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Alicia Huerta-Chagoya
Alicia Huerta-Chagoya
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Dirección de correo verificada de broadinstitute.org
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Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico
AL Williams, SBR Jacobs, H Moreno-Macías, A Huerta-Chagoya, ...
Nature 506 (7486), 97-101, 2014
5572014
The power of genetic diversity in genome-wide association studies of lipids
SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ...
Nature 600 (7890), 675-679, 2021
4042021
The trans-ancestral genomic architecture of glycemic traits
J Chen, CN Spracklen, G Marenne, A Varshney, LJ Corbin, J Luan, ...
Nature genetics 53 (6), 840-860, 2021
3742021
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
3032022
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
A Mahajan, CN Spracklen, W Zhang, MCY Ng, LE Petty, H Kitajima, ...
Nature genetics 54 (5), 560-572, 2022
2852022
Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population
K Estrada, I Aukrust, L Bjørkhaug, NP Burtt, JM Mercader, H García-Ortiz, ...
Jama 311 (22), 2305-2314, 2014
2712014
Multiethnic polygenic risk scores improve risk prediction in diverse populations
C Márquez‐Luna, PR Loh, ...
Genetic epidemiology 41 (8), 811-823, 2017
2342017
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
M Imamura, A Takahashi, T Yamauchi, K Hara, K Yasuda, N Grarup, ...
Nature communications 7 (1), 10531, 2016
1912016
Type 2 diabetes variants disrupt function of SLC16A11 through two distinct mechanisms
V Rusu, E Hoch, JM Mercader, DE Tenen, M Gymrek, CR Hartigan, ...
Cell 170 (1), 199-212. e20, 2017
1532017
Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population
MA Gamboa-Meléndez, A Huerta-Chagoya, H Moreno-Macías, ...
Diabetes 61 (12), 3314-3321, 2012
1302012
Genetic variants associated with quantitative glucose homeostasis traits translate to type 2 diabetes in Mexican Americans: the GUARDIAN (Genetics Underlying Diabetes in …
ND Palmer, MO Goodarzi, CD Langefeld, N Wang, X Guo, KD Taylor, ...
Diabetes 64 (5), 1853-1866, 2015
962015
Associations of autozygosity with a broad range of human phenotypes
DW Clark, Y Okada, KHS Moore, D Mason, N Pirastu, I Gandin, ...
Nature communications 10 (1), 4957, 2019
932019
Genetic determinants for gestational diabetes mellitus and related metabolic traits in Mexican women
A Huerta-Chagoya, P Vazquez-Cardenas, H Moreno-Macias, ...
PloS one 10 (5), e0126408, 2015
832015
A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes
JM Mercader, RG Liao, AD Bell, Z Dymek, K Estrada, T Tukiainen, ...
Diabetes 66 (11), 2903-2914, 2017
602017
A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes
JM Mercader, RG Liao, AD Bell, Z Dymek, K Estrada, T Tukiainen, ...
Diabetes 66 (11), 2903-2914, 2017
602017
Genome-wide association study of colorectal cancer in Hispanics
SL Schmit, FR Schumacher, CK Edlund, DV Conti, U Ihenacho, P Wan, ...
Carcinogenesis 37 (6), 547-556, 2016
412016
Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
A Mahajan, CN Spracklen, W Zhang, MCY Ng, LE Petty, H Kitajima, ...
MedRxiv, 2020.09. 22.20198937, 2020
312020
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
S Kanoni, SE Graham, Y Wang, I Surakka, S Ramdas, X Zhu, SL Clarke, ...
Genome biology 23 (1), 268, 2022
272022
The SLC16A11 risk haplotype is associated with decreased insulin action, higher transaminases and large-sized adipocytes
P Almeda-Valdes, D Gomez-Velasco, O Arellano-Campos, ...
European journal of endocrinology 1 (aop), 2018
242018
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
S Ramdas, J Judd, SE Graham, S Kanoni, Y Wang, I Surakka, B Wenz, ...
The American Journal of Human Genetics 109 (8), 1366-1387, 2022
212022
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