Christina Halgren Harding

Christina Halgren Harding

    Member of:

    • Psychiatry


    Publication year:
    All
    1 - 7 out of 7Page size: 10
    1. 2018
    2. Published

      Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes

      Halgren, C., Nielsen, N. M., Nazaryan-Petersen, L., Silahtaroglu, A., Collins, R. L., Lowther, C., Kjaergaard, S., Frisch, M., Kirchhoff, M., Brøndum-Nielsen, K., Lind-Thomsen, A., Mang, Y., El-Schich, Z., Boring, C. A., Mehrjouy, M. M., Jensen, P. K. A., Fagerberg, C., Krogh, L. N., Hansen, J., Bryndorf, T. & 5 others, Hansen, C., Talkowski, M. E., Bak, M., Tommerup, Niels & Bache, Iben, 2018, In: American Journal of Human Genetics. 102, 6, p. 1090-1103 14 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    3. 2017
    4. Published

      NGS mapped breakpoints in balanced chromosomal rearrangements including the first large cohort of healthy carriers

      Tommerup, N., Fonseca, A. C., Mehrjouy, M., Rasmussen, M. B., Bache, I., Halgren, C., Kroisel, P., Midyan, S., Vermeesch, J., Vianna-Morgante, A. M., Abe, K. T., Moretti-Ferreira, D., Paskulin, G., Angelova, L., Rajcan-Separovic, E., Sismani, C., Sedlacek, Z., Fagerberg, C., Brondum-Nielsen, K., Vogel, I. & 36 others, Bojesen, A., Ounap, K., Roht, L., Varilo, T., Luukkonen, T., Lespinasse, J., Beneteau, C., Kalscheuer, V. M., Ehmke, N., Daumer-Haas, C., Stefanou, E. G., Marta Czako, Kosztolanyi, G., Sheth, F., Zuffardi, O., Bonaglia, C., Novelli, A., Fannemel, M., Dias, P., Kokalj-Vokac, N., Ramos-Arroyo, M. A., Rodriguez Martinez, L., Guitart, M., Schinzel, A., Engelen, J., Silan, F., Akkari, Y., Batanian, J. R., Kim, H., Aristidou, C., De Almeida, C., Lewis, S., Moreno-Igoa, M., Hovhannisyan, A., Jacky, P. & Bak, M., 2017, In: Molecular Cytogenetics. 10, S1, p. 70 1 p., 7.P1.

      Research output: Contribution to journal › Conference abstract in journal › Research › peer-review

    5. 2014
    6. Published

      Neurodevelopmental disorders associated with dosage imbalance of ZBTB20 correlate with the morbidity spectrum of ZBTB20 candidate target genes

      Rasmussen, Malene Bøgehus, Nielsen, J. V., Lourenço, C. M., Melo, J. B., Harding, Christina Halgren, Geraldi, C. V. L., Marques, W., Rodrigues, G. R., Thomassen, M., Bak, M., Hansen, C., Ferreira, S. I., Venâncio, M., Henriksen, K. F., Lind-Thomsen, A., Carreira, I. M., Jensen, N. A. & Tommerup, Niels, Sep 2014, In: Journal of Medical Genetics. 51, 9, p. 605-613 9 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    7. Published

      Saturation of the Human Genome with Chromosomal Breakpoints

      Rasmussen, Malene Bøgehus, Schlechter, C. L., Mehrjouy, M. M., Bache, Iben, Lind-Thomsen, A., Silahtaroglu, Asli, Kjærgaard, S., Brondum-Nielsen, K., Jensen, P. K. A., Fagerberg, C., Krogh, L. N., Fonseca, A. C. D., Morgante, A. M. V., Abe, K. T., Harding, Christina Halgren, Bak, M., Jacky, P. & Tommerup, Niels, 2014, In: Cytogenetic and Genome Research. 142, 3, 2 p., 2.

      Research output: Contribution to journal › Conference abstract in journal › Research › peer-review

    8. 2012
    9. Published

      Haploinsufficiency of CELF4 at 18q12.2 is associated with developmental and behavioral disorders, seizures, eye manifestations, and obesity

      Harding, Christina Halgren, Bache, Iben, Bak, M., Myatt, M. W., Anderson, C. M., Brøndum-Nielsen, K. & Tommerup, Niels, Dec 2012, In: European Journal of Human Genetics. 20, 12, p. 1315-1319 5 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    10. Published

      Neurodevelopmental and Neuropsychiatric Disorders in Carriers of De Novo Balanced Chromosomal Rearrangements

      Harding, Christina Halgren, 30 Mar 2012

      Research output: Book/Report › Ph.D. thesis › Research

    11. 2011
    12. Published

      Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B

      Hansen, C. H., Kjaergaard, S., Bak, M., Hansen, C., Elschich, Z., Anderson, C. M., Henriksen, K. F., Hjalgrim, H., Kirchhoff, M., Bijlsma, E., Nielsen, M., den Hollander, N., Ruivenkamp, C., Isidor, B., Le Caignec, C., Zannolli, R., Mucciolo, M., Renieri, A., Mari, F., Anderlid, B-M. & 4 others, Andrieux, J., Dieux, A., Tommerup, Niels & Bache, Iben, 2011, In: Clinical Genetics. 82, 3, p. 248-55 8 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    ID: 14599793