Soberón, Xavier
National Institute of Genomic Medicine · University of Pennsylvania
5 papers on CoChatORCID 0000-0002-4498-5628
Most cited papers
- Verified
The genetics of Mexico recapitulates Native American substructure and affects biomedical traits
Moreno-Estrada, A., Gignoux, C. R., Fernández-López, J. C., Zakharia, F., Sikora, M., Contreras, A. V., Acuña-Alonzo, V., Sandoval, K., Eng, C., Romero-Hidalgo, S., et al. (2014) · Science
Forensic and Genetic ResearchGenetic diversity and population structure
Cited by 478
- Verified
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Platform, B. G., Flannick, J., DiscovEHR Collaboration, CHARGE, LuCamp, ProDiGY, GoT2D, ESP, SIGMA-T2D, T2D-GENES, et al. (2019) · Nature
Genetic Associations and EpidemiologyGenomics and Rare Diseases
Cited by 304
- Verified
Combining metagenomics, metatranscriptomics and viromics to explore novel microbial interactions: towards a systems-level understanding of human microbiome
Bikel, S., Valdez-Lara, A., Cornejo-Granados, F., Rico, K., Canizales-Quinteros, S., Soberón, X., Del Pozo-Yauner, L., & Ochoa-Leyva, A. (2015) · Computational and Structural Biotechnology Journal
Gut microbiota and healthGenomics and Phylogenetic Studies
Cited by 263
- Verified
Association of a Low-Frequency Variant in HNF1A With Type 2 Diabetes in a Latino Population
Estrada, K., Aukrust, I., Bjørkhaug, L., Burtt, N. P., Mercader, J. M., García-Ortiz, H., Huerta-Chagoya, A., Moreno-Macías, H., Walford, G., Flannick, J., et al. (2014) · JAMA
Genetic Associations and EpidemiologyDiabetes and associated disorders
Cited by 259
- Verified
Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms
Rusu, V., Hoch, E., Mercader, J. M., Tenen, D. E., Gymrek, M., Hartigan, C. R., DeRan, M., von Grotthuss, M., Fontanillas, P., Spooner, A., et al. (2017) · Cell
Genetic Associations and EpidemiologyMetabolism, Diabetes, and Cancer
Cited by 152
Go further with a free account
Verify every reference, keep papers in a library, and ask questions across them.
Sign up - it is free