Hans Rudolf Lytchoff Eiberg

Hans Rudolf Lytchoff Eiberg

Associate Professor


  1. Published

    A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth

    Hansen, L., Kreiborg, Sven, Jarlov, H., Niebuhr, E. & Eiberg, Hans Rudolf Lytchoff, 2007, In: European Journal of Oral Sciences. 115, 4, p. 330-333 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Published

    Branchio-oto-renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses

    Sanggaard, K. M., Rendtorff, N. D., Kjær, K. W., Eiberg, Hans Rudolf Lytchoff, Johnsen, T., Gimsing, S., Dyrmose, J., Nielsen, K. O., Lage, K. & Tranebjærg, Lisbeth, 2007, In: European Journal of Human Genetics. 15, 11, p. 1121-1131 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer.

    Margolin, S., Eiberg, Hans Rudolf Lytchoff, Lindblom, A. & Bisgaard, M. L., 2007, In: BMC Cancer. 7, p. 163

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Deficiency of mannan-binding lectin associated serine protease-2 due to missense polymorphisms

    Thiel, S., Steffensen, R., Christensen, I. J., Ip, W. K., Lau, Y. L., Reason, I. J. M., Eiberg, Hans Rudolf Lytchoff, Gadjeva, M., Ruseva, M. & Jensenius, J. C., 2007, In: Genes and Immunity. 8, 2, p. 154-163 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Fra forskning til forebyggelse i Grønland. Grønlandsmedicinsk Selskab

    Nielsen, I. M., Kern, P. & Eiberg, Hans Rudolf Lytchoff, 2007, In: Ugeskrift for læger. 169, 12, p. 1105-

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Genetic heterogeneity in microcornea-cataract: Five novel mutations in CRYAA, CRYGD, and GJA

    Hansen, Lars, Yao, W. L., Eiberg, Hans Rudolf Lytchoff, Kjær, K. W., Baggesen, K., Hejtmancik, J. F. & Rosenberg, T., 2007, In: Investigative Ophthalmology & Visual Science. 48, 9, p. 3937-3944 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    LOH at chromosome 9q34.3 and the Notch1 gene methylation are less involved in oral squamous cell carcinomas

    Gao, S., Krogdahl, A., Eiberg, Hans Rudolf Lytchoff, Liu, C. J. & Sørensen, J. A., 2007, In: Journal of Oral Pathology & Medicine. 36, 3, p. 173-176 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Non-disjunction of chromosome

    Bugge, Merete, Collins, A., Hertz, J. M., Eiberg, Hans Rudolf Lytchoff, Lundsteen, C., Brandt, C. A., Hansen, C., deLozier, C. D., Lespinasse, J., Tranebjærg, Lisbeth, Hahnemann, J. M. D., Rasmussen, K., Bruun-Petersen, G., Duprez, L., Tommerup, Niels & Petersen, M. B., 2007, In: Human Molecular Genetics. 16, 16, p. 2004-2010 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Novel MAF mutation in a family with congenital cataract-microcornea syndrome

    Hansen, L., Eiberg, Hans Rudolf Lytchoff & Rosenberg, T., 2007, In: Molecular Vision. 13, 223-27, p. 2019-2022 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the young

    Ellard, S., Thomas, K., Edghill, E. L., Owens, M., Ambye, L., Cropper, J., Little, J., Strachan, M., Stride, A., Ersoy, B., Pedersen, O., Shepherd, M. H., Hansen, T., Harries, L. W., Hattersley, A. T. & Eiberg, Hans Rudolf Lytchoff, 2007, In: Diabetologia. 50, 11, p. 2313-2317 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential

    Bross, P., Li, Z., Hansen, J., Hansen, J. J., Nielsen, M. N., Corydon, T. J., Georgopoulos, C., Ang, D., Lundemose, J. B., Niezen-Koning, K., Eiberg, Hans Rudolf Lytchoff, Yang, H., Kølvraa, S., Bolund, L. & Gregersen, N., 2007, In: Journal of Human Genetics. 52, 1, p. 56-65 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Suggestive linkage to a neighboring region of IRF6 in a cleft lip and palate multiplex family

    Jakobsen, L. P., Ullmann, R., Kjær, K. W., Knudsen, M. A., Tommerup, Niels & Eiberg, Hans Rudolf Lytchoff, 2007, In: American Journal of Medical Genetics. Part A. 143A, 22, p. 2716-2721 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  13. Published

    The ADULT-EEC spectrum: An R280C mutation with a borderline phenotype

    Kier-Swiatecka, E., Kock, M., Marker, P., Eiberg, Hans Rudolf Lytchoff & Kjær, K. W., 2007, In: American Journal of Medical Genetics. Part A. 143A, 8, p. 891-894 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  14. Published

    The CHEK2 1100delC variant in Swedish colorectal cancer.

    Djureinovic, T., Lindblom, A., Dalén, J., Dedorson, S., Edler, D., Hjern, F., Holm, J., Lenander, C., Lindforss, U., Lundqvist, N., Olivecrona, H., Olsson, L., Påhlman, L., Rutegård, J., Smedh, K., Törnqvist, A., Eiberg, Hans Rudolf Lytchoff & Bisgaard, M. L., 2007, In: Anticancer Research. 26, 6C, p. 4885-8 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  15. Published

    The functional Pro129Thr variant of the FAAH gene is not associated with various fat accumulation phenotypes in a population-based cohort of 5,801 whites

    Jensen, D. P., Lepola, Mette Andersen, Hansen, L., Eiberg, Hans Rudolf Lytchoff, Borch-Johnsen, K., Jørgensen, T., Hansen, Torben, Pedersen, Oluf Borbye & Andreasen, C. H., 2007, In: Journal of Molecular Medicine. 85, 5, p. 445-9 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 5291