| 1 | Genetic analysis of muscular dystrophies: our experience in Mexico | Coautor: Luna-Angulo, Alexandra Berenice, Escobar-Cedillo, Rosa Elena, Lopez-Hernandez, Luz Berenice, Miranda-Duarte, Antonio, et al. | 2021 | FOLIA NEUROPATHOLOGICA | WoS-id: 000705084900008
Scopus-id: 2-s2.0-85117047121
| 4 | 5 |
| 2 | Ursolic and oleanolic acids induce mitophagy in a549 human lung cancer cells | Coautor: Luna-Angulo A.B., Castrejón-Jiménez N.S., Leyva-Paredes K., Baltierra-Uribe S.L., et al. | 2019 | Molecules | WoS-id: 000496242300029
Scopus-id: 2-s2.0-85072572277
| 52 | 56 |
| 3 | Lack of delta-sarcoglycan (Sgcd) results in retinal degeneration | Coautor: Luna-Angulo, Alexandra, Perez-Ortiz, Andric C., Peralta-Ildefonso, Martha J., Lira-Romero, Esmeralda, et al. | 2019 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 000498946100238
Scopus-id: 2-s2.0-85074513789
| 5 | 5 |
| 4 | Significant association between variant in sgcd and age-related macular degeneration | 2ᵒ autor: Luna-Angulo A., Perez-Ortiz A.C., Zenteno J.C., Rendon A., et al. | 2018 | GENES | WoS-id: 000448656700005
Scopus-id: 2-s2.0-85054883682
| 3 | 3 |
| 5 | Pharmacogenetics of response to neoadjuvant paclitaxel treatment for locally advanced breast cancer | Coautor: Luna-Angulo, Alexandra, Perez-Ortiz, Andric C., Ramirez, Israel, Cruz-Lopez, Juan C., et al. | 2017 | Oncotarget | WoS-id: 000419534900040
Scopus-id: 2-s2.0-85036609036
| 6 | 8 |
| 6 | CFH and HTRA1 genes associated with AMD in Mexican population | Coautor: Berenice Luna-Angulo, Alexa, Martinez-Velasco, Antonieta, Christopher Perez-Ortiz, Andric, Carlos Zenteno, Juan, et al. | 2017 | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | WoS-id: 000432170306014
| 2 | 0 |
| 7 | Dysferlin quantification in monocytes for rapid screening for dysferlinopathies | Coautor: Luna-Angulo A., Sánchez-Chapul L., Ángel-Muñoz M.D., Ruano-Calderón L., et al. | 2016 | MUSCLE & NERVE | WoS-id: 000389625300014
Scopus-id: 2-s2.0-84995584816
| 2 | 2 |
| 8 | A new de novo mutation in a non-hot spot region at the DMD gene in a Mexican family | 1ᵉʳ autor: Luna-Angulo A.B., Gómez-Díaz B., Escobar-Cedillo R.E., Anaya-Segura M.A., et al. | 2015 | GENET COUNSEL | WoS-id: 000348956000012
Scopus-id: 2-s2.0-84923373849
| 2 | 2 |
| 9 | Comparison of mutation profiles in the duchenne muscular dystrophy gene among populations: Implications for potential molecular therapies | Coautor: Luna-Angulo A.B., López-Hernández L.B., Gómez-Díaz B., Anaya-Segura M., et al. | 2015 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 000352955500055
Scopus-id: 2-s2.0-84925852856
| 13 | 15 |
| 10 | Immunodetection analysis of muscular dystrophies in mexico | Coautor: Luna-Angulo A.B., Gómez-Díaz B., Rosas-Vargas H., Roque-Ramírez B., et al. | 2012 | MUSCLE & NERVE | WoS-id: 000300684600004
Scopus-id: 2-s2.0-84857067083
| 25 | 26 |
| 11 | A familial reciprocal translocation t(1;15) in three generations identified in a regular trisomy 21 patient | Coautor: Luna-Angulo, A, Garcia-Delgado, C, Bahena-Martinez, E, Aparicio-Onofre, A, et al. | 2010 | GENET COUNSEL | WoS-id: 000282665700006
Scopus-id: 2-s2.0-77957745560
| 4 | 3 |
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