Olaf Riess

发表

Genome search for susceptibility loci of common idiopathic generalised epilepsies.

T. Wienker, A. Sundquist, J. Prud'homme, 2000, Human molecular genetics.

SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene.

T. Klockgether, O. Riess, M. Macek, 1997, Human molecular genetics.

Cloning, sequencing and functional studies of the gene encoding human GTP cyclohydrolase I.

T. Werner, A. Bacher, O. Riess, 1996, Gene.

Extrapyramidal motor signs in degenerative ataxias.

R. Krüger, L. Schöls, H. Przuntek, 2000, Archives of neurology.

Replication Analysis of a Putative Susceptibility Locus (EGI) for Idiopathic Generalized Epilepsy on Chromosome 8q24

J. Epplen, G. Bauer, H. Schulz, 1998, Epilepsia.

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

M. Hayden, O. Riess, A. Noerremoelle, 1992, American journal of human genetics.

DNA analysis of Huntington’s disease

G. Schluter, C. Zühlke, D. Morris-Rosendahl, 1999, Neurology.

The α1-antichymotrypsin A-allele in German Parkinson disease patients

R. Krüger, M. Graeber, E. Grasbon-Frodl, 1999, Journal of Neural Transmission.

Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's disease.

R. Krüger, D. Berg, H. Przuntek, 2000, Neuroreport.

Spinocerebellar ataxia type 1: clinical and neurophysiological characteristics in German kindreds

L. Schöls, H. Przuntek, O. Riess, 1995, Acta neurologica Scandinavica.

Familial parkinsonism with synuclein pathology

R. Krüger, L. Schöls, K. Leenders, 2001, Neurology.

Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's disease

R. Krüger, L. Schöls, H. Przuntek, 2003, Journal of Neural Transmission.

Parkinson's disease--a multifactorial neurodegenerative disorder.

R. Krüger, O. Riess, Olaf Riess, 1999, Journal of neural transmission. Supplementum.

Spinocerebellar Ataxia Type 2: Genotype and Phenotype in German Kindreds

S. Pulst, L. Schöls, H. Przuntek, 1997 .

Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy.

A. Ziegler, O. Riess, J. Epplen, 1999, American journal of medical genetics.

Confidence intervals for predicted age of onset, given the size of (CAG)n repeat, in Huntington's disease

S. Hazout, F. Loirat, J. Epplen, 1995, Human Genetics.

Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study.

Í. Lopes-Cendes, S. Tsuji, A. Brice, 2001, American journal of human genetics.

Genetic dissection of familial Parkinson's disease.

R. Krüger, O. Riess, R. Jakes, 1998, Molecular medicine today.

Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease

R. Krüger, P. Bauer, D. Berg, 2004, Neurology.

Relationships of the 2642 deletion polymorphism (delta 2642) in the huntingtin gene with the CAG repeat expansion length and age at onset of the disease.

P. Roubertoux, I. Schmitt, G. Lucotte, 1996, Genetic counseling.

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6

T. Wienker, A. Ziegler, O. Riess, 1997, Neurology.

Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients.

L. Schöls, H. Przuntek, O. Riess, 1995, Human molecular genetics.

Expression of the Huntington disease gene in rodents: cloning the rat homologue and evidence for downregulation in non-neuronal tissues during development.

O. Riess, H. Hameister, J. Epplen, 1995, Human molecular genetics.

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

K. Fenger, O. Riess, J. Epplen, 1993, Human molecular genetics.

Polymorphisms of the α-synuclein promoter: expression analyses and association studies in Parkinson's disease

R. Krüger, L. Schöls, K. Berger, 2003, Journal of Neural Transmission.

Characterization of a human chromosome 4 flow-sorted cosmid library.

L. Deaven, O. Riess, J. Epplen, 1994, Cytogenetics and cell genetics.