| Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes S Kondo, BC Schutte, RJ Richardson, BC Bjork, AS Knight, Y Watanabe, ... Nature genetics 32 (2), 285-289, 2002 | 1068 | 2002 |
| Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate TM Zucchero, ME Cooper, BS Maher, S Daack-Hirsch, B Nepomuceno, ... New England Journal of Medicine 351 (8), 769-780, 2004 | 786 | 2004 |
| A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 TH Beaty, JC Murray, ML Marazita, RG Munger, I Ruczinski, JB Hetmanski, ... Nature genetics 42 (6), 525-529, 2010 | 677 | 2010 |
| Risk HLA-DQA1 and PLA2R1 Alleles in Idiopathic Membranous Nephropathy HC Stanescu, M Arcos-Burgos, A Medlar, D Bockenhauer, A Kottgen, ... New England Journal of Medicine 364 (7), 616-626, 2011 | 623 | 2011 |
| Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations D Bockenhauer, S Feather, HC Stanescu, S Bandulik, AA Zdebik, ... New England Journal of Medicine 360 (19), 1960-1970, 2009 | 611 | 2009 |
| Cognitive neuroscience of attention MI Posner Guilford Press, 2012 | 535 | 2012 |
| 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 | 465 | 1997 |
| Genetics of population isolates M Arcos‐Burgos, M Muenke Clinical genetics 61 (4), 233-247, 2002 | 355 | 2002 |
| 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 | 340 | 2010 |
| Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder R Kleta, E Romeo, Z Ristic, T Ohura, C Stuart, M Arcos-Burgos, MH Dave, ... Nature genetics 36 (9), 999-1002, 2004 | 328 | 2004 |
| 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 | 311 | 2004 |
| Young adult outcomes in the follow‐up of the multimodal treatment study of attention‐deficit/hyperactivity disorder: Symptom persistence, source discrepancy, and height suppression JM Swanson, LE Arnold, BSG Molina, MH Sibley, LT Hechtman, ... Journal of Child Psychology and Psychiatry 58 (6), 663-678, 2017 | 309 | 2017 |
| Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35 ML Marazita, JC Murray, AC Lidral, M Arcos-Burgos, ME Cooper, ... The American Journal of Human Genetics 75 (2), 161-173, 2004 | 309 | 2004 |
| Support for association between ADHD and two candidate genes: NET1 and DRD1 AJ Bobb, AM Addington, E Sidransky, MC Gornick, JP Lerch, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 134 …, 2005 | 292 | 2005 |
| 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 | 274 | 2008 |
| Myalgic encephalomyelitis/chronic fatigue syndrome: a comprehensive review M Cortes Rivera, C Mastronardi, CT Silva-Aldana, M Arcos-Burgos, ... Diagnostics 9 (3), 91, 2019 | 231 | 2019 |
| 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 | 220 | 1995 |
| 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 | 219 | 2010 |
| A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24. 2, 17q23 and 19q13 EJ Leslie, JC Carlson, JR Shaffer, E Feingold, G Wehby, CA Laurie, ... Human molecular genetics 25 (13), 2862-2872, 2016 | 214 | 2016 |
| FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate LM Moreno, MA Mansilla, SA Bullard, ME Cooper, TD Busch, J Machida, ... Human molecular genetics 18 (24), 4879-4896, 2009 | 181 | 2009 |
Francisco LoperaFull Professor of University of Antioquia在 gna.org.co 的电子邮件经过验证
