Publications

Max Planck Institute for Molecular Genetics

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

Satzger, I.; Marks, L.; Kerick, M.; Klages, S.; Berking, C.; Herbst, R.; Völker, B.; Schacht, V.; Timmermann, B.; Gutzmer, R.: Allele frequencies of BRAFV600 mutations in primary melanomas and matched metastases and their relevance for BRAF inhibitor therapy in metastatic melanoma. Oncotarget 2015, 5634 (2015)

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Heidari, A.; Tongsook, C.; Najafipour, R.; Musante, L.; Vasli, N.; Garshasbi, M.; Hu, H.; Mittal, K.; McNaughton, A. J.; Sritharan, K. et al.; Hudson, M.; Stehr, H.; Talebi, S.; Moradi, M.; Darvish, H.; Arshad Rafiq, M.; Mozhdehipanah, H.; Rashidinejad, A.; Samiei, S.; Ghadami, M.; Windpassinger, C.; Gillessen-Kaesbach, G.; Tzschach, A.; Ahmed, I.; Mikhailov, A.; Stavropoulos, D. J.; Carter, M. T.; Keshavarz, S.; Ayub, M.; Najmabadi, H.; Liu, X.; Ropers, H. H.; Macheroux, P.; Vincent, J. B.: Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability. Human Molecular Genetics 24 (20), pp. 5697 - 5710 (2015)

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Adegbola, A.; Musante, L.; Callewaert, B.; Maciel, P.; Hu, H.; Isidor, B.; Picker-Minh, S.; Le Caignec, C.; Delle Chiaie, B.; Vanakker, O. et al.; Menten, B.; Dheedene, A.; Bockaert, N.; Roelens, F.; Decaestecker, K.; Silva, J.; Soares, G.; Lopes, F.; Najmabadi, H.; Kahrizi, K.; Cox, G. F.; Angus, S. P.; Staropoli, J. F.; Fischer, U.; Suckow, V.; Bartsch, O.; Chess, A.; Ropers, H. H.; Wienker, T. F.; Hübner, C.; Kaindl, A. M.; Kalscheuer, V. M.: Redefining the MED13L syndrome. European journal of human genetics 23 (10), pp. 1308 - 1317 (2015)

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Egerer, J.; Emmerich, D.; Fischer-Zirnsak, B.; Chan, W. L.; Meierhofer, D.; Tuysuz, B.; Marschner, K.; Sauer, S.; Barr, F. A.; Mundlos, S. et al.; Kornak, U.: GORAB Missense Mutations Disrupt RAB6 and ARF5 Binding and Golgi Targeting. The Journal of Investigative Dermatology: an International Journal for Research in Cutaneous Biology 135 (10), pp. 2368 - 2376 (2015)

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Franic, S.; Groen-Blokhuis, M. M.; Dolan, C. V.; Kattenberg, M. V.; Pool, R.; Xiao, X.; Scheet, P. A.; Ehli, E. A.; Davies, G. E.; van der Sluis, S. et al.; Abdellaoui, A.; Hansell, N. K.; Martin, N. G.; Hudziak, J. J.; van Beijsterveldt, C. E.; Swagerman, S. C.; Hulshoff Pol, H. E.; de Geus, E. J.; Bartels, M.; Ropers, H. H.; Hottenga, J. J.; Boomsma, D. I.: Intelligence: shared genetic basis between Mendelian disorders and a polygenic trait. European journal of human genetics 23 (10), pp. 1378 - 1383 (2015)

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Ramirez, F.; Lingg, T.; Toscano, S.; Lam, K. C.; Georgiev, P.; Chung, H. R.; Lajoie, B. R.; de Wit, E.; Zhan, Y.; de Laat, W. et al.; Dekker, J.; Manke, T.; Akhtar, A.: High-Affinity Sites Form an Interaction Network to Facilitate Spreading of the MSL Complex across the X Chromosome in Drosophila. Molecular Cell 60 (1), pp. 146 - 162 (2015)

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Sauer, S.: Ligands for the Nuclear Peroxisome Proliferator-Activated Receptor Gamma. Trends in Pharmacological Sciences 36 (10), pp. 688 - 704 (2015)

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Schick, A.; Adam, R.; Vollmayr, B.; Kuehner, C.; Kanske, P.; Wessa, M.: Neural correlates of valence generalization in an affective conditioning paradigm. Behavioural Brain Research 292, pp. 147 - 156 (2015)

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Sudmant, P. H.; Rausch, T.; Gardner, E. J.; Handsaker, R. E.; Abyzov, A.; Huddleston, J.; The 1000 Genomes Project Consortium; Timmermann, B.; Herwig, R.; Lehrach, H.: An integrated map of structural variation in 2,504 human genomes. Nature 526 (7571), pp. 75 - 81 (2015)

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The 1000 Genome Project Consortium; Lehrach, H.; Amstislavskiy, V.; Lienhard, M.; Mertes, F.; Sultan, M.; Timmermann, B.; Yaspo, M.-L.; Herwig, R.: A global reference for human genetic variation. Nature 526 (7571), pp. 68 - 74 (2015)

