A polymorphic DNA marker at the D10S106 locus

Por Weber, B., Riess, O., Hayden, M.R.
Publicado em 1991

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

Por Holzmann, C, Saecker, A M, Epplen, J T, Riess, O
Publicado em 1997

A polymorphic DNA marker at the D8S131 locus

Por Weber, B., Riess, O., Kreklywich, C.N., Wood, S., Hayden, M.R.
Publicado em 1991

Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation.

Por Schöls, L, Amoiridis, G, Epplen, J T, Langkafel, M, Przuntek, H, Riess, O
Publicado em 1996

The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosa.

Por Riess, O, Noerremoelle, A, Weber, B, Musarella, M A, Hayden, M R
Publicado em 1992

Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds

Por Schols, L., Kruger, R., Amoiridis, G., Przuntek, H., Epplen, J., Riess, O.
Publicado em 1998

Isolation and characterization of the rat huntingtin promoter.

Por Holzmann, C, Mäueler, W, Petersohn, D, Schmidt, T, Thiel, G, Epplen, J T, Riess, O
Publicado em 1998

Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease region.

Por Weber, B, Hedrick, A, Andrew, S, Riess, O, Collins, C, Kowbel, D, Hayden, M R
Publicado em 1992

Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS)

Por WIECZOREK, D., KRAUSE, M., MAJEWSKI, F., ALBRECHT, B., MEINECKE, P., RIESS, O., GILLESSEN-KAESBAC..., G.
Publicado em 2000

Mirror-Image Asymmetry in Monozygotic Twins with Kabuki Syndrome

Por Riess, A., Dufke, A., Riess, O., Beck-Woedl, S., Fode, B., Skladny, H., Klaes, R., Tzschach, A.
Publicado em 2012

Machado-Joseph disease mutations as the genetic basis of most spinocerebellar ataxias in Germany.

Por Schöls, L, Amoiridis, G, Langkafel, M, Büttner, T, Przuntek, H, Riess, O, Vieira-Saecker, A M, Epplen, J T
Publicado em 1995

Genomic organization and complete sequence of the human gene encoding the beta-subunit of the cGMP phosphodiesterase and its localisation to 4p 16.3.

Por Weber, B, Riess, O, Hutchinson, G, Collins, C, Lin, B Y, Kowbel, D, Andrew, S, Schappert, K, Hayden, M R
Publicado em 1991

Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.

Por Fang, Y Y, Eyre, H J, Bohlander, S K, Estop, A, McPherson, E, Träger, T, Riess, O, Callen, D F
Publicado em 1995

Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD)

Por Klockgether, T., Schols, L., Abele, M., Burk, K., Topka, H., Andres, F., Amoiridis, G., Ludtke, R., Riess, O., Laccone, F., Dichgans, J.
Publicado em 1999

Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype

Por Bauer, P, Laccone, F, Rolfs, A, Wullner, U, Bosch, S, Peters, H, Liebscher, S, Scheible, M, Epplen, J, Weber, B, Holinski-Feder, E, Weirich-Schwaiger, H, Morris-Rosendahl, D, Andrich, J, Riess, O
Publicado em 2004

Mitochondrial proteolytic stress induced by loss of mortalin function is rescued by Parkin and PINK1

Por Burbulla, L F, Fitzgerald, J C, Stegen, K, Westermeier, J, Thost, A-K, Kato, H, Mokranjac, D, Sauerwald, J, Martins, L M, Woitalla, D, Rapaport, D, Riess, O, Proikas-Cezanne, T, Rasse, T M, Krüger, R
Publicado em 2014

Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias

Por Matilla-Dueñas, A., Ashizawa, T., Brice, A., Magri, S., McFarland, K. N., Pandolfo, M., Pulst, S. M., Riess, O., Rubinsztein, D. C., Schmidt, J., Schmidt, T., Scoles, D. R., Stevanin, G., Taroni, F., Underwood, B. R., Sánchez, I.
Publicado em 2014

Ancestral Origins of the Machado-Joseph Disease Mutation: A Worldwide Haplotype Study

Por Gaspar, C., Lopes-Cendes, I., Hayes, S., Goto, J., Arvidsson, K., Dias, A., Silveira, I., Maciel, P., Coutinho, P., Lima, M., Zhou, Y.-X., Soong, B.-W., Watanabe, M., Giunti, P., Stevanin, G., Riess, O., Sasaki, H., Hsieh, M., Nicholson, G. A., Brunt, E., Higgins, J. J., Lauritzen, M., Tranebjaerg, L., Volpini, V., Wood, N., Ranum, L., Tsuji, S., Brice, A., Sequeiros, J., Rouleau, G. A.
Publicado em 2001