Chabriat, Hugues
Inserm · Université Paris Cité · Hôpital Lariboisière · NeuroDiderot
43 papers on CoChatORCID 0000-0001-8436-6074
Most cited papers
- Verified
Neuroimaging standards for research into small vessel disease and its contribution to ageing and neurodegeneration
Wardlaw, J. M., Smith, E. E., Biessels, G. J., Cordonnier, C., Fazekas, F., Frayne, R., Lindley, R. I., O'Brien, J. T., Barkhof, F., Benavente, O. R., et al. (2013) · The Lancet Neurology
Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments
Cited by 5,544
- Verified
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
Joutel, A., Corpechot, C., Ducros, A., Vahedi, K., Chabriat, H., Mouton, P., Alamowitch, S., Domenga, V., Cécillion, M., Maréchal, E., et al. (1996) · Nature
Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments
Cited by 2,068
- Verified
Neuroimaging standards for research into small vessel disease—advances since 2013
Duering, M., Biessels, G. J., Brodtmann, A., Chen, C., Cordonnier, C., de Leeuw, F.-E., Debette, S., Frayne, R., Jouvent, E., Rost, N. S., et al. (2023) · The Lancet Neurology
Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments
Cited by 1,144
- Verified
CADASIL
Chabriat, H., Joutel, A., Dichgans, M., Tournier-Lasserve, E., & Bousser, M.-G. (2009) · The Lancet Neurology
Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments
Cited by 1,088
- Verified
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients
Joutel, A., Vahedi, K., Corpechot, C., Troesch, A., Chabriat, H., Vayssière, C., Cruaud, C., Maciazek, J., Weissenbach, J., Bousser, M.-G., et al. (1997) · The Lancet
Cerebrovascular and genetic disordersGenetic Neurodegenerative Diseases
Cited by 682
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Clinical spectrum of CADASIL: a study of 7 families
Chabriat, H., Vahedi, K., Bousser, M. G., Iba-Zizen, M. T., Joutel, A., Nibbio, A., Nagy, T. G., Tournier Lasserve, E., Krebs, M. O., Julien, J., et al. (1995) · The Lancet
Cerebrovascular and genetic disordersMigraine and Headache Studies
Cited by 669
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Changes in white matter as determinant of global functional decline in older independent outpatients: three year follow-up of LADIS (leukoaraiosis and disability) study cohort
Inzitari, D., Pracucci, G., Poggesi, A., Carlucci, G., Barkhof, F., Chabriat, H., Erkinjuntti, T., Fazekas, F., Ferro, J. M., Hennerici, M., et al. (2009) · BMJ
Cerebrovascular and genetic disordersDementia and Cognitive Impairment Research
Cited by 415
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A Novel Imaging Marker for Small Vessel Disease Based on Skeletonization of White Matter Tracts and Diffusion Histograms
Baykara, E., Gesierich, B., Adam, R., Tuladhar, A. M., Biesbroek, J. M., Koek, H. L., Ropele, S., Jouvent, E., Initiative, A. D. N., Chabriat, H., et al. (2016) · Annals of Neurology
Cerebrovascular and genetic disordersAdvanced Neuroimaging Techniques and Applications
Cited by 386
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Patterns of MRI lesions in CADASIL
Chabriat, H., Levy, C., Taillia, H., Iba-Zizen, M.-T., Vahedi, K., Joutel, A., Tournier-Lasserve, E., & Bousser, M.-G. (1998) · Neurology
Cerebrovascular and genetic disordersIntracerebral and Subarachnoid Hemorrhage Research
Cited by 339
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Severity of Dilated Virchow-Robin Spaces Is Associated With Age, Blood Pressure, and MRI Markers of Small Vessel Disease: A Population-Based Study
Zhu, Y.-C., Tzourio, C., Soumaré, A., Mazoyer, B., Dufouil, C., & Chabriat, H. (2010) · Stroke
Cerebrovascular and genetic disordersAdvanced MRI Techniques and Applications
Cited by 335
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Donepezil in patients with subcortical vascular cognitive impairment: a randomised double-blind trial in CADASIL
Dichgans, M., Markus, H. S., Salloway, S., Verkkoniemi, A., Moline, M., Wang, Q., Posner, H., & Chabriat, H. S. (2008) · The Lancet Neurology
Dementia and Cognitive Impairment ResearchNeurological Disease Mechanisms and Treatments
Cited by 264
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Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis
Joutel, A., Favrole, P., Labauge, P., Chabriat, H., Lescoat, C., Andreux, F., Domenga, V., Cécillon, M., Vahedi, K., Ducros, A., et al. (2001) · The Lancet
Cerebrovascular and genetic disordersVasculitis and related conditions
Cited by 252
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Incident subcortical infarcts induce focal thinning in connected cortical regions
