Anne Nørremølle

Anne Nørremølle

Associate Professor


  1. 2024
  2. Published

    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 journalJournal articleResearchpeer-review

  3. 2023
  4. Published

    The significance of mitochondrial haplogroups in preeclampsia risk

    Wendelboe Olsen, K., Hedley, P. L., Hagen, C. M., Rode, L., Placing, S., Wøjdemann, K. R., Shalmi, A. C., Sundberg, K., Nørremølle, Anne, Tabor, Ann, Elson, J. L. & Christiansen, M., 2023, In: Pregnancy Hypertension. 34, p. 146-151 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. 2022
  6. Published

    Progressive Mitochondrial Dysfunction of Striatal Synapses in R6/2 Mouse Model of Huntington's Disease

    Petersen, M. H., Willert, C. W., Andersen, Jens Velde, Madsen, M., Waagepetersen, Helle S., Skotte, Niels Henning & Nørremølle, Anne, 2022, In: Journal of Huntington's disease. 11, 2, p. 121-140

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. 2021
  8. Published

    Nicotinamide Adenine Dinucleotide Phosphate Oxidases Are Everywhere in Brain Disease, but Not in Huntington’s Disease?

    Duque Villegas, Luisana Carolina, Nørremølle, Anne, Freude, Kristine & Vilhardt, Frederik, 2021, In: Frontiers in Aging Neuroscience. 13, 20 p., 736734.

    Research output: Contribution to journalReviewResearchpeer-review

  9. 2020
  10. Published

    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 journalJournal articleResearchpeer-review

  11. Published

    Investigating the feasibility of using assessment and explanatory feedback in desktop virtual reality simulations

    Makransky, Guido, Mayer, R., Nørremølle, Anne, Cordoba, A. L., Wandall, J. & Bonde, M., 2020, In: Educational Technology Research and Development. 68, p. 293-317

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Paroxysmal Cranial Dyskinesia and Nail-Patella Syndrome Caused by a Novel Variant in the LMX1B Gene

    Bech, S., Løkkegaard, Annemette, Nielsen, T. T., Nørremølle, Anne, Grønborg, S., Hasholt, Lis Frydenreich, Steffensen, G. K., Graehn, G., Olesen, J. H., Tommerup, Niels, Mang, Y., Bak, M., Nielsen, Jørgen Erik, Eiberg, Hans Rudolf Lytchoff & Hjermind, L. E., 2020, In: Movement Disorders. 35, 12, p. 2343-2347

    Research output: Contribution to journalJournal articleResearchpeer-review

  13. Published

    Serotonin transporter gene (SLC6A4) variation and sensory processing sensitivity—Comparison with other anxiety-related temperamental dimensions

    Licht, C. L., Mortensen, Erik Lykke, Hjordt, L. V., Stenbæk, Dea Siggaard, Arentzen, T. E., Nørremølle, Anne & Knudsen, Gitte Moos, 2020, In: Molecular Genetics and Genomic Medicine. 8, 8, 10 p., e1352.

    Research output: Contribution to journalJournal articleResearchpeer-review

  14. 2019
  15. Published

    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 journalJournal articleResearchpeer-review

  16. Published

    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. 2449-2461

    Research output: Contribution to journalJournal articleResearchpeer-review

  17. Published

    Ghrelin-mediated improvements in the metabolic phenotype in the R6/2 mouse model of Huntington's disease

    Rudenko, Olga, Springer, C., Skov, Louise Julie, Madsen, A. N., Hasholt, Lis Frydenreich, Nørremølle, Anne & Holst, Birgitte, 2019, In: Journal of Neuroendocrinology. 31, 7 (SI), 14 p., e12699.

    Research output: Contribution to journalConference articleResearchpeer-review

  18. Published

    Haploinsufficiency of ARHGAP42 is associated with hypertension

    Fjorder, A. S., Rasmussen, Malene Bøgehus, Mehrjouy, M. M., Nazaryan, Lusine, Hansen, C., Bak, M., Grarup, Niels, Nørremølle, Anne, Larsen, Lars Allan, drb459, drb459, Hansen, Torben, Tommerup, Niels & Bache, Iben, 2019, In: European Journal of Human Genetics. 27, 8, p. 1296-1303 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  19. 2018
  20. Published

    The D313Y variant in the GLA gene - no evidence of a pathogenic role in Fabry disease in 2 Danish families

