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M. Anheim · SciRah

Researcher profile · Semantic Scholar

M. Anheim

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M. Anheim — researcher profile on SciRah

h-index: 57
Works: 217
Citations: 13K

Most-cited papers

Neurologic Features in Severe SARS-CoV-2 Infection
J. Helms, S. Kremer, Hamid Merdji, R. Clere-Jehl +8 more
2020New England Journal of Medicine2,325 citations Open access
Semantic Scholar
Brain MRI Findings in Severe COVID-19: A Retrospective Observational Study
S. Kremer, F. Lersy, J. de Sèze, Jean-Christophe Ferré +77 more
2020Radiology401 citations Open access
Semantic Scholar
Delirium and encephalopathy in severe COVID-19: a cohort analysis of ICU patients
J. Helms, S. Kremer, H. Merdji, M. Schenck +13 more
2020Critical Care299 citations Open access
Semantic Scholar
Neurologic and neuroimaging findings in patients with COVID-19: A retrospective multicenter study
S. Kremer, F. Lersy, M. Anheim, H. Merdji +46 more
2020142 citations
Semantic Scholar
Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 Disease
A. Traschütz, A. Cortese, S. Reich, N. Dominik +28 more
2021Neurology140 citations Open access
Semantic Scholar
Neurologic and neuroimaging findings in COVID-19 patients: A retrospective multicenter study.
S. Kremer, F. Lersy, M. Anheim, H. Merdji +56 more
2020Neurology89 citations
Semantic Scholar
The genetic nomenclature of recessive cerebellar ataxias
M. Rossi, M. Anheim, A. Durr, C. Klein +4 more
2018Movement Disorders80 citations
Semantic Scholar
A Phase 1 Randomized Trial of Specific Active α‐Synuclein Immunotherapies PD01A and PD03A in Multiple System Atrophy
W. Meissner, A. P. Traon, A. Foubert-Samier, G. Galabova +23 more
2020Movement Disorders75 citations Open access
Semantic Scholar
Characterization of Recessive Parkinson Disease in a Large Multicenter Study
S. Lesage, A. Lunati, Marion Houot, Sawssan Ben Romdhan +29 more
2020Annals of Neurology72 citations Open access
Semantic Scholar
Clinico-genetic, imaging and molecular delineation of COQ8A-ataxia: a multicenter study of 59 patients
A. Traschütz, T. Schirinzi, L. Laugwitz, Nathan H. Murray +38 more
2020Annals of Neurology70 citations Open access
Semantic Scholar
The inherited cerebellar ataxias: an update
Giulia Coarelli, T. Wirth, C. Tranchant, M. Koenig +2 more
2022Journal of Neurology69 citations Open access
Semantic Scholar
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia.
D. Ebrahimi-Fakhari, Julian Teinert, Robert Behne, Miriam Wimmer +84 more
2020Brain : a journal of neurology65 citations Open access
Semantic Scholar
Primary brain calcification: an international study reporting novel variants and associated phenotypes
E. Ramos, M. Carecchio, R. Lemos, J. Ferreira +33 more
2018European Journal of Human Genetics65 citations Open access
Semantic Scholar
Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype.
L. Grangeon, D. Wallon, C. Charbonnier, O. Quenez +25 more
2019Brain : a journal of neurology64 citations Open access
Semantic Scholar
Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions
Jean-Loup Méreaux, C. Davoine, D. Pellerin, Giulia Coarelli +43 more
2023EBioMedicine59 citations Open access
Semantic Scholar
Increased diagnostic yield in complex dystonia through exome sequencing.
T. Wirth, C. Tranchant, N. Drouot, B. Keren +20 more
2020Parkinsonism & Related Disorders59 citations Open access
Semantic Scholar
Early cognitive decline after bilateral subthalamic deep brain stimulation in Parkinson's disease patients with GBA mutations.
G. Mangone, S. Bekadar, F. Cormier-Dequaire, K. Tahiri +47 more
