| Vertical and horizontal smooth pursuit eye movements in children with developmental coordination disorder MP Robert, I Ingster‐Moati, E Albuisson, D Cabrol, B Golse, ... Developmental Medicine & Child Neurology 56 (6), 595-600, 2014 | 122 | 2014 |
| Oculomotor deficits indicate the progression of Huntington's disease SL Hicks, MPA Robert, CVP Golding, SJ Tabrizi, C Kennard Progress in brain research 171, 555-558, 2008 | 69 | 2008 |
| Dominant variants in the splicing factor PUF60 cause a recognizable syndrome with intellectual disability, heart defects and short stature S El Chehadeh, WS Kerstjens-Frederikse, J Thevenon, P Kuentz, ... European Journal of Human Genetics 25 (1), 43-51, 2017 | 61 | 2017 |
| Recent developments in the management of congenital cataract D Bremond-Gignac, A Daruich, MP Robert, S Valleix Annals of translational medicine 8 (22), 1545, 2020 | 55 | 2020 |
| Thromboembolism and congenital malformations: from Duane syndrome to thalidomide embryopathy CF Parsa, MP Robert JAMA ophthalmology 131 (4), 439-447, 2013 | 54 | 2013 |
| Congenital aniridia beyond black eyes: from phenotype and novel genetic mechanisms to innovative therapeutic approaches A Daruich, M Duncan, MP Robert, N Lagali, EV Semina, D Aberdam, ... Progress in Retinal and eye Research 95, 101133, 2023 | 47 | 2023 |
| Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti C Bodemer, A Diociaiuti, S Hadj‐Rabia, MP Robert, I Desguerre, ... Journal of the European Academy of Dermatology and Venereology 34 (7), 1415-1424, 2020 | 47 | 2020 |
| Recent innovations with drugs in clinical trials for neurotrophic keratitis and refractory corneal ulcers D Bremond-Gignac, A Daruich, MP Robert, F Chiambaretta Expert opinion on investigational drugs 28 (11), 1013-1020, 2019 | 36 | 2019 |
| Visual function in asymptomatic patients with homozygous sickle cell disease and temporal macular atrophy GC Martin, C Dénier, O Zambrowski, D Grévent, L Bruère, V Brousse, ... JAMA ophthalmology 135 (10), 1100-1105, 2017 | 31 | 2017 |
| Focal areas of high signal intensity in children with neurofibromatosis type 1: expected evolution on MRI S Calvez, R Levy, R Calvez, CJ Roux, D Grévent, Y Purcell, K Beccaria, ... American Journal of Neuroradiology 41 (9), 1733-1739, 2020 | 30 | 2020 |
| Saccadometry of conditional rules in presymptomatic Huntington's disease MPA Robert, PC Nachev, SL Hicks, CVP Golding, SJ Tabrizi, C Kennard Annals of the New York Academy of Sciences 1164 (1), 444-450, 2009 | 28 | 2009 |
| Thyroid-stimulating hormone receptor signaling restores skeletal muscle stem cell regeneration in rats with muscular dystrophy V Taglietti, K Kefi, L Rivera, O Bergiers, N Cardone, F Coulpier, S Gioftsidi, ... Science Translational Medicine 15 (685), eadd5275, 2023 | 27 | 2023 |
| Ophthalmological management in craniosynostosis R Touzé, D Bremond-Gignac, MP Robert Neurochirurgie 65 (5), 310-317, 2019 | 26 | 2019 |
| Ocular manifestations of cobalamin C type methylmalonic aciduria with homocystinuria LR Fuchs, M Robert, I Ingster-Moati, L Couette, JL Dufier, P de Lonlay, ... Journal of American Association for Pediatric Ophthalmology and Strabismus …, 2012 | 26 | 2012 |
| Craniofacial strategy for syndromic craniosynostosis E Arnaud, G Paternoster, S James, MP Morisseau-Durand, V Couloigner, ... Annales De Chirurgie Plastique Et Esthetique 61 (5), 408-419, 2016 | 25 | 2016 |
| Management of ocular involvement in the acute phase of Stevens-Johnson syndrome and toxic epidermal necrolysis: french national audit of practices, literature review, and … D Thorel, S Ingen-Housz-Oro, G Royer, A Delcampe, N Bellon, ... Orphanet Journal of Rare Diseases 15, 1-7, 2020 | 23 | 2020 |
| Neuroinflammatory disease following severe acute respiratory syndrome coronavirus 2 infection in children M Aubart, CJ Roux, C Durrleman, C Gins, M Hully, M Kossorotoff, ... The Journal of Pediatrics 247, 22-28. e2, 2022 | 22 | 2022 |
| Paramacular temporal atrophy in sickle cell disease occurs early in childhood GC Martin, E Albuisson, V Brousse, M de Montalembert, ... British Journal of Ophthalmology 103 (7), 906-910, 2019 | 22 | 2019 |
| Aripiprazole-induced chorioretinopathy: multimodal imaging and electrophysiological features C Faure, I Audo, C Zeitz, JB Letessier, MP Robert Documenta Ophthalmologica 131, 35-41, 2015 | 21 | 2015 |
| PRPS1 loss-of-function variants, from isolated hearing loss to severe congenital encephalopathy: New cases and literature review O Mercati, MT Abi Warde, G Lina-Granade, M Rio, S Heide, P de Lonlay, ... European Journal of Medical Genetics 63 (11), 104033, 2020 | 20 | 2020 |