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Correia, J. C.; Massart, J.; de Boer, J. F.; Porsmyr-Palmertz, M.; Martínez-Redondo, V.; Agudelo, L. Z.; Sinha, I.; Meierhofer, D.; Ribeiro, V.; Björnholm, M. et al.; Sauer, S.; Dahlman-Wright, K.; Zierath, J. R.; Groen, A. K.; Ruas, J. L.: Bioenergetic cues shift FXR splicing towards FXRα2 to modulate hepatic lipolysis and fatty acid metabolism. Molecular Metabolism 4 (12), pp. 891 - 901 (2015)

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Musahl, A.; Huang, X.; Rusakiewicz, S.; Ntini, E.; Marsico, A.; Kroemer, G.; Kepp, O.; Ørom, U. A.: A long non-coding RNA links calreticulin-mediated immunogenic cell removal to RB1 transcription. Oncogene 34 (39), pp. 5046 - 5054 (2015)

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Engen, H. G.; Singer, T.: Compassion-based emotion regulation up-regulates experienced positive affect and associated neural networks. Social, Cognitive and Affective Neuroscience 10 (9), pp. 1291 - 1301 (2015)

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Fischer-Zirnsak, B.; Escande-Beillard, N.; Ganesh, J.; Tan, Y. X.; Bughaili, M. A.; Lin, A. E.; Sahai, I.; Bahena, P.; Reichert, S. L.; Loh, A. et al.; Wright, G. D.; Liu, J.; Rahikkala, E.; Pivnick, E. K.; Choudhri, A. F.; Krüger, U.; Zemojtel, T.; van Ravenswaaij-Arts, C.; Mostafavi, R.; Stolte-Dijkstra, I.; Symoens, S.; Pajunen, L.; Al-Gazali, L.; Meierhofer, D.; Robinson, P. N.; Mundlos, S.; Villarroel, C. E.: Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa. The American Journal of Human Genetics 97 (3), pp. 483 - 492 (2015)

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Bernhardt, B. C.; Bonilha, L.; Gross, D. W.: Network analysis for a network disorder: The emerging role of graph theory in the study of epilepsy. Epilepsy and Behavior 50, pp. 162 - 170 (2015)

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Böckler, A.; van der Wel, R. P.; Welsh, T. N.: Eyes only? Perceiving eye contact is neither sufficient nor necessary for attentional capture by face direction. Acta Psychologica 160, pp. 134 - 140 (2015)

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Eduati, F.; Mangravite, L. M.; Wang, T.; Tang, H.; Bare, J. C.; Huang, R.; Norman, T.; Kellen, M.; Menden, M. P.; Yang, J. et al.; Zhan, X.; Zhong, R.; Xiao, G.; Xia, M.; Abdo, N.; Kosyk, O.; Collaboration, N.-N.-U. D. T.; van Bömmel, A.; Caffrey, B.; Heinig, M.; Huska, M.; Mammana, A.; Perner, J.; Vingron, M.; Friend, S.; Dearry, A.; Simeonov, A.; Tice, R. R.; Rusyn, I.; Wright, F. A.; Stolovitzky, G.; Xie, Y.; Saez-Rodriguez, J.: Prediction of human population responses to toxic compounds by a collaborative competition. Nat Biotechnol 33 (9), pp. 933 - 940 (2015)

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Fischer, U.; Forster, M.; Rinaldi, A.; Risch, T.; Sungalee, S.; Warnatz, H. J.; Bornhauser, B.; Gombert, M.; Kratsch, C.; Stutz, A. M. et al.; Sultan, M.; Tchinda, J.; Worth, C. L.; Amstislavskiy, V.; Badarinarayan, N.; Baruchel, A.; Bartram, T.; Basso, G.; Canpolat, C.; Cario, G.; Cave, H.; Dakaj, D.; Delorenzi, M.; Dobay, M. P.; Eckert, C.; Ellinghaus, E.; Eugster, S.; Frismantas, V.; Ginzel, S.; Haas, O. A.; Heidenreich, O.; Hemmrich-Stanisak, G.; Hezaveh, K.; Holl, J. I.; Hornhardt, S.; Husemann, P.; Kachroo, P.; Kratz, C. P.; Kronnie, G. T.; Marovca, B.; Niggli, F.; McHardy, A. C.; Moorman, A. V.; Panzer-Grumayer, R.; Petersen, B. S.; Raeder, B.; Ralser, M.; Rosenstiel, P.; Schäfer, D.; Schrappe, M.; Schreiber, S.; Schutte, M.; Stade, B.; Thiele, R.; Weid, N.; Vora, A.; Zaliova, M.; Zhang, L.; Zichner, T.; Zimmermann, M.; Lehrach, H.; Borkhardt, A.; Bourquin, J. P.; Franke, A.; Korbel, J. O.; Stanulla, M.; Yaspo, M. L.: Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options. Nature Genetics 47 (9), pp. 1020 - 1029 (2015)

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Lamm, C.; Silani, G.; Singer, T.: Distinct neural networks underlying empathy for pleasant and unpleasant touch. Cortex 70 (Special issue: Neuro-cognitive mechanisms of social interaction), pp. 79 - 89 (2015)

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Conrad, T.; Ørom, U. A.: Insight into miRNA biogenesis with RNA sequencing. Oncotarget 6 (29), pp. 26546 - 26547 (2015)

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