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 (116)

Journal Article

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

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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, pp. 1398 - 1414 (2016)

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Journal Article

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)

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Journal Article

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), pp. 94 - 102 (2016)

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Journal Article

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)

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Journal Article

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), pp. 133 - 148 (2016)

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Journal Article

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

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Journal Article

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

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Journal Article

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), pp. 185 - 200 (2016)

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Journal Article

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), pp. 120 - 127 (2016)

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Journal Article

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), pp. 1231 - 1244 (2016)

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Journal Article

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)

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Journal Article

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)

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Journal Article

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), pp. 32 - 42 (2016)

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Journal Article

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)

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Journal Article

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)

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Book (1)

Book

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)

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Book Chapter (3)

Book Chapter

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

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Book Chapter

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 (Ed. Benfenati , E.) (2016)

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Book Chapter

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

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