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F. Dubas · SciRah

Researcher profile · Semantic Scholar

F. Dubas

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F. Dubas — researcher profile on SciRah

h-index: 28
Works: 131
Citations: 4,135

Most-cited papers

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy
A. Rovelet-Lecrux, D. Hannequin, G. Raux, N. Le Meur +9 more
2006Nature Genetics1,280 citations
Semantic Scholar
A Clinicopathological Study
M. Baudrimont, F. Dubas
2005264 citations
Semantic Scholar
Idiopathic acute transverse myelitis: Application of the recent diagnostic criteria
J. de Sèze, C. Lanctin, C. Lebrun, I. Malikova +10 more
2005Neurology156 citations
Semantic Scholar
Executive functioning in normal aging: a study of action planning using the Zoo Map Test.
P. Allain, S. Nicoleau, K. Pinon, F. Etcharry-Bouyx +4 more
2005Brain and Cognition130 citations
Semantic Scholar
Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations.
J. Cassereau, A. Chevrollier, N. Gueguen, V. Desquiret +7 more
2011Experimental Neurology104 citations
Semantic Scholar
Fibromuscular Dysplasia May Herald Symptomatic Recurrence of Cervical Artery Dissection
J. de Bray, G. Marc, V. Pautot, B. Vielle +3 more
2007Cerebrovascular Diseases104 citations
Semantic Scholar
Ultrasonic features of extracranial carotid dissections: 47 cases studied by angiography.
J. de Bray, P. Lhoste, F. Dubas, J. Emile +1 more
1994Journal of ultrasound in medicine94 citations Open access
Semantic Scholar
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation.
C. Verny, N. Guegen, V. Desquiret, A. Chevrollier +8 more
2011Mitochondrion (Amsterdam. Print)90 citations
Semantic Scholar
Psychiatric side effects of interferon-β in multiple sclerosis
J. Goeb, C. Even, G. Nicolas, B. Gohier +2 more
2006European psychiatry86 citations
Semantic Scholar
Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)
J. Cassereau, A. Chevrollier, N. Gueguen, M. Malinge +10 more
2009Neurogenetics83 citations
Semantic Scholar
MULTIPLE SCLEROSIS–LIKE DISORDER IN OPA1-RELATED AUTOSOMAL DOMINANT OPTIC ATROPHY
C. Verny, D. Loiseau, C. Scherer, P. Lejeune +7 more
2008Neurology66 citations
Semantic Scholar
Myotilinopathy in a family with late onset myopathy.
I. Pénisson-Besnier, K. Talvinen, C. Dumez, A. Vihola +5 more
2006Neuromuscular Disorders64 citations
Semantic Scholar
Psychiatric side effects of interferon-beta in multiple sclerosis.
J. Goeb, C. Even, G. Nicolas, B. Gohier +2 more
2006European psychiatry53 citations
Semantic Scholar
mtDNA haplogroup J: a contributing factor of optic neuritis
P. Reynier, I. Pénisson-Besnier, C. Moreau, F. Savagner +4 more
1999European Journal of Human Genetics53 citations
Semantic Scholar
A second pedigree with autosomal dominant nemaline myopathy caused by TPM3 mutation: a clinical and pathological study.
I. Pénisson-Besnier, N. Monnier, A. Toutain, F. Dubas +1 more
2007Neuromuscular Disorders48 citations
Semantic Scholar
Recurrent brain hematomas in MELAS associated with an ND5 gene mitochondrial mutation
I. Pénisson-Besnier, P. Reynier, P. Asfar, O. Douay +4 more
2000Neurology46 citations
Semantic Scholar
Accuracy of Color-Doppler in the Quantification of Proximal Vertebral Artery Stenoses
J. de Bray, A. Pasco, F. Tranquart, X. Papon +4 more
2001Cerebrovascular Diseases45 citations
Semantic Scholar
Pseudometabolic expression and phenotypic variability of calpain deficiency in two siblings
I. Pénisson-Besnier, I. Richard, F. Dubas, J. Beckmann +1 more
