Romero-Hidalgo S, Sagaceta-Mejia J, Villalobos-Comparan M, Tejero ME, Dominguez-Perez M, Jacobo-Albavera L, Posadas-Sanchez R, Vargas-Alarcon G, Posadas-Romero C, Macias-Kauffer L, Vadillo-Ortega F, Contreras-Sieck MA, Acuna-Alonzo V, Barquera R, Macin G, Binia A, Guevara-Chavez JG, Sebastian-Medina L, Menjivar M, Canizales-Quinteros S, Carnevale A, Villarreal-Molina T. Selection scan in Native Americans of Mexico identifies FADS2 rs174616: Evidence of gene-diet interactions affecting lipid levels and Delta-6-desaturase activity. Heliyon. 2024 Aug 15; 10(15):e35477.

Gonzalez-Garrido A, Rosas-Madrigal S, Rojo-Dominguez A, Arellanes-Robledo J, Lopez-Mora E, Carnevale A, Arregui L, Rosendo-Gutierrez R, Romero-Hidalgo S, Villarreal-Molina MT. Leukocyte Nuclear Morphology Alterations in Dilated Cardiomyopathy Caused by a Lamin AC Truncating Mutation (LMNA/Ser431*) Are Modified by the Presence of a LAP2 Missense Polymorphism (TMPO/Arg690Cys). Int J Mol Sci. 2022 Nov 7; 23(21):.

Ramirez-Garcia MA, de Montellano DJDO, Martinez-Ruano L, Ochoa-Morales A, Romero-Hidalgo S, Zenteno JC, Yescas-Gomez P. Clinical and molecular findings of intermediate allele carriers in the HTT gene from the Mexican Mestizo population. Am J Med Genet. 2022 NOV; 22(1):34 - 41.

Caballero-Sanchez U, Roman-Lopez TV, Silva-Pereyra JF, Polo-Romero A, Romero-Hidalgo S, Mendez-Diaz M, Prospero-Garcia O, Ruiz-Contreras AE. Brain electrophysiological responses associated with the retrieval of temporal and spatial contexts in episodic memory. Behav Brain Res. 2022 Aug 12; :114057.

Rosas-Madrigal S, Villarreal-Molina MT, Flores-Rivera J, Rivas-Alonso V, Macias-Kauffer LR, Ordonez G, Chima-Galan MDC, Acuna-Alonzo V, Macin-Perez G, Barquera R, Granados J, Valle-Rios R, Corona T, Carnevale A, Romero-Hidalgo S. Interaction of HLA Class II rs9272219 and TMPO rs17028450 (Arg690Cys) Variants Affects Neuromyelitis Optica Spectrum Disorder Susceptibility in an Admixed Mexican Population. Front Genet. 2021; 12:647343.

Leon-Mimila P, Villamil-Ramirez H, Macias-Kauffer LR, Jacobo-Albavera L, Lopez-Contreras BE, Posadas-Sanchez R, Posadas-Romero C, Romero-Hidalgo S, Moran-Ramos S, Dominguez-Perez M, Olivares-Arevalo M, Lopez-Montoya P, Nieto-Guerra R, Acuna-Alonzo V, Macin-Perez G, Barquera-Lozano R, Del-Rio-Navarro BE, Gonzalez-Gonzalez I, Campos-Perez F, Gomez-Perez F, Valdes VJ, Sampieri A, Reyes-Garcia JG, Carrasco-Portugal MDC, Flores-Murrieta FJ, Aguilar-Salinas CA, Vargas-Alarcon G, Shih D, Meikle PJ, Calkin AC, Drew BG, Vaca L, Lusis AJ, Huertas-Vazquez A, Villarreal-Molina T, Canizales-Quinteros S. Genome-Wide Association Study Identifies a Functional SIDT2 Variant Associated With HDL-C (High-Density Lipoprotein Cholesterol) Levels and Premature Coronary Artery Disease. Arterioscler Thromb Vasc Biol. 2021 Jul 8; :ATVBAHA120315391.

