| 1 | Plasma MicroRNAs Related to Metabolic Syndrome in Mexican Women | 2ᵒ autor: Córdova E.J., Ramírez-Solano M.A., Orozco L., Tejero M.E. | 2023 | Lifestyle Genomics | WoS-id: 001071439000001
Scopus-id: 2-s2.0-85180539757
| 0 | 0 |
| 2 | Rare coding variants in 35 genes associate with circulating lipid levels?A multi-ancestry analysis of 170,000 exomes | Coautor: Córdova E.J., Hindy G., Dornbos P., Chaffin M.D., et al. | 2022 | AMERICAN JOURNAL OF HUMAN GENETICS | WoS-id: 000748493200007
Scopus-id: 2-s2.0-85122004213
| 21 | 21 |
| 3 | Exome Sequencing Data Analysis and a Case-Control Study in Mexican Population Reveals Lipid Trait Associations of New and Known Genetic Variants in Dyslipidemia-Associated Loci | Coautor: Cordova, Emilio J., Jurado-Camacho, Pedro A., Cid-Soto, Miguel A., Barajas-Olmos, Francisco, et al. | 2022 | Frontiers in Genetics | WoS-id: 000806612000001
Scopus-id: 2-s2.0-85131733069
| 2 | 3 |
| 4 | Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review | Coautor: Cordova, E. J., Martinez-Hernandez, A., Martinez-Anaya, D., Duran-McKinster, C., et al. | 2022 | BMC MEDICAL GENOMICS | WoS-id: 000877014900002
Scopus-id: 2-s2.0-85140943693
| 0 | 0 |
| 5 | The genomic landscape of Mexican Indigenous populations brings insights into the peopling of the Americas | Coautor: Córdova E.J., García-Ortiz H., Barajas-Olmos F., Contreras-Cubas C., et al. | 2021 | NATURE COMMUNICATIONS | WoS-id: 000706749500019
Scopus-id: 2-s2.0-85117232577
| 26 | 29 |
| 6 | Metabolic syndrome in indigenous communities in Mexico: A descriptive and cross-sectional study | Coautor: Córdova E.J., Mendoza-Caamal E.C., Barajas-Olmos F., Garciá-Ortiz H., et al. | 2020 | Bmc Public Health | WoS-id: 000521311600003
Scopus-id: 2-s2.0-85082025059
| 27 | 30 |
| 7 | A homozygous CEP57 c.915_925dupCAATGTTCAGC mutation in a patient with mosaic variegated aneuploidy syndrome with rhizomelic shortening in the upper and lower limbs and a narrow thorax | Coautor: Córdova E.J., De la Torre-García O., Mar-Aldama R., Salgado-Sangri R., et al. | 2019 | EUROPEAN JOURNAL OF MEDICAL GENETICS | WoS-id: 000457638200008
Scopus-id: 2-s2.0-85049879950
| 8 | 7 |
| 8 | Curcumin induces p53-independent inactivation of Nrf2 during oxidative stress?induced apoptosis | Coautor: Córdova E.J., Méndez-García L.A., Martínez-Castillo M., Villegas-Sepúlveda N., et al. | 2019 | HUMAN & EXPERIMENTAL TOXICOLOGY | WoS-id: 000476722600007
Scopus-id: 2-s2.0-85064931603
| 30 | 33 |
| 9 | Analysis of the dynamic aberrant landscape of DNA methylation and gene expression during arsenic-induced cell transformation | Coautor: Córdova-Alarcón E.J., Barajas-Olmos F.M., Ortiz-Sánchez E., Imaz-Rosshandler I., et al. | 2019 | Gene | WoS-id: 000479025300011
Scopus-id: 2-s2.0-85068035379
| 11 | 13 |
| 10 | Genetic variability of five ADRB2 polymorphisms among Mexican Amerindian ethnicities and the Mestizo population | Coautor: Cordova E.J., Salas-Martínez M.G., Saldaña-Alvarez Y., Mendiola-Soto D.K., et al. | 2019 | PLOS ONE | WoS-id: 000533930800022
Scopus-id: 2-s2.0-85075803215
| 4 | 6 |
| 11 | Altered DNA methylation in liver and adipose tissues derived from individuals with obesity and type 2 diabetes | Coautor: Cordova E.J., Barajas-Olmos F., Centeno-Cruz F., Zerrweck C., et al. | 2018 | BMC MEDICAL GENETICS | WoS-id: 000426095300001
Scopus-id: 2-s2.0-85042417139
| 33 | 35 |
| 12 | GSTT1 and GSTM1 null variants in mestizo and amerindian populations from Northwestern Mexico and a literature review | 2ᵒ autor: Córdova E.J., Palma-Cano L.E., Orozco L., Martínez-Hernández A., et al. | 2017 | Genetics And Molecular Biology | Scopus-id: 2-s2.0-85035749703
| 0 | 15 |
| 13 | A subpopulation of the K562 cells are killed by curcumin treatment after G2/M arrest and mitotic catastrophe | Coautor: Cordova E.J., Martinez-Castillo M., Bonilla-Moreno R., Aleman-Lazarini L., et al. | 2016 | PLOS ONE | WoS-id: 000387725000049
Scopus-id: 2-s2.0-84994475818
| 16 | 21 |
| 14 | The rs61764370 functional variant in the KRAS oncogene is associated with chronic myeloid leukemia risk in women | Coautor: Cordova E.J., Gutiérrez-Malacatt H., Ayala-Sanchez M., Aquino-Ortega X., et al. | 2016 | ASIAN PACIFIC JOURNAL OF CANCER PREVENTION | Scopus-id: 2-s2.0-84973130135
| 0 | 13 |
| 15 | Association of HMOX1 and NQO1 polymorphisms with metabolic syndrome components | 2ᵒ autor: Córdova E.J., Martínez-Hernández A., Rosillo-Salazar O., García-Ortíz H., et al. | 2015 | PLOS ONE | WoS-id: 000353887100019
Scopus-id: 2-s2.0-84929121316
| 22 | 28 |
| 16 | The NRF2-KEAP1 pathway is an early responsive gene network in arsenic exposed lymphoblastoid cells | 1ᵉʳ autor: Córdova E.J., Martínez-Hernández A., Uribe-Figueroa L., Centeno F., et al. | 2014 | PLOS ONE | WoS-id: 000330834400027
Scopus-id: 2-s2.0-84895739598
| 21 | 20 |
| 17 | Nuclear factor erythroid 2-related factor gene variants and susceptibility of arsenic-related skin lesions | 1ᵉʳ autor: Cordova E.J., Valenzuela O.L., Sánchez-Peña L.C., Escamilla-Guerrero G., et al. | 2014 | HUMAN & EXPERIMENTAL TOXICOLOGY | WoS-id: 000337597200004
Scopus-id: 2-s2.0-84901386299
| 5 | 5 |
| 18 | HMOX1 promoter (GT)n polymorphism is associated with childhood-onset systemic lupus erythematosus but not with juvenile rheumatoid arthritis in a Mexican population | 1ᵉʳ autor: Córdova E.J., Martínez-Hernández A., Ramírez-Bello J., Velázquez-Cruz R., et al. | 2012 | CLINICAL AND EXPERIMENTAL RHEUMATOLOGY | WoS-id: 000303905800026
Scopus-id: 2-s2.0-84863732055
| 11 | 11 |
