Larissa Arning
Department of Human Genetics
Ruhr-University Bochum
Germany
Name/email consistency: high
- PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease. Taherzadeh-Fard, E., Saft, C., Akkad, D.A., Wieczorek, S., Haghikia, A., Chan, A., Epplen, J.T., Arning, L. Mol. Neurodegener (2011)
- Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease. Arning, L., Haghikia, A., Taherzadeh-Fard, E., Saft, C., Andrich, J., Pula, B., Höxtermann, S., Wieczorek, S., Akkad, D.A., Perrech, M., Gold, R., Epplen, J.T., Chan, A. J. Mol. Med. (2010)
- PGC-1alpha as modifier of onset age in Huntington disease. Taherzadeh-Fard, E., Saft, C., Andrich, J., Wieczorek, S., Arning, L. Mol. Neurodegener (2009)
- ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease. Arning, L., Monté, D., Hansen, W., Wieczorek, S., Jagiello, P., Akkad, D.A., Andrich, J., Kraus, P.H., Saft, C., Epplen, J.T. J. Mol. Med. (2008)
- Identification and characterisation of a large senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2). Arning, L., Schöls, L., Cin, H., Souquet, M., Epplen, J.T., Timmann, D. Neurogenetics (2008)
- NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner. Arning, L., Saft, C., Wieczorek, S., Andrich, J., Kraus, P.H., Epplen, J.T. Hum. Genet. (2007)
- NR2A and NR2B receptor gene variations modify age at onset in Huntington disease. Arning, L., Kraus, P.H., Valentin, S., Saft, C., Andrich, J., Epplen, J.T. Neurogenetics (2005)
- Age at onset of Huntington disease is not modulated by the R72P variation in TP53 and the R196K variation in the gene coding for the human caspase activated DNase (hCAD). Arning, L., Kraus, P.H., Saft, C., Andrich, J., Epplen, J.T. BMC Med. Genet. (2005)
- Glutathione S-Transferase Omega 1 variation does not influence age at onset of Huntington's disease. Arning, L., Jagiello, P., Wieczorek, S., Saft, C., Andrich, J., Epplen, J.T. BMC Med. Genet. (2004)