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Article

Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico.

Nature - 6 Feb 2014

Williams Amy L, Jacobs Suzanne B R, Moreno-Macías Hortensia, Huerta-Chagoya Alicia, Churchhouse Claire, Márquez-Luna Carla, García-Ortíz Humberto, Gómez-Vázquez María José, Burtt Noël P, Aguilar-Salinas Carlos A, González-Villalpando Clicerio, Florez Jose C, Orozco Lorena, Haiman Christopher A, Tusié-Luna Teresa, Altshuler David

Abstract excerpt

Performing genetic studies in multiple human populations can identify disease risk alleles that are common in one population but rare in others, with the potential to illuminate pathophysiology, health disparities, and the population genetic origins of disease alleles. Here we analysed 9.2 million single nucleotide polymorphisms (SNPs) in each of 8,214 Mexicans and other Latin Americans: 3,848 with type 2...

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Identifiers

PMID: 24390345
DOI: 10.1038/nature12828
PMCID: PMC4127086

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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