Jørgen Erik Nielsen
Clinical Professor
Department of Clinical Medicine
Rigshospitalet - Neurocentret, Blegdamsvej 9, 2100 København Ø
- Published
Antisense gene silencing : therapy for neurodegenerative disorders? / Nielsen, Troels T; Nielsen, Jørgen E.
In: Genes, Vol. 4, No. 3, 10.09.2013, p. 457-84.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Cognitive impairment in the preclinical stage of dementia in FTD-3 CHMP2B mutation carriers : A longitudinal prospective study. / Stokholm, Jette; Teasdale, Thomas W; Johannsen, Peter; Nielsen, Jorgen E; Nielsen, Troels Tolstrup; Isaacs, Adrian; Brown, Jerry M; Gade, Anders; and the Frontotemporal dementia Research in Jutland Association (FReJA) consortium.
In: Journal of Neurology, Neurosurgery and Psychiatry, Vol. 84, No. 2, 02.2013, p. 170-176.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease. / Lindquist, Sg; Duno, M; Batbayli, M; Puschmann, A; Braendgaard, H; Mardosiene, S; Svenstrup, K; Pinborg, Lh; Vestergaard, K; Hjermind, LE; Stokholm, J; Andersen, Bb; Johannsen, P; Nielsen, Jørgen Erik.
In: Clinical Genetics, Vol. 83, No. 3, 03.2013, p. 279-283.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Germ-line CAG repeat instability causes extreme CAG repeat expansion with infantile-onset spinocerebellar ataxia type 2. / Vinther-Jensen, Tua; Ek, Jakob; Duno, Morten; Skovby, Flemming; Hjermind, Lena E; Nielsen, Jørgen E; Nielsen, Troels Tolstrup.
In: European Journal of Human Genetics, Vol. 21, No. 6, 2013, p. 626-9.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients. / Metzger, Silke; Walter, Carolin; Riess, Olaf; Roos, Raymund A C; Nielsen, Jørgen E; Craufurd, David; Nguyen, Huu Phuc; REGISTRY Investigators of the European Huntington’s Disease Network.
In: PLOS ONE, Vol. 8, No. 7, 07.2013, p. e68951.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
Published -
141
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Generation of a human induced pluripotent stem cell line via CRISPR-Cas9 mediated integration of a site-specific heterozygous mutation in CHMP2B
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
140
downloads
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