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C. Tranchant · SciRah

Researcher profile · Semantic Scholar

C. Tranchant

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C. Tranchant — researcher profile on SciRah

h-index: 63
Works: 331
Citations: 12K

Most-cited papers

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.
S. Lesage, Valérie Drouet, E. Majounie, V. Deramecourt +38 more
2016American Journal of Human Genetics418 citations Open access
Semantic Scholar
Trial of Deferiprone in Parkinson's Disease.
D. Devos, J. Labreuche, O. Rascol, J. Corvol +61 more
2022New England Journal of Medicine190 citations Open access
Semantic Scholar
Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex
L. Parodi, S. Fenu, M. Barbier, G. Banneau +42 more
2018Brain : a journal of neurology102 citations Open access
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
Quality of life in Parkinson’s disease improved by apomorphine pump: the OPTIPUMP cohort study
S. Drapier, A. Eusebio, B. Degos, M. Vérin +12 more
2016Journal of Neurology75 citations
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
The inherited cerebellar ataxias: an update
Giulia Coarelli, T. Wirth, C. Tranchant, M. Koenig +2 more
2022Journal of Neurology69 citations Open access
Semantic Scholar
Assessment of a Targeted Gene Panel for Identification of Genes Associated With Movement Disorders
S. Montaut, C. Tranchant, N. Drouot, G. Rudolf +11 more
2018JAMA Neurology69 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
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
Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues
V. Biancalana, Sophie Scheidecker, M. Miguet, A. Laquérriere +40 more
2017Acta Neuropathologica58 citations
Semantic Scholar
Movement disorders in mitochondrial diseases.
C. Tranchant, M. Anheim
2016Revue neurologique (Paris)58 citations
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
Outcome of deep brain stimulation in slowly progressive multiple system atrophy: A clinico-pathological series and review of the literature.
W. Meissner, C. Laurencin, C. Tranchant, T. Witjas +11 more
2016Parkinsonism & Related Disorders51 citations
Semantic Scholar
Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effect
Y. Nadjar, Ana Lucia Hütter-Moncada, P. Latour, X. Ayrignac +16 more
2018Orphanet Journal of Rare Diseases50 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
Comparison of Corticosteroid Tapering Regimens in Myasthenia Gravis: A Randomized Clinical Trial.
T. Sharshar, R. Porcher, S. Demeret, C. Tranchant +8 more
2021JAMA Neurology45 citations Open access
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
Deciphering the causes of sporadic late-onset cerebellar ataxias: a prospective study with implications for diagnostic work
O. Gebus, S. Montaut, B. Monga, T. Wirth +26 more
2017Journal of Neurology42 citations
Semantic Scholar
Autophagy-Lysosomal Pathway as Potential Therapeutic Target in Parkinson’s Disease
S. R. Bonam, C. Tranchant, S. Muller
2021Cells41 citations Open access
Semantic Scholar
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment
T. Roux, M. Barbier, M. Papin, C. Davoine +17 more
2020Genetics in Medicine41 citations Open access
Semantic Scholar
Mini‐Exome Coupled to Read‐Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias
C. Marelli, C. Guissart, C. Hubsch, M. Renaud +30 more
2016Human Mutation40 citations Open access
Semantic Scholar
Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1
M. Renaud, M. Moreira, Bondo Ben Monga, D. Rodriguez +39 more
2018JAMA Neurology38 citations Open access
Semantic Scholar
A Placebo‐Controlled Trial of AQW051 in Patients With Moderate to Severe Levodopa‐Induced Dyskinesia
C. Trenkwalder, D. Berg, O. Rascol, K. Eggert +29 more
2016Movement Disorders38 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
Intermediate repeat expansions of TBP and STUB1: Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?
M. Barbier, C. Davoine, Emilien Petit, M. Porché +18 more
2022Genetics in Medicine36 citations Open access
Semantic Scholar
Suggestive association between OPRM1 and impulse control disorders in Parkinson's disease
F. Cormier-Dequaire, S. Bekadar, M. Anheim, Said Lebbah +31 more
2018Movement Disorders36 citations
Semantic Scholar
A recessive ataxia diagnosis algorithm for the next generation sequencing era
M. Renaud, C. Tranchant, Juan Vicente Torres Martin, F. Mochel +75 more
2017Annals of Neurology36 citations Open access
Semantic Scholar
A randomized, double‐blind, placebo‐controlled trial evaluating cysteamine in Huntington's disease
C. Verny, A. Bachoud-Lévi, A. Durr, C. Goizet +16 more
2017Movement Disorders36 citations
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
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
The hidden Niemann-Pick type C patient: clinical niches for a rare inherited metabolic disease
C. Hendriksz, M. Anheim, P. Bauer, O. Bonnot +23 more
2017Current Medical Research and Opinion31 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
Ability of pulmonary function decline to predict death in amyotrophic lateral sclerosis patients
I. Enache, C. Pistea, M. Fleury, M. Schaeffer +5 more
2017Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration30 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
Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia
M. Renaud, C. Guissart, M. Mallaret, S. Ferdinandusse +7 more
2016Journal of Neurology28 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
Mutations in KARS cause a severe neurological and neurosensory disease with optic neuropathy
Sophie Scheidecker, S. Bär, C. Stoetzel, Véronique Geoffroy +13 more
2019Human Mutation27 citations Open access
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
Low cancer prevalence in polyglutamine expansion diseases
Giulia Coarelli, Alhassane Diallo, M. S. Thion, D. Rinaldi +16 more
2017Neurology26 citations
Semantic Scholar
Parkinsonian-Pyramidal syndromes: A systematic review.
C. Tranchant, M. Koob, M. Anheim
2017Parkinsonism & Related Disorders26 citations
Semantic Scholar
Fluoxetine for the Symptomatic Treatment of Multiple System Atrophy: The MSA‐FLUO Trial
O. Rascol, Valérie Cochen de Cock, Anne Pavy-Le Traon, A. Foubert-Samier +18 more
2021Movement Disorders24 citations Open access
Semantic Scholar
Hemophagocytic Lymphohistiocytosis Gene Mutations in Adult Patients Presenting With CLIPPERS-Like Syndrome
G. Taieb, E. Kaphan, C. Duflos, C. Lebrun-Frénay +14 more
2021Neurology: Neuroimmunology & Neuroinflammation23 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

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