Niels Tommerup
Professor, dr.med., Professor
Department of Cellular and Molecular Medicine
Blegdamsvej 3, Building: 22.4.28
2200 2200 København N
Medical Genetics Program
Blegdamsvej 3
2200 København N.
- 2015
- Published
Dysregulation of FOXG1 by ring chromosome 14
Alosi, Daniela, Klitten, L. L., Bak, M., Hjalgrim, H., Møller, R. S. & Tommerup, Niels, Apr 2015, In: Molecular Cytogenetics. 8, 24, 7 p., 24.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The phenotypic spectrum of SCN8A encephalopathy
Larsen, J., Carvill, G. L., Gardella, E., Kluger, G., Schmiedel, G., Barisic, N., Depienne, C., Brilstra, E., Mang, Y., Nielsen, J. E. K., Kirkpatrick, M., Goudie, D., Goldman, R., Jähn, J. A., Jepsen, B., Gill, D., Döcker, M., Biskup, S., McMahon, J. M., Koeleman, B. & 18 others, , 3 Feb 2015, In: Neurology. 84, 5, p. 480-9 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Complete re-sequencing of a 2Mb topological domain encompassing the FTO/IRXB genes identifies a novel obesity-associated region upstream of IRX5
Hunt, L. E., Noyvert, B., Bhaw-Rosun, L., Sesay, A. K., Paternoster, L., Nohr, E. A., Davey Smith, G., Tommerup, Niels, Sørensen, Thorkild I.A. & Elgar, G., 2015, In: Genome Medicine. 7, 1, p. 1-14 14 p., 126.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Partial USH2A deletions contribute to Usher syndrome in Denmark
Dad, S., Rendtorff, N. D., Kann, E., Albrechtsen, Anders, M. Mehrjouy, M., Bak, M., Tommerup, Niels, Tranebjærg, Lisbeth, Rosenberg, T., Jensen, H. & Møller, L. B., 2015, In: European Journal of Human Genetics. 23, p. 1646-1651 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The small RNA content of human sperm reveals pseudogene-derived piRNAs complementary to protein-coding genes
Pantano, L., Jodar, M., Bak, M., Ballescà, J. L., Tommerup, Niels, Oliva, R. & Vavouri, T., 2015, In: R N A. 21, 6, p. 1085-95 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2014
- Published
Epigenetic remodelling and dysregulation of DLGAP4 is linked with early-onset cerebellar ataxia
Minocherhomji, S., Hansen, C., Kim, H., Mang, Y., Bak, M., Guldberg, P., Papadopoulos, N., Eiberg, Hans Rudolf Lytchoff, Doh, G. D., Møllgård, Kjeld, Hertz, J. M., Nielsen, Jørgen Erik, Ropers, H., Tümer, Asuman Zeynep, Tommerup, Niels, Kalscheuer, V. M. & Silahtaroglu, Asli, 1 Dec 2014, In: Human Molecular Genetics. 23, 23, p. 6163-6176 14 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Aberrant expression of miR-218 and miR-204 in human mesial temporal lobe epilepsy and hippocampal sclerosis-Convergence on axonal guidance
Kaalund, S. S., Venø, M. T., Bak, M., Møller, R. S., Laursen, H., Madsen, F., Broholm, H., Quistorff, B., Uldall, P., Tommerup, Niels, Kauppinen, S., Sabers, A., Fluiter, K., Møller, L. B., Nossent, Anne Yaël, Silahtaroglu, Asli, Kjems, J., Aronica, E. & Tümer, Asuman Zeynep, Dec 2014, In: Epilepsia. 55, 12, p. 2017-2027 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The myosin chaperone UNC45B is involved in lens development and autosomal dominant juvenile cataract
Hansen, Lars, Comyn, S., Mang, Y., Lind-Thomsen, A., Myhre, L., Jean, F., Eiberg, Hans Rudolf Lytchoff, Tommerup, Niels, Rosenberg, T. & Pilgrim, D., Nov 2014, In: European Journal of Human Genetics. 22, 11, p. 1290-1297 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Neural correlates of taste perception in congenital olfactory impairment
Gagnon, L., Vestergaard, M., Madsen, K., Karstensen, H. G., Siebner, Hartwig Roman, Tommerup, Niels, Kupers, Ron & Ptito, Maurice, Sep 2014, In: Neuropsychologia. 62, p. 297-305 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Neurodevelopmental disorders associated with dosage imbalance of ZBTB20 correlate with the morbidity spectrum of ZBTB20 candidate target genes
Rasmussen, Malene Bøgehus, Nielsen, J. V., Lourenço, C. M., Melo, J. B., Harding, Christina Halgren, Geraldi, C. V. L., Marques, W., Rodrigues, G. R., Thomassen, M., Bak, M., Hansen, C., Ferreira, S. I., Venâncio, M., Henriksen, K. F., Lind-Thomsen, A., Carreira, I. M., Jensen, N. A. & Tommerup, Niels, Sep 2014, In: Journal of Medical Genetics. 51, 9, p. 605-613 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 5189
Most downloads
-
2623
downloads
Dysfunction of the heteromeric KV7.3/KV7.5 potassium channel is associated with autism spectrum disorders
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
1901
downloads
A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
1157
downloads
Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans
Research output: Contribution to journal › Journal article › Research › peer-review
Published