Riess O - Search Results

1

Intronic enhancers of the human SNCA gene predominantly regulate its expression in brain in vivo.

Cheng F, Zheng W, Liu C, Barbuti PA, Yu-Taeger L, Casadei N, Huebener-Schmid J, Admard J, Boldt K, Junger K, Ueffing M, Houlden H, Sharma M, Kruger R, Grundmann-Hauser K, Ott T, Riess O. Cheng F, et al. Among authors: riess o. Sci Adv. 2022 Nov 25;8(47):eabq6324. doi: 10.1126/sciadv.abq6324. Epub 2022 Nov 23. Sci Adv. 2022. PMID: 36417521 Free PMC article.

2

Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson's disease.

Rahner N, Holzmann C, Krüger R, Schöls L, Berger K, Riess O. Rahner N, et al. Among authors: riess o. Brain Res. 2002 Sep 27;951(1):82-6. doi: 10.1016/s0006-8993(02)03138-4. Brain Res. 2002. PMID: 12231460

3

Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.

Kobayashi H, Krüger R, Markopoulou K, Wszolek Z, Chase B, Taka H, Mineki R, Murayama K, Riess O, Mizuno Y, Hattori N. Kobayashi H, et al. Among authors: riess o. Brain. 2003 Jan;126(Pt 1):32-42. doi: 10.1093/brain/awg010. Brain. 2003. PMID: 12477695

4

14-3-3 protein is a component of Lewy bodies in Parkinson's disease-mutation analysis and association studies of 14-3-3 eta.

Ubl A, Berg D, Holzmann C, Krüger R, Berger K, Arzberger T, Bornemann A, Riess O. Ubl A, et al. Among authors: riess o. Brain Res Mol Brain Res. 2002 Dec;108(1-2):33-9. doi: 10.1016/s0169-328x(02)00510-7. Brain Res Mol Brain Res. 2002. PMID: 12480176

5

Spectrum of phenotypes and genotypes in Parkinson's disease.

Riess O, Krüger R, Schulz JB. Riess O, et al. J Neurol. 2002 Oct;249 Suppl 3:III/15-20. doi: 10.1007/s00415-002-1303-2. J Neurol. 2002. PMID: 12522566 Review.

6

Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease.

Marx FP, Holzmann C, Strauss KM, Li L, Eberhardt O, Gerhardt E, Cookson MR, Hernandez D, Farrer MJ, Kachergus J, Engelender S, Ross CA, Berger K, Schöls L, Schulz JB, Riess O, Krüger R. Marx FP, et al. Among authors: riess o. Hum Mol Genet. 2003 Jun 1;12(11):1223-31. doi: 10.1093/hmg/ddg134. Hum Mol Genet. 2003. PMID: 12761037

7

Therapeutic strategies for Parkinson's disease based on data derived from genetic research.

Riess O, Berg D, Krüger R, Schulz JB. Riess O, et al. J Neurol. 2003 Feb;250 Suppl 1:I3-10. doi: 10.1007/s00415-003-1101-3. J Neurol. 2003. PMID: 12761628 Review.

8

Mutation analysis of the neurofilament M gene in Parkinson's disease.

Krüger R, Fischer C, Schulte T, Strauss KM, Müller T, Woitalla D, Berg D, Hungs M, Gobbele R, Berger K, Epplen JT, Riess O, Schöls L. Krüger R, et al. Among authors: riess o. Neurosci Lett. 2003 Nov 13;351(2):125-9. doi: 10.1016/s0304-3940(03)00903-0. Neurosci Lett. 2003. PMID: 14583397

9

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease.

Strauss KM, Martins LM, Plun-Favreau H, Marx FP, Kautzmann S, Berg D, Gasser T, Wszolek Z, Müller T, Bornemann A, Wolburg H, Downward J, Riess O, Schulz JB, Krüger R. Strauss KM, et al. Among authors: riess o. Hum Mol Genet. 2005 Aug 1;14(15):2099-111. doi: 10.1093/hmg/ddi215. Epub 2005 Jun 16. Hum Mol Genet. 2005. PMID: 15961413

10

Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease.

Abahuni N, Gispert S, Bauer P, Riess O, Krüger R, Becker T, Auburger G. Abahuni N, et al. Among authors: riess o. Neurosci Lett. 2007 Mar 6;414(2):126-9. doi: 10.1016/j.neulet.2006.12.053. Epub 2007 Jan 11. Neurosci Lett. 2007. PMID: 17267121

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