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 (190)

Journal Article
Dedovic, K.; Duchesne, A.; Engert, V.; Lue, S. D.; Andrews, J.; Efanov, S. I.; Beaudry, T.; Pruessner, J. C.: Psychological, endocrine and neural responses to social evaluation in subclinical depression. Social Cognitive and Affective Neuroscience 9 (10), pp. 1632 - 1644 (2014)
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Lohan, S.; Spielmann, M.; Doelken, S. C.; Flottmann, R.; Muhammad, F.; Baig, S. M.; Wajid, M.; Hulsemann, W.; Habenicht, R.; Kjaer, K. W. et al.; Patil, S. J.; Girisha, K. M.; Abarca-Barriga, H. H.; Mundlos, S.; Klopocki, E.: Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndrome. Clinical Genetics: an international journal of genetics in medicine 86 (4), pp. 318 - 325 (2014)
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Wolkenstein, L.; Zeiller, M.; Kanske, P.; Plewnia, C.: Induction of a depression-like negativity bias by cathodal transcranial direct current stimulation. Cortex 59, pp. 103 - 112 (2014)
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Liao, J.; Jijon, H. B.; Kim, I. R.; Goel, G.; Doan, A.; Sokol, H.; Bauer, H.; Herrmann, B. G.; Lassen, K. G.; Xavier, R. J.: An Image-Based Genetic Assay Identifies Genes in T1D Susceptibility Loci Controlling Cellular Antiviral Immunity in Mouse. PLoS One 9 (9), e108777 (2014)
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Liu, T.; Li, S.-C.; Papenberg, G.; Schröder, J.; Roehr, J. T.; Nietfeld, W.; Lindenberger, U.; Bertram, L.: No association between CTNNBL1 and episodic memory performance. Translational Psychiatry 4, e454 (2014)
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Röthlein, C.; Miettinen, M. S.; Borwankar, .; Bürger, J.; Mielke, T.; Kumke, M. U.; Ignatova, Z.: Architecture of polyglutamine-containing fibrils from time-resolved fluorescence decay. The Journal of Biological Chemistry 289 (39), pp. 26817 - 26828 (2014)
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Stange, K.; Thieme, T.; Hertel, K.; Kuhfahl, S.; Janecke, A. R.; Piza-Katzer, H.; Penttinen, M.; Hietala, M.; Dathe, K.; Mundlos, S. et al.; Schwarz, E.; Seemann, P.: Molecular analysis of two novel missense mutations in the GDF5 proregion that reduce protein activity and are associated with brachydactyly type C. Journal of Molecular Biology 426 (19), pp. 3221 - 3231 (2014)
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Singer, T.; Klimecki, O.: Empathy and compassion. Current Biology 24 (18), pp. R875 - R878 (2014)
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Vrticka, P.; Sander, D.; Anderson, B.; Badoud, D.; Eliez, S.; Dabenne, M.: Social feedback processing from early to late adolescence: Influence of sex, age, and attachment style. Brain and Behavior 4 (5), pp. 703 - 720 (2014)
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Kumar, V.; Cheng, S.-C.; Johnson, M. D.; Smeekens, S.; Wojtowicz, A.; Giamarellos-Bourboulis, E.; Karjalainen, J.; Franke, L.; Withoff, S.; Plantinga, T. S. et al.; van de Veerdonk, F.; van der Meer, J.; Joosten, L. A. B.; Sokol, H.; Bauer, H.; Herrmann, B. G.; Bochud, P.-Y.; Marchetti, O.; Perfect, J. R.; Xavier, R.; Kullberg, B. J.; Wijmenga, C.; Netea, M.: Immunochip SNP array identifies novel genetic variants conferring susceptibility to candidaemia. Nature Communications 5, Article 4675 (2014)
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Ibn-Salem, J.; Köhler, S.; Love, M. I.; Chung, H.-R.; Huang, N.; Hurles, M. E.; Haendel, M.; Washington, N. L.; Smedley, D.; Mungall, C. J. et al.; Lewis, S. E.; Ott, C. E.; Bauer, S.; Schofield, P. N.; Mundlos, S.; Spielmann, M.; Robinson, P. N.: Deletions of chromosomal regulatory boundaries are associated with congenital disease. Genome Biology: Biology for the Post-Genomic Era 15, 15:423 (2014)