1998Muscle and Nerve42 citations
Semantic Scholar
Detection of vertebrobasilar intracranial stenoses: transcranial Doppler sonography versus angiography
J. de Bray, A. Missoum, F. Dubas, J. Emile +1 more
1997Journal of ultrasound in medicine41 citations Open access
Semantic Scholar
Compound heterozygous mutations of the TNXB gene cause primary myopathy.
I. Pénisson-Besnier, V. Allamand, P. Beurrier, Ludovic Martin +11 more
2013Neuromuscular Disorders38 citations
Semantic Scholar
Monitoring processes and metamemory experience in patients with dysexecutive syndrome.
K. Pinon, Phillipe Allain, Mohamed Zied Kefi, F. Dubas +1 more
2005Brain and Cognition38 citations
Semantic Scholar
Acute delirium, delusion, and depression during IFN-beta-1a therapy for multiple sclerosis: a case report.
J. Goeb, A. Cailleau, P. Laine, F. Etcharry-Bouyx +6 more
2003Clinical neuropharmacology38 citations
Semantic Scholar
Coincidence of two genetic forms of Charcot–Marie–Tooth disease in a single family
Christophe Verny, N. Ravisé, A. Leutenegger, F. Pouplard +6 more
2004Neurology34 citations
Semantic Scholar
Colour Doppler and duplex sonography and angiography of the carotid artery bifurcations
J. Bray, F. Galland, P. Lhoste, S. Nicolau +3 more
1995Neuroradiology28 citations
Semantic Scholar
Intravascular malignant lymphomatosis (so-called malignant angioendotheliomatosis): a case confined to the lumbosacral spinal cord and nerve roots.
F. Dubas, J. Saint-André, A. Pouplard-Barthelaix, F. Delestre +1 more
1990Clinical Neuropathology26 citations
Semantic Scholar
Script representation in patients with Alzheimer's disease.
P. Allain, D. Le Gall, C. Foucher, F. Etcharry-Bouyx +3 more
2008Cortex; a journal devoted to the study of the nervous system and behavior25 citations
Semantic Scholar
Executive functions in normal aging: an examination of script sequencing, script sorting, and script monitoring.
P. Allain, G. Berrut, F. Etcharry-Bouyx, J. Barré +2 more
2007The journals of gerontology. Series B, Psychological sciences and social sciences25 citations
Semantic Scholar
Diagnosis of myotubular myopathy in the oldest known manifesting female carrier: a clinical and genetic study.
I. Pénisson-Besnier, V. Biancalana, P. Reynier, M. Cossée +1 more
2007Neuromuscular Disorders25 citations
Semantic Scholar
Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathy
C. Lamirel, J. Cassereau, I. Cochereau, C. Vignal-Clermont +8 more
2010Journal of Neurology Neurosurgery & Psychiatry22 citations
Semantic Scholar
Autosomal dominant late adult onset distal leg myopathy.
I. Pénisson-Besnier, C. Dumez, D. Château, F. Dubas +1 more
1997Neuromuscular Disorders21 citations
Semantic Scholar
Myoclonic encephalopathy after exposure to aluminium
K. Hoang-Xuan, P. Perrotte, F. Dubas, J. Philippon +1 more
199620 citations
Semantic Scholar
Uneven distribution of mitochondrial DNA mutation in MERRF dizygotic twins.
I. Pénisson-Besnier, Françoise Degoul, C. Desnuelle, F. Dubas +3 more
1992Journal of Neurological Sciences18 citations
Semantic Scholar
Effect of subclavian syndrome on the basilar artery
J. Bray, J. P. Zenglein, J. Laroche, P. Joseph +4 more
1994Acta Neurologica Scandinavica17 citations Open access
Semantic Scholar
[Demyelinating neuropathy during anti-TNF alpha treatment with a review of the literature].
M. Hamon, G. Nicolas, F. Devière, F. Letournel +1 more
2007Revue neurologique (Paris)16 citations
Semantic Scholar
