Journal Article (2847)

  1. 21.
    Journal Article
    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 (2019)
  2. 22.
    Journal Article
    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)
  3. 23.
    Journal Article
    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)
  4. 24.
    Journal Article
    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)
  5. 25.
    Journal Article
    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.; Ragert, 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 (2019)
  6. 26.
    Journal Article
    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)
  7. 27.
    Journal Article
    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 (2019)
  8. 28.
    Journal Article
    Hoehe, M. R.; Herwig, R.; Mao , Q.; Peters , B. A.; Drmanac , R.; Church, G. M.; Huebsch, T.: Significant abundance of cis configurations of coding variants in diploid human genomes. Nucleic Acids Research (London) (2019)
  9. 29.
    Journal Article
    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) (2019)
  10. 30.
    Journal Article
    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)
  11. 31.
    Journal Article
    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)
  12. 32.
    Journal Article
    Klein, H.-U.; McCabe, C.; Gjoneska, E.; Sarah 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)
  13. 33.
    Journal Article
    Hildebrandt, L. K.; McCall, C.; Singer, T.: Socioaffective versus sociocognitive mental trainings differentially affect emotion regulation strategies. Emotion (2018)
  14. 34.
    Journal Article
    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)
  15. 35.
    Journal Article
    Engert, V.; Linz, R.; Grant, J.: Embodied stress: The physiological resonance of psychosocial stress. Psychoneuroendocrinology (2018)
  16. 36.
    Journal Article
    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)
  17. 37.
    Journal Article
    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)
  18. 38.
    Journal Article
    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) (2018)
  19. 39.
    Journal Article
    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)
  20. 40.
    Journal Article
    Kazeminasab, S.; Taskiran, I.; Fattahi, Z.; Bazazzadegan, N.; Hosseini, M.; Rahimi, M.; Oladnabi, M.; Haddadi, M.; Celik, A.; Ropers, H. H. et al.; Najmabadi, H.; Kahrizi, K.: CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability. Am J Med Genet B Neuropsychiatr Genet 177 (8), pp. 691 - 699 (2018)
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