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)

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Cohrs, S.; Rodenbeck, A.; Riemann, D.; Szagun, B.; Jaehne, A.; Brinkmeyer, J.; Grunder, G.; Wienker, T. F.; Diaz-Lacava, A.; Mobascher, A. et al.; Dahmen, N.; Thuerauf, N.; Kornhuber, J.; Kiefer, F.; Gallinat, J.; Wagner, M.; Kunz, D.; Grittner, U.; Winterer, G.: Impaired sleep quality and sleep duration in smokers-results from the German Multicenter Study on Nicotine Dependence. Addiction Biology 19 (3), pp. 486 - 496 (2014)
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Lill, C. M.; Schilling, M.; Ansaloni, S.; Schröder, J.; Jaedicke, M.; Luessi, F.; Schjeide, B.-M.; Mashychev, A.; Graetz, C.; Akkad, D. A. et al.; Gerdes, L.-A.; Kroner, A.; Blaschke, P.; Hoffjan, S.; Winkelmann, A.; Dörner, T.; Rieckmann, P.; Steinhagen-Thiessen, E.; Lindenberger, U.; Chan, A.; Hartung, H.-P.; Aktas, O.; Lohse, P.; Buttmann, M.; Kümpfel, T.; Kubisch, C.; Zettl, U. K.; Epplen, J. T.; Zipp, F.; Bertram, L.: Assessment of microRNA-related SNP effects in the 3' untranslated region of the IL22RA2 risk locus in multiple sclerosis. Neurogenetics 15 (2), pp. 129 - 134 (2014)
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Mendes, N.; Call, J.: Chimpanzees form long-term memories for food locations after limited exposure. American Journal of Primatology 76 (5), pp. 485 - 495 (2014)
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Møller, R. S.; Jensen, L. R.; Maas, S. M.; Filmus, J.; Capurro, M.; Hansen, C.; Marcelis, C. L.; Ravn, K.; Andrieux, J.; Mathieu, M. et al.; Kirchhoff, M.; Rodningen, O. K.; de Leeuw, N.; Yntema, H. G.; Froyen, G.; Vandewalle, J.; Ballon, K.; Klopocki, E.; Joss, S.; Tolmie, J.; Knegt, A. C.; Lund, A. M.; Hjalgrim, H.; Kuss, A. W.; Tommerup, N.; Ullmann, R.; de Brouwer, A. P.; Stromme, P.; Kjaergaard, S.; Tumer, Z.; Kleefstra, T.: X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome. Human Genetics 133 (5), pp. 625 - 638 (2014)
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Papenberg, G.; Li, S. C.; Nagel, I. E.; Nietfeld, W.; Schjeide, B. M.; Schröder, J.; Bertram, L.; Heekeren, H. R.; Lindenberger, U.; Bäckman, L.: Dopamine and glutamate receptor genes interactively influence episodic memory in old age. Neurobiology of Aging 35 (5), pp. 1213.e3 - 1213.e8 (2014)
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Sotnik, N. V.; Osovets, S. V.; Schertan, H.; Azizova, T. V.: mFISH analysis of chromosome aberrations in workers occupationally exposed to mixed radiation. Radiation and Environmental Biophysics 53 (2), pp. 347 - 354 (2014)
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Hussong, M.; Börno, S.; Kerick, M.; Wunderlich, A.; Franz, A.; Sültmann, H.; Timmermann, B.; Lehrach, H.; Hirsch-Kauffmann, M.; Schweiger, M. R.: The bromodomain protein BRD4 regulates the KEAP1/NRF2-dependent oxidative stress response. Cell Death and Disease 5, 5:e1195 (2014)
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Hussong, M.; Börno, S. T.; Kerick, M.; Wunderlich, A.; Franz, A.; Sültmann, H.; Timmermann, B.; Lehrach, H.; Hirsch-Kauffmann, M.; Schweiger, M. R.: The bromodomain protein BRD4 regulates the KEAP1/NRF2 dependent oxidative stress response. Cell Death and Disease 2014 (5), e1195 (2014)
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Bernhardt, B. C.; Smallwood, J.; Tusche, A.; Ruby, F. J. M.; Engen, H. G.; Steinbeis, N.; Singer, T.: Medial prefrontal and anterior cingulate cortical thickness predicts shared individual differences in self-generated thought and temporal discounting. NeuroImage 90, pp. 290 - 297 (2014)
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Hampel, H.; Lista, S.; Teipel, S. J.; Garaci, F.; Nistico, R.; Blennow, K.; Zetterberg, H.; Bertram, L.; Duyckaerts, C.; Bakardjian, H. et al.; Drzezga, A.; Colliot, O.; Epelbaum, S.; Broich, K.; Lehericy, S.; Brice, A.; Khachaturian, Z. S.; Aisen, P. S.; Dubois, B.: Perspective on future role of biological markers in clinical therapy trials of Alzheimer's disease: A long-range point of view beyond 2020. Biochemical Pharmacology 88 (4), pp. 426 - 449 (2014)
