| Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements P Liu, A Erez, SCS Nagamani, SU Dhar, KE Kołodziejska, ... Cell 146 (6), 889-903, 2011 | 459 | 2011 |
| 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 | 30 | 2019 |
| 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 |
| Maternal folic acid intake and methylation status of genes associated with ventricular septal defects in children: Case–control study SM González-Peña, G Calvo-Anguiano, LE Martínez-de-Villarreal, ... Nutrients 13 (6), 2071, 2021 | 12 | 2021 |
| Detection of Turner Syndrome by Quantitative PCR of SHOX and VAMP7 Genes M Ibarra-Ramírez, MJ Zamudio-Osuna, LD Campos-Acevedo, ... Genetic testing and molecular biomarkers 19 (2), 88-92, 2015 | 11 | 2015 |
| Phenotypic Variation in patients with homozygous c. 1678G> T mutation in EVC Gene: report of two mexican families with ellis-van creveld syndrome M Ibarra-Ramirez, LD Campos-Acevedo, J Lugo-Trampe, ... The American Journal of Case Reports 18, 1325, 2017 | 8 | 2017 |
| A novel phenotype characterized by digital abnormalities, intellectual disability, and short stature in a Mexican family maps to Xp11. 4–p11. 21 MC Barboza‐Cerda, LD Campos‐Acevedo, R Rangel, ... American Journal of Medical Genetics Part A 161 (2), 237-243, 2013 | 7 | 2013 |
| Dosage of sex chromosomal genes in blood deposited on filter paper for neonatal screening of sex chromosome aneuploidy LD Campos-Acevedo, M Ibarra-Ramirez, J de Jesús Lugo-Trampe, ... Genetic Testing and Molecular Biomarkers 20 (12), 786-790, 2016 | 6 | 2016 |
| Displasia tanatofórica en un embarazo gemelar: Hallazgos prenatales y revisión de la literatura D Campos-Acevedo, A Martínez-Mendoza, R Ambriz-López, ... Perinatología y Reproducción Humana 24 (1), 36-41, 2010 | 5 | 2010 |
| Molecular characterization of associated pathogens in febrile patients during inter-epidemic periods of urban arboviral diseases in Tapachula southern Mexico G Calvo-Anguiano, JJ Lugo-Trampe, G Ponce-García, A Lugo-Trampe, ... Pathogens 10 (11), 1450, 2021 | 3 | 2021 |
| A case series of infants with increased VAMP7 gene dosage at birth and virilization defects S Chávez-López, J de Jesús Lugo-Trampe, M Ibarra-Ramírez, ... Journal of Pediatric Urology 16 (4), 423. e1-423. e6, 2020 | 3 | 2020 |
| Gene Copy Number Quantification of SHOX, VAMP7, and SRY for the Detection of Sex Chromosome Aneuploidies in Neonates M Ibarra-Ramírez, JJ Lugo-Trampe, LD Campos-Acevedo, ... Genetic testing and molecular biomarkers 24 (6), 352-358, 2020 | 2 | 2020 |
| Congenital Heart Diseases: Genetic Risk Variants and Their Methylation Status M Calzada-Dávila, G Calvo-Anguiano, LE Martínez-de-Villarreal, ... Genes 13 (11), 2115, 2022 | 1 | 2022 |
| Bloom syndrome sans characteristic facial features in a Mestizo patient-a diagnostic challenge S Chavez-Alvarez, A Villarreal-Martinez, MDR Velasco-Campos, ... Indian Journal of Dermatology, Venereology and Leprology 85, 130, 2019 | 1 | 2019 |
| Clinical and molecular analysis in a series of mexican patients with clinical diagnosis of fibrodysplasia ossificans progressiva (FOP) LHB Flores-Gallegos, A Casas-Avila, L de Leon-Suarez, ... Int J Clin Exp Med 9 (1), 423-432, 2016 | 1 | 2016 |
| Optic nerve abnormalities in female-restricted Wieacker-Wolff syndrome by a novel variant in the ZC4H2 gene M Ibarra-Ramírez, ML Fernandez-de-Luna, LD Campos-Acevedo, ... Ophthalmic Genetics 44 (5), 465-468, 2023 | | 2023 |
| Chromosomal Abnormalities of Interest in Turner Syndrome: An Update M Ibarra-Ramírez, LD Campos-Acevedo, LEM de Villarreal Journal of Pediatric Genetics, 2023 | | 2023 |
| Molecular diagnosis of Retinal Dystrophies in Mexican patients. ML Fernandez-de Luna, MI Ramirez, LD Campos-Acevedo, ... Investigative Ophthalmology & Visual Science 64 (8), 1530-1530, 2023 | | 2023 |
| Consulta génetica y asesoramiento IP Rodríguez Sánchez, LD Campos Acevedo, M Ibarra Ramírez, ... Biología y Sociedad 2 (3), 45-54, 2019 | | 2019 |
Laura MARTINEZ de VillarrealProfesor Universidad Autónoma de Nuevo LeónAdresse e-mail validée de uanl.edu.mx
