Anne Nørremølle

Anne Nørremølle

Associate professor, Associate Professor


  1. 1992
  2. Published

    Exclusion of DNA changes in the *GB-subunit of the C-GMP phosphodiesterase gene as the cause for Huntington's disease. / Riess, Olaf; Nørremølle, Anne; Collins, Colin; Mah, Diana; Weber, Bernhard; Hayden, Michael R.

    In: Nature Genetics, No. 1, 1992, p. 104-108.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Linkage studies and mutation analysis of the PDEB gene in 23 families with Leber congenital amaurosis. / Riess, O; Weber, B; Nørremølle, Anne; Shaikh, R A; Hayden, M R; Musarella, M A.

    In: Human Mutation, Vol. 1, No. 6, 1992, p. 478-85.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Nucleotide sequence and PCR-amplification of a polymorphic MboI site in human DNA marker D4S95 linked to the Huntington disease locus. / Nørremølle, Anne; Sørensen, Sven Asger; Arctander, Peter.

    In: Clinical Genetics, Vol. 42, 1992, p. 210-211.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosa. / Riess, O; Noerremoelle, A; Weber, B; Musarella, M A; Hayden, M R.

    In: American Journal of Human Genetics, Vol. 51, No. 4, 1992, p. 755-62.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. 1993
  7. Published

    DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington's disease. / Andrew, S.; Theilmann, J.; Almquist, E.; Nørremølle, Anne; Lucotte, G.; Anvret, M.; Sørensen, S.A.; Turpin, J.C.; Hayden, Michael R.

    In: Clinical Genetics, No. 43, 1993, p. 286-294.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease. / Riess, O; Noerremoelle, A; Sørensen, Sven Asger; Epplen, J T.

    In: Human Molecular Genetics, Vol. 2, No. 6, 1993, p. 637.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Mapping of the human NMDA receptor subunit (NMDAR1) and the proposed NMDA receptor glutamate-binding subunit (NMDARA1) to chromosomes 9q34.3 and chromosome 8, respectively. / Collins, C; Duff, C; Duncan, A M; Planells-Cases, R; Sun, W; Nørremølle, Anne; Michaelis, E; Montal, M; Worton, R; Hayden, M R.

    In: Genomics, Vol. 17, No. 1, 1993, p. 237-9.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Trinucleotide repeat elongation in the Huntington gene in Huntington Disease patients from 71 Danish families. / Nørremølle, Anne; Riess, O.; Epplen, J.T.; Fenger, Kirsten; Hasholt, L.; Sørensen, S.A.

    In: Human Molecular Genetics, No. 2, 1993, p. 1475-1476.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. 1995
  12. Published

    Correlation between magnitude of CAG repeat length alterations and length of the paternal repeat in paternally inherited Huntington's disease. / Nørremølle, Anne; Sørensen, S.A.; Fenger, Kirsten; Hasholt, L.

    In: Clinical Genetics, No. 47, 1995, p. 113-117.

    Research output: Contribution to journalJournal articleResearchpeer-review

  13. Published

    Elongated CAG repeats of the B37 gene in a Danish family with dentatorubro-pallido-luysian atrophy. / Nørremølle, Anne; Nielsen, J.E.; Sørensen, S.A.; Hasholt, Lis Frydenreich.

    In: Human Genetics, No. 95, 1995, p. 313-318.

    Research output: Contribution to journalJournal articleResearchpeer-review

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