| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1366 | 2018 |
| Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine P Gormley, V Anttila, BS Winsvold, P Palta, T Esko, TH Pers, KH Farh, ... Nature genetics 48 (8), 856-866, 2016 | 721 | 2016 |
| Herpes simplex virus encephalitis is a trigger of brain autoimmunity T Armangue, F Leypoldt, I Málaga, M Raspall‐Chaure, I Marti, C Nichter, ... Annals of neurology 75 (2), 317-323, 2014 | 478 | 2014 |
| Genome-wide association analysis identifies susceptibility loci for migraine without aura T Freilinger, V Anttila, B De Vries, R Malik, M Kallela, GM Terwindt, ... Nature genetics 44 (7), 777-782, 2012 | 404 | 2012 |
| The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome FM Santorelli, S Shanske, A Macaya, DC DeVivo, S DiMauro Annals of Neurology: Official Journal of the American Neurological …, 1993 | 311 | 1993 |
| TuberOus SClerosis registry to increase disease Awareness (TOSCA)–baseline data on 2093 patients JC Kingswood, GB d’Augères, E Belousova, JC Ferreira, T Carter, ... Orphanet journal of rare diseases 12, 1-13, 2017 | 216 | 2017 |
| Clinical and biochemical spectrum of D‐bifunctional protein deficiency S Ferdinandusse, S Denis, PAW Mooyer, C Dekker, M Duran, ... Annals of neurology 59 (1), 92-104, 2006 | 196 | 2006 |
| AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders V Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ... Nature communications 10 (1), 3094, 2019 | 184 | 2019 |
| Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor S Mardy, Y Miura, F Endo, I Matsuda, L Sztriha, P Frossard, A Moosa, ... The American Journal of Human Genetics 64 (6), 1570-1579, 1999 | 183 | 1999 |
| Identification of necrotic cell death by the TUNEL assay in the hypoxic-ischemic neonatal rat brain C de Torres, F Munell, I Ferrer, J Reventós, A Macaya Neuroscience letters 230 (1), 1-4, 1997 | 183 | 1997 |
| Clinical course of sly syndrome (mucopolysaccharidosis type VII) AM Montaño, N Lock-Hock, RD Steiner, BH Graham, M Szlago, ... Journal of medical genetics 53 (6), 403-418, 2016 | 180 | 2016 |
| Evidence of nuclear DNA fragmentation following hypoxia‐ischemia in the infant rat brain, and transient forebrain ischemia in the adult gerbil I Ferrer, A Tortosa, A Macaya, A Sierra, D Moreno, F Munell, R Blanco, ... Brain pathology 4 (2), 115-122, 1994 | 169 | 1994 |
| Apoptosis in substantia nigra following developmental striatal excitotoxic injury. A Macaya, F Munell, RM Gubits, RE Burke Proceedings of the National Academy of Sciences 91 (17), 8117-8121, 1994 | 165 | 1994 |
| Epilepsy in tuberous sclerosis complex: findings from the TOSCA Study R Nabbout, E Belousova, MP Benedik, T Carter, V Cottin, P Curatolo, ... Epilepsia open 4 (1), 73-84, 2019 | 155 | 2019 |
| TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study PJ De Vries, E Belousova, MP Benedik, T Carter, V Cottin, P Curatolo, ... Orphanet journal of rare diseases 13, 1-13, 2018 | 124 | 2018 |
| Fusion of the human gene for the polyubiquitination coeffector UEV1 with Kua, a newly identified gene TM Thomson, JJ Lozano, N Loukili, R Carrió, F Serras, B Cormand, ... Genome research 10 (11), 1743-1756, 2000 | 119 | 2000 |
| Naturally occurring cell death in the developing cerebral cortex of the rat. Evidence of apoptosis-associated internucleosomal DNA fragmentation I Ferrer, A Tortosa, R Blanco, F Martin, T Serrano, A Planas, A Macaya Neuroscience letters 182 (1), 77-79, 1994 | 119 | 1994 |
| Both apoptosis and necrosis occur following intrastriatal administration of excitotoxins I Ferrer, F Martin, T Serrano, J Reiriz, E Perez-Navarro, J Alberch, ... Acta neuropathologica 90, 504-510, 1995 | 114 | 1995 |
| Neonatal hypoxic-ischemic or excitotoxic striatal injury results in a decreased adult number of substantia nigra neurons RE Burke, A Macaya, D DeVivo, N Kenyon, EM Janec Neuroscience 50 (3), 559-569, 1992 | 102 | 1992 |
| Common variant burden contributes to the familial aggregation of migraine in 1,589 families P Gormley, MI Kurki, ME Hiekkala, K Veerapen, P Häppölä, AA Mitchell, ... Neuron 98 (4), 743-753. e4, 2018 | 97 | 2018 |
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