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Hooli , B. V.; Parrado, A. R.; Mullin , K.; Yip , W. K.; Liu , T.; Roehr , J.; Qiao , D.; Jessen , F.; Peters , O.; Becker , T. et al.; Ramirez , A.; Lange, C.; Bertram, L.; Tanzi, R. E.: The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk. Neurology 83 (15), pp. 1353 - 1358 (2014)
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Zemojtel, T.; Köhler, S.; Mackenroth, L.; Jäger, M.; Hecht, J.; Krawitz, P.; Graul-Neumann, L.; Doelken, S.; Ehmke, N.; Spielmann, M. et al.; Oien, N. C.; Schweiger, M. R.; Krüger, U.; Frommer, G.; Fischer, B.; Kornak, U.; Flöttmann, R.; Ardeshirdavani, A.; Moreau, Y.; Lewis, S. E.; Haendel, M.; Smedley, D.; Horn, D.; Mundlos, S.; Robinson, P. N.: Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome. Science Translational Madicine 6 (252), 252ra123 (2014)
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Carrell, D. T.; Rajpert-De Meyts, E.; Krausz, C.; Jannini, E. A.; Liu, P. Y.; Gerton, G. L.; La Salle, S.; Amaral, A.: The need of continuous focus on improved mentoring of trainees and young investigators in the field of andrology: highlights of current programs and opportunities for the future. Andrology 2 (5), pp. 649 - 651 (2014)
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Grant, J. A.: What constitutes pain? Comment on “Facing the experience of pain: A neuropsychological perspective” by Franco Fabbro and Cristiano Crescentini. Physics of Life Reviews 11 (3), pp. 553 - 554 (2014)
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Henderson, D.; Ogilvie, L. A.; Hoyle, N.; Keilholz, U.; Lange, B.; Lehrach, H.; OncoTrack, C.; Yaspo, M. L.: Personalized medicine approaches for colon cancer driven by genomics and systems biology: OncoTrack. Biotechnology Journal 9 (9), pp. 1104 - 1114 (2014)
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Krawitz, P. M.; Schiska, D.; Krüger, U.; Appelt, S.; Heinrich, V.; Parkhomchuk, D.; Timmermann, B.; Millan, J. M.; Robinson, P. N.; Mundlos, S. et al.; Hecht, J.; Gross, M.: Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndrome. Molecular Genetics and Genomic Medicine 2 (5), pp. 393 - 401 (2014)
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Kühnisch, J.; Seto, J.; Lange, C.; Stumpp, S.; Kobus, K.; Grohmann, J.; Elefteriou, F.; Fratzl, P.; Mundlos, S.; Kolanczyk, M.: Neurofibromin inactivation impairs osteocyte development in Nf1Prx1 and Nf1Col1 mouse models. Bone 66, pp. 155 - 162 (2014)
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Misra, N.; Szczurek, E.; Vingron, M.: Inferring the paths of somatic evolution in cancer. Bioinformatics 30 (17), pp. 2456 - 2463 (2014)
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Nalls, M. A.; Pankratz, N.; Lill, C. M.; Do, C. B.; Hernandez, D. G.; Saad, M.; DeStefano, A. L.; Kara, E.; Bras, J.; Sharma, M. et al.; Schulte, C.; Keller, M. F.; Arepalli, S.; Letson, C.; Edsall, C.; Stefansson, H.; Liu, X.; Pliner, H.; Lee, J. H.; Cheng, R.; Ikram, M. A.; Ioannidis, J. P.A.; Hadjigeorgiou, G. M.; Bis, J. C.; Martinez, M.; Perlmutter, J. S.; Goate, A.; Marder, K.; Fiske, B.; Sutherland, M.; Xiromerisiou, G.; Myers, R. H.; Clark, L. N.; Stefansson, K.; Hardy, J. A.; Heutink, P.; Chen, H.; Wood, N. W.; Houlden, H.; Payami, H.; Brice, A.; Scott, W. K.; Gasser, T.; Bertram, L.; Eriksson, N.; Foroud, T.; Singleton, A. B.: Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease. Nature Genetics 46 (9), pp. 989 - 993 (2014)
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