Böckler, A.; Eskenazi, T.; Sebanz, N.; Rueschemeyer, S.-A.: (How) observed eye-contact modulates gaze following: An fMRI study. Cognitive Neuroscience 7 (1-4 ), S. 55 - 66 (2016)

Chen, L.; Ge, B.; Casale, F. P.; Vasquez, L.; Kwan, T.; Garrido-Martin, D.; Watt, S.; Yan, Y.; Kundu, K.; Ecker, S. et al.; Datta, A.; Richardson, D.; Burden, F.; Mead, D.; Mann, A. L.; Fernandez, J. M.; Rowlston, S.; Wilder, S. P.; Farrow, S.; Shao, X.; Lambourne, J. J.; Redensek, A.; Albers, C. A.; Amstislavskiy, V.; Ashford, S.; Berentsen, K.; Bomba, L.; Bourque, G.; Bujold, D.; Busche, S.; Caron, M.; Chen, S. H.; Cheung, W.; Delaneau, O.; Dermitzakis, E. T.; Elding, H.; Colgiu, I.; Bagger, F. O.; Flicek, P.; Habibi, E.; Iotchkova, V.; Janssen-Megens, E.; Kim, B.; Lehrach, H.; Lowy, E.; Mandoli, A.; Matarese, F.; Maurano, M. T.; Morris, J. A.; Pancaldi, V.; Pourfarzad, F.; Rehnstrom, K.; Rendon, A.; Risch, T.; Sharifi, N.; Simon, M. M.; Sultan, M.; Valencia, A.; Walter, K.; Wang, S. Y.; Frontini, M.; Antonarakis, S. E.; Clarke, L.; Yaspo, M. L.; Beck, S.; Guigo, R.; Rico, D.; Martens, J. H. A.; Ouwehand, W. H.; Kuijpers, T. W.; Paul, D. S.; Stunnenberg, H. G.; Stegle, O.; Downes, K.; Pastinen, T.; Soranzo, N.: Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells. Cell 167 (5), e24, S. 1398 - 1414 (2016)

Esmaeeli-Nieh, S.; Fenckova, M.; Porter, I. M.; Motazacker, M. M.; Nijhof, B.; Castells-Nobau, A.; Asztalos, Z.; Weissmann, R.; Behjati, F.; Tzschach, A. et al.; Felbor, U.; Scherthan, H.; Sayfati, S. M.; Ropers, H. H.; Kahrizi, K.; Najmabadi, H.; Swedlow, J. R.; Schenck, A.; Kuss, A. W.: BOD1 Is Required for Cognitive Function in Humans and Drosophila. PLoS Genetics 12 (5), e1006022 (2016)

Hackmann, K.; Rump, A.; Haas, S. A.; Lemke, J. R.; Fryns, J. P.; Tzschach, A.; Wieczorek, D.; Albrecht, B.; Kuechler, A.; Ripperger, T. et al.; Kobelt, A.; Oexle, K.; Tinschert, S.; Schrock, E.; Kalscheuer, V. M.; Di Donato, N.: Tentative clinical diagnosis of Lujan-Fryns syndrome-A conglomeration of different genetic entities? American Journal of Medical Genetics Part A 170 (1), S. 94 - 102 (2016)

Hartmann, B.; Wai, T.; Hu, H.; MacVicar, T.; Musante, L.; Fischer-Zirnsak, B.; Stenzel, W.; Graf, R.; van den Heuvel, L.; Ropers, H. H. et al.; Wienker, T. F.; Hübner, C.; Langer, T.; Kaindl, A. M.: Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation. eLife 5, e16078 (2016)

Hu, H.; Haas, S. A.; Chelly, J.; Van Esch, H.; Raynaud, M.; de Brouwer, A. P. M.; Weinert, S.; Froyen, G.; Frints, S. G. M.; Laumonnier, F. et al.; Zemojtel, T.; Love, M. I.; Richard, H.; Emde, A.-K.; Bienek, M.; Jensen, C.; Hambrock, M.; Fischer, U.; Langnick, C.; Feldkamp, M.; Wissink-Lindhout, W.; Lebrun, N.; Castelnau, L.; Rucci, J.; Montjean, R.; Dorseuil, O.; Billuart, P.; Stuhlmann, T.; Shaw, M.; Corbett, M. A.; Gardner, A.; Willis-Owen, S.; Tan, C.; Friend, K. L.; Belet, S.; van Roozendaal, K. E. P.; Jimenez-Pocquet, M.; Moizard, M.-P.; Ronce, N.; Sun, R.; O'Keeffe, S.; Chenna, R.; van Bömmel, A.; Göke, J.; Hackett, A.; Field, M.; Christie, L.; Boyle, J.; Haan, E.; Nelson, J.; Turner, G.; Baynam, G.; Gillessen-Kaesbach, G.; Müller, U.; Steinberger, D.; Budny, B.; Badura-Stronka, M.; Latos-Bieleńska, A.; Ousager, L. B.; Wieacker, P.; Rodríguez Criado, G.; Bondeson, M.-L.; Annerén, G.; Dufke, A.; Cohen, M.; Van Maldergem, L.; Vincent-Delorme, C.; Echenne, B.; Simon-Bouy, B.; Kleefstra, T.; Willemsen, M.; Fryns, J.-P.; Devriendt, K.; Ullmann, R.; Vingron, M.; Wrogemann, K.; Wienker, T. F.; Tzschach, A.; van Bokhoven, H.; Gecz, J.; Jentsch, T. J.; Chen, W.; Ropers, H.-H.; Kalscheuer, V. M.: X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes. Molecular Psychiatry 21 (1), S. 133 - 148 (2016)

