas, S. A.; Piccini, G.; Karl, T.; Klauck, S. M. et al.; Bellacchio, E.; Emma, F.; Cappa, M.; Bertini, E.; Breitenbach-Koller, L.: A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal Dysplasia. Human Mutation 36 (12), pp. 1155 - 1158 (2015)

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Kärst, S.; Arends, D.; Heise, S.; Trost, J.; Yaspo-Lehrach, M.-L.; Amstislavskiy, V.; Risch, T.; Lehrach, H.; Brockmann, G.: Erratum. BMC Genomics 16, p. 1018 - 1018 (2015)

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Spier, I.; Drichel, D.; Kerick, M.; Kirfel, J.; Horpaopan, S.; Laner, A.; Holzapfel, S.; Peters, S.; Adam, R.; Zhao, B. et al.; Becker, T.; Lifton, R. P.; Perner, S.; Hoffmann, P.; Kristiansen, G.; Timmermann, B.; Nöthen, M. M.; Holinski-Feder, E.; Schweiger, M. R.; Aretz, S.: Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases. Journal of Medical Genetics, 103468 (2015)

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Ganbari, M.; Lasserre, J.; Vingron, M.: Reconstruction of gene networks using prior knowledge. BMC Systems Biology 9, 9:84 (2015)

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Kanske, P.; Böckler, A.; Trautwein, F.-M.; Singer, T.: Dissecting the social brain: Introducing the EmpaToM to reveal distinct neural networks and brain-behavior relations for empathy and Theory of Mind. NeuroImage 122, pp. 6 - 19 (2015)

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Mertes, F.; Lichtner, B.; Kuhl, H.; Blattner , M.; Otte, J.; Wruck, W.; Timmermann, B.; Lehrach, H.; Adjaye, J.: Combined ultra-low input mRNA and whole-genome sequencing of human embryonic stem cells. BMC Genomics 16, 16:925 (2015)

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Kulaga-Yoskovitz, J.; Bernhardt, B. C.; Hong, S.-J.; Mansi, T.; Liang, K. E.; Van der Kouwe, A. J.W.; Smallwood, J.; Bernasconi, A.; Bernasconi, N.: Multi-contrast submillimetric 3 Tesla hippocampal subfield segmentation protocol and dataset. Scientific Data 2, 150059 (2015)

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Kärst, S.; Arends, D.; Heise, S.; Trost, J.; Yaspo-Lehrach, M.-L.; Amstislavskiy, V.; Risch, T.; Lehrach, H.: The direction of cross affects [corrected] obesity after puberty in male but not female offspring. BMC Genomics 16, p. 904 (2015)

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Lehrach, H.: Virtual Clinical Trials, an Essential Step in Increasing the Effectiveness of the Drug Development Process. Public Health Genomics 18 (6), pp. 366 - 371 (2015)

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Reiter, C.; Heise, F.; Chung, H.-R.; Ehrenhofer-Murray, A. E.: A link between Sas2-mediated H4 K16 acetylation, chromatin assembly in S-phase by CAF-I and Asf1, and nucleosome assembly by Spt6 during transcription. FEMS Yeast Research 15 (7), fov073 (2015)

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Zinchenko, A.; Kanske, P.; Obermeier, C.; Schröger, E.; Kotz, S. A.: Emotion and goal-directed behavior: ERP evidence on cognitive and emotional conflict. Social Cognitive and Affective Neuroscience 10 (11), pp. 1577 - 1587 (2015)

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