Engen, H. G.; Singer, T.: Affect and motivation are critical in constructive meditation. Trends in Cognitive Sciences 20 (3), S. 159 - 160 (2016)

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), S. 615 - 621 (2016)

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), S. 392 - 399 (2016)

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), S. 549 - 561 (2016)

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), S. 78 - 83 (2016)

Smith, Z. D.; Sindhu, C.; Meissner, A.: Molecular features of cellular reprogramming and development. Nature Reviews Molecular Cell Biology 17 (3), S. 139 - 154 (2016)

Bonhage, C.; Weber, F.; Exner, C.; Kanske, P.: Thinking about thinking: Neural mechanisms and effects on memory. NeuroImage 127, S. 203 - 214 (2016)

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), S. 1794 - 1796 (2016)

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), S. 1246 - 1257 (2016)

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), S. 57 - 62 (2016)

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)

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), S. 637 - 648 (2016)

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), S. 515 - 524 (2016)

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), S. 183 - 191 (2016)

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)

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, S. 1 - 8 (2016)

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)

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), S. 438 - 451 (2016)

Saggar, M.; Vrticka, P.; Reiss, A. L.: Understanding the influence of personality on dynamic social gesture processing: An fMRI study. Neuropsychologia 80, S. 71 - 78 (2016)

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), S. 1183 - 1193 (2016)