Anne Nørremølle
Associate Professor
Medical Genetics Program
Blegdamsvej 3
2200 København N.
- Published
4p16.3 haplotype modifying age at onset of Huntington disease
Nørremølle, Anne, Budtz-Joergensen, Esben, Fenger, K., Nielsen, Jørgen Erik, Sørensen, S. A. & Hasholt, Lis Frydenreich, 2009, In: Clinical Genetics. 75, 3, p. 244-50 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A SNP in the HTT promoter alters NF-κB binding and is a bidirectional genetic modifier of Huntington disease
Bečanović, K., Nørremølle, A., Neal, S. J., Kay, C., Collins, J. A., Arenillas, D., Lilja, T., Gaudenzi, G., Manoharan, S., Doty, C. N., Beck, J., Lahiri, N., Portales-Casamar, E., Warby, S. C., Connolly, C., De Souza, R. A. G., Tabrizi, S. J., Hermanson, O., Langbehn, D. R., Hayden, M. R. & 3 others, , Jun 2015, In: Nature Neuroscience. 18, 6, p. 807-816 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A clinical classification acknowledging neuropsychiatric and cognitive impairment in Huntingtons disease
Vinther-Jensen, T., Larsen, I. U., Hjermind, L. E., Budtz-Joergensen, Esben, Nielsen, T. T., Nørremølle, Anne, Nielsen, Jørgen Erik & Vogel, Asmus, 17 Jul 2014, In: Orphanet Journal of Rare Diseases. 9, 1, p. 1-9 9 p., 114.Research output: Contribution to journal › Journal article › Research › peer-review
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A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment
Lindquist, S. G., Hasholt, Lis Frydenreich, Bahl, J. M. C., Heegaard, N. H. H., Andersen, B. B., Nørremølle, Anne, Stokholm, J., Schwartz, M., Batbayli, M., Laursen, H., Pardossi-Piquard, R., Chen, F., George-Hyslop, P. S., Waldemar, Gunhild & Nielsen, J. E., 2008, In: European Journal of Neurology. 15, 10, p. 1135-1139 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Antisense downregulation of mutant huntingtin in a cell model
Hasholt, Lis Frydenreich, Abell, K., Nørremølle, Anne, Nellemann, C., Fenger, K. & Sørensen, S. A., 2003, In: Journal of Gene Medicine. Vol. 5, p. 528-538Research output: Contribution to journal › Journal article › Research › peer-review
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CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion
Lee, J-M., Ramos, E. M., Lee, J-H., Gillis, T., Mysore, J. S., Hayden, M. R., Warby, S. C., Morrison, P., Nance, M., Ross, C. A., Margolis, R. L., Squitieri, F., Orobello, S., Di Donato, S., Gomez-Tortosa, E., Ayuso, C., Suchowersky, O., Trent, R. J. A., McCusker, E., Novelletto, A. & 22 others, , Mar 2012, In: Neurology. 78, 10, p. 690-5 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Cells exposed to a huntingtin fragment containing an expanded polyglutamine tract show no sign of ion channel formation: results arguing against the ion channel hypothesis.
Nørremølle, Anne, Grunnet, Morten, Hasholt, Lis Frydenreich & Sørensen, S. A., 2003, In: Journal of Neuroscience Research. 71, 1, p. 132-7 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Central 5-HT4 receptor binding as biomarker of serotonergic tonus in humans: a [11C]SB207145 PET study
Haahr, M. E., Fisher, P. M., Jensen, C. G., Frøkjær, Vibe Gedsø, Mahon, B. M., Madsen, K., Baaré, W. F. C., Lehel, S., Nørremølle, Anne, Rabiner, E. A. & Knudsen, G. M., Apr 2014, In: Molecular Psychiatry. 19, 4, p. 427-32 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Compromised IGF signaling causes caspase-6 activation in Huntington disease
Skotte, Niels Henning, Pouladi, M. A., Ehrnhoefer, D. E., Huynh, K., Qiu, X., Nielsen, S. M. B., Nielsen, T. T., Nørremølle, Anne & Hayden, M. R., 2020, In: Experimental Neurology. 332, 113396.Research output: Contribution to journal › Journal article › Research › peer-review
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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, K. & Hasholt, L., 1995, In: Clinical Genetics. 47, p. 113-117Research output: Contribution to journal › Journal article › Research › peer-review
ID: 3886
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252
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Integrative Characterization of the R6/2 Mouse Model of Huntington's Disease Reveals Dysfunctional Astrocyte Metabolism
Research output: Contribution to journal › Journal article › Research › peer-review
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147
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Serotonin transporter gene (SLC6A4) variation and sensory processing sensitivity—Comparison with other anxiety-related temperamental dimensions
Research output: Contribution to journal › Journal article › Research › peer-review
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22
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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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