Anne Nørremølle
Associate Professor
Medical Genetics Program
Blegdamsvej 3
2200 København N.
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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, M. R., 1993, In: Clinical Genetics. 43, p. 286-294Research output: Contribution to journal › Journal article › Research › peer-review
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Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation Danish family.
Nielsen, Jørgen Erik, Sørensen, S. A., Hasholt, Lis Frydenreich & Nørremølle, Anne, 1996, In: Movement Disorders. 11, 5, p. 533-541 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Discrepancies in reporting the CAG repeat lengths for Huntington's disease
Quarrell, O. W., Handley, O., O'Donovan, K., Dumoulin, C., Ramos-Arroyo, M., Biunno, I., Bauer, P., Kline, M., Landwehrmeyer, G. B., Hjermind, L. E., Hasholt, Lis Frydenreich, Nørremølle, Anne, Nielsen, Jørgen Erik & European Huntington’s Disease Network, E. H. D. N., Aug 2011, In: European Journal of Human Genetics. 20, 1, p. 20-6 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model
Aidt, F. H., Nielsen, S. M. B., Kanters, Jørgen K., Pesta, D., Nielsen, T. T., Nørremølle, Anne, Hasholt, Lis Frydenreich, Christiansen, M. & Hagen, C. M., 2013, In: PLoS Currents. 5Research output: Contribution to journal › Journal article › Research › peer-review
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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, 1995, In: Human Genetics. 95, p. 313-318Research output: Contribution to journal › Journal article › Research › peer-review
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Enhanced cerebral branched-chain amino acid metabolism in R6/2 mouse model of Huntington's disease
Andersen, Jens Velde, Skotte, Niels Henning, Aldana, Blanca, Nørremølle, Anne & Waagepetersen, Helle S., 2019, In: Cellular and Molecular Life Sciences. 76, 12, p. 2449-2461Research output: Contribution to journal › Journal article › Research › peer-review
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Exclusion of DNA changes in the *GB-subunit of the C-GMP phosphodiesterase gene as the cause for Huntington's disease
Riess, O., Nørremølle, Anne, Collins, C., Mah, D., Weber, B. & Hayden, M. R., 1992, In: Nature Genetics. 1, p. 104-108Research output: Contribution to journal › Journal article › Research › peer-review
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Fabry disease mimicking hypertrophic cardiomyopathy: genetic screening needed for establishing the diagnosis in women
Havndrup, O., Christiansen, M., Stoevring, B., Jensen, M., Hoffman-Bang, J., Andersen, P. S., Hasholt, L., Nørremølle, A., Feldt-Rasmussen, U., Køber, L., Bundgaard, H., Havndrup, O., Christiansen, M., Stoevring, B., Jensen, M., Hofman-Bang, J., Andersen, P. S., Hasholt, L. F., Nørremølle, A., Feldt-Rasmussen, U. & 2 others, , 1 Jun 2010, In: European Journal of Heart Failure. 12, 6, p. 535-40 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Functional Differences between Synaptic Mitochondria from the Striatum and the Cerebral Cortex
Petersen, M. H., Willert, C. W., Andersen, Jens Velde, Waagepetersen, Helle S., Skotte, Niels Henning & Nørremølle, Anne, May 2019, In: Neuroscience. 406, p. 432-443 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Generation of three isogenic gene-edited Huntington’s disease human embryonic stem cell lines with DOX-inducible NGN2 expression cassette in the AAVS1 safe locus
Duque Villegas, Luisana Carolina, Chandrasekaran, Abinaya, Flintholm Andersen, S. A., Nørremølle, Anne, Schmid, B., Pouladi, M. A. & Freude, Kristine, 2024, In: Stem Cell Research. 77, 6 p., 103408.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 3886
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Integrative Characterization of the R6/2 Mouse Model of Huntington's Disease Reveals Dysfunctional Astrocyte Metabolism
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151
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Serotonin transporter gene (SLC6A4) variation and sensory processing sensitivity—Comparison with other anxiety-related temperamental dimensions
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Nicotinamide Adenine Dinucleotide Phosphate Oxidases Are Everywhere in Brain Disease, but Not in Huntington’s Disease?
Research output: Contribution to journal › Review › Research › peer-review
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