Riess O - Search Results

1

Allelic distribution of CTG18.1 in Caucasian populations: association studies in bipolar disorder, schizophrenia, and ataxia.

McInnis MG, Swift-Scanlanl T, Mahoney AT, Vincent J, Verheyen G, Lan TH, Oruc L, Riess O, Van Broeckhoven C, Chen H, Kennedy JL, MacKinnon DF, Margolis RL, Simpson SG, McMahon FJ, Gershon E, Nurnberger J, Reich T, DePaulo JR, Ross CA. McInnis MG, et al. Among authors: riess o. Mol Psychiatry. 2000 Jul;5(4):439-42. doi: 10.1038/sj.mp.4000747. Mol Psychiatry. 2000. PMID: 10889556

2

Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.

Holmes SE, O'Hearn EE, McInnis MG, Gorelick-Feldman DA, Kleiderlein JJ, Callahan C, Kwak NG, Ingersoll-Ashworth RG, Sherr M, Sumner AJ, Sharp AH, Ananth U, Seltzer WK, Boss MA, Vieria-Saecker AM, Epplen JT, Riess O, Ross CA, Margolis RL. Holmes SE, et al. Among authors: o hearn ee, riess o. Nat Genet. 1999 Dec;23(4):391-2. doi: 10.1038/70493. Nat Genet. 1999. PMID: 10581021 No abstract available.

3

Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.

Schöls L, Krüger R, Amoiridis G, Przuntek H, Epplen JT, Riess O. Schöls L, et al. Among authors: riess o. J Neurol Neurosurg Psychiatry. 1998 Jan;64(1):67-73. doi: 10.1136/jnnp.64.1.67. J Neurol Neurosurg Psychiatry. 1998. PMID: 9436730 Free PMC article.

4

CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2).

Hayes S, Turecki G, Brisebois K, Lopes-Cendes I, Gaspar C, Riess O, Ranum LP, Pulst SM, Rouleau GA. Hayes S, et al. Among authors: riess o. Hum Mol Genet. 2000 Jul 22;9(12):1753-8. doi: 10.1093/hmg/9.12.1753. Hum Mol Genet. 2000. PMID: 10915763

5

Genetic background of apparently idiopathic sporadic cerebellar ataxia.

Schöls L, Szymanski S, Peters S, Przuntek H, Epplen JT, Hardt C, Riess O. Schöls L, et al. Among authors: riess o. Hum Genet. 2000 Aug;107(2):132-7. doi: 10.1007/s004390000346. Hum Genet. 2000. PMID: 11030410

6

Avoiding errors in the diagnosis of (CAG)n expansion in the huntingtin gene.

Holzmann C, Saecker AM, Epplen JT, Riess O. Holzmann C, et al. Among authors: riess o. J Med Genet. 1997 Mar;34(3):264. doi: 10.1136/jmg.34.3.264. J Med Genet. 1997. PMID: 9132504 Free PMC article. No abstract available.

7

Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German origin.

Zühlke C, Riess O, Schröder K, Siedlaczck I, Epplen JT, Engel W, Thies U. Zühlke C, et al. Among authors: riess o. Hum Mol Genet. 1993 Sep;2(9):1467-9. doi: 10.1093/hmg/2.9.1467. Hum Mol Genet. 1993. PMID: 8242072 No abstract available.

8

Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease.

Riess O, Noerremoelle A, Soerensen SA, Epplen JT. Riess O, et al. Hum Mol Genet. 1993 Sep;2(9):1523. Hum Mol Genet. 1993. PMID: 8242095 No abstract available.

9

Toward the complete genomic map and molecular pathology of human chromosome 4.

Riess O, Winkelmann B, Epplen JT. Riess O, et al. Hum Genet. 1994 Jul;94(1):1-18. doi: 10.1007/BF02272834. Hum Genet. 1994. PMID: 8034286 Review.

10

Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish families.

Nørremølle A, Riess O, Epplen JT, Fenger K, Hasholt L, Sørensen SA. Nørremølle A, et al. Among authors: riess o. Hum Mol Genet. 1993 Sep;2(9):1475-6. doi: 10.1093/hmg/2.9.1475. Hum Mol Genet. 1993. PMID: 8242074

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