Riess O - Search Results

1

Genome-wide association study reveals genetic risk underlying Parkinson's disease.

Simón-Sánchez J, Schulte C, Bras JM, Sharma M, Gibbs JR, Berg D, Paisan-Ruiz C, Lichtner P, Scholz SW, Hernandez DG, Krüger R, Federoff M, Klein C, Goate A, Perlmutter J, Bonin M, Nalls MA, Illig T, Gieger C, Houlden H, Steffens M, Okun MS, Racette BA, Cookson MR, Foote KD, Fernandez HH, Traynor BJ, Schreiber S, Arepalli S, Zonozi R, Gwinn K, van der Brug M, Lopez G, Chanock SJ, Schatzkin A, Park Y, Hollenbeck A, Gao J, Huang X, Wood NW, Lorenz D, Deuschl G, Chen H, Riess O, Hardy JA, Singleton AB, Gasser T. Simón-Sánchez J, et al. Among authors: riess o. Nat Genet. 2009 Dec;41(12):1308-12. doi: 10.1038/ng.487. Epub 2009 Nov 15. Nat Genet. 2009. PMID: 19915575 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

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

4

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.

5

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

6

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.

7

Specification of 14-3-3 proteins in Lewy bodies.

Berg D, Riess O, Bornemann A. Berg D, et al. Among authors: riess o. Ann Neurol. 2003 Jul;54(1):135. doi: 10.1002/ana.10621. Ann Neurol. 2003. PMID: 12838532 No abstract available.

8

14-3-3 proteins in the nervous system.

Berg D, Holzmann C, Riess O. Berg D, et al. Among authors: riess o. Nat Rev Neurosci. 2003 Sep;4(9):752-62. doi: 10.1038/nrn1197. Nat Rev Neurosci. 2003. PMID: 12951567 Review. No abstract available.

9

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

10

Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7).

Hering R, Strauss KM, Tao X, Bauer A, Woitalla D, Mietz EM, Petrovic S, Bauer P, Schaible W, Müller T, Schöls L, Klein C, Berg D, Meyer PT, Schulz JB, Wollnik B, Tong L, Krüger R, Riess O. Hering R, et al. Among authors: riess o. Hum Mutat. 2004 Oct;24(4):321-9. doi: 10.1002/humu.20089. Hum Mutat. 2004. PMID: 15365989

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

527 results

Search Page