Clinical characteristics and brain PET findings in 3 cases of dissociative amnesia: disproportionate retrograde deficit and posterior middle temporal gyrus hypometabolism.
Catherine Thomas-Antérion, F. Dubas, M. Decousus, C. Jeanguillaume +1 more
2014Neurophysiologie clinique15 citations
Semantic Scholar
Focal adherent thrombus in the common carotid artery: clinical, ultrasonographic, and pathogenic aspects in two cases.
G. Devuyst, J. de Bray, P. Despland, P. Maeder +5 more
2000Journal of ultrasound in medicine15 citations
Semantic Scholar
Myopathy caused by anoctamin 5 mutations and necrotizing vasculitis
I. Pénisson-Besnier, J. Saint-André, D. Hicks, A. Sarkozy +4 more
2012Journal of Neurology14 citations Open access
Semantic Scholar
The neural substrates of script knowledge deficits as revealed by a PET study in Huntington's disease.
P. Allain, V. Gaura, L. Fasotti, Valérie Chauviré +8 more
2011Neuropsychologia14 citations Open access
Semantic Scholar
[Cerebrovascular complications of cancers].
F. Dubas, I. Serre
1992Revue neurologique (Paris)14 citations
Semantic Scholar
Isolated Horner’s Syndrome May Herald Stroke
J. de Bray, R. Baumgartner, B. Guillon, V. Pautot +13 more
2005Cerebrovascular Diseases13 citations
Semantic Scholar
Anti-NGF autoantibodies and NGF in sera of Alzheimer patients and in normal subjects in relation to age.
E. Dicou, P. Vermersch, I. Pénisson-Besnier, F. Dubas +1 more
1997Autoimmunity13 citations
Semantic Scholar
[Histological demonstration of the process of paraspinal muscle denervation in a case of reducible lumbar kyphosis (camptocormia)].
I. Pénisson-Besnier, P. Menei, F. Dubas, C. Bregeon
1994Revue du rhumatisme13 citations
Semantic Scholar
Arithmetic word-problem-solving in Huntington's disease.
P. Allain, C. Verny, G. Aubin, K. Pinon +3 more
2005Brain and Cognition12 citations
Semantic Scholar
Selective decrease in axonal nerve growth factor and insulin-like growth factor I immunoreactivity in axonopathies of unknown etiology
C. Fressinaud, I. Jean, F. Dubas
2003Acta Neuropathologica12 citations
Semantic Scholar
Middle Cerebral Artery Dissection Gives Rise to Giant Serpentine Aneurysm
C. Verny, G. Marc, A. Pasco, F. Dubas
2008Cerebrovascular Diseases11 citations Open access
Semantic Scholar
Clinical commentary with video sequences Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome
B. Ricard-Mousnier, S. N'guyen, F. Dubas, F. Pouplard +1 more
200711 citations
Semantic Scholar
Obsessive-compulsive disorders in association with focal brain lesions
F. Etcharry-Bouyx, F. Dubas, J. Bogousslavsky, J. Cummings
200011 citations
Semantic Scholar
Refsum's disease may mimic familial Guillain Barre syndrome.
C. Verny, Adriana Prundean, G. Nicolas, V. Pautot +4 more
2006Neuromuscular Disorders10 citations
Semantic Scholar
Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African origin
J. Cassereau, C. Lavigne, F. Letournel, A. Ghali +4 more
2008Journal of the peripheral nervous system9 citations
Semantic Scholar
[An OPA3 gene mutation is responsible for the disease associating optic atrophy and cataract with extrapyramidal signs].
C. Verny, P. Amati-Bonneau, F. Dubas, Y. Malthiéry +2 more
2005Revue neurologique (Paris)8 citations
Semantic Scholar

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P. Reynier×9
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J. Emile — researcher profile on SciRah

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J. de Bray — researcher profile on SciRah

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