| Genetics of homocysteine metabolism and associated disorders S Brustolin, R Giugliani, TM Felix Brazilian Journal of Medical and Biological Research 43, 1-7, 2010 | 330 | 2010 |
| Medical sequencing of candidate genes for nonsyndromic cleft lip and palate AR Vieira, JR Avila, S Daack-Hirsch, E Dragan, TM Félix, F Rahimov, ... PLoS genetics 1 (6), e64, 2005 | 324 | 2005 |
| The genetic basis of DOORS syndrome: an exome-sequencing study PM Campeau, D Kasperaviciute, JT Lu, LC Burrage, C Kim, M Hori, ... The Lancet Neurology 13 (1), 44-58, 2014 | 279 | 2014 |
| Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association … ML Marazita, AC Lidral, JC Murray, LL Field, BS Maher, ... Human heredity 68 (3), 151-170, 2009 | 177 | 2009 |
| Thalidomide, a current teratogen in South America EE Castilla, P Ashton‐Prolla, E Barreda‐Mejia, D Brunoni, DP Cavalcanti, ... Teratology 54 (6), 273-277, 1996 | 150 | 1996 |
| TBC1D24 genotype–phenotype correlation: Epilepsies and other neurologic features S Balestrini, M Milh, C Castiglioni, K Lüthy, MJ Finelli, P Verstreken, ... Neurology 87 (1), 77-85, 2016 | 119 | 2016 |
| A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects FP Favaro, L Alvizi, RM Zechi-Ceide, D Bertola, TM Felix, J de Souza, ... The American Journal of Human Genetics 94 (1), 120-128, 2014 | 118 | 2014 |
| Polymorphisms in genes MTHFR, MTR and MTRR are not risk factors for cleft lip/palate in South Brazil APC Brandalize, E Bandinelli, JB Borba, TM Felix, I Roisenberg, ... Brazilian Journal of Medical and Biological Research 40, 787-791, 2007 | 101 | 2007 |
| Genetic causes of intellectual disability in a birth cohort: A population‐based study SM Karam, M Riegel, SL Segal, TM Félix, AJD Barros, IS Santos, ... American Journal of Medical Genetics Part A 167 (6), 1204-1214, 2015 | 91 | 2015 |
| The role of methylenetetrahydrofolate reductase in acute lymphoblastic leukemia in a Brazilian mixed population CW Zanrosso, A Hatagima, M Emerenciano, F Ramos, A Figueiredo, ... Leukemia research 30 (4), 477-481, 2006 | 91 | 2006 |
| Defining new guidelines for screening the 22q11. 2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature FP Monteiro, TP Vieira, IC Sgardioli, MC Molck, AP Damiano, J Souza, ... European journal of pediatrics 172, 927-945, 2013 | 84 | 2013 |
| An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects WD Fakhouri, F Rahimov, C Attanasio, EN Kouwenhoven, ... Human molecular genetics 23 (10), 2711-2720, 2014 | 71 | 2014 |
| High dosage folic acid supplementation, oral cleft recurrence and fetal growth GL Wehby, TM Félix, N Goco, A Richieri-Costa, H Chakraborty, J Souza, ... International journal of environmental research and public health 10 (2 …, 2013 | 63 | 2013 |
| A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population TK de Araujo, R Secolin, TM Félix, LT De Souza, MÍB Fontes, IL Monlleó, ... Journal of Cranio-Maxillofacial Surgery 44 (1), 16-20, 2016 | 60 | 2016 |
| Muscle strength, joint range of motion, and gait in children and adolescents with osteogenesis imperfecta E Brizola, ALP Staub, TM Félix Pediatric Physical Therapy 26 (2), 245-252, 2014 | 57 | 2014 |
| Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern Brazil TM Félix, S Leistner, R Giugliani Birth Defects Research Part A: Clinical and Molecular Teratology 70 (7), 459-463, 2004 | 54 | 2004 |
| Oral cleft prevention program (OCPP) GL Wehby, N Goco, D Moretti-Ferreira, T Felix, A Richieri-Costa, ... BMC pediatrics 12, 1-33, 2012 | 53 | 2012 |
| Intellectual disability in a birth cohort: prevalence, etiology, and determinants at the age of 4 years SM Karam, AJD Barros, A Matijasevich, IS Dos Santos, L Anselmi, ... Public Health Genomics 19 (5), 290-297, 2016 | 50 | 2016 |
| Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly FR Vargas, E Roessler, K Gaudenz, E Belloni, AS Whitehead, PN Kirke, ... Human genetics 102, 387-392, 1998 | 50 | 1998 |
| Rare variants in the epithelial cadherin gene underlying the genetic etiology of nonsyndromic cleft lip with or without cleft palate LA Brito, GL Yamamoto, S Melo, C Malcher, SG Ferreira, J Figueiredo, ... Human mutation 36 (11), 1029-1033, 2015 | 49 | 2015 |