2020Parkinsonism & Related Disorders59 citations Open access
Semantic Scholar
Natural History and Phenotypic Spectrum of GAA‐FGF14 Sporadic Late‐Onset Cerebellar Ataxia (SCA27B)
T. Wirth, G. Clément, Clarisse Delvallée, C. Bonnet +16 more
2023Movement Disorders57 citations Open access
Semantic Scholar
Early-Onset Parkinsonism Is a Manifestation of the PPP2R5D p.E200K Mutation
Christine Y Kim, T. Wirth, C. Hubsch, A. Nemeth +12 more
2020Annals of Neurology57 citations Open access
Semantic Scholar
Highlighting the Dystonic Phenotype Related to GNAO1
T. Wirth, Giacomo Garone, M. Kurian, A. Piton +40 more
2022Movement Disorders56 citations Open access
Semantic Scholar
Apathy in Parkinson’s Disease: Clinical Patterns and Neurobiological Basis
M. Béreau, Vincent Van Waes, Mathieu Servant, E. Magnin +2 more
2023Cells55 citations Open access
Semantic Scholar
Safety and efficacy of subcutaneous night-time only apomorphine infusion to treat insomnia in patients with Parkinson's disease (APOMORPHEE): a multicentre, randomised, controlled, double-blind crossover study.
V. D. De Cock, P. Dodet, Smaranda Leu-Semenescu, C. Aerts +23 more
2022Lancet Neurology53 citations Open access
Semantic Scholar
The spectrum of functional tic‐like behaviours: Data from an international registry
D. Martino, T. Hedderly, Tara L. Murphy, K. Müller-Vahl +18 more
2022European Journal of Neurology52 citations
Semantic Scholar
Critical illness-associated cerebral microbleeds for patients with severe COVID-19: etiologic hypotheses
F. Lersy, T. Willaume, J. Brisset, O. Collange +8 more
2020Journal of Neurology51 citations Open access
Semantic Scholar
Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with SPG7.
Giulia Coarelli, Rebecca Schule, B. C. van de Warrenburg, P. de Jonghe +32 more
2019Neurology49 citations Open access
Semantic Scholar
Intronic FGF14 GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathy
D. Pellerin, C. Wilke, A. Traschütz, Sara Nagy +18 more
2023Journal of Neurology Neurosurgery & Psychiatry48 citations Open access
Semantic Scholar
Efficacy of Caffeine in ADCY5‐Related Dyskinesia: A Retrospective Study
A. Méneret, S. Mohammad, L. Cif, D. Doummar +22 more
2022Movement Disorders48 citations
Semantic Scholar
Impact of Subthalamic Deep Brain Stimulation on Impulse Control Disorders in Parkinson's Disease: A Prospective Study
M. Santin, P. Voulleminot, A. Vrillon, É. Hainque +29 more
2020Movement Disorders43 citations
Semantic Scholar
Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center Cohort
S. Lesage, Marion Houot, G. Mangone, C. Tesson +21 more
2020Frontiers in Neurology42 citations Open access
Semantic Scholar
Cerebral vasculitis of medium-sized vessels as a possible mechanism of brain damage in COVID-19 patients
F. Lersy, M. Anheim, T. Willaume, A. Chammas +3 more
2020Journal of neuroradiology = Journal de neuroradiologie39 citations Open access
Semantic Scholar
Functional classification of ATM variants in ataxia‐telangiectasia patients
A. Fiévet, D. Bellanger, Guillaume Rieunier, C. Dubois d'Enghien +42 more
2019Human Mutation39 citations Open access
Semantic Scholar
Loss‐of‐Function Mutations in NR4A2 Cause Dopa‐Responsive Dystonia Parkinsonism
T. Wirth, L. Mariani, G. Bergant, M. Baulac +11 more
2020Movement Disorders37 citations
Semantic Scholar
Responsiveness of the Scale for the Assessment and Rating of Ataxia and Natural History in 884 Recessive and Early Onset Ataxia Patients
A. Traschütz, A. Adarmes-Gómez, M. Anheim, J. Baets +20 more
2023Annals of Neurology35 citations Open access
Semantic Scholar
Biallelic RFC1-expansion in a French multicentric sporadic ataxia cohort
S. Montaut, Nadège Diedhiou, P. Fahrer, C. Marelli +22 more
