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Olaf Rieß (1959-)

Arzt

Name	Olaf Rieß
Time	1959- (Date of birth and death)
Place	Großenhain (Geburtsort) Rostock (Professor für Medizinische Genetik) (1999-2001) (Wirkungsort) Tübingen (Professor für Medizinische Genetik) (seit 2001-) (Wirkungsort) Deutschland
Gender	männlich
Academic degree	Prof. Dr. med.
Profession	Arzt (characteristic profession)
Variant	Olaf Riess Olaf Horst Riess
Related	Universität Rostock Eberhard Karls Universität Tübingen. Institut für Anthropologie und Humangenetik
Source	Internet
Record type	Person
GND-Identifier	120266008
Record ID	120266008
Involved in show all The parkin V380L variant is a genetic modifier of Machado–Joseph disease with impact on mitophagy Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings Model matchmaking via the Solve-RD Rare Disease Models & Mechanisms Network (RDMM-Europe) Genomes in clinical care Overexpression of human alpha-Synuclein leads to dysregulated microbiome/metabolites with ageing in a rat model of Parkinson disease TR-FRET-Based Immunoassay to Measure Ataxin-2 as a Target Engagement Marker in Spinocerebellar Ataxia Type 2 KPNB1 modulates the Machado–Joseph disease protein ataxin-3 through activation of the mitochondrial protease CLPP Recommendations for whole genome sequencing in diagnostics for rare diseases Calpains as novel players in the molecular pathogenesis of spinocerebellar ataxia type 17 PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot study A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 Dystonia Improved diagnosis of rare disease patients through systematic detection of runs of homozygosity Evidence for bidirectional and trans-synaptic parasympathetic and sympathetic propagation of alpha-synuclein in rats α-Synuclein in Parkinson’s disease: causal or bystander? Silhouette-Length-Scaled Gait Parameters for Motor Functional Analysis in Mice and Rats RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases Dynamic footprints of α-synucleinopathic mice recorded by CatWalk gait analysis Dynamic footprints of α-synucleinopathic mice recorded by CatWalk gait analysis = Dynamic footprints of [alpha]-synucleinopathic mice recorded by CatWalk gait analysis Early Alterations in Operant Performance and Prominent Huntingtin Aggregation in a Congenic F344 Rat Line of the Classical CAGn51trunc Model of Huntington Disease Qualitative und quantitative Analyse der Huntingtin-Aggregatbildung im transgenen Chorea-Huntington-Rattenmodell BACHD TG22 RD-connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases Capturing schizophrenia-like prodromal symptoms in a spinocerebellar ataxia-17 transgenic rat Overexpression of synphilin-1 promotes clearance of soluble and misfolded alpha-synuclein without restoring the motor phenotype in aged A30P transgenic mice Medizinische Genetik für die Praxis : Diagnostik, Beratung, Fallbeispiele Medizinische Genetik für die Praxis : Diagnostik, Beratung, Fallbeispiele Medizinische Genetik für die Praxis : Diagnostik, Beratung, Fallbeispiele First German Academy for Further Medical Training on Rare Diseases (FAKSE,http://www.fakse.info) Angewandte Humangenetik Indirect DNA/gene diagnoses via electrophoresis – an obsolete principle? Simple repetitive (GAA) n loci in the human genome Neurogenetik : molekulargenetische Diagnostik neurologischer und psychiatrischer Erkrankungen Genetic background of apparently idiopathic sporadic cerebellar ataxia Neurogenetik : Molekulargenetische Diagnostik neurologischer Erkrankungen Neurogenetik : molekulargenetische Diagnostik neurologischer Erkrankungen ; mit 59 Tabellen SCA2 trinucleotide expansion in German SCA patients Transmission distortion of the mutant alleles in spinocerebellar ataxia DNA-Diganostik in der Humangenetik : Voraussetzungen und Tendenzen Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25 Gene von Chromosom-4 des Menschen als Kandidaten für die Auslösung von Erkrankungen RELP-discordance within the human phenylalanine hydroxylase locus DNA-Analyse von Phenylketonuriefamilien mit einer menschlichen Phenylalaninhydroxylase-cDNA-Sonde zur Einführung der genomischen pränatalen Diagnostik bei der PKU

