Olaf Riess

Olaf Riess

Eberhard Karls Universität Tübingen

H-index: 98

Europe-Germany

Contact Olaf Riess

About Olaf Riess

Olaf Riess, With an exceptional h-index of 98 and a recent h-index of 55 (since 2020), a distinguished researcher at Eberhard Karls Universität Tübingen, specializes in the field of Humangenetik.

His recent articles reflect a diverse array of research interests and contributions to the field:

RFC1 repeat expansions in downbeat nystagmus syndromes: frequency and phenotypic profile

Community effort to unravel the complex human neuronal landscape exemplified for the striatum

Diagnostic genome sequencing improves diagnostic yield: a prospective single-centre study in 1000 patients with inherited eye diseases

Stage‐dependent biomarker changes in spinocerebellar ataxia type 3

Augmenting MEK inhibitor efficacy in BRAF wild-type melanoma: synergistic effects of disulfiram combination therapy

A further case of AFG2B‐related neurodevelopmental disorder with hearing loss and microcephaly allows further clarification of pathogenicity of the variant c.1313T …

A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy

Resequencing the complete SNCA locus in Indian patients with Parkinson’s disease

Olaf Riess Information

University	Eberhard Karls Universität Tübingen
Position	Professor der Humangenetik
Citations(all)	41071
Citations(since 2020)	14359
Cited By	30548
hIndex(all)	98
hIndex(since 2020)	55
i10Index(all)	387
i10Index(since 2020)	249
Email	Access Email
University Profile Page	Eberhard Karls Universität Tübingen
Google Scholar	View Google Scholar Profile

Olaf Riess Skills & Research Interests

Humangenetik

Top articles of Olaf Riess

RFC1 repeat expansions in downbeat nystagmus syndromes: frequency and phenotypic profile

Journal of Neurology

2024/2/21

Olaf Riess

H-Index: 50

Community effort to unravel the complex human neuronal landscape exemplified for the striatum

2024/2/20

Joachim Schultze

H-Index: 58

Stefan Czemmel

H-Index: 12

Matthias Becker

H-Index: 4

Lorenzo Bonaguro

H-Index: 5

Sören Franzenburg

H-Index: 11

Andreas Dahl

H-Index: 32

Thomas Ulas

H-Index: 27

Diagnostic genome sequencing improves diagnostic yield: a prospective single-centre study in 1000 patients with inherited eye diseases

Journal of Medical Genetics

2024/2/1

Olaf Riess

H-Index: 50

Stage‐dependent biomarker changes in spinocerebellar ataxia type 3

Annals of neurology

2024/2

Moritz Berger

H-Index: 2

Patrick Silva

H-Index: 0

Gulin Oz

H-Index: 28

Olaf Riess

H-Index: 50

Matthias Schmid

H-Index: 2

Augmenting MEK inhibitor efficacy in BRAF wild-type melanoma: synergistic effects of disulfiram combination therapy

Journal of Experimental & Clinical Cancer Research

2024/1/23

Lukas Flatz

H-Index: 24

Boris Macek

H-Index: 41

Thomas Eigentler

H-Index: 45

A further case of AFG2B‐related neurodevelopmental disorder with hearing loss and microcephaly allows further clarification of pathogenicity of the variant c.1313T …

Molecular Genetics & Genomic Medicine

2024/1

Olaf Riess

H-Index: 50

A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy

Nature Genetics

2024/4/29

Naseebullah Kakar

H-Index: 12

Thomas Klopstock

H-Index: 52

Olaf Riess

H-Index: 50

Resequencing the complete SNCA locus in Indian patients with Parkinson’s disease

npj Parkinson's Disease

2024/4/15

Ravi Yadav

H-Index: 5

Peter Bauer

H-Index: 15

Olaf Riess

H-Index: 50

Manu Sharma

H-Index: 8

A Novel PINK1 p.F385S Loss‐of‐Function Mutation in an Indian Family with Parkinson's Disease

Movement Disorders

2024/4/8

Karan Sharma

H-Index: 1

Francesco Raimondi

H-Index: 18

Olaf Riess

H-Index: 50

Manu Sharma

H-Index: 8

Genomes in clinical care

2024/3/14

Olaf Riess

H-Index: 50

Christopher Schroeder

H-Index: 5

p62, the Receptor for Selective Autophagy, Contributes in ATXN3 Aggregate Formation in Spinocerebellar Ataxia Type 3

