Jørgen Erik Nielsen
Clinical Professor
- 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 Novel TTBK2 De Novo Mutation in a Danish Family with Early-Onset Spinocerebellar Ataxia
Lindquist, S. G., Møller, L. B., Dali, C. I., Marner, L., Kamsteeg, E. J., Nielsen, Jørgen Erik & Hjermind, L. E., Feb 2017, In: Cerebellum. 16, 1, p. 268-271 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunction
Puschmann, A., Ross, O. A., Vilariño-Güell, C., Lincoln, S. J., Kachergus, J. M., Cobb, S. A., Lindquist, Suzanne Granhøj, Nielsen, Jørgen Erik, Wszolek, Z. K., Farrer, M., Widner, H., van Westen, D., Hägerström, D., Markopoulou, K., Chase, B. A., Nilsson, K., Reimer, J. & Nilsson, C., 2009, In: Parkinsonism & Related Disorders. 15, 9, p. 627-32 5 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
- Published
A proteomics analysis of 5xFAD mouse brain regions reveals the lysosome-associated protein Arl8b as a candidate biomarker for Alzheimer’s disease
Boeddrich, A., Haenig, C., Neuendorf, N., Blanc, E., Ivanov, A., Kirchner, M., Schleumann, P., Bayraktaroğlu, I., Richter, M., Molenda, C. M., Sporbert, A., Zenkner, M., Schnoegl, S., Suenkel, C., Schneider, L. S., Rybak-Wolf, A., Kochnowsky, B., Byrne, L. M., Wild, E. J., Nielsen, J. E. & 4 others, , 2023, In: Genome Medicine. 15, 1, 32 p., 50.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
ATXN2 with intermediate-length CAG/CAA repeats does not seem to be a risk factor in hereditary spastic paraplegia
Nielsen, T. T., Svenstrup, K., Budtz-Joergensen, Esben, Eiberg, Hans Rudolf Lytchoff, Hasholt, Lis Frydenreich & Nielsen, Jørgen Erik, Oct 2012, In: Journal of the Neurological Sciences. 321, 1-2, p. 100-2 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Allogenic hematopoietic stem cell transplantation in two siblings with adult metachromatic leukodystrophy and a systematic literature review
Videbæk, C., Stokholm, J., Sengeløv, Henrik, Fjeldborg, L. U., Larsen, V. A., Krarup, Christian, Nielsen, Jørgen Erik & Grønborg, S., 2021, In: JIMD Reports. 60, 1, p. 96-104 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Amyloid-related biomarkers and axonal damage proteins in parkinsonian syndromes
Bech, S., Hjermind, L. E., Salvesen, Lisette, Nielsen, Jørgen Erik, Heegaard, N. H. H., Jørgensen, Henrik Løvendahl, Rosengren, L., Blennow, K., Zetterberg, H. & Winge, K., 2012, In: Parkinsonism & Related Disorders. 18, 1, p. 69-72 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
An Exploratory Study Investigating Autonomy in Huntington's Disease Gene Expansion Carriers
Hendel, Rebecca K., Hellem, M. N. N., Hjermind, L. E., Nielsen, Jørgen Erik & Vogel, Asmus, 2022, In: Journal of Huntington's disease. 11, 4, p. 373-381 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Anlægsbærere for fragilt X-syndrom kan udvise et bredt spektrum af kliniske manifestationer
Jønch, A. E., Grønskov, K., Carlsen Lunding, J. M., Nielsen, Jørgen Erik & Brøndum-Nielsen, K., 23 Jun 2014, In: Ugeskrift for Laeger. 176, 26, p. 2-6 5 p., V02140099.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 9689629
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Patient iPSC-derived neurons for disease modeling of frontotemporal dementia with mutation in CHMP2B
Research output: Contribution to journal › Journal article › Research › peer-review
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329
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Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.A11
Research output: Contribution to journal › Journal article › Research › peer-review
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297
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Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.B11
Research output: Contribution to journal › Journal article › Research › peer-review
Published