2026 Maria Stamelou: Neuroscience Researcher – H-Index, Publications & Awards

Discipline name	D-Index	World Ranking	Current World Ranking	National Ranking	Current National Ranking	Publications	Citations
Neuroscience	55	4639	4267	3	3	269	15494

Discipline name

D-Index

World Ranking

Current World Ranking

National Ranking

Current National Ranking

Publications

Citations

Neuroscience

4639

4267

269

15494

Research.com Recognitions

2026 - Research.com Neuroscience in Greece Leader Award

Best Publications

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

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

2243
Citations
Consensus Statement on the classification of tremors. from the task force on tremor of the International Parkinson and Movement Disorder Society

Kailash P Bhatia;Peter Bain;Nin Bajaj;Rodger J Elble

1429
Citations
The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy

Unknown

905
Citations
Past, present, and future of Parkinson's disease: A special essay on the 200th Anniversary of the Shaking Palsy

J.A. Obeso;M. Stamelou;M. Stamelou;C.G. Goetz;W. Poewe

890
Citations
Dopaminergic reward system: a short integrative review

Oscar Arias-Carrión;Oscar Arias-Carrión;Maria Stamelou;Eric Murillo-Rodríguez;Manuel Menéndez-González

586
Citations
The phenotypic spectrum of progressive supranuclear palsy: a retrospective multicenter study of 100 definite cases.

Gesine Respondek;Gesine Respondek;Gesine Respondek;Maria Stamelou;Maria Stamelou;Carolin Kurz;Carolin Kurz;Leslie W Ferguson

402
Citations
Reward Pays the Cost of Noise Reduction in Motor and Cognitive Control.

Sanjay G. Manohar;Trevor T.-J. Chong;Trevor T.-J. Chong;Matthew A.J. Apps;Matthew A.J. Apps;Amit Batla

360
Citations
The non-motor syndrome of primary dystonia: clinical and pathophysiological implications.

Maria Stamelou;Mark J. Edwards;Mark Hallett;Kailash P. Bhatia

347
Citations
Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis.

Gavin Charlesworth;Vincent Plagnol;Kira M. Holmström;Jose Bras

287
Citations
Radiological biomarkers for diagnosis in PSP: Where are we and where do we need to be?

Jennifer L Whitwell;Günter U Höglinger;Günter U Höglinger;Angelo Antonini;Yvette Bordelon

247
Citations
The expanding universe of disorders of the basal ganglia

Jose A Obeso;Maria C Rodriguez-Oroz;Maria Stamelou;Maria Stamelou;Kailash P Bhatia

233
Citations
Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers

Niccolò E. Mencacci;Niccolò E. Mencacci;Ioannis U. Isaias;Martin M. Reich;Christos Ganos;Christos Ganos

221
Citations
PRRT2 gene mutations: From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine

Alice R. Gardiner;Kailash P. Bhatia;Maria Stamelou;Russell C. Dale

206
Citations
AFQ056 treatment of levodopa-induced dyskinesias: Results of 2 randomized controlled trials

Daniela Berg;Jana Godau;Claudia Trenkwalder;Karla Eggert

195
Citations
Which Ante Mortem Clinical Features Predict Progressive Supranuclear Palsy Pathology

Gesine Respondek;Carolin Kurz;Thomas Arzberger;Yaroslau Compta

193
Citations
The clinical and genetic heterogeneity of paroxysmal dyskinesias.

Alice R. Gardiner;Fatima Jaffer;Russell C. Dale;Robyn Labrum

181
Citations
What do patients with scans without evidence of dopaminergic deficit (SWEDD) have? New evidence and continuing controversies

Roberto Erro;Susanne A Schneider;Maria Stamelou;Niall P Quinn

161
Citations
Continuous jejunal levodopa infusion in patients with advanced parkinson disease: practical aspects and outcome of motor and non-motor complications.

Karla Eggert;Christoph Schrader;Michaela Hahn;Maria Stamelou

158
Citations
Dystonia with Brain Manganese Accumulation Resulting From SLC30A10 Mutations: A New Treatable Disorder

Maria Stamelou;Karin Tuschl;W. K. Chong;Andrew K. Burroughs

158
Citations
Differentiation of neurodegenerative parkinsonian syndromes by volumetric magnetic resonance imaging analysis and support vector machine classification.

Hans-Jürgen Huppertz;Leona Möller;Martin Südmeyer;Rüdiger Hilker

148
Citations

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Maria Stamelou

D-Index & Metrics

D-Index & Metrics

Neuroscience

Research.com Recognitions

Best Publications

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

Consensus Statement on the classification of tremors. from the task force on tremor of the International Parkinson and Movement Disorder Society

The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy

Past, present, and future of Parkinson's disease: A special essay on the 200th Anniversary of the Shaking Palsy

Dopaminergic reward system: a short integrative review

The phenotypic spectrum of progressive supranuclear palsy: a retrospective multicenter study of 100 definite cases.

Reward Pays the Cost of Noise Reduction in Motor and Cognitive Control.

The non-motor syndrome of primary dystonia: clinical and pathophysiological implications.

Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis.

Radiological biomarkers for diagnosis in PSP: Where are we and where do we need to be?

The expanding universe of disorders of the basal ganglia

Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers

PRRT2 gene mutations: From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine

AFQ056 treatment of levodopa-induced dyskinesias: Results of 2 randomized controlled trials

Which Ante Mortem Clinical Features Predict Progressive Supranuclear Palsy Pathology

The clinical and genetic heterogeneity of paroxysmal dyskinesias.

What do patients with scans without evidence of dopaminergic deficit (SWEDD) have? New evidence and continuing controversies

Continuous jejunal levodopa infusion in patients with advanced parkinson disease: practical aspects and outcome of motor and non-motor complications.

Dystonia with Brain Manganese Accumulation Resulting From SLC30A10 Mutations: A New Treatable Disorder

Differentiation of neurodegenerative parkinsonian syndromes by volumetric magnetic resonance imaging analysis and support vector machine classification.

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