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Page 1
The genomic landscape of Mexican Indigenous populations brings insights into the peopling of the Americas.
García-Ortiz H, Barajas-Olmos F, Contreras-Cubas C, Cid-Soto MÁ, Córdova EJ, Centeno-Cruz F, Mendoza-Caamal E, Cicerón-Arellano I, Flores-Huacuja M, Baca P, Bolnick DA, Snow M, Flores-Martínez SE, Ortiz-Lopez R, Reynolds AW, Blanchet A, Morales-Marín M, Velázquez-Cruz R, Kostic AD, Galaviz-Hernández C, García-Zapién AG, Jiménez-López JC, León-Reyes G, Salas-Bautista EG, Lazalde-Ramos BP, Jiménez-Ruíz JL, Salas-Martínez G, Ramos-Madrigal J, Mirzaeicheshmeh E, Saldaña-Alvarez Y, Del Carmen Abrahantes-Pérez M, Loeza-Becerra F, Mojica-Espinosa R, Sánchez-Quinto F, Rangel-Villalobos H, Sosa-Macías M, Sánchez-Corona J, Rojas-Martinez A, Martínez-Hernández A, Orozco L. García-Ortiz H, et al. Nat Commun. 2021 Oct 12;12(1):5942. doi: 10.1038/s41467-021-26188-w. Nat Commun. 2021. PMID: 34642312 Free PMC article.
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico.
SIGMA Type 2 Diabetes Consortium; Williams AL, Jacobs SB, Moreno-Macías H, Huerta-Chagoya A, Churchhouse C, Márquez-Luna C, García-Ortíz H, Gómez-Vázquez MJ, Burtt NP, Aguilar-Salinas CA, González-Villalpando C, Florez JC, Orozco L, Haiman CA, Tusié-Luna T, Altshuler D. SIGMA Type 2 Diabetes Consortium, et al. Nature. 2014 Feb 6;506(7486):97-101. doi: 10.1038/nature12828. Epub 2013 Dec 25. Nature. 2014. PMID: 24390345 Free PMC article.
WNT3A gene polymorphisms are associated with bone mineral density variation in postmenopausal mestizo women of an urban Mexican population: findings of a pathway-based high-density single nucleotide screening.
Velázquez-Cruz R, García-Ortiz H, Castillejos-López M, Quiterio M, Valdés-Flores M, Orozco L, Villarreal-Molina T, Salmerón J. Velázquez-Cruz R, et al. Age (Dordr). 2014 Jun;36(3):9635. doi: 10.1007/s11357-014-9635-2. Epub 2014 Mar 3. Age (Dordr). 2014. PMID: 24584697 Free PMC article.
Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population.
SIGMA Type 2 Diabetes Consortium; Estrada K, Aukrust I, Bjørkhaug L, Burtt NP, Mercader JM, García-Ortiz H, Huerta-Chagoya A, Moreno-Macías H, Walford G, Flannick J, Williams AL, Gómez-Vázquez MJ, Fernandez-Lopez JC, Martínez-Hernández A, Jiménez-Morales S, Centeno-Cruz F, Mendoza-Caamal E, Revilla-Monsalve C, Islas-Andrade S, Córdova EJ, Soberón X, González-Villalpando ME, Henderson E, Wilkens LR, Le Marchand L, Arellano-Campos O, Ordóñez-Sánchez ML, Rodríguez-Torres M, Rodríguez-Guillén R, Riba L, Najmi LA, Jacobs SB, Fennell T, Gabriel S, Fontanillas P, Hanis CL, Lehman DM, Jenkinson CP, Abboud HE, Bell GI, Cortes ML, Boehnke M, González-Villalpando C, Orozco L, Haiman CA, Tusié-Luna T, Aguilar-Salinas CA, Altshuler D, Njølstad PR, Florez JC, MacArthur DG. SIGMA Type 2 Diabetes Consortium, et al. JAMA. 2014 Jun 11;311(22):2305-14. doi: 10.1001/jama.2014.6511. JAMA. 2014. PMID: 24915262 Free PMC article.
Genomewide admixture study in Mexican Mestizos with multiple sclerosis.
Ordoñez G, Romero S, Orozco L, Pineda B, Jiménez-Morales S, Nieto A, García-Ortiz H, Sotelo J. Ordoñez G, et al. Clin Neurol Neurosurg. 2015 Mar;130:55-60. doi: 10.1016/j.clineuro.2014.11.026. Epub 2014 Dec 24. Clin Neurol Neurosurg. 2015. PMID: 25577161
Association of HMOX1 and NQO1 Polymorphisms with Metabolic Syndrome Components.
Martínez-Hernández A, Córdova EJ, Rosillo-Salazar O, García-Ortíz H, Contreras-Cubas C, Islas-Andrade S, Revilla-Monsalve C, Salas-Labadía C, Orozco L. Martínez-Hernández A, et al. PLoS One. 2015 May 1;10(5):e0123313. doi: 10.1371/journal.pone.0123313. eCollection 2015. PLoS One. 2015. PMID: 25933176 Free PMC article.
Gender-Dependent Association of FTO Polymorphisms with Body Mass Index in Mexicans.
Saldaña-Alvarez Y, Salas-Martínez MG, García-Ortiz H, Luckie-Duque A, García-Cárdenas G, Vicenteño-Ayala H, Cordova EJ, Esparza-Aguilar M, Contreras-Cubas C, Carnevale A, Chávez-Saldaña M, Orozco L. Saldaña-Alvarez Y, et al. PLoS One. 2016 Jan 4;11(1):e0145984. doi: 10.1371/journal.pone.0145984. eCollection 2016. PLoS One. 2016. PMID: 26726774 Free PMC article.
Analysis of protein-coding genetic variation in 60,706 humans.
Lek M, Karczewski KJ, Minikel EV, Samocha KE, Banks E, Fennell T, O'Donnell-Luria AH, Ware JS, Hill AJ, Cummings BB, Tukiainen T, Birnbaum DP, Kosmicki JA, Duncan LE, Estrada K, Zhao F, Zou J, Pierce-Hoffman E, Berghout J, Cooper DN, Deflaux N, DePristo M, Do R, Flannick J, Fromer M, Gauthier L, Goldstein J, Gupta N, Howrigan D, Kiezun A, Kurki MI, Moonshine AL, Natarajan P, Orozco L, Peloso GM, Poplin R, Rivas MA, Ruano-Rubio V, Rose SA, Ruderfer DM, Shakir K, Stenson PD, Stevens C, Thomas BP, Tiao G, Tusie-Luna MT, Weisburd B, Won HH, Yu D, Altshuler DM, Ardissino D, Boehnke M, Danesh J, Donnelly S, Elosua R, Florez JC, Gabriel SB, Getz G, Glatt SJ, Hultman CM, Kathiresan S, Laakso M, McCarroll S, McCarthy MI, McGovern D, McPherson R, Neale BM, Palotie A, Purcell SM, Saleheen D, Scharf JM, Sklar P, Sullivan PF, Tuomilehto J, Tsuang MT, Watkins HC, Wilson JG, Daly MJ, MacArthur DG; Exome Aggregation Consortium. Lek M, et al. Nature. 2016 Aug 18;536(7616):285-91. doi: 10.1038/nature19057. Nature. 2016. PMID: 27535533 Free PMC article.
55 results