    Feldt-Rasmussen, Ulla, Hasholt, Lis Frydenreich, Ballegaard, Martin, Christiansen, M., Law, Ian, Lund, A., Nørremølle, Anne, Ravn, K., Rasmussen, A. K., Tuemer, Z., Bundgård, Henning & Wibrand, F., Feb 2018, In: Molecular Genetics and Metabolism. 123, 2, p. S44-S44 1 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  21. Published

    Integrative Characterization of the R6/2 Mouse Model of Huntington's Disease Reveals Dysfunctional Astrocyte Metabolism

    Skotte, Niels Henning, Andersen, Jens Velde, Santos, A., Aldana, Blanca, Willert, C. W., Nørremølle, Anne, Waagepetersen, Helle S. & Nielsen, Michael Lund, 2018, In: Cell Reports. 23, 7, p. 2211-2224 14 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  22. Published

    Perturbations in the p53/miR-34a/SIRT1 pathway in the R6/2 Huntington's disease model

    Reynolds, R. H., Petersen, M. H., Willert, C. W., Heinrich, M., Nymann, N., Dall, M., Treebak, Jonas Thue, Björkqvist, M., Silahtaroglu, Asli, Hasholt, Lis Frydenreich & Nørremølle, Anne, 2018, In: Molecular and Cellular Neuroscience. 88, p. 118-129

    Research output: Contribution to journalJournal articleResearchpeer-review

  23. 2017
  24. Published

    TMEM106B and ApoE polymorphisms in CHMP2B-mediated frontotemporal dementia (FTD-3)

    Rostgaard, N., Roos, P., Budtz-Joergensen, Esben, Johannsen, P., Waldemar, Gunhild, Nørremølle, Anne, Lindquist, S. G., Gydesen, S., Brown, J. M., Collinge, J., Isaacs, A. M., Nielsen, T. T., Nielsen, Jørgen Erik & FReJA collaboration, F. C., Nov 2017, In: Neurobiology of Aging. 59, p. 221.e1-221.e7 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  25. Published

    The D313Y variant in the GLA gene–no evidence of a pathogenic role in Fabry disease

    Hasholt, Lis Frydenreich, Ballegaard, Martin, Bundgård, Henning, Christiansen, M., Law, Ian, Lund, Allan Meldgaard, Nørremølle, Anne, Krogh Rasmussen, A., Ravn, K., Tümer, Asuman Zeynep, Wibrand, F. & Feldt-Rasmussen, Ulla, 2017, In: Scandinavian Journal of Clinical and Laboratory Investigation. 77, 8, p. 617-621 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  26. 2016
  27. Published

    Liver function in Huntington's disease assessed by blood biochemical analyses in a clinical setting

    Nielsen, S. M. B., Vinther-Jensen, T., Nielsen, Jørgen Erik, Nørremølle, Anne, Hasholt, Lis Frydenreich, Hjermind, L. E. & Josefsen, K., 15 Mar 2016, In: Journal of the Neurological Sciences. 362, p. 326-332 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  28. Published

    Psychiatric and cognitive symptoms in Huntington's disease are modified by polymorphisms in catecholamine regulating enzyme genes

    Vinther-Jensen, T., Nielsen, T. T., Budtz-Joergensen, Esben, Larsen, I. U., Hansen, M. M., Hasholt, Lis Frydenreich, Hjermind, L. E., Nielsen, J. E. & Nørremølle, Anne, Mar 2016, In: Clinical Genetics. 89, 3, p. 320-327 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  29. Published

    Simulation based virtual learning environment in medical genetics counseling: an example of bridging the gap between theory and practice in medical education

    Makransky, Guido, Bonde, M. T., Wulff, J. S. G., Wandall, J., Hood, M., Creed, P. A., Bache, Iben, Silahtaroglu, Asli & Nørremølle, Anne, Mar 2016, In: B M C Medical Education. 16, 1, p. 1-9 9 p., 98.

