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 (116)

Journal Article
Engen, H. G.; Singer, T.: Affect and motivation are critical in constructive meditation. Trends in Cognitive Sciences 20 (3), pp. 159 - 160 (2016)
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Ibrahim, D.; Tayebi, N.; Knaus, A.; Stiege, A. C.; Sahebzamani, A.; Hecht, J.; Mundlos, S.; Spielmann, M.: A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation. American Journal of Medical Genetics Part A 170 (3), pp. 615 - 621 (2016)
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Iqbal, Z.; Püttmann, L.; Musante, L.; Razzaq, A.; Zahoor, M. Y.; Hu, H.; Wienker, T. F.; Garshasbi, M.; Fattahi, Z.; Gilissen, C. et al.; Vissers, L. E.; de Brouwer, A. P.; Veltman, J. A.; Pfundt, R.; Najmabadi, H.; Ropers, H. H.; Riazuddin, S.; Kahrizi, K.; van Bokhoven, H.: Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration. European journal of human genetics 24 (3), pp. 392 - 399 (2016)
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Mueller, J. C.; Kuhl, H.; Timmermann, B.; Kempenaers, B.: Characterization of the genome and transcriptome of the blue tit Cyanistes caeruleus: polymorphisms, sex-biased expression and selection signals. Molecular Ecology Resources 16 (2), pp. 549 - 561 (2016)
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Olech, E. M.; Zemojtel, T.; Sowinska-Seidler, A.; Mundlos, S.; Robinson, P. N.; Karczewski, M.; Jamsheer, A.: Identification of a molecular defect in a stillborn fetus with perinatal lethal hypophosphatasia using a disease-associated genome sequencing approach. Polish Journal of Pathology 67 (1), pp. 78 - 83 (2016)
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Smith, Z. D.; Sindhu, C.; Meissner, A.: Molecular features of cellular reprogramming and development. Nature Reviews Molecular Cell Biology 17 (3), pp. 139 - 154 (2016)
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Bonhage, C.; Weber, F.; Exner, C.; Kanske, P.: Thinking about thinking: Neural mechanisms and effects on memory. NeuroImage 127, pp. 203 - 214 (2016)
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Veenvliet, J. V.: Studying Mesodiencephalic Dopaminergic Neuron Development In Vivo to Improve Stem Cell Therapy in Parkinson’s Disease. The Journal of Neuroscience 36 (6), pp. 1794 - 1796 (2016)
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Juan, D.; Perner, J.; Carrillo de Santa Pau, E.; Marsili, S.; Ochoa, D.; Chung, H. R.; Vingron, M.; Rico, D.; Valencia, A.: Epigenomic Co-localization and Co-evolution Reveal a Key Role for 5hmC as a Communication Hub in the Chromatin Network of ESCs. Cell Reports 14 (5), pp. 1246 - 1257 (2016)
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Lin, C. Y.; Erkek, S.; Tong, Y.; Yin, L.; Federation, A. J.; Zapatka, M.; Haldipur, P.; Kawauchi, D.; Risch, T.; Warnatz, H. J. et al.; Worst, B. C.; Ju, B.; Orr, B. A.; Zeid, R.; Polaski, D. R.; Segura-Wang, M.; Waszak, S. M.; Jones, D. T.; Kool, M.; Hovestadt, V.; Buchhalter, I.; Sieber, L.; Johann, P.; Chavez, L.; Groschel, S.; Ryzhova, M.; Korshunov, A.; Chen, W.; Chizhikov, V. V.; Millen, K. J.; Amstislavskiy, V.; Lehrach, H.; Yaspo, M. L.; Eils, R.; Lichter, P.; Korbel, J. O.; Pfister, S. M.; Bradner, J. E.; Northcott, P. A.: Active medulloblastoma enhancers reveal subgroup-specific cellular origins. Nature 530 (7588), pp. 57 - 62 (2016)
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Alam, M. T.; Zelezniak, A.; Mülleder, M.; Shliaha, P.; Schwarz, R.; Capuano, F.; Vowinckel, J.; Radmanesfahar , E.; Krüger, A.; Calvani , E. et al.; Michel, S.; Börno, S. T.; Christen, S.; Patil , K. R.; Timmermann, B.; Lilley, K. S.; Ralser, M.: The metabolic background is a global player in Saccharomyces gene expression epistasis. Nature Microbiology 2016, 15030 (2016)
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Hoffmann, F.; Köhne, S.; Steinbeis, N.; Dziobek, I.; Singer, T.: Preserved self-other distinction during empathy in autism is linked to network integrity of right supramarginal gyrus. Journal of Autism and Developmental Disorders 46 (2), pp. 637 - 648 (2016)
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Liu, M.; Bernhardt, B. C.; Bernasconi, A.; Bernasconi, N.: Gray matter structural compromise is equally distributed in left and right temporal lobe epilepsy. Human Brain Mapping 37 (2), pp. 515 - 524 (2016)
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Spielmann, M.; Kakar, N.; Tayebi, N.; Leettola, C.; Nürnberg, G.; Sowada, N.; Lupiáñez, D. G.; Harabula, I.; Flöttmann, R.; Horn, D. et al.; Chan, W. L.; Wittler, L.; Yilmaz, R.; Altmüller, J.; Thiele, H.; van Bokhoven,, H.; Schwartz, C. E.; Nürnberg, P.; Bowie, J. U.; Ahmad, J.; Kubisch, C.; Mundlos, S.: Exome Sequencing and CRISPR/Cas Genome Editing Identify Mutations of ZAK as a Cause of Limb Defects in Humans and Mice. Genome Research 26 (2), pp. 183 - 191 (2016)
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Steinbeis, N.: The role of self–other distinction in understanding others' mental and emotional states: Neurocognitive mechanisms in children and adults. Philosophical Transactions of the Royal Society of London, Series B: Biological Sciences 371 (1688), 20150547 (2016)
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Spier, I.; Kerick, M.; Drichel, D.; Horpaopan, S.; Altmüller, J.; Laner, A.; Holzapfel, S.; Peters, S.; Adam, R.; Zhao, B. et al.; Becker, T.; Lifton, R. P.; Holinski-Feder, E.; Perner, S.; Thiele, H.; Nöthen, M. M.; Hoffmann, P.; Timmermann, B.; Schweiger, M. R.; Aretz, S.: Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis. Famillial Cancer 2016, pp. 1 - 8 (2016)
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Kalscheuer, V. M.; James, V. M.; Himelright, M. L.; Long, P.; Oegema, R.; Jensen, C.; Bienek, M.; Hu, H.; Haas, S. A.; Topf, M. et al.; Hoogeboom, A. J.; Harvey, K.; Walikonis, R.; Harvey, R. J.: Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family. Frontiers in Molecular Neuroscience 8, 8:85 (2016)
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Marks, M.; Pennimpede, T.; Lange, L.; Grote, P.; Herrmann, B. G.; Wittler, L.: Analysis of the Fam181 gene family during mouse development reveals distinct strain-specific expression patterns, suggesting a role in nervous system development and function. Gene 575 (2 Pt 2), pp. 438 - 451 (2016)
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Saggar, M.; Vrticka, P.; Reiss, A. L.: Understanding the influence of personality on dynamic social gesture processing: An fMRI study. Neuropsychologia 80, pp. 71 - 78 (2016)
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Ancherbak, S.; Kuruoglu, E. E.; Vingron, M.: Time-Dependent Gene Network Modelling by Sequential Monte Carlo. IEEE ACM Transactions on Computational Biology and Bioinformatics 13 (6), pp. 1183 - 1193 (2016)
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