Ortega-Mora EI, Caballero-Sanchez U, Roman-Lopez TV, Rosas-Escobar CB, Gonzalez-Barrios JA, Romero-Hidalgo S, Mendez-Diaz M, Prospero-Garcia OE, Ruiz-Contreras AE. Allele-dosage genetic polymorphisms of cannabinoid receptor 1 predict attention, but not working memory performance in humans. Acta Psychol (Amst). 2021 Mar 31; 216:103299.

Carnevale A, Rosas-Madrigal S, Rosendo-Gutierrez R, Lopez-Mora E, Romero-Hidalgo S, Avila-Vazzini N, Jacobo-Albavera L, Dominguez-Perez M, Vargas-Alarcon G, Perez-Villatoro F, Navarrete-Martinez JI, Villarreal-Molina MT. Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing. Mol Genet Genomic Med. 2020 Nov; 8(11):e1504.

Romero-Hidalgo S, Flores-Rivera J, Rivas-Alonso V, Barquera R, Villarreal-Molina MT, Antuna-Puente B, Macias-Kauffer LR, Villalobos-Comparan M, Ortiz-Maldonado J, Yu N, Lebedeva TV, Alosco SM, Garcia-Rodriguez JD, Gonzalez-Torres C, Rosas-Madrigal S, Ordonez G, Guerrero-Camacho JL, Trevino-Frenk I, Escamilla-Tilch M, Garcia-Lechuga M, Tovar-Mendez VH, Pacheco-Ubaldo H, Acuna-Alonzo V, Bortolini MC, Gallo C, Bedoya G, Rothhammer F, Gonzalez-Jose R, Ruiz-Linares A, Canizales-Quinteros S, Yunis E, Granados J, Corona T. Native American ancestry significantly contributes to neuromyelitis optica susceptibility in the admixed Mexican population. Sci Rep. 2020 Aug 13; 10(1):13706.

Barquera R, Hernandez-Zaragoza DI, Bravo-Acevedo A, Arrieta-Bolanos E, Clayton S, Acuna-Alonzo V, Martinez-Alvarez JC, Lopez-Gil C, Adalid-Sainz C, Vega-Martinez MDR, Escobedo-Ruiz A, Juarez-Cortes ED, Immel A, Pacheco-Ubaldo H, Gonzalez-Medina L, Lona-Sanchez A, Lara-Riegos J, Sanchez-Fernandez MGJ, Diaz-Lopez R, Guizar-Lopez GU, Medina-Escobedo CE, Arrazola-Garcia MA, Montiel-Hernandez GD, Hernandez-Hernandez O, Ramos-de la Cruz FDR, Juarez-Nicolas F, Pantoja-Torres JA, Rodriguez-Munguia TJ, Juarez-Barreto V, Delgado-Aguirre H, Escutia-Gonzalez AB, Gone-Vazquez I, Benitez-Arvizu G, Arellano-Prado FP, Garcia-Arias VE, Rodriguez-Lopez ME, Mendez-Mani P, Garcia-Alvarez R, Gonzalez-Martinez MDR, Aquino-Rubio G, Escareno-Montiel N, Vazquez-Castillo TV, Uribe-Duarte MG, Ruiz-Corral MJ, Ortega-Yanez A, Bernal-Felipe N, Gomez-Navarro B, Arriaga-Perea AJ, Martinez-Bezies V, Macias-Medrano RM, Aguilar-Campos JA, Solis-Martinez R, Serrano-Osuna R, Sandoval-Sandoval MJ, Jaramillo-Rodriguez Y, Salgado-Adame A, Juarez-de la Cruz F, Novelo-Garza B, Pavon-Vargas MLA, Salgado-Galicia N, Bortolini MC, Gallo C, Bedoya G, Rothhammer F, Gonzalez-Jose R, Ruiz-Linares A, Canizales-Quinteros S, Romero-Hidalgo S, Krause J, Zuniga J, Yunis EJ, Bekker-Mendez C, Granados J. The immunogenetic diversity of the HLA system in Mexico correlates with underlying population genetic structure. Hum Immunol. 2020 Jul 7; :.

