| Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia A Joutel, C Corpechot, A Ducros, K Vahedi, H Chabriat, P Mouton, ... Nature 383 (6602), 707-710, 1996 | 2044 | 1996 |
| Cadasil H Chabriat, A Joutel, M Dichgans, E Tournier-Lasserve, MG Bousser The Lancet Neurology 8 (7), 643-653, 2009 | 920 | 2009 |
| Clinical spectrum of CADASIL: a study of 7 families H Chabriat, K Vahedi, MG Bousser, MT Iba-Zizen, A Joutel, A Nibbio, ... The Lancet 346 (8980), 934-939, 1995 | 755 | 1995 |
| Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12 E Tournier-Lasserve, A Joutel, J Melki, J Weissenbach, GM Lathrop, ... Nature genetics 3 (3), 256-259, 1993 | 722 | 1993 |
| Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients A Joutel, K Vahedi, C Corpechot, A Troesch, H Chabriat, C Vayssière, ... The Lancet 350 (9090), 1511-1515, 1997 | 671 | 1997 |
| The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel A Ducros, C Denier, A Joutel, M Cecillon, C Lescoat, K Vahedi, F Darcel, ... New England Journal of Medicine 345 (1), 17-24, 2001 | 589 | 2001 |
| The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients A Joutel, F Andreux, S Gaulis, V Domenga, M Cecillon, N Battail, N Piga, ... The Journal of clinical investigation 105 (5), 597-605, 2000 | 557 | 2000 |
| Notch3 is required for arterial identity and maturation of vascular smooth muscle cells V Domenga, P Fardoux, P Lacombe, M Monet, J Maciazek, LT Krebs, ... Genes & development 18 (22), 2730-2735, 2004 | 493 | 2004 |
| Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas S Laberge-le Couteulx, HH Jung, P Labauge, JP Houtteville, C Lescoat, ... Nature genetics 23 (2), 189-193, 1999 | 456 | 1999 |
| A gene for familial hemiplegic migraine maps to chromosome 19 A Joutel, MG Bousser, V Biousse, P Labauge, H Chabriat, A Nibbio, ... Nature genetics 5 (1), 40-45, 1993 | 433 | 1993 |
| Patterns of MRI lesions in CADASIL H Chabriat, C Levy, H Taillia, MT Iba-Zizen, K Vahedi, A Joutel, ... Neurology 51 (2), 452-457, 1998 | 361 | 1998 |
| Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study. M Baudrimont, F Dubas, A Joutel, E Tournier-Lasserve, MG Bousser Stroke 24 (1), 122-125, 1993 | 341 | 1993 |
| Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease A Joutel, M Monet-Leprêtre, C Gosele, C Baron-Menguy, A Hammes, ... The Journal of clinical investigation 120 (2), 433-445, 2010 | 282 | 2010 |
| Characterization of Notch3‐deficient mice: Normal embryonic development and absence of genetic interactions with a Notch1 mutation LT Krebs, Y Xue, CR Norton, JP Sundberg, P Beatus, U Lendahl, A Joutel, ... genesis 37 (3), 139-143, 2003 | 278 | 2003 |
| Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis A Joutel, P Favrole, P Labauge, H Chabriat, C Lescoat, F Andreux, ... The Lancet 358 (9298), 2049-2051, 2001 | 268 | 2001 |
| Mapping of a second locus for familial hemiplegic migraine to 1q21–q23 and evidence of further heterogeneity A Ducros, A Joutel, M Cecillon, E Tournier‐Lasserve, K Vahedi, ... Annals of Neurology: Official Journal of the American Neurological …, 1997 | 260 | 1997 |
| Notch signalling pathway and human diseases A Joutel, E Tournier-Lasserve Seminars in cell & developmental biology 9 (6), 619-625, 1998 | 236 | 1998 |
| High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2 C Denier, A Ducros, K Vahedi, A Joutel, P Thierry, A Ritz, G Castelnovo, ... Neurology 52 (9), 1816-1816, 1999 | 226 | 1999 |
| Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy MM Ruchoux, V Domenga, P Brulin, J Maciazek, S Limol, ... The American journal of pathology 162 (1), 329-342, 2003 | 216 | 2003 |
| Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia A Ducros, C Denier, A Joutel, K Vahedi, A Michel, F Darcel, M Madigand, ... The American Journal of Human Genetics 64 (1), 89-98, 1999 | 200 | 1999 |