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Hampel, H.; Listab, S.; Teipelc, S. J.; Garacie, F.; Nisticòg, .; Blennowi, K.; Zetterbergi, H.; Bertram, L.; Duyckaertsl, .; Bakardjianm, H. et al.; Drzezgao, .; Colliotp, O.; Epelbaumu, S.; Broich, K.; Lehéricy, S.; Brice, A.; Khachaturian, Z. S.; Aisen , P. S.; Dubois , B.: Perspective on future role of biological markers in clinical therapy trials of Alzheimer's disease: a long-range point of view beyond 2020. Biochemical Pharmacology 88 (4), pp. 426 - 449 (2014)
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Philips, A. K.; Siren, A.; Avela, K.; Somer, M.; Peippo, M.; Ahvenainen, M.; Doagu, F.; Arvio, M.; Kaariainen, H.; Van Esch, H. et al.; Froyen, G.; Haas, S. A.; Hu, H.; Kalscheuer, V. M.; Jarvela, I.: X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes. Orphanet Journal of Rare Diseases 9, 9:49 (2014)
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Siewert, C.; Luge, T.; Duduk, B.; Seemüller, E.; Büttner, C.; Sauer, S.; Kube, M.: Analysis of expressed genes of the bacterium 'Candidatus phytoplasma Mali' highlights key features of virulence and metabolism. PLoS One 9 (4), e94391 (2014)
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Bokemeyer, A.; Eckert, C.; Meyr, F.; Koerner, G.; von Stackelberg, A.; Ullmann, R.; Türkmen, S.; Henze, G.; Seeger, K.: Copy number genome alterations are associated with treatment response and outcome in relapsed childhood ETV6/RUNX1-positive acute lymphoblastic leukemia. Haematologica 99 (4), pp. 706 - 714 (2014)
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Bokemeyer, A.; Eckert, C.; Meyr, F.; Koerner, G.; von Stackelberg, A.; Ullmann, R.; Turkmen, S.; Henze, G.; Seeger, K.: Copy number genome alterations are associated with treatment response and outcome in relapsed childhood ETV6/RUNX1-positive acute lymphoblastic leukemia. Haematologica 99 (4), pp. 706 - 714 (2014)
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de Brouwer, A. P.; Nabuurs, S. B.; Verhaart, I. E.; Oudakker, A. R.; Hordijk, R.; Yntema, H. G.; Hordijk-Hos, J. M.; Voesenek, K.; de Vries, B. B.; van Essen, T. et al.; Chen, W.; Hu, H.; Chelly, J.; den Dunnen, J. T.; Kalscheuer, V. M.; Aartsma-Rus, A. M.; Hamel, B. C.; van Bokhoven, H.; Kleefstra, T.: A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy. European journal of human genetics 22 (4), pp. 480 - 485 (2014)
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Fernandez-Cuesta, L.; Plenker, D.; Osada, H.; Sun, R.; Menon, R.; Leenders, F.; Ortiz-Cuaran, S.; Peifer, M.; Bos, M.; Dassler, J. et al.; Malchers, F.; Schöttle, J.; Vogel, W.; Dahmen, I.; Koker, M.; Ullrich, R. T.; Wright, G. M.; Russell, P. A.; Wainer, Z.; Solomon, B.; Brambilla, E.; Nagy-Mignotte, H.; Moro-Sibilot, D.; Brambilla, C. G.; Lantuejoul, S.; Altmüller, J.; Becker, C.; Nürnberg, P.; Heuckmann, J. M.; Stoelben, E.; Petersen, I.; Clement, J. H.; Sänger, J.; Muscarella, L. A.; la Torre, A.; Fazio, V. M.; Lahortiga, I.; Perera, T.; Ogata, S.; Parade, M.; Brehmer, D.; Vingron, M.; Heukamp, L. C.; Buettner, R.; Zander, T.; Wolf, J.; Perner, S.; Ansen, S.; Haas, S. A.; Yatabe, Y.; Thomas, R. K.: CD74-NRG1 Fusions in Lung Adenocarcinoma. Cancer Discovery 4 (4), pp. 415 - 422 (2014)
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Girisha, K. M.; Bidchol, A. M.; Kamath, P. S.; Shah, K. H.; Mortier, G. R.; Mundlos, S.; Shah, H.: A novel mutation (g.106737G>T) in zone of polarizing activity regulatory sequence (ZRS) causes variable limb phenotypes in Werner mesomelia. American Journal of Medical Genetics Part A 164A (4), pp. 898 - 906 (2014)
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Jamsheer, A.; Smigiel, R.; Jakubiak, A.; Zemojtel, T.; Socha, M.; Robinson, P. N.; Mundlos, S.: Further evidence for FGF16 truncating mutations as the cause of X-linked recessive fusion of metacarpals 4 / 5. Birth Defects Research Part A: Clinical and Molecular Teratology 100 (4), pp. 314 - 318 (2014)
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Reiner, G.; Bertsch, N.; Hoeltig, D.; Selke, M.; Willems, H.; Gerlach, G. F.; Tuemmler, B.; Probst, I.; Herwig, R.; Drungowski, M. et al.; Waldmann, K. H.: Identification of QTL affecting resistance/susceptibility to acute Actinobacillus pleuropneumoniae infection in swine. Mammalian Genome 25 (3-4), pp. 180 - 191 (2014)
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