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 (3387)

Journal Article
Charron, Y.; Willert, J.; Lipkowitz, B.; Kusecek, B.; Herrmann, B. G.; Bauer, H.: Two isoforms of the RAC-specific guanine nucleotide exchange factor TIAM2 act oppositely on transmission ratio distortion by the mouse t-haplotype. PLOS Genetics 15 (2), e1007964 (2019)
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van Jaarsveld, M.; Deng, D.; Wiemer, E. A. C.; Zi, Z.: Tissue-Specific Chk1 Activation Determines Apoptosis by Regulating the Balance of p53 and p21. iScience 12, pp. 27 - 40 (2019)
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Millera, J. G.; Vrticka, P.; Cui, X.; Shrestha, S.; Hosseini, S.M. H.; Baker, J. M.; Reiss, A. L.: Inter-brain synchrony in mother-child dyads during cooperation: An fNIRS hyperscanning study. Neuropsychologia 124, pp. 117 - 124 (2019)
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Khayat, W.; Hackett , A.; Shaw, M.; Ilie , A.; Dudding-Byth , T.; Kalscheuer, V. M.; Christie , L.; Corbett , M. A.; Juusola , J.; Friend, K. L. et al.; Kirmse , B. M.; Gecz , J.; Field, M.; Orlowski, J.: A recurrent missense variant in SLC9A7 causes nonsyndromic X-linked intellectual disability with alteration of Golgi acidification and aberrant glycosylation. Human Molecular Genetics 28 (4), pp. 598 - 614 (2019)
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Krols, M.; Asselbergh, B.; De Rycke, R.; De Winter, V.; Seyer, A.; Müller, F.-J.; Kurth, I.; Bultynck, G.; Timmerman, V.; Janssens, S.: Sensory neuropathy-causing mutations in ATL3 affect ER-mitochondria contact sites and impair axonal mitochondrial distribution. Human Molecular Genetics 28 (4), pp. 615 - 627 (2019)
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Mendes, N.; Oligschläger, S.; Lauckner, M.; Golchert, J.; Huntenburg, J. M.; Falkiewicz, M.; Ellamil, M.; Krause , S.; Baczkowski, B.; Cozatl, R. et al.; Osoianu, A.; Kumral, D.; Pool, J.; Golz, L.; Paerisch, M.; Haueis, P.; Jost , R.; Kramarenko, Y.; Engen, H. G.; Ohrnberger, K.; Gorgolewski, K. J.; Farrugia, N.; Babayan, A.; Reiter, A.; Schaare, H. L.; Reinelt, J.; Röbbig, J.; Uhlig, M.; Erbey, M.; Gaebler, M.; Smallwood, J.; Villringer, A.; Margulies, D. S.: A functional connectome phenotyping dataset including cognitive state and personality measures. Scientific Data 6, 180307 (2019)
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Hinohara, K.; Wu, H.-J.; Vigneau, S.; McDonald, T. O.; Igarashi, K. J.; Yamamoto, K. N.; Madsen, T.; Fassl, A.; Egri, S. B.; Papanastasiou, M. et al.; Ding, L.; Peluffo, G.; Cohen, O.; Kales, S. C.; Lal-Nag, M.; Rai, G.; Maloney, D. J.; Jadhav, A.; Simeonov, A.; Wagle, N.; Brown, M.; Meissner, A.; Sicinski, P.; Jaffe, J. D.; Jeselsohn, R.; Gimelbrant, A. A.; Michor, F.; Polyak, K.: KDM5 Histone Demethylase Activity Links Cellular Transcriptomic Heterogeneity to Therapeutic Resistance. Cancer Cell 35 (2), pp. 330 - 332 (2019)
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Preckel, K.; Trautwein, M.; Paulus, F. M.; Kirsch, P.; Krach, S.; Singer, T.; Kanske, P.: Neural mechanisms of affective matching across faces and scenes. Scientific Reports 9, 1492 (2019)
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Bhushan, R.; Altinbas, L.; Jäger, M.; Zaradzki, M.; Lehmann, D.; Timmermann, B.; Clayton, N. P.; Zhu, Y.; Kallenbach, K.; Kararigas, G. et al.; Robinson, P. N.: An integrative systems approach identifies novel candidates in Marfan syndrome-related pathophysiology. Journal of Cellular and Molecular Medicine 23 (4), pp. 2526 - 2535 (2019)
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Yi, G.; Wierenga, A. T. J.; Petraglia, F.; Narang, P.; Janssen-Megens, E. M.; Mandoli, A.; Merkel, A.; Berentsen, K.; Kim, B.; Matarese, F. et al.; Singh, A. A.; Habibi, E.; Prange, K. H. M.; Mulder, A. B.; Jansen, J. H.; Clarke, L.; Heath, S.; van der Reijden, B. A.; Flicek, P.; Yaspo, M.-L.; Gut, I.; Bock, C.; Schuringa, J. J.; Altucci, L.; Vellenga, E.; Stunnenberg, H. G.; Martens, J. H. A.: Chromatin-Based Classification of Genetically Heterogeneous AMLs into Two Distinct Subtypes with Diverse Stemness Phenotypes. Cell Reports 26 (4), pp. 1059 - 1069 (2019)
