| 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, 2010 | 360 | 2010 |
| Linear clinical progression, independent of age of onset, in Niemann–Pick disease, type C NM Yanjanin, JI Vélez, A Gropman, K King, SE Bianconi, SK Conley, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153 …, 2010 | 227 | 2010 |
| Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly E Roessler, MV Ouspenskaia, JD Karkera, JI Vélez, A Kantipong, ... The American Journal of Human Genetics 83 (1), 18-29, 2008 | 196 | 2008 |
| Executive Function and Theory of Mind in Children with ADHD: A Systematic Review W Pineda-Alhucema, E Aristizabal, J Escudero-Cabarcas, J Acosta-López, ... Neuropsychology Review, 1-9, 2018 | 181 | 2018 |
| Analysis of genotype–phenotype correlations in human holoprosencephaly BD Solomon, S Mercier, JI Vélez, DE Pineda‐Alvarez, A Wyllie, N Zhou, ... American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2010 | 162 | 2010 |
| APOE*E2 allele delays age of onset in PSEN1 E280A Alzheimer’s disease JI Vélez, F Lopera, D Sepulveda-Falla, HR Patel, AS Johar, A Chuah, ... Molecular Psychiatry 21 (7), 916, 2016 | 141 | 2016 |
| Robotic approach for cervical cancer: Comparison with laparotomy A case control study A Maggioni, L Minig, V Zanagnolo, M Peiretti, F Sanguineti, L Bocciolone, ... Gynecologic oncology 115 (1), 60-64, 2009 | 137 | 2009 |
| Symptomatology of autism spectrum disorder in a population with neurofibromatosis type 1 KS Walsh, JI Vélez, PG Kardel, DM Imas, M Muenke, RJ Packer, ... Developmental Medicine & Child Neurology 55 (2), 131-138, 2013 | 136 | 2013 |
| Comparison between SVM and logistic regression: Which one is better to discriminate? DA Salazar, JI Vélez, JC Salazar Revista Colombiana de Estadística 35 (2), 223-237, 2012 | 129 | 2012 |
| Analysis of component findings in 79 patients diagnosed with VACTERL association BD Solomon, DE Pineda‐Alvarez, MS Raam, SM Bous, AA Keaton, ... American Journal of Medical Genetics Part A 152 (9), 2236-2244, 2010 | 120 | 2010 |
| Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function F Lacbawan, BD Solomon, E Roessler, K El-Jaick, S Domené, JI Velez, ... Journal of medical genetics 46 (6), 389, 2009 | 107 | 2009 |
| Exosomes: Potential Disease Biomarkers and New Therapeutic Targets MI Mosquera-Heredia, LC Morales, OM Vidal, E Barceló, ... Biomedicines 9, 1061, 2021 | 100 | 2021 |
| The mutational spectrum of holoprosencephaly‐associated changes within the SHH gene in humans predicts loss‐of‐function through either key structural … E Roessler, KB El‐Jaick, C Dubourg, JI Vélez, BD Solomon, ... Human mutation 30 (10), E921-E935, 2009 | 97 | 2009 |
| A common genetic network underlies substance use disorders and disruptive or externalizing disorders M Arcos-Burgos, JI Vélez, BD Solomon, M Muenke Human Genetics, 1-13, 2012 | 95 | 2012 |
| Validity and Reliability of the Multidimensional Scale of Perceived Social Support in Colombian Adolescents AM Trejos-Herrera, MJ Bahamón, Y Alarcón-Vásquez, JI Vélez, ... Psychosocial Intervention 27 (1), 56-63, 2018 | 90 | 2018 |
| Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals BD Solomon, F Lacbawan, S Mercier, NJ Clegg, MR Delgado, ... Journal of medical genetics 47 (8), 513-524, 2010 | 90 | 2010 |
| Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly E Roessler, W Pei, MV Ouspenskaia, JD Karkera, JI Veléz, ... Molecular genetics and metabolism 98 (1-2), 225-234, 2009 | 84 | 2009 |
| A new approach to the Box–Cox transformation JI Vélez, JC Correa, F Marmolejo-Ramos Frontiers in Applied Mathematics and Statistics 1, 12, 2015 | 80 | 2015 |
| A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD M Jain, JI Vélez, MT Acosta, LG Palacio, J Balog, E Roessler, D Pineda, ... Molecular Psychiatry, 2011 | 80 | 2011 |
| The PHF21B gene is associated with major depression and modulates the stress response ML Wong, M Arcos-Burgos, S Liu, JI Velez, C Yu, BT Baune, MC Jawahar, ... Molecular Psychiatry, 2016 | 68 | 2016 |
Mauricio Arcos-Burgos MD, PhD.Universidad de Antioquiaایمیل تأیید شده در udea.edu.co