Francisco Lopera
Francisco Lopera
Full Professor of University of Antioquia
Verified email at - Homepage
Cited by
Cited by
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
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
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
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
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
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
Reviews of evidence regarding interventions to reduce tobacco use and exposure to environmental tobacco smoke
DP Hopkins, PA Briss, CJ Ricard, CG Husten, VG Carande-Kulis, ...
American journal of preventive medicine 20 (2), 16-66, 2001
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
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
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
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
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
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
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
Funciones ejecutivas: aspectos clínicos
FJL Restrepo
Revista Neuropsicología, Neuropsiquiatría y Neurociencias 8 (1), 59-76, 2008
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
Prevalence estimations of attention-deficit/hyperactivity disorder: differential diagnoses and comorbidities in a Colombian sample
DA Pineda, F Lopera, JD Palacio, D Ramirez, GC Henao
International Journal of Neuroscience 113 (1), 49-71, 2003
Hippocampal hyperactivation in presymptomatic familial Alzheimer's disease
YT Quiroz, AE Budson, K Celone, A Ruiz, R Newmark, G Castrillón, ...
Annals of neurology 68 (6), 865-875, 2010
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
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
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