Zeynep Tümer

Zeynep Tümer

Clinical Professor

Member of:

  • Clinical Genetics


Publication year:
All
1 - 10 out of 10Page size: 10
  1. 2013
  2. Published

    An association study between the norepinephrine transporter gene and depression

    Buttenschøn, H. N., Jacobsen, I. S., Grynderup, M. B., Hansen, Åse Marie, Kolstad, H. A., Kaerlev, L., Thomsen, Jane Frølund, Nordentoft, Merete, Silahtaroglu, Asli, Tommerup, Niels, Tümer, Asuman Zeynep, Krogh, J., Børglum, A. & Mors, O., Oct 2013, In: Psychiatric Genetics. 23, 5, p. 217-21 5 p.

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

  3. Published

    SLC26A4 mutation frequency and spectrum in 109 Danish Pendred syndrome/DFNB4 probands and a report of nine novel mutations

    Rendtorff, N. D., Schrijver, I., Lodahl, M., Rodriguez-Paris, J., Johnsen, T., Hansén, E., Nickelsen, L., Tümer, Asuman Zeynep, Fagerheim, T., Wetke, R. & Tranebjærg, Lisbeth, Oct 2013, In: Clinical Genetics. 84, 4, p. 388-391 4 p.

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

  4. Published

    A homozygous mutation in a consanguineous family consolidates the role of ALDH1A3 in autosomal recessive microphthalmia

    Roos, L., Fang, M., Dali, C., Jensen, H., Christoffersen, N., Wu, B., Zhang, J., Xu, R., Harris, P., Xu, X., Grønskov, K. & Tümer, Asuman Zeynep, 11 Sep 2013, In: Clinical Genetics.

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

  5. Published

    Ring chromosome 9 in a girl with developmental delay and dysmorphic features: case report and review of the literature

    la Cour Sibbesen, E., Jespersgaard, C., Alosi, Daniela, Bisgaard, A. & Tümer, Asuman Zeynep, Jun 2013, In: American Journal of Medical Genetics. Part A. 161, 6, p. 1447-52 6 p.

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

  6. Published

    Sequence analysis of SLITRK1 for var321 in Danish patients with Tourette syndrome and review of the literature

    Yasmeen, S., Melchior, L., Bertelsen, B., Skov, L., Debes, Nanette M Monique Mol & Tümer, Asuman Zeynep, Jun 2013, In: Psychiatric Genetics. 23, 3, p. 130-3 4 p.

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

  7. Published

    An overview and update of ATP7A mutations leading to menkes disease and occipital horn syndrome

    Tümer, Asuman Zeynep, Mar 2013, In: Human Mutation. 34, 3, p. 417-29 13 p.

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

  8. Published

    Transient neonatal diabetes, ZFP57, and hypomethylation of multiple imprinted loci: a detailed follow-up

    Boonen, S. E., Mackay, D. J. G., Hahnemann, J. M. D., Docherty, L., Grønskov, K., Lehmann, A., Larsen, L. G., Haemers, A. P., Kockaerts, Y., Dooms, L., Vu, D. C., Ngoc, C. T. B., Nguyen, P. B., Kordonouri, O., Sundberg, F., Dayanikli, P., Puthi, V., Acerini, C., Massoud, A. F., Tümer, Z. & 1 others, Temple, I. K., Mar 2013, In: Diabetes Care. 36, 3, p. 505-12 8 p.

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

  9. Published

    Chromosomal rearrangements in Tourette syndrome: implications for identification of candidate susceptibility genes and review of the literature

    Bertelsen, B., Debes, Nanette M Monique Mol, Hjermind, L. E., Skov, L., Brøndum-Nielsen, K. & Tümer, Asuman Zeynep, 2013, In: Neurogenetics. 14, 3-4, p. 197-203 7 p.

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

  10. Published

    Dysfunction of the heteromeric KV7.3/KV7.5 potassium channel is associated with autism spectrum disorders

    Nielsen, M. G., Rasmussen, Hanne Borger, Callø, Kirstine, F. Sequeira, A., Baretto, M., Oliveira, G., Almeida, J., B. Lauritsen, M., Ullmann, R., Boonen, S. E., Brøndum-Nielsen, K., M. Kalscheuer, V., Tümer, Asuman Zeynep, M. Vicente, A., Schmitt, Nicole & Tommerup, Niels, 2013, In: Frontiers in Genetics. 4, 54, p. 1-13 13 p.

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

  11. Published

    Microduplication of 15q13.3 and Xq21.31 in a family with tourette syndrome and comorbidities

    Melchior, L., Bertelsen, B., Debes, Nanette M Monique Mol, Groth, C., Skov, L., Mikkelsen, Jens D., Brøndum-Nielsen, K. & Tümer, Asuman Zeynep, 2013, In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics. 162, 8, p. 825-831 7 p.

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

ID: 7071