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Hosseini, M.; Fattahi, Z.; Abedini, S. S.; Hu, H.; Ropers, H. H.; Kalscheuer, V. M.; Najmabadi, H.; Kahrizi, K.: GPR126: A novel candidate gene implicated in autosomal recessive intellectual disability. Am J Med Genet A 179 (1), pp. 13 - 19 (2019)
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Kahrizi, K.; Hu, H.; Hosseini, M.; Kalscheuer, V. M.; Fattahi, Z.; Beheshtian, M.; Suckow, V.; Mohseni, M.; Lipkowitz, B.; Mehvari, S. et al.; Mehrjoo, Z.; Akhtarkhavari, T.; Ghaderi, Z.; Rahimi, M.; Arzhangi, S.; Jamali, P.; Falahat Chian, M.; Nikuei , P.; Sabbagh Kermani, F.; Sadeghinia, F.; Jazayeri , R.; Tonekaboni, S. H.; Khoshaeen, A.; Habibi, H.; Pourfatemi, F.; Mojahedi , F.; Khodaie‐Ardakani, M.; Najafipour, R.; Wienker, T. F.; Najmabadi , H.; Ropers, H.-H.: Effect of inbreeding on intellectual disability revisited by Trio sequencing. Clinical Genetics: an international journal of genetics in medicine 95 (1), pp. 151 - 159 (2019)
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Klein, H.-U.; McCabe, C.; Gjoneska, E.; Sullivan, S. E.; Kaskow, B. J.; Tang, A.; Smith, R. V.; Xu, J.; Pfenning, A. R.; Bernstein, B. E. et al.; Meissner, A.; Schneider, J. A.; Mostafavi, S.; Tsai, L.-H.; Young-Pearse, T. L.; Bennett, D. A.; De Jager, P. L.: Epigenome-wide study uncovers large-scale changes in histone acetylation driven by tau pathology in aging and Alzheimer's human brains. Nature Neuroscience 22 (1), pp. 37 - 46 (2019)
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Hildebrandt, L. K.; McCall, C.; Singer, T.: Socioaffective versus sociocognitive mental trainings differentially affect emotion regulation strategies. Emotion (2018)
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Hernandez-Miranda, L. R.; Ibrahim, D.; Ruffault, P.-L.; Larrosa, M.; Balueva, K.; Müller, T.; Weerd, W. d.; Stolte-Dijkstra, I.; Hostra, R. M. W.; Brunet, J.-F. et al.; Fortin, G.; Mundlos, S.; Birchmeier, C.: Mutation in LBX1/Lbx1 precludes transcription factor cooperativity and causes congenital hypoventilation in humans and mice. Proceedings of the National Academy of Sciences of the United States of America 115 (51), pp. 13021 - 13026 (2018)
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Engert, V.; Linz, R.; Grant, J.: Embodied stress: The physiological resonance of psychosocial stress. Psychoneuroendocrinology (2018)
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Gerhauser, C.; Favero, F.; Risch, T.; Simon, R.; Feuerbach, L.; Assenov, Y.; Heckmann, D.; Sidiropoulos, N.; Waszak, S. M.; Hübschmann, D. et al.; Urbanucci, A.; Girma, E. G.; Kuryshev, V.; Klimczak, L. J.; Saini, N.; Stütz, A. M.; Weichenhan, D.; Böttcher, L.-M.; Toth, R.; Hendriksen, J. D.; Koop, C.; Lutsik, P.; Matzk, S.; Warnatz, H.-J.; Amstislavskiy, V.; Feuerstein, C.; Raeder, B.; Bogatyrova, O.; Schmitz, E.-M.; Hube-Magg, C.; Kluth, M.; Huland, H.; Graefen, M.; Lawerenz, C.; Henry, G. H.; Yamaguchi, T. N.; Malewska, A.; Meiners, J.; Schilling, D.; Reisinger, E.; Eils, R.; Schlesner, M.; Strand, D. W.; Bristow, R. G.; Boutros, P. C.; von Kalle, C.; Gordenin, D.; Sültmann, H.; Brors, B.; Sauter, G.; Plass, C.; Yaspo, M.-L.; Korbel, J. O.; Schlomm, T.; Weischenfeldt, J.: Molecular Evolution of Early-Onset Prostate Cancer Identifies Molecular Risk Markers and Clinical Trajectories. Cancer Cell 34 (6), pp. 996 - 1011 (2018)
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Adachi, K.; Kopp, W.; Wu, G.; Heising, S.; Greber, B.; Stehling, M.; Araúzo-Bravo, M. J.; Boerno, S. T.; Timmermann, B.; Vingron, M. et al.; Schöler, H. R.: Esrrb Unlocks Silenced Enhancers for Reprogramming to Naive Pluripotency - Correction. Cell Stem Cell 23 (6), pp. 900 - 904 (2018)
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Flis, J.; Holm, M.; Rundlet, E. J.; Loerke, J.; Hilal, T.; Dabrowski, M.; Bürger, J.; Mielke, T.; Blanchard, S. C.; Spahn, C. M.T. et al.; Budkevich, T. V.: tRNA Translocation by the Eukaryotic 80S Ribosome and the Impact of GTP Hydrolysis. Cell Reports 25 (10), e7, pp. 2676 - 2688 (2018)
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Banzhaf, C.; Hoffmann, F.; Kanske, P.; Fan, Y.; Walter, H.; Spengler, S.; Schreiter, S.; Singer, T.; Bermpohl, F.: Interacting and dissociable effects of alexithymia and depression on empathy. Psychiatry Research 270, pp. 631 - 638 (2018)
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