| Analysis of shared heritability in common disorders of the brain V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ... Science 360 (6395), eaap8757, 2018 | 1484 | 2018 |
| Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture LK Davis, D Yu, CL Keenan, ER Gamazon, AI Konkashbaev, EM Derks, ... PLoS genetics 9 (10), e1003864, 2013 | 339 | 2013 |
| Genome-wide association study of Tourette's syndrome JM Scharf, D Yu, CA Mathews, BM Neale, SE Stewart, JA Fagerness, ... Molecular psychiatry 18 (6), 721-728, 2013 | 232 | 2013 |
| Genetic make up and structure of Colombian populations by means of uniparental and biparental DNA markers W Rojas, MV Parra, O Campo, MA Caro, JG Lopera, W Arias, C Duque, ... American journal of physical anthropology 143 (1), 13-20, 2010 | 210 | 2010 |
| Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette’s syndrome and OCD D Yu, CA Mathews, JM Scharf, BM Neale, LK Davis, ER Gamazon, ... American Journal of Psychiatry 172 (1), 82-93, 2015 | 153 | 2015 |
| CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1 A Nag, EG Bochukova, B Kremeyer, DD Campbell, H Muller, ... Plos one 8 (3), e59061, 2013 | 102 | 2013 |
| Whole-genome analysis of Azoarcus sp. strain CIB provides genetic insights to its different lifestyles and predicts novel metabolic features Z Martín-Moldes, MT Zamarro, C Del Cerro, A Valencia, MJ Gómez, ... Systematic and Applied Microbiology 38 (7), 462-471, 2015 | 74 | 2015 |
| A CLN5 mutation causing an atypical neuronal ceroid lipofuscinosis of juvenile onset N Pineda-Trujillo, W Cornejo, J Carrizosa, RB Wheeler, S Munera, ... Neurology 64 (4), 740-742, 2005 | 65 | 2005 |
| Association of DRD2 variants and Gilles de la Tourette syndrome in a family-based sample from a South American population isolate I Herzberg, AV Valencia-Duarte, VA Kay, DJ White, H Müller, IC Rivas, ... Psychiatric genetics 20 (4), 179-183, 2010 | 57 | 2010 |
| Genotype imputation performance of three reference panels using African ancestry individuals C Vergara, MM Parker, L Franco, MH Cho, AV Valencia-Duarte, TH Beaty, ... Human genetics 137, 281-292, 2018 | 45 | 2018 |
| Multi-ancestry genome-wide association study of spontaneous clearance of hepatitis C virus C Vergara, CL Thio, E Johnson, AH Kral, TR O’brien, JJ Goedert, ... Gastroenterology 156 (5), 1496-1507. e7, 2019 | 43 | 2019 |
| Mutations in FOXL2 underlying BPES (types 1 and 2) in Colombian families JL Ramírez‐Castro, N Pineda‐Trujillo, AV Valencia, CM Muneton, ... American journal of medical genetics 113 (1), 47-51, 2002 | 34 | 2002 |
| Analysis of antibody binding specificities in twin and SNP-genotyped cohorts reveals that antiviral antibody epitope selection is a heritable trait T Venkataraman, C Valencia, M Mangino, W Morgenlander, SJ Clipman, ... Immunity 55 (1), 174-184. e5, 2022 | 32 | 2022 |
| Neurocognitive subtypes of schizophrenia A Rangel, C Munoz, MV Ocampo, C Quintero, M Escobar, S Botero, ... Actas Españolas de Psiquiatría 43 (3), 80-90, 2015 | 22 | 2015 |
| Association and interaction of AGT, AGTR1, ACE, ADRB2, DRD1, ADD1, ADD2, ATP2B1, TBXA2R and PTGS2 genes on the risk of hypertension in Antioquian population DM Valencia, CA Naranjo, MV Parra, MA Caro, AV Valencia, CJ Jaramillo, ... Biomedica 33 (4), 598-614, 2013 | 21 | 2013 |
| Memoria de trabajo verbal en individuos con esquizofrenia y sus familiares de primer grado: relación con los síntomas negativos y desorganizados. S Botero, C Muñoz, MV Ocampo, M Escobar, A Rangel, C Quintero, ... Actas Españolas de Psiquiatría 41 (3), 106-114, 2013 | 14* | 2013 |
| Producción del conocimiento a través de las tesis doctorales. Estudio de algunas tesis de la generación 2004-2008 del doctorado en educación de la Universidad de Guadalajara ML Chavoya, AC Valencia Miradas analíticas sobre la educación superior, 473-496, 2013 | 12 | 2013 |
| Trans-ancestral fine-mapping of MHC reveals key amino acids associated with spontaneous clearance of hepatitis C in HLA-DQβ1 A Valencia, C Vergara, CL Thio, N Vince, V Douillard, A Grifoni, AL Cox, ... The American Journal of Human Genetics, 2022 | 11 | 2022 |
| Desenlaces cardiovasculares adversos mayores en pacientes con síndrome coronario agudo temprano DA Echeverri-Marín, K Betancur-Salazar, CI Saldarriaga-Giraldo, ... Revista Colombiana de Cardiología 26 (1), 10-16, 2019 | 11 | 2019 |
| Efecto de la hiperglucemia en el síndrome coronario agudo y sus implicaciones en el tratamiento antiagregante plaquetario JP Pérez-Bedoya, N Gallego-Lopera, CA Velarde-Hoyos, ... Iatreia 32 (2), 113-125, 2019 | 10 | 2019 |
Gabriel Bedoya BerríoProfessor of Population GeneticsDirección de correo verificada de udea.edu.co
