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The Capital Region of Denmark - a part of Copenhagen University Hospital
  1. 2018
  2. Published

    Altered auditory processing and effective connectivity in 22q11.2 deletion syndrome

    Larsen, K. M., Mørup, M., Birknow, M. R., Fischer, E., Hulme, O., Vangkilde, A., Schmock, H., Baaré, W. F. C., Didriksen, M., Olsen, L., Werge, T., Siebner, H. R. & Garrido, M. I., 30 Jan 2018, In: Schizophrenia Research.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. 2017
  4. Published
  5. Published

    Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study

    Hoeffding, L. K., Trabjerg, B. B., Olsen, L., Mazin, W., Sparsø, T., Vangkilde, A., Mortensen, P. B., Pedersen, C. B. & Werge, T., 18 Jan 2017, In: JAMA Psychiatry.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. 2016
  7. Published
  8. Published

    Schizophrenia Spectrum Disorders in a Danish 22q11.2 Deletion Syndrome Cohort Compared to the Total Danish Population-A Nationwide Register Study

    Vangkilde, A., Olsen, L., Hoeffding, L. K., Pedersen, C. B., Mortensen, P. B., Werge, T. & Trabjerg, B., May 2016, In: Schizophrenia Bulletin. 42, 3, p. 824-831

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Risk of Mental Disorders in 22q11.2 Deletion and Duplication Syndrome: A Nation-wide Study.

    Høffding, L. K. E., Olsen, L., Mazin, W., Vangkilde, A. & Werge, T. M., 2016.

    Research output: Contribution to conferenceConference abstract for conferenceCommunication

  10. 2015
  11. Published

    The Danish 22q11 research initiative

    Schmock, H., Vangkilde, A., Larsen, K. M., Fischer, E., Birknow, M. R., Jepsen, J. R. M., Olesen, C., Skovby, F., Plessen, K. J., Mørup, M., Hulme, O., Baaré, W. F. C., Didriksen, M., Siebner, H. R., Werge, T. & Olsen, L., 2015, In: B M C Psychiatry. 15, 1, p. 220

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. 2013
  13. Published

    Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes

    Delio, M., Guo, T., McDonald-McGinn, D. M., Zackai, E., Herman, S., Kaminetzky, M., Higgins, A. M., Coleman, K., Chow, C., Jalbrzikowski, M., Jarlbrzkowski, M., Bearden, C. E., Bailey, A., Vangkilde, A., Olsen, L., Olesen, C., Skovby, F., Werge, T. M., Templin, L., Busa, T., Philip, N., Swillen, A., Vermeesch, J. R., Devriendt, K., Schneider, M., Dahoun, S., Eliez, S., Schoch, K., Hooper, S. R., Shashi, V., Samanich, J., Marion, R., van Amelsvoort, T., Boot, E., Klaassen, P., Duijff, S. N., Vorstman, J., Yuen, T., Silversides, C., Chow, E., Bassett, A., Frisch, A., Weizman, A., Gothelf, D., Niarchou, M., van den Bree, M., Owen, M. J., Suñer, D. H., Andreo, J. R., Armando, M., Vicari, S., Digilio, M. C., Auton, A., Kates, W. R., Wang, T., Shprintzen, R. J., Emanuel, B. S. & Morrow, B. E., 7 Mar 2013, In: American Journal of Human Genetics. 92, 3, p. 439-47 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 42706222