Zeynep Tümer

Zeynep Tümer

Clinical Professor

Member of:

  • Clinical Genetics


Publication year:
All
1 - 7 out of 7Page size: 10
  1. 2007
  2. Published

    A human phenome-interactome network of protein complexes implicated in genetic disorders

    Lage, K., Karlberg, E. O., Størling, Z. M., Olason, P. I., Pedersen, A. G., Rigina, O., Hinsby, A. M., Tümer, Asuman Zeynep, Pociot, Flemming, Tommerup, Niels, Moreau, Y. & Brunak, S., 2007, In: Nature Biotechnology. 25, 3, p. 309-16 7 p.

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

  3. Published

    Cytogenetically invisible microdeletions involving PITX2 in Rieger syndrome

    Ladegaard, E. L. E., Saraiva, J., Carreira, I., Ramos, L., Ropers, H. H., Silva, E., Tommerup, Niels & Tümer, Asuman Zeynep, 2007, In: Clinical Genetics. 72, 5, p. 464-470 6 p.

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

  4. Published

    Det genetiske grundlag for epilepsi: Dansk Epilepsi Selskab

    Hansen, C. P., Møller, R., Tümer, Asuman Zeynep & Tommerup, Niels, 2007, In: Ugeskrift for læger. 169, 12, p. 1102-

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

  5. Published

    Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome

    Belloso, J. M., Bache, Iben, Guitart, M., Caballin, M. R., Halgren, C., Kirchhoff, M., Ropers, H. H., Tommerup, Niels & Tümer, Asuman Zeynep, 2007, In: European Journal of Human Genetics. 15, 6, p. 711-713 2 p.

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

  6. Published

    Interstitial deletion of chromosome 4p associated with mild mental retardation, epilepsy and polymicrogyria of the left temporal lobe

    Møller, R. S., Hansen, C. P., Jackson, G. D., Ullmann, R., Ropers, H. H., Tommerup, Niels & Tümer, Asuman Zeynep, 2007, In: Clinical Genetics. 72, 6, p. 593-598 5 p.

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

  7. Published

    Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2

    Jakobsen, L. P., Ullmann, R., Christensen, S. B., Jensen, K. E., Molsted, K., Henriksen, K. F., Hansen, C., Knudsen, M. A. F., Larsen, Lars Allan, Tommerup, Niels & Tümer, Asuman Zeynep, 2007, In: Journal of Medical Genetics. 44, 6, p. 381-386 5 p.

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

  8. Published

    The variant inv(2)(p11.2q13) is a genuinely recurrent rearrangement but displays some breakpoint heterogeneity

    Fickelscher, I., Liehr, T., Watts, K., Bryant, V., Barber, J. C. K., Heidemann, S., Siebert, R., Hertz, J. M., Tümer, Asuman Zeynep & Thomas, N. S., 2007, In: American Journal of Human Genetics. 81, 4, p. 847-856 9 p.

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

ID: 7071