Duering, M., Righart, R., Csanadi, E., Jouvent, E., Hervé, D., Chabriat, H., & Dichgans, M. (2012) · Neurology
Cerebrovascular and genetic disordersAdvanced Neuroimaging Techniques and Applications
Cited by 218
- Verified · note
Clinical Severity in CADASIL Related to Ultrastructural Damage in White Matter: In Vivo Study With Diffusion Tensor MRI
Chabriat, H., Pappata, S., Poupon, C., Clark, C. A., Vahedi, K., Poupon, F., Mangin, J. F., Pachot-Clouard, M., Jobert, A., Le Bihan, D., et al. (1999) · Stroke
Cerebrovascular and genetic disordersAdvanced Neuroimaging Techniques and Applications
Cited by 214
- Verified
Strategic role of frontal white matter tracts in vascular cognitive impairment: a voxel-based lesion-symptom mapping study in CADASIL
Duering, M., Zieren, N., Hervé, D., Jouvent, E., Reyes, S., Peters, N., Pachai, C., Opherk, C., Chabriat, H., & Dichgans, M. (2011) · Brain
Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments
Cited by 200
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Incident lacunes preferentially localize to the edge of white matter hyperintensities: insights into the pathophysiology of cerebral small vessel disease
Duering, M., Csanadi, E., Gesierich, B., Jouvent, E., Herve, D., Seiler, S., Belaroussi, B., Ropele, S., Schmidt, R., Chabriat, H., et al. (2013) · Brain
Cerebrovascular and genetic disordersIntracerebral and Subarachnoid Hemorrhage Research
Cited by 183
- Verified
Frequency and location of dilated Virchow-Robin spaces in elderly people: a population-based 3D MR imaging study
Zhu, Y.-C., Dufouil, C., Mazoyer, B., Soumaré, A., Ricolfi, F., Tzourio, C., & Chabriat, H. (2011) · American Journal of Neuroradiology
Advanced MRI Techniques and ApplicationsCerebrovascular and genetic disorders
Cited by 181
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The effect of NOTCH3 pathogenic variant position on CADASIL disease severity: NOTCH3 EGFr 1-6 pathogenic variant are associated with a more severe phenotype and lower survival compared with EGFr 7-34 pathogenic variant
Rutten, J. W., Van Eijsden, B. J., Duering, M., Jouvent, E., Opherk, C., Pantoni, L., Federico, A., Dichgans, M., Markus, H. S., Chabriat, H., et al. (2019) · Genetics in Medicine
Cerebrovascular and genetic disordersGenetic Neurodegenerative Diseases
Cited by 169
- Verified
Lacunar lesions are independently associated with disability and cognitive impairment in CADASIL
Viswanathan, A., Gschwendtner, A., Guichard, J. P., Buffon, F., Cumurciuc, R., O'Sullivan, M., Holtmannspötter, M., Pachai, C., Bousser, M. G., Dichgans, M., et al. (2007) · Neurology
Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments
Cited by 155
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Strategic white matter tracts for processing speed deficits in age-related small vessel disease
Duering, M., Gesierich, B., Seiler, S., Pirpamer, L., Gonik, M., Hofer, E., Jouvent, E., Duchesnay, E., Chabriat, H., Ropele, S., et al. (2014) · Neurology
Cerebrovascular and genetic disordersDementia and Cognitive Impairment Research
Cited by 143
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Impact of MRI markers in subcortical vascular dementia: A multi-modal analysis in CADASIL
Viswanathan, A., Godin, O., Jouvent, E., O’Sullivan, M., Gschwendtner, A., Peters, N., Duering, M., Guichard, J.-P., Holtmannspötter, M., Dufouil, C., et al. (2010) · Neurobiology of Aging
Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments
Cited by 139
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Cortical neuronal apoptosis in CADASIL
Viswanathan, A., Gray, F., Bousser, M.-G., Baudrimont, M., & Chabriat, H. (2006) · Stroke
Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments
Cited by 119
- Verified · note
Monitoring Disease Progression in CADASIL With Diffusion Magnetic Resonance Imaging: A Study With Whole Brain Histogram Analysis
Molko, N., Pappata, S., Mangin, J.-F., Poupon, F., LeBihan, D., Bousser, M.-G., & Chabriat, H. (2002) · Stroke
Cerebrovascular and genetic disordersAdvanced Neuroimaging Techniques and Applications
Cited by 116
- Verified
Brain atrophy is related to lacunar lesions and tissue microstructural changes in CADASIL
Jouvent, E., Viswanathan, A., Mangin, J.-F., O’Sullivan, M., Guichard, J.-P., Gschwendtner, A., Cumurciuc, R., Buffon, F., Peters, N., Pachaï, C., et al. (2007) · Stroke
Cerebrovascular and genetic disordersIntracerebral and Subarachnoid Hemorrhage Research
Cited by 109
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