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Katalog der Deutschen Nationalbibliothek

Olaf Rieß (1959-)

The parkin V380L variant is a genetic modifier of Machado–Joseph disease with impact on mitophagy

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

Model matchmaking via the Solve-RD Rare Disease Models & Mechanisms Network (RDMM-Europe)

Genomes in clinical care

Overexpression of human alpha-Synuclein leads to dysregulated microbiome/metabolites with ageing in a rat model of Parkinson disease

TR-FRET-Based Immunoassay to Measure Ataxin-2 as a Target Engagement Marker in Spinocerebellar Ataxia Type 2

KPNB1 modulates the Machado–Joseph disease protein ataxin-3 through activation of the mitochondrial protease CLPP

Recommendations for whole genome sequencing in diagnostics for rare diseases

Calpains as novel players in the molecular pathogenesis of spinocerebellar ataxia type 17

PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot study

A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome

Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 Dystonia

Improved diagnosis of rare disease patients through systematic detection of runs of homozygosity

Evidence for bidirectional and trans-synaptic parasympathetic and sympathetic propagation of alpha-synuclein in rats

α-Synuclein in Parkinson’s disease: causal or bystander?

Silhouette-Length-Scaled Gait Parameters for Motor Functional Analysis in Mice and Rats

RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases

Dynamic footprints of α-synucleinopathic mice recorded by CatWalk gait analysis

Dynamic footprints of α-synucleinopathic mice recorded by CatWalk gait analysis = Dynamic footprints of [alpha]-synucleinopathic mice recorded by CatWalk gait analysis

Early Alterations in Operant Performance and Prominent Huntingtin Aggregation in a Congenic F344 Rat Line of the Classical CAGn51trunc Model of Huntington Disease

Qualitative und quantitative Analyse der Huntingtin-Aggregatbildung im transgenen Chorea-Huntington-Rattenmodell BACHD TG22

RD-connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases

Capturing schizophrenia-like prodromal symptoms in a spinocerebellar ataxia-17 transgenic rat

Overexpression of synphilin-1 promotes clearance of soluble and misfolded alpha-synuclein without restoring the motor phenotype in aged A30P transgenic mice

Medizinische Genetik für die Praxis : Diagnostik, Beratung, Fallbeispiele

Medizinische Genetik für die Praxis : Diagnostik, Beratung, Fallbeispiele

Medizinische Genetik für die Praxis : Diagnostik, Beratung, Fallbeispiele

First German Academy for Further Medical Training on Rare Diseases (FAKSE,http://www.fakse.info)

Angewandte Humangenetik

Indirect DNA/gene diagnoses via electrophoresis – an obsolete principle?

Simple repetitive (GAA) n loci in the human genome

Neurogenetik : molekulargenetische Diagnostik neurologischer und psychiatrischer Erkrankungen

Genetic background of apparently idiopathic sporadic cerebellar ataxia

Neurogenetik : Molekulargenetische Diagnostik neurologischer Erkrankungen

Neurogenetik : molekulargenetische Diagnostik neurologischer Erkrankungen ; mit 59 Tabellen

SCA2 trinucleotide expansion in German SCA patients

Transmission distortion of the mutant alleles in spinocerebellar ataxia

DNA-Diganostik in der Humangenetik : Voraussetzungen und Tendenzen

Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25

Gene von Chromosom-4 des Menschen als Kandidaten für die Auslösung von Erkrankungen

RELP-discordance within the human phenylalanine hydroxylase locus

DNA-Analyse von Phenylketonuriefamilien mit einer menschlichen Phenylalaninhydroxylase-cDNA-Sonde zur Einführung der genomischen pränatalen Diagnostik bei der PKU