Author

Paulina Cunha

Observed names: Cunha, Paulina R, Paulina R Cunha, Paulina Rodrigues Cunha

Institutions: Centre National de la Recherche Scientifique, Institut national de recherche en sciences et technologies du numérique, Inserm, Sorbonne Université, Assistance Publique – Hôpitaux de Paris, Institut du Cerveau

Observed institutions: Centre National de la Recherche Scientifique, Institut national de recherche en sciences et technologies du numérique, Institut de la Vision, Inserm, Universidade de São Paulo, Sorbonne Université, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, Institut du Cerveau, Hôpital Charles-Foix, Centre d'Acquisition et de Traitement des Images, Universidade Estadual Paulista (Unesp)

ORCID: 0000-0003-4910-2297

Observed ORCID: 0000-0003-4910-2297

OpenAlex ID: A5047946641

Safety and Outcomes of Dentate Nucleus Deep Brain Stimulation for Cerebellar Ataxia

2021 · Rubens Gisbert Cury, Carina França, et al. · The Cerebellum · 40

Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias

2023 · Paulina Cunha, Emilien Petit, et al. · The American Journal of Human Genetics · 33

Longitudinal Changes of Clinical, Imaging, and Fluid Biomarkers in Preataxic and Early Ataxic Spinocerebellar Ataxia Type 2 and 7 Carriers

2024 · Giulia Coarelli, Charlotte Dubec-Fleury, et al. · Neurology · 19

Prevalence, Severity, and Progression of Cerebellar Cognitive-Affective Syndrome in Patients With Spinocerebellar Ataxias

2025 · Emilien Petit, Daniel López Domínguez, et al. · Neurology · 10

Patient-Relevant Digital-Motor Outcomes for Clinical Trials in Hereditary Spastic Paraplegia Type 7

2024 · Lukas Beichert, Jens Seemann, et al. · Neurology · 9

Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia.

2022 · Fernando Freua, Mariana Espíndola de Castro Almeida, et al. · Molecular Case Studies · 9

Predictive models for ataxia progression and conversion in spinocerebellar ataxia type 1 and 3

2025 · Emilien Petit, Giulia Coarelli, et al. · Brain · 8

Expanding the phenotypic spectrum of CLCN2-related leucoencephalopathy and ataxia

2023 · Paulo R Nóbrega, Anderson R. B. de Paiva, et al. · Brain Communications · 6

Ceroid lipofuscinosis type 5: novel pathogenic variants and unexpected phenotypic findings

2023 · Anderson Rodrigues Brandão de Paiva, André Luiz Santos Pessoa, et al. · Journal of Neurology Neurosurgery & Psychiatry · 6

Hippocampal Damage and Atrophy Secondary to Status Epilepticus in a Patient with Schizophrenia

2017 · Elaine Keiko Fujisao, Nathalia Raquel Cristaldo, et al. · Frontiers in Neurology · 6

IRF2BPL Causes Mild Intellectual Disability Followed by Late-Onset Ataxia

2023 · Solveig Heide, Claire-Sophie Davoine, et al. · Neurology Genetics · 5

Freezing of gait (FOG) in Parkinson’s disease patients—the contribution of Garcin and Melaragno

2021 · Hélio A. G. Teive, Paulina Cunha, et al. · Neurological Sciences · 4

Predictive Models for Ataxia Progression and Conversion in Sca1 and Sca3

2024 · Emilien Petit, Giulia Coarelli, et al. · SSRN Electronic Journal

F29 Pyramidal involvement in Huntington disease

2022 · Théo Dominot, Emilien Petit, et al.

Works count: 15

Citation count: 155

H-index: 7

I10-index: 4