Villarreal-mMolina MT, Rosas-Madrigal S, Lopez-Mora E, Calderon-Avila AL, Rodriguez-Zanella H, Romero-Hidalgo S, Rosendo-Gutierrez R, Carnevale A. Homozygous Fukutin Missense Mutation in Two Mexican Siblings with Dilated Cardiomyopathy. Rev Invest Clin. 2020 May 7; 73(5):None.

Romero-Romero S, Balleza D. Voltage vs. Ligand II: Structural insights of the intrinsic flexibility in cyclic nucleotide-gated channels. Channels (Austin). 2019 Dec; 13(1):382-399.

Macias-Kauffer LR, Villamil-Ramirez H, Leon-Mimila P, Jacobo-Albavera L, Posadas-Romero C, Posadas-Sanchez R, Lopez-Contreras BE, Moran-Ramos S, Romero-Hidalgo S, Acuna-Alonzo V, Del-Rio-Navarro BE, Bortolini MC, Gallo C, Bedoya G, Rothhammer F, Gonzalez-Jose R, Ruiz-Linares A, Stephens CR, Velazquez-Cruz R, Fernandez Del Valle-Laisequilla C, Reyes-Garcia JG, Barranco Garduno LM, Carrasco-Portugal MDC, Flores-Murrieta FJ, Vargas-Alarcon G, Aguilar-Salinas CA, Villarreal-Molina T, Canizales-Quinteros S. Genetic contributors to serum uric acid levels in Mexicans and their effect on premature coronary artery disease. Int J Cardiol. 2019 Oct 1; 279:.

Rivera-Paredez B, Macias-Kauffer L, Fernandez-Lopez JC, Villalobos-Comparan M, Martinez-Aguilar MM, de la Cruz-Montoya A, Ramirez-Salazar EG, Villamil-Ramirez H, Quiterio M, Ramirez-Palacios P, Romero-Hidalgo S, Villarreal-Molina MT, Denova-Gutierrez E, Flores YN, Canizales-Quinteros S, Salmeron J, Velazquez-Cruz R. Influence of Genetic and Non-Genetic Risk Factors for Serum Uric Acid Levels and Hyperuricemia in Mexicans. Nutrients. 2019 Jun 14; 11(6):.

Grijalva-Pérez A., Esmer C., Romero-Hidalgo S., Rojo-Dominguez A., Rosas-Madrigal S., Velázquez-Cruz R Villarreal-Molina T., Acuña-Alonzo V., Bravo-Oro A., Carnevale A.. Prevalence and ancestral origin of the c.1987delC GAA gene mutation causing Pompe disease in Central Mexico. Am J Med Genet. 2018 2018; 15:None.

Romero-Hidalgo S, Ochoa-Leyva A, Garciarrubio A, Acuna-Alonzo V, Antunez-Arguelles E, Balcazar-Quintero M, Barquera-Lozano R, Carnevale A, Cornejo-Granados F, Fernandez-Lopez JC, Garcia-Herrera R, Garcia-Ortiz H, Granados-Silvestre A, Granados J, Guerrero-Romero F, Hernandez-Lemus E, Leon-Mimila P, Macin-Perez G, Martinez-Hernandez A, Menjivar M, Morett E, Orozco L, Ortiz-Lopez G, Perez-Villatoro F, Rivera-Morales J, Riveros-McKay F, Villalobos-Comparan M, Villamil-Ramirez H, Villarreal-Molina T, Canizales-Quinteros S, Soberon X. Demographic history and biologically relevant genetic variation of Native Mexicans inferred from whole-genome sequencing. Nat Commun. 2017 Oct 18; 8(1):1005.

Ortiz-Rodriguez MA, Yanez-Velasco L, Carnevale A, Romero-Hidalgo S, Bernal D, Aguilar-Salinas C, Rojas R, Villa A, Tur JA. Prevalence of metabolic syndrome among elderly Mexicans. Arch Gerontol Geriatr. 2017 Nov; 73:288-293.

