Our publications listed in the Puplication Repository of the Max Planck Society (PuRe)

Journal Article (190)

41.
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)
42.
Journal Article
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)
43.
Journal Article
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)
44.
Journal Article
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)
45.
Journal Article
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)
46.
Journal Article
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)
47.
Journal Article
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)
48.
Journal Article
Singer, T.; Klimecki, O.: Empathy and compassion. Current Biology 24 (18), pp. R875 - R878 (2014)
49.
Journal Article
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)
50.
Journal Article
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)
51.
Journal Article
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)
52.
Journal Article
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)
53.
Journal Article
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)
54.
Journal Article
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)
55.
Journal Article
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)
56.
Journal Article
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)
57.
Journal Article
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)
58.
Journal Article
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)
59.
Journal Article
Misra, N.; Szczurek, E.; Vingron, M.: Inferring the paths of somatic evolution in cancer. Bioinformatics 30 (17), pp. 2456 - 2463 (2014)
60.
Journal Article
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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