2021Journal of Neurology35 citations
Semantic Scholar
Autosomal Recessive Cerebellar Ataxias With Elevated Alpha‐Fetoprotein: Uncommon Diseases, Common Biomarker
M. Renaud, C. Tranchant, M. Koenig, M. Anheim
2020Movement Disorders34 citations Open access
Semantic Scholar
Safety and efficacy of riluzole in spinocerebellar ataxia type 2 in France (ATRIL): a multicentre, randomised, double-blind, placebo-controlled trial.
Giulia Coarelli, Anna Heinzmann, C. Ewenczyk, C. Fischer +16 more
2022Lancet Neurology33 citations Open access
Semantic Scholar
A randomized controlled double-blind study of rotigotine on neuropsychiatric symptoms in de novo PD
A. Castrioto, S. Thobois, M. Anheim, J. Quesada +15 more
2020npj Parkinson's Disease33 citations Open access
Semantic Scholar
High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families
M. Benkirane, C. Marelli, C. Guissart, A. Roubertie +81 more
2021Genetics in Medicine32 citations Open access
Semantic Scholar
Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesia
D. Doummar, C. Dentel, Romane Lyautey, J. Métreau +24 more
2020European Journal of Human Genetics32 citations Open access
Semantic Scholar
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias.
Paulina Cunha, Emilien Petit, Marie Coutelier, Giulia Coarelli +68 more
2023American Journal of Human Genetics31 citations Open access
Semantic Scholar
Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxia.
A. Rebelo, I. Eidhof, V. Cintra, Léna Guillot-Noel +17 more
2021Brain : a journal of neurology30 citations
Semantic Scholar
Limbic Stimulation Drives Mania in STN‐DBS in Parkinson Disease: A Prospective Study
S. Prange, Zheng-Yu Lin, Mikail Nourredine, T. Danaila +15 more
2022Annals of Neurology28 citations Open access
Semantic Scholar
The ARCA Registry: A Collaborative Global Platform for Advancing Trial Readiness in Autosomal Recessive Cerebellar Ataxias
A. Traschütz, S. Reich, Astrid D. Adarmes, M. Anheim +31 more
2021Frontiers in Neurology27 citations Open access
Semantic Scholar
Expanding the clinical spectrum of STIP1 homology and U-box containing protein 1-associated ataxia
J. Ravel, M. Benkirane, N. Calmels, C. Marelli +24 more
2021Journal of Neurology27 citations
Semantic Scholar
Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective study
T. Bogdan, T. Wirth, A. Iosif, A. Schalk +27 more
2022Journal of Neurology26 citations
Semantic Scholar
Coronavirus Disease 2019: Associated Multiple Organ Damage
O. Collange, C. Tacquard, X. Delabranche, I. Léonard-Lorant +12 more
2020Open Forum Infectious Diseases26 citations Open access
Semantic Scholar
Motivational and cognitive predictors of apathy after subthalamic nucleus stimulation in Parkinson's disease.
M. Béreau, A. Kibleur, Mathieu Servant, Gautier Clément +31 more
2023Brain : a journal of neurology24 citations Open access
Semantic Scholar
Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome
C. Depienne, S. Ciura, O. Trouillard, D. Bouteiller +19 more
2019Tremor and Other Hyperkinetic Movements23 citations Open access
Semantic Scholar
Spastic paraplegia due to recessive or dominant mutations in ERLIN2 can convert to ALS
M. del Mar Amador, F. Muratet, E. Teyssou, G. Banneau +11 more
2019Neurology: Genetics23 citations Open access
Semantic Scholar
Cerebral perfusion using ASL in patients with COVID-19 and neurological manifestations: A retrospective multicenter observational study
F. Ardellier, S. Baloglu, M. Sokolska, V. Noblet +87 more
2023Journal of neuroradiology = Journal de neuroradiologie20 citations Open access
Semantic Scholar

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