Villalobos-Comparan M, Jimenez-Ortega RF, Estrada K, Parra-Torres AY, Gonzalez-Mercado A, Patino N, Castillejos-Lopez M, Quiterio M, Fernandez-Lopez JC, Ibarra B, Romero-Hidalgo S, Salmeron J, Velazquez-Cruz R. A Pilot Genome-Wide Association Study in Postmenopausal Mexican-Mestizo Women Implicates the RMND1/CCDC170 Locus Is Associated with Bone Mineral Density. Int J Genomics. 2017; 2017:5831020.

Villalobos-Comparan M, Antuna-Puente B, Villarreal-Molina MT, Canizales-Quinteros S, Velazquez-Cruz R, Leon-Mimila P, Villamil-Ramirez H, Gonzalez-Barrios JA, Merino-Garcia JL, Thompson-Bonilla MR, Jarquin D, Sanchez-Hernandez OE, Rodriguez-Arellano ME, Posadas-Romero C, Vargas-Alarcon G, Campos-Perez F, Quiterio M, Salmeron-Castro J, Carnevale A, Romero-Hidalgo S. Interaction between FTO rs9939609 and the Native American-origin ABCA1 rs9282541 affects BMI in the admixed Mexican population. BMC Med Genet. 2017 May 02; 18(1):46.

Villamil-Ramirez H, Leon-Mimila P, Macias-Kauffer LR, Canizalez-Roman A, Villalobos-Comparan M, Leon-Sicairos N, Vega-Badillo J, Sanchez-Munoz F, Lopez-Contreras B, Moran-Ramos S, Villarreal-Molina T, Zurita LC, Campos-Perez F, Huertas-Vazquez A, Bojalil R, Romero-Hidalgo S, Aguilar-Salinas CA, Canizales-Quinteros S. A combined linkage and association strategy identifies a variant near the GSTP1 gene associated with BMI in the Mexican population. J Hum Genet. 2016 Nov 24; :.

Ruiz-Contreras AE, Roman-Lopez TV, Caballero-Sanchez U, Rosas-Escobar CB, Ortega-Mora EI, Barrera-Tlapa MA, Romero-Hidalgo S, Carrillo-Sanchez K, Hernandez-Morales S, Vadillo-Ortega F, Gonzalez-Barrios JA, Mendez-Diaz M, Prospero-Garcia O. Because difficulty is not the same for everyone: the impact of complexity in working memory is associated with cannabinoid 1 receptor genetic variation in young adults. Memory. 2016 Apr 25; 35:1-9.

Jacobo-Albavera L, Posadas-Romero C, Vargas-Alarcon G, Romero-Hidalgo S, Posadas-Sanchez R, Gonzalez-Salazar MD, Carnevale A, Canizales-Quinteros S, Medina-Urrutia A, Antunez-Arguelles E, Villarreal-Molina T. Dietary fat and carbohydrate modulate the effect of the ATP-binding cassette A1 () R230C variant on metabolic risk parameters in premenopausal women from the Genetics of Atherosclerotic Disease (GEA) Study. Nutr Metab (Lond). 2015; 12:45.

Palacios-Gonzalez B, Vadillo-Ortega F, Polo-Oteyza E, Sanchez T, Ancira-Moreno M, Romero-Hidalgo S, Meraz N, Antuna-Puente B. Irisin levels before and after physical activity among school-age children with different BMI: A direct relation with leptin. Obesity (Silver Spring). 2015 Apr; 23(4):729-32.

