Formación académica
Trayectoria profesional y docente
Distinciones y premios
Reconocimiento como Estudiante distinguido de Posgrado 2013, Facultad de Medicina UANL.
Mención Summa Cum Laude. Doctorado en Ciencias 2018. UANL.
Publicaciones
1. C Córdova-Fletes, H Rivera, TA Aguayo-Orozco, LA Martínez-Jacobo. (2022) A chromoanagenesis-driven ultra-complex t (5; 7; 21) dn truncates neurodevelopmental genes in a disabled boy as revealed by wholegenome sequencing. European Journal of Medical Genetics 65 (10), 104579.
2. Daniela Martinez-Chapoy, Francisco J Cruz-Arroyo, Francisco D Ancer-Leal, Regina A Rodriguez-Leal, Bianka D Camacho-Zamora, Daniela A Guzman-Sanchez, Nelly A Espinoza-Gonzalez, Lizeth Martinez-Jacobo, Ivan A Marino-Martinez (2022). Pilot study: genetic distribution of AR, FGF5, SULT1A1 and CYP3A5 polymorphisms in male Mexican population with androgenetic alopecia. International Journal of Molecular Epidemiology and Genetics 13 (3).
3. Carlos Córdova-Fletes, Martha M Rangel-Sosa, Lizeth A Martínez-Jacobo, et al. (2020). Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositis. Autoimmunity 53 (6), 344-352.
4. Martínez-Jacobo Lizeth, et al. (2020). Global expression profile and global genome methylation signatures in male patients with androgenetic alopecia. Journal of the European Academy of Dermatology and Venereology 34 (5), e216-e218.
5. Félix R Cedillo-Salazar, Lizeth Martínez-Jacobo, Yadira X Pérez-Páramo, et al. (2019). Association of CYP2C19* 2 polymorphism with clopidogrel resistance among patients with high cardiovascular risk in Northeastern Mexico. Archivos de cardiologia de Mexico 89 (4), 324-329.
6. CD Villarreal‐Villarreal, RD Sinclair, L Martínez‐Jacobo, et al. (2019). Prostaglandins in androgenetic alopecia in 12 men and four female. Journal of the European Academy of Dermatology and Venereology 33 (5), e214-e215.
7. César Daniel Villarreal‐Villarreal, Jesus Ancer‐Arellano, Estefania Boland‐Rodríguez, Lizeth Martínez‐ Jacobo, Jorge Ocampo‐Candiani. (2019). A giant and atypical port‐wine stain with facial deformity. JDDG: Journal der Deutschen Dermatologischen Gesellschaft 17 (1), 68-69.
8. MM Rangel‐Sosa, LE Figuera‐Villanueva, IA González‐Ramos, YX Pérez‐Páramo, LA Martínez‐Jacobo, L Arnaud‐López, JA Nastasi‐Catanese, AM Rivas‐Estilla, KA Galán‐Huerta, A Rojas‐Martínez, R Ortiz‐López, C Córdova‐Fletes. Exome sequencing reveals three homozygous missense variants in SNRPA in two sisters with syndromic intellectual disability. (2018). Clinical Genetics 93(6), 1229-33.
9. Martínez-Jacobo et al. (2018). Genetic and molecular aspects of androgenetic alopecia. Indian Journal of Dermatology, Venereology, and Leprology 84 (3), 263.
10. Martínez-Jacobo et al. (2018). Evaluation of the expression of genes associated with inflammation and apoptosis in androgenetic alopecia by targeted RNA-seq. Skin Appendage Disord 2018;4:268–273. https://doi.org/10.1159/000484530
11. Santuario-Facio SK, Cardona-Huerta S, Perez-Paramo YX, Trevino V, Hernandez-Cabrera F, Rojas-Martinez A, Uscanga-Perales G, Martinez-Rodriguez JL, Martinez-Jacobo L, Padilla-Rivas G, Muñoz-Maldonado G, Gonzalez-Guerrero JF, Valero-Gomez J, Vazquez-Guerrero AL, Martinez-Rodriguez HG, Barboza-Quintana A, Barboza-Quintana O, Garza-Guajardo R, Ortiz-Lopez R.(2017). A New Gene Expression Signature for Triple Negative Breast Cancer Using Frozen Fresh Tissue before Neoadjuvant Chemotherapy. Mol Med: 4;23. doi: 10.2119/molmed.2016.00257
12. Córdova-Fletes C1, Rivera H, Garza-Villarreal EA, Vázquéz-Cárdenas NA, Martínez-Jacobo LA, MorenoAndrade T. 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. Clin Dysmorphol. 2017 Jan;26(1):33-37.
13. Lizeth Martínez-Jacobo, Rocío Ortíz-López, Alfredo Rizo-Méndez, Viridiana García-Molina, Sandra K.Santuario-Facio, Fernando Rivas, Augusto Rojas-Martínez.(2015). Clinical and molecular delineation of duplication 9p24.3q21.11 in a patient with psychotic behavior. Gene. doi:10.1016/j.gene.2015.02.010.
14. L. Martínez-Jacobo, C. Córdova-Fletes , R. Ortiz-López, F. Rivas-Solís, C. Saucedo-Carrasco, A. RojasMartinez. (2013). Delineation of a de novo 7q21 . 3q31 . 1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma. Molecular Syndromology, 1–7. doi:10.1159/000353510