    Research output: Contribution to journalJournal articleResearchpeer-review

  30. 2015
  31. Published

    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, Wasserman, W. W., Leavitt, B. R. & REGISTRY Investigators of the European Huntington's Disease Network, R. I. O. T. E. H. D. N., Jun 2015, In: Nature Neuroscience. 18, 6, p. 807-816 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  32. Published

    Progressive Impairment of Lactate-based Gluconeogenesis in the Huntington's Disease Mouse Model R6/2

    Nielsen, S. M. B., Hasholt, Lis Frydenreich, Nørremølle, Anne & Josefsen, K. E., 20 Apr 2015, In: PLoS Currents. 7

    Research output: Contribution to journalConference abstract in journalResearchpeer-review

  33. 2014
  34. Published

    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 journalJournal articleResearchpeer-review

  35. Published

    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 journalJournal articleResearchpeer-review

  36. Published

    Reduction in mitochondrial DNA copy number in peripheral leukocytes after onset of Huntington's disease

    Petersen, M. H., Budtz-Joergensen, Esben, Sørensen, S. A., Nielsen, Jørgen Erik, Hjermind, L. E., Vinther-Jensen, T., Nielsen, S. M. B. & Nørremølle, Anne, 2014, In: Mitochondrion. 17, p. 14-21 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  37. 2013
  38. Published

    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. 5

    Research output: Contribution to journalJournal articleResearchpeer-review

  39. 2012
  40. Published

    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, Frontali, M., Jones, R., Ashizawa, T., Frank, S., Saint-Hilaire, M. H., Hersch, S. M., Rosas, H. D., Lucente, D., Harrison, M. B., Zanko, A., Abramson, R. K., Marder, K., Sequeiros, J., Paulsen, J. S., Landwehrmeyer, G. B., Myers, R. H., MacDonald, M. E., Gusella, J. F., Hasholt, Lis Frydenreich, Nørremølle, Anne, Nielsen, Jørgen Erik & PREDICT-HD study of the Huntington Study Group (HSG), P. S. O. T. H. S. G. (., Mar 2012, In: Neurology. 78, 10, p. 690-5 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  41. 2011
  42. Published

    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 journalJournal articleResearchpeer-review

  43. Published

    The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders

    Bech, S., Nørremølle, Anne, Winge, K., Hasholt, Lis Frydenreich, Tommerup, Niels, Svenstrup, K., Nielsen, Jørgen Erik & Hjermind, L. E., 1 Jun 2011, In: Parkinsonism & Related Disorders. 17, 5, p. 398-9 2 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  44. Published

    Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY

    Orth, M., Handley, O. J., Schwenke, C., Dunnett, S., Wild, E. J., Tabrizi, S. J., Landwehrmeyer, G. B., Hasholt, Lis Frydenreich, Hjermind, L. E., Nørremølle, Anne, Nielsen, Jørgen Erik & European Huntington's Disease Network, E. H. D. N., 2011, In: The Egyptian Journal of Neurology, Psychiatry, and Neurosurgery. 82, 12, p. 1409-12 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  45. 2010
  46. Published

    Reduced gluconeogenesis and lactate clearance in Huntington's disease

    Josefsen, K., Nielsen, S. M. B., Campos, A., Seifert, T., Hasholt, Lis Frydenreich, Nielsen, Jørgen Erik, Nørremølle, Anne, Skotte, Niels Henning, Secher, Niels H. & Quistorff, B., 1 Dec 2010, In: Neurobiology of Disease. 40, 3, p. 656-62 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  47. Published

    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, Køber, Lars Valeur & Bundgaard, H., 1 Jun 2010, In: European Journal of Heart Failure. 12, 6, p. 535-40 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  48. Published

    Huntington's disease-like and ataxia syndromes: identification of a family with a de novo SCA17/TBP mutation

    Bech, S., Petersen, T., Nørremølle, Anne, Gjedde, Albert, Ehlers, L., Eiberg, Hans Rudolf Lytchoff, Hjermind, L. E., Hasholt, Lis Frydenreich, Lundorf, E. & Nielsen, Jørgen Erik, 2010, In: Parkinsonism & Related Disorders. 16, 1, p. 12-5 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  49. 2009
  50. 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 journalJournal articleResearchpeer-review

  51. Published

    Huntington's disease does not appear to increase the risk of diabetes mellitus

    Boesgaard, T. W., Nielsen, T. T., Josefsen, K. E., Hansen, T., Jørgensen, T., Pedersen, O., Nørremølle, Anne, Nielsen, Jørgen Erik & Hasholt, Lis Frydenreich, 2009, In: Journal of Neuroendocrinology. 21, 9, p. 770-6 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  52. Published

    Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia

    Svenstrup, K., Bross, P., Koefoed, P., Hjermind, L. E., Eiberg, H., Born, A. P., Vissing, J., Gyllenborg, J., Nørremølle, A., Hasholt, L., Nielsen, J. E., Svenstrup, K., Bross, P., Koefoed, P., Hjermind, L. E., Eiberg, H., Born, A. P., Vissing, J., Gyllenborg, J., Nørremølle, A. & 2 others, Hasholt, L. & Nielsen, J. E., 2009, In: Journal of the Neurological Sciences. 284, 1-2, p. 90-5 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  53. 2008
  54. Published

    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 journalJournal articleResearchpeer-review

  55. Published

    Impaired glucose tolerance in the R6/1 transgenic mouse model of Huntington's disease

    Josefsen, K., Nielsen, M. D., Jorgensen, K. H., Bock, T., Nørremølle, Anne, Sørensen, S. A., Naver, B. & Hasholt, Lis Frydenreich, 2008, In: Journal of Neuroendocrinology. 20, 2, p. 165-172 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  56. Published

    Inhibition of endoplasmic reticulum stress counteracts neuronal cell death and protein aggregation caused by N-terminal mutant huntingtin proteins

    Reijonen, S., Putkonen, N., Nørremølle, Anne, Lindholm, D. & Korhonen, L., 2008, In: Experimental Cell Research. 314, 5, p. 950-960 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  57. 2006
  58. Published

    Meiotic CAG repeat instability in spinocerebellar ataxia type 6: Maternally transmitted elongation in a presumed sporadic case

    Lindquist, S. G., Nørremølle, Anne, Hjermind, L. E., Hasholt, Lis Frydenreich & Nielsen, J. E., 2006, In: Journal of the Neurological Sciences. 241, 1-2, p. 95-98 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  59. Published

    MicroRNAs in mammalian brain

    Christensen, M., Bak, M., Silahtaroglu, A., Kloosterman, W., Skryapin, B., Nolting, D., Nørremølle, Anne, Lassen, A., Halsholm, L., Brosius, J., Tommerup, Niels, Plasterk, R. & Kauppinen, M. S., 2006, p. 1.

    Research output: Working paperResearch

  60. 2004
  61. Published

    Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.

    Nielsen, Jørgen Erik, Johnson, B., Koefoed, P., Scheuer, K. H., Grønbech-Jensen, M., Law, I., Krabbe, K., Nørremølle, Anne, Eiberg, Hans Rudolf Lytchoff, Søndergård, H., Dam, M., Rehfeld, J. F., Krarup, C., Paulson, Olaf B., Hasholt, Lis Frydenreich & Sørensen, S. A., 2004, In: European Journal of Neurology. 11, 12, p. 817-824 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  62. Published

    Mosaicism of the CAG repeat sequence in the Huntington disease gene in a pair of monozygotic twins

    Nørremølle, Anne, Hasholt, Lis Frydenreich, Petersen, C. B., Eiberg, Hans Rudolf Lytchoff, Hasselbalch, S. G., Gideon, P., Nielsen, J. E. & Sørensen, S. A., 2004, In: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Vol. 130, p. 154-159

    Research output: Contribution to journalJournal articleResearchpeer-review

  63. Published

    Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG4) using direct mutation detection

    Nielsen, Jørgen Erik, Koefoed, P., Kjaergaard, S., Jensen, L. N., Nørremølle, Anne & Hasholt, Lis Frydenreich, 2004, In: Prenatal Diagnosis. 24, 5, p. 363-6 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  64. 2003
  65. Published

    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. 528-538

    Research output: Contribution to journalJournal articleResearchpeer-review

  66. Published

    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 journalJournal articleResearchpeer-review

  67. Published

    Sekventering

    Nørremølle, Anne, 2003, DNA og RNA. En håndbog. København: Gad, p. 161-180

    Research output: Chapter in Book/Report/Conference proceedingReport chapterResearch

  68. 2000
  69. Published

    Inhibition of Huntingtin synthesis by antisense oligodeoxynucleotides

    Nellemann, C. L., Abell, K., Nørremølle, Anne, Løkkegaard, T., Naver, B., Röpke, C., Rygaard, J., Sørensen, S. A. & Hasholt, Lis Frydenreich, 2000, In: Molecular and Cellular Neuroscience. 16, p. 313-323

    Research output: Contribution to journalJournal articleResearchpeer-review

  70. 1996
  71. Published

    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 journalJournal articleResearchpeer-review

  72. 1995
  73. 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, K. & Hasholt, L., 1995, In: Clinical Genetics. 47, p. 113-117

    Research output: Contribution to journalJournal articleResearchpeer-review

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