2024/3/7

Jonasz Jeremiasz Weber

H-Index: 11

Olaf Riess

H-Index: 50

Blood and cerebellar abundance of ATXN3 splice variants in spinocerebellar ataxia type 3/Machado-Joseph disease

Neurobiology of Disease

2024/2/27

Rebecca Tagett

H-Index: 12

Olaf Riess

H-Index: 50

ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations

Brain

2024/2/22

Lucia Laugwitz

H-Index: 5

Helen Cox

H-Index: 40

Stephanie Efthymiou

H-Index: 14

David Murphy

H-Index: 10

Faisal Zafar

H-Index: 2

Hamid Ghaedi

H-Index: 16

Mina Zamani

H-Index: 6

Samira Molaei Ramshe

H-Index: 1

Ali Zare

H-Index: 1

Behnam Alipoor

H-Index: 13

Olaf Riess

H-Index: 50

Reza Maroofian

H-Index: 16

UV-radiation and MC1R germline mutations are risk factors for the development of conventional and spitzoid melanomas in children and adolescents

EBioMedicine

2023/10/1

Hannah Wild

H-Index: 5

Christian Seitz

H-Index: 2

Olaf Riess

H-Index: 50

Christopher Schroeder

H-Index: 5

Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patients

European Journal of Human Genetics

2023/10

Christopher Schroeder

H-Index: 5

Peter Lang

H-Index: 2

Julia Skokowa

H-Index: 18

Olaf Riess

H-Index: 50

Embracing monogenic Parkinson's disease: the MJFF Global Genetic PD cohort

Movement Disorders

2023/2

Stanley Fahn

H-Index: 8

Norbert Brüggemann

H-Index: 25

Max Borsche

H-Index: 4

Leonidas Stefanis

H-Index: 39

Pablo Mir

H-Index: 35

David Crosiers

H-Index: 15

Kenya Nishioka

H-Index: 21

Manabu Funayama

H-Index: 25

Marta Camacho

H-Index: 7

Pichet Termsarasab

H-Index: 13

Andreas Puschmann

H-Index: 24

Mathias Toft

H-Index: 26

Anthony E Lang

H-Index: 97

Vitor Tumas

H-Index: 23

Juliane Winkelmann

H-Index: 51

Mika Martikainen

H-Index: 13

Olaf Riess

H-Index: 50

Enza Maria Valente

H-Index: 45

Kathrin Brockmann

H-Index: 30

Christine Klein

H-Index: 57

Blood transcriptome sequencing identifies biomarkers able to track disease stages in spinocerebellar ataxia type 3

Brain

2023/10

Olaf Riess

H-Index: 50

Frequency and Phenotype of RFC1 Repeat Expansions in Bilateral Vestibulopathy

Neurology

2023/9/5

Muhammad Bilal

H-Index: 1

Olaf Riess

H-Index: 50

Andreas Zwergal

H-Index: 23

TMB and BRAF mutation status are independent predictive factors in high-risk melanoma patients with adjuvant anti-PD-1 therapy

Journal of Cancer Research and Clinical Oncology

2023/2

Christopher Schroeder

H-Index: 5

Thomas Eigentler

H-Index: 45

Lukas Flatz

H-Index: 24

Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

Human Genetics and Genomics Advances

2023/4/13

Karen Low

H-Index: 6

Simon Lovell

H-Index: 25

E Williams

H-Index: 18

Olaf Riess

H-Index: 50

Christoph Kessler

H-Index: 13

Hans Scheffer

H-Index: 39

Alexander Hoischen

H-Index: 56

Christian Gilissen

H-Index: 58

Colin Veal

H-Index: 14

Spencer Gibson

H-Index: 32

Mehdi Mehtarizadeh

H-Index: 1

Volker Straub

H-Index: 56

Siddharth Banka

H-Index: 33

Yannis Duffourd

H-Index: 23

See List of Professors in Olaf Riess University(Eberhard Karls Universität Tübingen)

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