| Discriminative accuracy of plasma phospho-tau217 for Alzheimer disease vs other neurodegenerative disorders S Palmqvist, S Janelidze, YT Quiroz, H Zetterberg, F Lopera, E Stomrud, ... Jama 324 (8), 772-781, 2020 | 680 | 2020 |
| The E280A presenilin 1 Alzheimer mutation produces increased Aβ42 deposition and severe cerebellar pathology CA Lemere, F LoPERA, KS Kosik, CL Lendon, J OssA, TC Saido, ... Nature medicine 2 (10), 1146-1150, 1996 | 651 | 1996 |
| Brain imaging and fluid biomarker analysis in young adults at genetic risk for autosomal dominant Alzheimer's disease in the presenilin 1 E280A kindred: a case-control study EM Reiman, YT Quiroz, AS Fleisher, K Chen, C Velez-Pardo, ... The Lancet Neurology 11 (12), 1048-1056, 2012 | 584 | 2012 |
| A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome B Kremeyer, F Lopera, JJ Cox, A Momin, F Rugiero, S Marsh, CG Woods, ... Neuron 66 (5), 671-680, 2010 | 486 | 2010 |
| Symptom onset in autosomal dominant Alzheimer disease: a systematic review and meta-analysis DC Ryman, N Acosta-Baena, PS Aisen, T Bird, A Danek, NC Fox, A Goate, ... Neurology 83 (3), 253-260, 2014 | 474 | 2014 |
| Clinical features of early-onset Alzheimer disease in a large kindred with an E280A presenilin-1 mutation F Lopera, A Ardilla, A Martínez, L Madrigal, JC Arango-Viana, CA Lemere, ... Jama 277 (10), 793-799, 1997 | 434 | 1997 |
| Alzheimer's Prevention Initiative: a plan to accelerate the evaluation of presymptomatic treatments EM Reiman, J Langbaum, AS Fleisher, RJ Caselli, K Chen, N Ayutyanont, ... Journal of Alzheimer's Disease 26 (s3), 321-329, 2011 | 392 | 2011 |
| Resistance to autosomal dominant Alzheimer’s disease in an APOE3 Christchurch homozygote: a case report JF Arboleda-Velasquez, F Lopera, M O’Hare, S Delgado-Tirado, C Marino, ... Nature medicine 25 (11), 1680-1683, 2019 | 365 | 2019 |
| A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication M Arcos-Burgos, M Jain, MT Acosta, S Shively, H Stanescu, D Wallis, ... Molecular psychiatry 15 (11), 1053-1066, 2010 | 328 | 2010 |
| Visual short-term memory binding deficits in familial Alzheimer’s disease MA Parra, S Abrahams, RH Logie, LG Méndez, F Lopera, S Della Sala Brain 133 (9), 2702-2713, 2010 | 312 | 2010 |
| Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13. 2, 5q33. 3, 11q22, and 17p11 M Arcos-Burgos, FX Castellanos, D Pineda, F Lopera, JD Palacio, ... The American Journal of Human Genetics 75 (6), 998-1014, 2004 | 307 | 2004 |
| World‐Wide FINGERS Network: a global approach to risk reduction and prevention of dementia M Kivipelto, F Mangialasche, HM Snyder, R Allegri, S Andrieu, H Arai, ... Alzheimer's & dementia 16 (7), 1078-1094, 2020 | 282 | 2020 |
| Pre-dementia clinical stages in presenilin 1 E280A familial early-onset Alzheimer's disease: a retrospective cohort study N Acosta-Baena, D Sepulveda-Falla, CM Lopera-Gómez, ... The Lancet Neurology 10 (3), 213-220, 2011 | 266 | 2011 |
| Funciones ejecutivas: aspectos clínicos FL Restrepo Revista Neuropsicología, Neuropsiquiatría y Neurociencias 8 (1), 59-76, 2008 | 264 | 2008 |
| Florbetapir PET analysis of amyloid-β deposition in the presenilin 1 E280A autosomal dominant Alzheimer's disease kindred: a cross-sectional study AS Fleisher, K Chen, YT Quiroz, LJ Jakimovich, MG Gomez, CM Langois, ... The Lancet Neurology 11 (12), 1057-1065, 2012 | 262 | 2012 |
| Meta‐analysis of genome‐wide linkage scans of attention deficit hyperactivity disorder K Zhou, A Dempfle, M Arcos‐Burgos, SC Bakker, T Banaschewski, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147 …, 2008 | 261 | 2008 |
| Hippocampal hyperactivation in presymptomatic familial Alzheimer's disease YT Quiroz, AE Budson, K Celone, A Ruiz, R Newmark, G Castrillon, ... Annals of neurology 68 (6), 865-875, 2010 | 249 | 2010 |
| Apolipoprotein Eε4 modifies Alzheimer's disease onset in an E280A PS1 kindred P Pastor, CM Roe, A Villegas, G Bedoya, S Chakraverty, G García, ... Annals of neurology 54 (2), 163-169, 2003 | 229 | 2003 |
| The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families RF Clark, M Hutton, M Fuldner, S Froelich, E Karran, C Talbot, R Crook, ... Nature genetics 11 (2), 219-222, 1995 | 215 | 1995 |
| Confirmación de la alta prevalencia del trastorno por déficit de atención en una comunidad colombiana DA Pineda, F Lopera, GC Henao, JD Palacio, FX Castellanos, ... Revista de neurología 32 (3), 217-222, 2001 | 208 | 2001 |
Mauricio Arcos-Burgos MD, PhD.Universidad de AntioquiaDirección de correo verificada de udea.edu.co
