Norbert Brüggemann

Norbert Brüggemann publication distribution in Neuroscience in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Neuroscience in 2026. The highlighted bar marks where Norbert Brüggemann sits on this spectrum.

Norbert Brüggemann D-index placement in Neuroscience in 2026

The chart shows the D-index (discipline H-index) distribution of Neuroscience scientists ranked by Research.com in 2026. The highlighted bar marks where Norbert Brüggemann sits on this spectrum.

Best Publications

• Clinical manifestations of the anti-IgLON5 disease.

  Carles Gaig;Francesc Graus;Yarko Compta;Birgit Högl

  412
  Citations

• An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA50/ATX-FGF14.

  Unknown

  199
  Citations

• Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study.

  Ana Djarmati;Susanne A Schneider;Katja Lohmann;Susen Winkler

  194
  Citations

• Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene

  Katja Lohmann;Robert A. Wilcox;Susen Winkler;Alfredo Ramirez;Alfredo Ramirez

  182
  Citations

• Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects

  Eunju Seong;Ryan Insolera;Marija Dulovic;Erik Jan Kamsteeg

  177
  Citations

• Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism.

  Max Borsche;Inke R König;Sylvie Delcambre;Simona Petrucci;Simona Petrucci

  172
  Citations

• Etiology of musician's dystonia: familial or environmental?

  A. Schmidt;H. C. Jabusch;H. C. Jabusch;E. Altenmüller;J. Hagenah

  150
  Citations

• Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystonia

  Norbert Brüggemann;Andrea Kühn;Susanne A. Schneider;Christoph Kamm

  139
  Citations

• Dopa-responsive dystonia revisited: diagnostic delay, residual signs, and nonmotor signs.

  Vera Tadic;Meike Kasten;Norbert Brüggemann;Sophie Stiller

  134
  Citations

• Clinical spectrum of Kufor-Rakeb syndrome in the Chilean kindred with ATP13A2 mutations.

  Maria I. Behrens;Maria I. Behrens;Norbert Brüggemann;Pedro Chana;Pablo Venegas

  127
  Citations

• Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease.

  Carles Gaig;Yaroslau Compta;Anna Heidbreder;Maria J Marti

  107
  Citations

• The Rostock International Parkinson's Disease (ROPAD) Study: Protocol and Initial Findings.

  Volha Skrahina;Hanaa Gaber;Eva-Juliane Vollstedt;Toni M Förster

  103
  Citations

• Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype.

  Norbert Brüggemann;Johann Hagenah;Kathrin Reetz;Alexander Schmidt

  99
  Citations

• Mutations in GNAL: A Novel Cause of Craniocervical Dystonia

  Kishore R. Kumar;Katja Lohmann;Ikuo Masuho;Ryosuke Miyamoto

  97
  Citations

• Nonmotor symptoms in genetic Parkinson disease.

  Meike Kasten;Lena Kertelge;Norbert Brüggemann;Joyce van der Vegt

  96
  Citations

• Gaucher Disease Ascertained through a Parkinson’s Center: Imaging and Clinical Characterization

  Rachel Saunders‐Pullman;Rachel Saunders‐Pullman;Johann Hagenah;Vijay Dhawan;Kaili Stanley

  95
  Citations

• Dominantly transmitted focal dystonia in families of patients with musician’s cramp

  A. Schmidt;H. C. Jabusch;E. Altenmüller;J. Hagenah

  94
  Citations

• Psychiatric associations of adult-onset focal dystonia phenotypes

  Brian D. Berman;Johanna Junker;Erika Shelton;Stefan H. Sillau

  93
  Citations

• A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism.

  Ana Westenberger;Charles Jourdan Reyes;Gerard Saranza;Valerija Dobricic

  88
  Citations

• ATP13A2 variants in early-onset Parkinson's disease patients and controls.

  Ana Djarmati;Johann Hagenah;Kathrin Reetz;Susen Winkler

  84
  Citations