| Global surveillance of trends in cancer survival 2000–14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 … C Allemani, T Matsuda, V Di Carlo, R Harewood, M Matz, M Nikšić, ... The Lancet 391 (10125), 1023-1075, 2018 | 4618 | 2018 |
| Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease C Paisán-Ruı́z, S Jain, EW Evans, WP Gilks, J Simón, M Van Der Brug, ... Neuron 44 (4), 595-600, 2004 | 2776 | 2004 |
| New insights into the genetic etiology of Alzheimer’s disease and related dementias C Bellenguez, F Küçükali, IE Jansen, L Kleineidam, S Moreno-Grau, ... Nature genetics 54 (4), 412-436, 2022 | 1022 | 2022 |
| Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions VM Van Deerlin, PMA Sleiman, M Martinez-Lage, A Chen-Plotkin, ... Nature genetics 42 (3), 234-239, 2010 | 606 | 2010 |
| Association between total, processed, red and white meat consumption and all-cause, CVD and IHD mortality: a meta-analysis of cohort studies I Abete, D Romaguera, AR Vieira, AL de Munain, T Norat British Journal of Nutrition 112 (5), 762-775, 2014 | 530 | 2014 |
| Burden and centralised treatment in Europe of rare tumours: results of RARECAREnet—a population-based study G Gatta, R Capocaccia, L Botta, S Mallone, R De Angelis, E Ardanaz, ... The Lancet Oncology 18 (8), 1022-1039, 2017 | 497 | 2017 |
| Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy JM Morante-Redolat, A Gorostidi-Pagola, S Piquer-Sirerol, A Sáenz, ... Human molecular genetics 11 (9), 1119-1128, 2002 | 382 | 2002 |
| A small noncoding RNA signature found in exosomes of GBM patient serum as a diagnostic tool L Manterola, E Guruceaga, JG Pérez-Larraya, M González-Huarriz, ... Neuro-oncology 16 (4), 520-527, 2014 | 364 | 2014 |
| Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A S Baghdiguian, M Martin, I Richard, F Pons, C Astier, N Bourg, RT Hay, ... Nature medicine 5 (5), 503-511, 1999 | 354 | 1999 |
| Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy C Fugier, AF Klein, C Hammer, S Vassilopoulos, Y Ivarsson, A Toussaint, ... Nature medicine 17 (6), 720-725, 2011 | 351 | 2011 |
| Clinical correlations with Lewy body pathology in LRRK2-related Parkinson disease LV Kalia, AE Lang, LN Hazrati, S Fujioka, ZK Wszolek, DW Dickson, ... JAMA neurology 72 (1), 100-105, 2015 | 324 | 2015 |
| Differential micro RNA expression in PBMC from multiple sclerosis patients D Otaegui, SE Baranzini, R Armañanzas, B Calvo, M Muñoz-Culla, ... PloS one 4 (7), e6309, 2009 | 309 | 2009 |
| A multicentre validation study of the diagnostic value of plasma neurofilament light NJ Ashton, S Janelidze, A Al Khleifat, A Leuzy, EL van der Ende, ... Nature communications 12 (1), 3400, 2021 | 297 | 2021 |
| Genetic and epigenetic modifications of Sox2 contribute to the invasive phenotype of malignant gliomas MM Alonso, R Diez-Valle, L Manterola, A Rubio, D Liu, N Cortes-Santiago, ... PloS one 6 (11), e26740, 2011 | 275 | 2011 |
| 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 | 274 | 1997 |
| Oncogenicity of the developmental transcription factor Sox9 A Matheu, M Collado, C Wise, L Manterola, L Cekaite, AJ Tye, ... Cancer research 72 (5), 1301-1315, 2012 | 255 | 2012 |
| Calpainopathy—a survey of mutations and polymorphisms I Richard, C Roudaut, A Saenz, R Pogue, J Grimbergen, LVB Anderson, ... The American Journal of Human Genetics 64 (6), 1524-1540, 1999 | 235 | 1999 |
| ALS: A bucket of genes, environment, metabolism and unknown ingredients M Zufiria, FJ Gil-Bea, R Fernandez-Torron, JJ Poza, JL Muñoz-Blanco, ... Progress in neurobiology 142, 104-129, 2016 | 214 | 2016 |
| Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain). M Urtasun, A Saenz, C Roudaut, JJ Poza, JA Urtizberea, AM Cobo, ... Brain: a journal of neurology 121 (9), 1735-1747, 1998 | 213 | 1998 |
| Progression of somatic CTG repeat length heterogeneity in the blood cells of myotonic dystrophy patients L Martorell, DG Monckton, J Gamez, KJ Johnson, I Gich, AL de Munain, ... Human molecular genetics 7 (2), 307-312, 1998 | 200 | 1998 |