Moreno-Estrada A, Gignoux CR, Fernandez-Lopez JC, Zakharia F, Sikora M, Contreras AV, Acuna-Alonzo V, Sandoval K, Eng C, Romero-Hidalgo S, Ortiz-Tello P, Robles V, Kenny EE, Nuno-Arana I, Barquera-Lozano R, Macin-Perez G, Granados-Arriola J, Huntsman S, Galanter JM, Via M, Ford JG, Chapela R, Rodriguez-Cintron W, Rodriguez-Santana JR, Romieu I, Sienra-Monge JJ, del Rio Navarro B, London SJ, Ruiz-Linares A, Garcia-Herrera R, Estrada K, Hidalgo-Miranda A, Jimenez-Sanchez G, Carnevale A, Soberon X, Canizales-Quinteros S, Rangel-Villalobos H, Silva-Zolezzi I, Burchard EG, Bustamante CD. Human genetics. The genetics of Mexico recapitulates Native American substructure and affects biomedical traits. Science. 2014 Jun 13; 344(6189):1280-5.

Larrieta-Carrasco E, Acuna-Alonzo V, Velazquez-Cruz R, Barquera-Lozano R, Leon-Mimila P, Villamil-Ramirez H, Menjivar M, Romero-Hidalgo S, Mendez-Sanchez N, Cardenas V, Banuelos-Moreno M, Flores YN, Quiterio M, Salmeron J, Sanchez-Munoz F, Villarreal-Molina T, Aguilar-Salinas CA, Canizales-Quinteros S. PNPLA3 I148M polymorphism is associated with elevated alanine transaminase levels in Mexican Indigenous and Mestizo populations. Mol Biol Rep. 2014 Apr 2; 41(7):4705-11.

Garcia-Velazquez LE, Canizales-Quinteros S, Romero-Hidalgo S, Ochoa-Morales A, Martinez-Ruano L, Marquez-Luna C, Acuna-Alonzo V, Villarreal-Molina MT, Alonso-Vilatela ME, Yescas-Gomez P. Founder effect and ancestral origin of the spinocerebellar ataxia type 7 (SCA7) mutation in Mexican families. Neurogenetics. 2013 Dec 28; 15(1):13-7.

Williams AL, Jacobs SB, Moreno-Macias H, Huerta-Chagoya A, Churchhouse C, Marquez-Luna C, Garcia-Ortiz H, Jose Gomez-Vazquez M, Burtt NP, Aguilar-Salinas CA, Gonzalez-Villalpando C, Florez JC, Orozco L, Haiman CA, Tusie-Luna T, Altshuler D, Ripke S, Manning AK, Neale B, Reich D, Stram DO, Fernandez-Lopez JC, Romero-Hidalgo S, Patterson N, Aguilar-Delfin I, Martinez-Hernandez A, Centeno-Cruz F, Revilla-Monsalve C, Islas-Andrade S, Cordova E, Rodriguez-Arellano E, Soberon X, Gonzalez-Villalpando ME, Henderson BE, Monroe K, Wilkens L, Kolonel LN, Le Marchand L, Riba L, Ordonez-Sanchez ML, Rodriguez-Guillen R, Cruz-Bautista I, Rodriguez-Torres M, Munoz-Hernandez LL, Saenz T, Gomez D, Alvirde U, Onofrio RC, Brodeur WM, Gage D, Murphy J, Franklin J, Mahan S, Ardlie K, Crenshaw AT, Winckler W, Prufer K, Shunkov MV, Sawyer S, Stenzel U, Kelso J, Lek M, Sankararaman S, Macarthur DG, Derevianko AP, Paabo S, Gopal S, Grammatikos JA, Smith IC, Bullock KH, Deik AA, Souza AL, Pierce KA, Clish CB, Fennell T, Farjoun Y, Genomics Platform B, Gabriel S, Gross MD, Pereira MA, Seielstad M, Koh WP, Tai ES, Flannick J, Fontanillas P, Morris A, Teslovich TM, Atzmon G, Blangero J, Bowden DW, Chambers J, Shin Cho Y, Duggirala R, Glaser B, Hanis C, Kooner J, Laakso M, Lee JY, Ying Teo Y, Wilson JG, Puppala S, Farook VS, Thameem F, Abboud HE, Defronzo RA, Jenkinson CP, Lehman DM, Curran JE, Cortes ML. Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico. Nature. 2013 Dec 25; 506(7486):97-101.