Huska, M.; Vingron, M.: Improved Prediction of Non-methylated Islands in Vertebrates Highlights Different Characteristic Sequence Patterns. PLoS Computational Biology 12 (12), e1005249 (2016)

Imkeller, K.; Arndt, P. F.; Wardemann, H.; Busse, C. E.: sciReptor: analysis of single-cell level immunoglobulin repertoires. BMC Bioinformatics 17, 67 (2016)

Muino, J. M.; de Bruijn, S.; Pajoro, A.; Geuten, K.; Vingron, M.; Angenent, G. C.; Kaufmann, K.: Evolution of DNA-Binding Sites of a Floral Master Regulatory Transcription Factor. Molecular Biology and Evolution 33 (1), S. 185 - 200 (2016)

Palmer, E. E.; Leffler, M.; Rogers, C.; Shaw, M.; Carroll, R.; Earl, J.; Cheung, N. W.; Champion, B.; Hu, H.; Haas, S. A. et al.; Kalscheuer, V. M.; Gecz, J.; Field, M.: New insights into Brunner syndrome and potential for targeted therapy. Clinical Genetics: an international journal of genetics in medicine 89 (1), S. 120 - 127 (2016)

Perdomo-Sabogal, A.; Nowick, K.; Piccini, I.; Sudbrak, R.; Lehrach, H.; Yaspo, M. L.; Warnatz, H. J.; Querfurth, R.: Human Lineage-Specific Transcriptional Regulation through GA-Binding Protein Transcription Factor Alpha (GABPa). Molecular Biology and Evolution 33 (5), S. 1231 - 1244 (2016)

Schöne, S.; Jurk, M.; Helabad, M. B.; Dror, I.; Lebars, I.; Kieffer, B.; Imhof, P.; Rohs, R.; Vingron, M.; Thomas-Chollier, M. et al.; Meijsing, S.: Corrigendum: Sequences flanking the core-binding site modulate glucocorticoid receptor structure and activity. Nature Communications 7, 13784 (2016)

Schöne, S.; Jurk, M.; Helabad, M. B.; Dror, I.; Lebars, I.; Kieffer, B.; Imhof, P.; Rohs, R.; Vingron, M.; Thomas-Chollier, M. et al.; Meijsing, S.: Sequences flanking the core-binding site modulate glucocorticoid receptor structure and activity. Nature Communications 7, 12621 (2016)

Steinbeis, N.; Haushofer, J.; Fehr, E.; Singer, T.: Development of behavioural control and associated vmPFC-DLPFC connectivity explains children’s increased resistance to temptation in intertemporal choice. Cerebral Cortex 26 (1), S. 32 - 42 (2016)

Volckmar, A. L.; Han, C. T.; Putter, C.; Haas, S.; Vogel, C. I.; Knoll, N.; Struve, C.; Gobel, M.; Haas, K.; Herrfurth, N. et al.; Jarick, I.; Grallert, H.; Schurmann, A.; Al-Hasani, H.; Hebebrand, J.; Sauer, S.; Hinney, A.: Analysis of Genes Involved in Body Weight Regulation by Targeted Re-Sequencing. PLoS One 11 (2), e0147904 (2016)

Williams, L. S.; Kim, H. G.; Kalscheuer, V. M.; Tuck, J. M.; Chorich, L. P.; Sullivan, M. E.; Falkenstrom, A.; Reindollar, R. H.; Layman, L. C.: A balanced chromosomal translocation involving chromosomes 3 and 16 in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome reveals new candidate genes at 3p22.3 and 16p13.3. Molecular Cytogenetics 9, 9:57 (2016)

Singer, T.; Kok, B. E.; Bornemann, B.; Zurborg, S.; Bolz, M.; Bochow, C.: The ReSource Project: Background, design, samples, and measurements. Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig (2016)

Feng, Z.; Zi, Z.; Liu, X.: Measuring TGF-β Ligand Dynamics in Culture Medium. In: TGF-β Signaling: methods and protocols (Hg. Feng, X.-H.; Xu, P.; Lin, X.) (2016)

Hebels, D. G.; Rasche, A.; Herwig, R.; van Westen, G. J.; Jennen, D. G.; Kleinjans, J. C.: A Systems Biology Approach for Identifying Hepatotoxicant Groups Based on Similarity in Mechanisms of Action and Chemical Structure. In: In Silico Methods for Predicting Drug Toxicity (Hg. Benfenati , E.) (2016)

Lienhard, M.; Chavez, L.: Quantitative Comparison of Large-Scale DNA Enrichment Sequencing Data. In: Statistical Genomics (Hg. Mathé, E.; Davis, S.) (2016)