1 | Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits | Coautor: Huerta-Chagoya, A, Petty, LE, Chen, HH, Frankel, EG, et al. | 2025 | NATURE COMMUNICATIONS | WoS-id: 001465426800011 Scopus-id: 2-s2.0-105003323438
| 0 | 0 |
2 | The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes | 1ᵉʳ autor: Huerta-Chagoya A., Schroeder P., Mandla R., Deutsch A.J., et al. | 2023 | Diabetologia | WoS-id: 000992603500001 Scopus-id: 2-s2.0-85158950110
| 7 | 7 |
3 | Correction to: The power of genetic diversity in genome-wide association studies of lipids (Nature, (2021), 600, 7890, (675-679), 10.1038/s41586-021-04064-3) | Coautor: Huerta-Chagoya A., Graham S.E., Clarke S.L., Wu K.-H.H., et al. | 2023 | Nature | WoS-id: 001008939200001 Scopus-id: 2-s2.0-85161084469
| 10 | 4 |
4 | Imputation Performance in Latin American Populations: Improving Rare Variants Representation With the Inclusion of Native American Genomes | Coautor: Huerta-Chagoya, Alicia, Jimenez-Kaufmann, Andres, Chong, Amanda Y., Cortes, Adrian, et al. | 2022 | Frontiers in Genetics | WoS-id: 000745703100001 Scopus-id: 2-s2.0-85123123221
| 9 | 9 |
5 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation | Coautor: Huerta-Chagoya, Alicia, Mahajan, Anubha, Spracklen, Cassandra N., Zhang, Weihua, et al. | 2022 | NATURE GENETICS | WoS-id: 000794118000004 Scopus-id: 2-s2.0-85130637871
| 358 | 358 |
6 | A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids | Coautor: Huerta-Chagoya A., Ramdas S., Judd J., Graham S.E., et al. | 2022 | AMERICAN JOURNAL OF HUMAN GENETICS | WoS-id: 000850681500003 Scopus-id: 2-s2.0-85135598739
| 21 | 23 |
7 | A saturated map of common genetic variants associated with human height | Coautor: Huerta-Chagoya, Alicia, Yengo, Loic, Vedantam, Sailaja, Marouli, Eirini, et al. | 2022 | Nature | WoS-id: 000866362700001 Scopus-id: 2-s2.0-85139748621
| 316 | 342 |
8 | Recessive Genome-Wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes | Coautor: Huerta-Chagoya A., O'Connor M.J., Schroeder P., Cortés-Sánchez P., et al. | 2022 | Diabetes | WoS-id: 000883311700019 Scopus-id: 2-s2.0-85125212528
| 14 | 16 |
9 | Familial hypertriglyceridemia: an entity with distinguishable features from other causes of hypertriglyceridemia | 2ᵒ autor: Huerta-Chagoya, Alicia, Cruz-Bautista, Ivette, Moreno-Macias, Hortensia, Rodriguez-Guillen, Rosario, et al. | 2021 | LIPIDS IN HEALTH AND DISEASE | WoS-id: 000620219200002 Scopus-id: 2-s2.0-85101485953
| 8 | 11 |
10 | The trans-ancestral genomic architecture of glycemic traits | Coautor: Huerta-Chagoya, Alicia, Chen, Ji, Spracklen, Cassandra N., Marenne, Gaelle, et al. | 2021 | NATURE GENETICS | WoS-id: 000656384400001 Scopus-id: 2-s2.0-85108020584
| 426 | 434 |
11 | The power of genetic diversity in genome-wide association studies of lipids | Coautor: Huerta-Chagoya, Alicia, Graham, Sarah E., Clarke, Shoa L., Wu, Kuan-Han H., et al. | 2021 | Nature | WoS-id: 000728504500001 Scopus-id: 2-s2.0-85121605114
| 468 | 471 |
12 | Contribution of Known Genetic Risk Variants to Dyslipidemias and Type 2 Diabetes in Mexico: A Population-Based Nationwide Study | 1ᵉʳ autor: Huerta-Chagoya, Alicia, Moreno-Macias, Hortensia, Sevilla-Gonzalez, Magdalena, Rodriguez-Guillen, Rosario, et al. | 2020 | GENES | WoS-id: 000514898000041 Scopus-id: 2-s2.0-85078260878
| 8 | 8 |
13 | A panel of 32 AIMs suitable for population stratification correction and global ancestry estimation in Mexican mestizos 06 Biological Sciences 0604 Genetics | 1ᵉʳ autor: Huerta-Chagoya A., Moreno-Macías H., Carlos Fernandez-Lopez, Juan, Luisa Ordonez-Sanchez, Maria, et al. | 2019 | BMC GENETICS | WoS-id: 000455208900002 Scopus-id: 2-s2.0-85059768837
| 9 | 10 |
14 | The SLC16A11 risk haplotype is associated with decreased insulin action, higher transaminases and large-size adipocytes | Coautor: Huerta-Chagoya A., Almeda-Valdes P., Velasco D.V.G., Campos O.A., et al. | 2019 | EUROPEAN JOURNAL OF ENDOCRINOLOGY | WoS-id: 000457062800008 Scopus-id: 2-s2.0-85058857855
| 19 | 16 |
15 | Associations of autozygosity with a broad range of human phenotypes | Coautor: Huerta-Chagoya, Alicia, Clark, David W., Okada, Yukinori, Moore K.H.S., et al. | 2019 | NATURE COMMUNICATIONS | WoS-id: 000493438700005 Scopus-id: 2-s2.0-85074297784
| 77 | 82 |
16 | Identification of population-stratified coding variants for low and high serum triglycerides in Mexicans | Coautor: Huerta-Chagoya, Alicia, Ko, Arthur, Nikkola, Elina, Garske, Kristina, et al. | 2018 | HUMAN GENOMICS | WoS-id: 000427728400061
| 0 | 0 |
17 | A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes | Coautor: Huerta-Chagoya, Alicia, Mercader, Josep M., Liao, Rachel G., Bell, Avery D., et al. | 2017 | Diabetes | WoS-id: 000413559100019 Scopus-id: 2-s2.0-85037582424
| 44 | 45 |
18 | Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes | Coautor: Huerta-Chagoya, Alicia, Imamura, Minako, Takahashi, Atsushi, Yamauchi, Toshimasa, et al. | 2016 | NATURE COMMUNICATIONS | WoS-id: 000369024700002 Scopus-id: 2-s2.0-84956612031
| 127 | 131 |
19 | Genetic determinants for gestational diabetes mellitus and related metabolic traits in Mexican women | 1ᵉʳ autor: Huerta-Chagoya A., Vázquez-Cárdenas P., Moreno-Macías H., Tapia-Maruri L., et al. | 2015 | PLOS ONE | WoS-id: 000354545600050 Scopus-id: 2-s2.0-84929346819
| 65 | 66 |
20 | Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes | Coautor: Huerta-Chagoya A., Majithia A.R., Flannick J., Shahinian P., et al. | 2014 | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | WoS-id: 000341625600043 Scopus-id: 2-s2.0-84907013152
| 139 | 145 |
21 | Seasonal variations in the levels of PAH-DNA adducts in young adults living in Mexico City | 2ᵒ autor: Huerta-Chagoya A., García-Suástegui W.A., Carrasco-Colín K.L., Pratt M.M., et al. | 2011 | Mutagenesis | WoS-id: 000289843000003 Scopus-id: 2-s2.0-79955461999
| 44 | 49 |