| PSMB8 encoding the β5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome AK Agarwal, C Xing, GN DeMartino, D Mizrachi, MD Hernandez, ... The American Journal of Human Genetics 87 (6), 866-872, 2010 | 354 | 2010 |
| Hypospadias prevalence and trends in international birth defect surveillance systems, 1980–2010 X Yu, N Nassar, P Mastroiacovo, M Canfield, B Groisman, ... European urology 76 (4), 482-490, 2019 | 102 | 2019 |
| An autosomal recessive syndrome of joint contractures, muscular atrophy, microcytic anemia, and panniculitis-associated lipodystrophy A Garg, MD Hernandez, AB Sousa, L Subramanyam, ... The Journal of Clinical Endocrinology & Metabolism 95 (9), E58-E63, 2010 | 100 | 2010 |
| Decline of neural tube defects cases after a folic acid campaign in Nuevo Leon, Mexico L Martínez de Villarreal, JZV Pérez, PA Vázquez, RH Herrera, ... Teratology 66 (5), 249-256, 2002 | 80 | 2002 |
| The phenotype, psychotype and genotype of bruxism N Cruz‑Fierro, M Martínez‑Fierro, RM Cerda‑Flores, MA Gómez‑Govea, ... Biomedical reports 8 (3), 264-268, 2018 | 56 | 2018 |
| Prevalence, mortality, and spatial distribution of gastroschisis in Mexico VM Salinas-Torres, RA Salinas-Torres, RM Cerda-Flores, ... Journal of pediatric and adolescent gynecology 31 (3), 232-237, 2018 | 45 | 2018 |
| Plasma and urine metabolic profiles are reflective of altered beta-oxidation in non-diabetic obese subjects and patients with type 2 diabetes mellitus JZ Villarreal-Pérez, JZ Villarreal-Martínez, FJ Lavalle-González, ... Diabetology & metabolic syndrome 6, 1-8, 2014 | 45 | 2014 |
| Weekly administration of folic acid and epidemiology of neural tube defects LE Martínez de Villarreal, P Arredondo, R Hernández, JZ Villarreal Maternal and child health journal 10, 397-401, 2006 | 44 | 2006 |
| Tamiz metabólico neonatal por espectrometría de masas en tándem: dos años de experiencia en Nuevo León, México MR Torres-Sepúlveda, LE Martínez-de Villarreal, C Esmer, ... Salud pública de México 50 (3), 200-206, 2008 | 43 | 2008 |
| Clinical and genetic aspects of Turner's syndrome M Ibarra-Ramírez, LE Martínez-de-Villarreal Medicina universitaria 18 (70), 42-48, 2016 | 40 | 2016 |
| Programación fetal de enfermedades expresadas en la etapa adulta LE Martínez de Villarreal Medicina universitaria 10 (39), 108-113, 2008 | 36 | 2008 |
| Analysis of the pathogenic variants of BRCA1 and BRCA2 using next-generation sequencing in women with familial breast cancer: a case–control study OA Zayas-Villanueva, LD Campos-Acevedo, JJ Lugo-Trampe, ... BMC cancer 19, 1-8, 2019 | 31 | 2019 |
| Efecto de la administración semanal de ácido fólico sobre los valores sanguíneos LE Martínez-de Villarreal, C Limón-Benavides, R Valdez-Leal, ... salud pública de méxico 43, 103-107, 2001 | 28 | 2001 |
| Folic acid levels, homocysteine and polymorphism of methylenetetrahydrofolate reductase enzyme (MTHFR) in patients with pre-eclampsia and eclampsia LE Martínez de Villarreal Ginecologia y Obstetricia de Mexico 69, 6-11, 2001 | 24 | 2001 |
| Aumento de la incidencia de gastrosquisis en un hospital de alta especialidad al norte de México. D Hernández Almaguer, G Elizondo Cárdenas, C Barrón Gámez, ... Medicina Universitaria 12 (48), 159-164, 2010 | 18 | 2010 |
| Evaluation of familial factors in a Mexican population-based setting with gastroschisis: Further evidence for an underlying genetic susceptibility VM Salinas-Torres, RA Salinas-Torres, RM Cerda-Flores, ... Journal of Pediatric Surgery 53 (3), 521-524, 2018 | 17 | 2018 |
| Familial occurrence of gastroschisis: a population-based overview on recurrence risk, sex-dependent influence, and geographical distribution VM Salinas-Torres, RA Salinas-Torres, RM Cerda-Flores, ... Pediatric Surgery International 34, 277-282, 2018 | 17 | 2018 |
| Identification of novel mutations in Mexican patients with Aarskog–Scott syndrome M Pérez‐Coria, JJ Lugo‐Trampe, M Zamudio‐Osuna, ... Molecular Genetics & Genomic Medicine 3 (3), 197-202, 2015 | 17 | 2015 |
| GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico AA Hernández-Juárez, J de Jesús Lugo-Trampe, LD Campos-Acevedo, ... International Journal of Pediatric Otorhinolaryngology 78 (12), 2107-2112, 2014 | 17 | 2014 |
| Genética y la enfermedad de Parkinson: Revisión de actualidades G Elizondo-Cárdenas, MA Déctor-Carrillo, HR Martínez-Rodríguez, ... Med. Univer 13 (51), 96-100, 2011 | 17 | 2011 |
