| Genetic and molecular aspects of androgenetic alopecia L Martinez-Jacobo, CD Villarreal-Villarreal, R Ortiz-López, ... Indian journal of dermatology, venereology and leprology 84, 263, 2018 | 80 | 2018 |
| A new gene expression signature for triple-negative breast cancer using frozen fresh tissue before neoadjuvant chemotherapy SK Santuario-Facio, S Cardona-Huerta, YX Perez-Paramo, V Trevino, ... Molecular Medicine 23, 101-111, 2017 | 51 | 2017 |
| Prostaglandins in androgenetic alopecia in 12 men and four female CD Villarreal‐Villarreal, RD Sinclair, L Martínez‐Jacobo, ... Journal of the European Academy of Dermatology and Venereology 33 (5), e214-e215, 2019 | 15 | 2019 |
| Evaluation of the expression of genes associated with inflammation and apoptosis in androgenetic alopecia by targeted RNA-seq L Martinez-Jacobo, CI Ancer-Arellano, R Ortiz-Lopez, ... Skin Appendage Disorders 4 (4), 268-273, 2018 | 12 | 2018 |
| Clinical and molecular delineation of duplication 9p24. 3q21. 11 in a patient with psychotic behavior L Martínez-Jacobo, R Ortíz-López, A Rizo-Méndez, V García-Molina, ... Gene 560 (1), 124-127, 2015 | 12 | 2015 |
| Association of CYP2C19* 2 polymorphism with clopidogrel resistance among patients with high cardiovascular risk in Northeastern Mexico FR Cedillo-Salazar, L Martínez-Jacobo, YX Pérez-Páramo, ... Archivos de cardiología de México 89 (4), 324-329, 2019 | 10 | 2019 |
| Delineation of a de novo 7q21. 3q31. 1 deletion by CGH-SNP arrays in a girl with multiple congenital anomalies including severe glaucoma L Martínez-Jacobo, C Córdova-Fletes, R Ortiz-López, F Rivas, ... Molecular syndromology 4 (6), 285-291, 2013 | 9 | 2013 |
| A rare co-occurrence of intestinal malrotation and Hirschsprung's disease in a neonate with 13q21. 31q33. 1 interstitial deletion including the EDNRB gene T Chatmethakul, R Phaltas, G Minzes, J Martinez, R Bhat Journal of Pediatric Genetics 8 (03), 142-146, 2019 | 5 | 2019 |
| Exome sequencing reveals three homozygous missense variants in SNRPA in two sisters with syndromic intellectual disability MM Rangel‐Sosa, LE Figuera‐Villanueva, IA González‐Ramos, ... Clinical Genetics 93 (6), 1229-1233, 2018 | 5 | 2018 |
| Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositis C Córdova-Fletes, MM Rangel-Sosa, LA Martínez-Jacobo, ... Autoimmunity 53 (6), 344-352, 2020 | 4 | 2020 |
| A del (13)(q21. 32q31. 2) dn refined to 21.9 Mb in a female toddler with irides heterochromia and hypopigmentation: appraisal of interstitial mid-13q deletions C Córdova-Fletes, H Rivera, EA Garza-Villarreal, NA Vázquéz-Cárdenas, ... Clinical Dysmorphology 26 (1), 33-37, 2017 | 3 | 2017 |
| Global expression profile and global genome methylation signatures in male patients with androgenetic alopecia LA Martinez-Jacobo, CI Ancer-Arellano, CD Villarreal-Villarreal, ... J Eur Acad Dermatol Venereol 34 (5), e216-e218, 2020 | 2 | 2020 |
| A chromoanagenesis-driven ultra-complex t (5; 7; 21) dn truncates neurodevelopmental genes in a disabled boy as revealed by whole-genome sequencing C Córdova-Fletes, H Rivera, TA Aguayo-Orozco, LA Martínez-Jacobo, ... European Journal of Medical Genetics 65 (10), 104579, 2022 | 1 | 2022 |
| Pilot study: genetic distribution of AR, FGF5, SULT1A1 and CYP3A5 polymorphisms in male Mexican population with androgenetic alopecia D Martinez-Chapoy, FJ Cruz-Arroyo, FD Ancer-Leal, RA Rodriguez-Leal, ... International Journal of Molecular Epidemiology and Genetics 13 (3), 32, 2022 | | 2022 |
| Großes und atypisches Feuermal mit Gesichtsdeformität CD Villarreal-Villarreal, J Ancer-Arellano, E Boland-Rodríguez, ... JDDG: Journal der Deutschen Dermatologischen Gesellschaft 17 (1), 68-70, 2019 | | 2019 |
| A giant and atypical port‐wine stain with facial deformity CD Villarreal‐Villarreal, J Ancer‐Arellano, E Boland‐Rodríguez, ... JDDG: Journal der Deutschen Dermatologischen Gesellschaft 17 (1), 68-69, 2019 | | 2019 |
| Análisis del perfil de expresión global y metilación del genoma en pacientes masculinos con alopecia androgenética LA Martínez Jacobo Universidad Autónoma de Nuevo León, 2017 | | 2017 |
| Caracterización molecular por aCGH de alteraciones genómicas en pacientes con discapacidad intelectual y malformaciones múltiples de etiología desconocida LA Martínez Jacobo Universidad Autónoma de Nuevo León, 2013 | | 2013 |
| Word count: 630 Tables: 1 Figures CD Villarreal-Villarreal, RD Sinclair, L Martínez-Jacobo, R Ortiz-Lopez, ... | | |
