World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
100
Citations
33642
World Ranking
756
National Ranking
375

Medicine

D-Index
103
Citations
34891
World Ranking
7424
National Ranking
3881

Overview

Ulrich Müller is affiliated with Johns Hopkins University School of Medicine in the United States. Their research focus spans the fields of Biochemistry, Genetics and Molecular Biology, and Neuroscience, with particular emphasis on Neurology, Genetics, and Molecular Biology as subfields. They have contributed substantially to topics such as Parkinson's Disease Mechanisms and Treatments, Neurological Diseases and Metabolism, RNA Regulation and Disease, Genetic Neurodegenerative Diseases, Genomics and Rare Diseases, Genetics and Neurodevelopmental Disorders, and Mitochondrial Function and Pathology.

Ulrich Müller's recent publications include:

  • Spinocerebellar ataxias (SCAs) caused by common mutations, 2021, Neurogenetics
  • Identifying genetic modifiers of age-associated penetrance in X-linked dystonia-parkinsonism, 2021, Nature Communications
  • Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes, 2024, Nature Communications
  • Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy, 2024, Molecular Neurodegeneration
  • Mutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxia, 2021, Journal of Neurology

The scientist frequently collaborates with the following coauthors:

  • Günter U. Höglinger
  • Dennis W. Dickson
  • Owen A. Ross
  • Kurt Farrell
  • Timothy S. Chang

Ulrich Müller's work is primarily published in these venues:

  • Nature Communications
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Molecular Neurodegeneration
  • Movement Disorders
  • Schwäbische Heimat

Best Publications

  • Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria

    Günter U Höglinger;Gesine Respondek;Maria Stamelou;Carolin Kurz

  • Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

    Stephan Niemann;Ulrich Müller

  • A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

    Ethylin Wang Jabs;Ulrich Müller;Xiang Li;Liang Ma

  • Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells.

    Piotr Kazmierczak;Hirofumi Sakaguchi;Joshua Tokita;Elizabeth M. Wilson-Kubalek

  • Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

    Günter U. Höglinger;Nadine M. Melhem;Dennis W. Dickson;Patrick M A Sleiman

  • β1-Class Integrins Regulate the Development of Laminae and Folia in the Cerebral and Cerebellar Cortex

    Diana Graus-Porta;Sandra Blaess;Mathias Senften;Amanda Littlewood-Evans

  • Specific interference with gene expression induced by long, double-stranded RNA in mouse embryonal teratocarcinoma cell lines

    Eric Billy;Vincent Brondani;Haidi Zhang;Ulrich Müller

  • Microarrayed allergen molecules: diagnostic gatekeepers for allergy treatment.

    Reinhard Hiller;Sylvia Laffer;Christian Harwanegg;Martin Huber

  • Cadherin 23 is a component of the tip link in hair-cell stereocilia.

    Jan Siemens;Concepcion Lillo;Rachel A. Dumont;Anna Reynolds

  • Targeted disruption of β1-integrin in a transgenic mouse model of human breast cancer reveals an essential role in mammary tumor induction

    Donald E. White;Natasza A. Kurpios;Dongmei Zuo;John A. Hassell

  • Mechanotransduction by Hair Cells: Models, Molecules, and Mechanisms

    Peter G. Gillespie;Ulrich Müller

  • Friedreich's ataxia: Point mutations and clinical presentation of compound heterozygotes

    Mireille Cossée;A Dürr;M. Schmitt;N Dahl

  • Extracellular Matrix: Functions in the Nervous System

    Claudia S. Barros;Santos J. Franco;Ulrich Müller

  • Integrin α8β1 Is Critically Important for Epithelial–Mesenchymal Interactions during Kidney Morphogenesis

    Ulrich Müller;Denan Wang;Sumiko Denda;Juanito J. Meneses

  • β1 Integrins Regulate Myoblast Fusion and Sarcomere Assembly

    Martin Schwander;Marco Leu;Michael Stumm;Olivier M. Dorchies

  • HOMOZYGOUS WNT3 MUTATION CAUSES TETRA-AMELIA IN A LARGE CONSANGUINEOUS FAMILY

    Stephan Niemann;Chengfeng Zhao;Filon Pascu;Ulrich Stahl

  • Conditional disruption of β1 integrin in Schwann cells impedes interactions with axons

    M. Laura Feltri;Diana Graus Porta;Stefano C. Previtali;Alessandro Nodari

  • Reelin, Disabled 1, and β1 integrins are required for the formation of the radial glial scaffold in the hippocampus

    Eckart Förster;Albrecht Tielsch;Barbara Saum;Karl Heinz Weiss

  • Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells

    Christian Söllner;Gerd-Jörg Rauch;Jan Siemens;Robert Geisler

  • Fate-Restricted Neural Progenitors in the Mammalian Cerebral Cortex

    Santos J. Franco;Cristina Gil-Sanz;Isabel Martinez-Garay;Ana Espinosa

Frequent Co-Authors

Günter U. Höglinger
Günter U. Höglinger Ludwig Maximilian University of Munich
Gerard D. Schellenberg
Gerard D. Schellenberg University of Pennsylvania
Anthony P. Monaco
Anthony P. Monaco Tufts University
Ole A. Andreassen
Ole A. Andreassen Oslo University Hospital
John B. Mulliken
John B. Mulliken Boston Children's Hospital
Christopher L. Cunningham
Christopher L. Cunningham University of Pittsburgh
Louis F. Reichardt
Louis F. Reichardt University of California, San Francisco
Nicola T. Lautenschlager
Nicola T. Lautenschlager University of Melbourne
Jamel Chelly
Jamel Chelly Institute of Genetics and Molecular and Cellular Biology
Bechara Kachar
Bechara Kachar National Institutes of Health

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