| 1 | Germline mutations in pediatric cancer cohort with mixed-ancestry Mexicans | Coautor: Mendoza-Caamal E.C., Alonso-Luna O., Mercado-Celis G.E., Melendez-Zajgla J., et al. | 2024 | Molecular Genetics & Genomic Medicine | WoS-id: 001126236200001
Scopus-id: 2-s2.0-85179709004
| 0 | 0 |
| 2 | CFTR pathogenic variants spectrum in a cohort of Mexican patients with cystic fibrosis | 2ᵒ autor: Mendoza-Caamal E.C., Martínez-Hernández A., Mendiola-Vidal N.G., Barajas-Olmos F., et al. | 2024 | Heliyon | WoS-id: 001226662900001
Scopus-id: 2-s2.0-85189700727
| 1 | 1 |
| 3 | The genetic era of childhood cancer: Identification of high-risk patients and germline sequencing approaches | Coautor: Mendoza-Caamal, Elvia, Alonso-Luna, Oscar, Mercado-Celis, Gabriela E., Melendez-Zajgla, Jorge, et al. | 2023 | ANNALS OF HUMAN GENETICS | WoS-id: 000946671400001
Scopus-id: 2-s2.0-85150654300
| 4 | 6 |
| 4 | Rare coding variants in 35 genes associate with circulating lipid levels?A multi-ancestry analysis of 170,000 exomes | Coautor: Mendoza-Caamal E., 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 |
| 5 | 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: Mendoza-Caamal, Elvia C., 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
| 3 | 3 |
| 6 | Frequency of germline mutations in Mexican children with cancer | Coautor: Mendoza Caamal, Elvia Cristina, Alonso Luna, Oscar, Melendez Zajgla, Jorge, Zapata Tarres, Marta, et al. | 2022 | CANCER RESEARCH | WoS-id: 000892509502478
| 0 | 0 |
| 7 | Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes | Coautor: Mendoza-Caamal, Elvia, Goodrich, Julia K., Singer-Berk, Moriel, Son, Rachel, et al. | 2021 | NATURE COMMUNICATIONS | WoS-id: 000664874700036
Scopus-id: 2-s2.0-85107774343
| 48 | 52 |
| 8 | Two novel variants in DYRK1B causative of AOMS3: expanding the clinical spectrum | 1ᵉʳ autor: Mendoza-Caamal E.C., Barajas-Olmos F., Mirzaeicheshmeh E., Ilizaliturri-Flores I., et al. | 2021 | ORPHANET JOURNAL OF RARE DISEASES | WoS-id: 000671281100001
Scopus-id: 2-s2.0-85108990517
| 8 | 8 |
| 9 | The L125F MATE1 variant enriched in populations of Amerindian origin is associated with increased plasma levels of metformin and lactate | Coautor: Mendoza-Caamal, Elvia C., Morales-Rivera, Monserrat I., Alemon-Medina, Radames, Martinez-Hernandez, Angelica, et al. | 2021 | BIOMEDICINE & PHARMACOTHERAPY | WoS-id: 000700360700001
Scopus-id: 2-s2.0-85112274358
| 3 | 3 |
| 10 | The genomic landscape of Mexican Indigenous populations brings insights into the peopling of the Americas | Coautor: Mendoza-Caamal E., García-Ortiz H., Barajas-Olmos F., Contreras-Cubas C., et al. | 2021 | NATURE COMMUNICATIONS | WoS-id: 000706749500019
Scopus-id: 2-s2.0-85117232577
| 27 | 31 |
| 11 | Alterations of DNA methylation during adipogenesis differentiation of mesenchymal stem cells isolated from adipose tissue of patients with obesity is associated with type 2 diabetes | Coautor: Mendoza-Caamal, Elvia C., Mirzaeicheshmeh, Elaheh, ZERRWECK, CARLOS, Centeno-Cruz, Federico, et al. | 2021 | Adipocyte | WoS-id: 000711201500001
Scopus-id: 2-s2.0-85118329024
| 6 | 6 |
| 12 | Metabolic syndrome in indigenous communities in Mexico: A descriptive and cross-sectional study | 1ᵉʳ autor: Mendoza-Caamal E.C., Barajas-Olmos F., Garciá-Ortiz H., Cicerón-Arellano I., et al. | 2020 | Bmc Public Health | WoS-id: 000521311600003
Scopus-id: 2-s2.0-85082025059
| 30 | 33 |
| 13 | Next-generation sequencing for identifying a novel/de novo pathogenic variant in a Mexican patient with cystic fibrosis: a case report | Coautor: Mendoza-Caamal E.C., Martínez-Hernández A., Larrosa J., Barajas-Olmos F., et al. | 2019 | BMC MEDICAL GENOMICS | WoS-id: 000468792300002
Scopus-id: 2-s2.0-85066442854
| 4 | 4 |
| 14 | Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls | Coautor: Mendoza-Caamal, Elvia, Flannick, Jason, Mercader, Josep M., Fuchsberger, Christian, et al. | 2019 | Nature | WoS-id: 000470149000041
Scopus-id: 2-s2.0-85066251977
| 212 | 211 |
| 15 | Genetic variability of five ADRB2 polymorphisms among Mexican Amerindian ethnicities and the Mestizo population | Coautor: Mendoza-Caamal E.C., Salas-Martínez M.G., Saldaña-Alvarez Y., Cordova E.J., et al. | 2019 | PLOS ONE | WoS-id: 000533930800022
Scopus-id: 2-s2.0-85075803215
| 5 | 6 |
| 16 | Genomics of a pediatric ovarian fibrosarcoma. Association with the DICER1 syndrome | Coautor: Mendoza-Caamal E., Melendez-Zajgla J., Mercado-Celis G.E., Gaytan-Cervantes J., et al. | 2018 | SCIENTIFIC REPORTS | WoS-id: 000425380900035
Scopus-id: 2-s2.0-85042224135
| 20 | 22 |
| 17 | ERBIN deficiency links STAT3 and TGF-ß pathway defects with atopy in humans | Coautor: Mendoza-Caamal E., Lyons J.J., Liu Y., Ma C.A., et al. | 2017 | JOURNAL OF EXPERIMENTAL MEDICINE | WoS-id: 000395828600008
Scopus-id: 2-s2.0-85027530748
| 79 | 82 |
| 18 | Correction: ERBIN deficiency links STAT3 and TGF-ß pathway defects with atopy in humans [The Journal of Experimental Medicine, 214, 3, March, (2017) (669-680)]doi 10.1084/jem.20161435 | Coautor: Mendoza-Caamal E., Lyons J.J., Liu Y., Ma C.A., et al. | 2017 | JOURNAL OF EXPERIMENTAL MEDICINE | Scopus-id: 2-s2.0-85021982222
| 0 | 7 |