Ruiz-Contreras AE, Carrillo-Sanchez K, Ortega-Mora I, Barrera-Tlapa MA, Roman-Lopez TV, Rosas-Escobar CB, Flores-Barrera L, Caballero-Sanchez U, Munoz-Torres Z, Romero-Hidalgo S, Hernandez-Morales S, Gonzalez-Barrios JA, Vadillo-Ortega F, Mendez-Diaz M, Aguilar-Roblero R, Prospero-Garcia O. Performance in working memory and attentional control is associated with the rs2180619 SNP in the CNR1 gene. Genes Brain Behav. 2013 Oct 23; 13(2):173-8.

Leon-Mimila P, Villamil-Ramirez H, Villalobos-Comparan M, Villarreal-Molina T, Romero-Hidalgo S, Lopez-Contreras B, Gutierrez-Vidal R, Vega-Badillo J, Jacobo-Albavera L, Posadas-Romeros C, Canizalez-Roman A, Rio-Navarro BD, Campos-Perez F, Acuna-Alonzo V, Aguilar-Salinas C, Canizales-Quinteros S. Contribution of common genetic variants to obesity and obesity-related traits in mexican children and adults. PLoS One. 2013; 8(8):e70640.

Larrieta-Carrasco E, Leon-Mimila P, Villarreal-Molina T, Villamil-Ramirez H, Romero-Hidalgo S, Jacobo-Albavera L, Gutierrez-Vidal R, Lopez-Contreras BE, Guillen-Pineda LE, Sanchez-Munoz F, Bojalil R, Mejia-Dominguez AM, Mendez-Sanchez N, Dominguez-Lopez A, Aguilar-Salinas CA, Canizales-Quinteros S. Association of the I148M/PNPLA3 Variant with Elevated Alanine Transaminase Levels in Normal-weight and Overweight/Obese Mexican Children. Gene. 2013 Mar 16; 520(2):185-8.

Ramirez-Martinez G, Cruz-Lagunas A, Jimenez-Alvarez L, Espinosa E, Ortiz-Quintero B, Santos-Mendoza T, Herrera MT, Canche-Pool E, Mendoza C, Banales JL, Garcia-Moreno SA, Moran J, Cabello C, Orozco L, Aguilar-Delfin I, Hidalgo-Miranda A, Romero S, Suratt BT, Selman M, Zuniga J. Seasonal and pandemic influenza H1N1 viruses induce differential expression of SOCS-1 and RIG-I genes and cytokine/chemokine production in macrophages. Cytokine. 2013 Feb 20; 62(1):151-119.

Jacobo-Albavera L, Aguayo-de la Rosa PI, Maria Teresa Villareal Molina, Villamil-Ramirez H, Leon-Mimila P, Sandra Romero Hidalgo, Lopez-Contreras BE, Sanchez-Munoz F, Bojalil R, Gonzalez-Barrios JA, Aguilar-Salinas CA, Canizales-Quinteros S. VNN1 gene expression levels and the G-137T polymorphism are associated with HDL-C levels in Mexican prepubertal children.. PLoS One. 2012; 7(11):e49818.

Maria Teresa Villareal Molina, Posadas-Romero C, Sandra Romero Hidalgo, Antunez-Arguelles E, Bautista-Grande A, Vargas-Alarcon G, Kimura-Hayama E, Canizales-Quinteros S, Juarez-Rojas JG, Posadas-Sanchez R, Cardoso-Saldana G, Medina-Urrutia A, Gonzalez-Salazar Mdel C, Martinez-Alvarado R, Jorge-Galarza E, Alessandra Carnevale. The ABCA1 gene R230C variant is associated with decreased risk of premature coronary artery disease: the genetics of atherosclerotic disease (GEA) study.. PLoS One. 2012; 7(11):e49285.

Villalobos-Comparan M, Villamil-Ramirez H, Maria Teresa Villareal Molina, Larrieta-Carrasco E, Leon-Mimila P, Sandra Romero Hidalgo, Jacobo-Albavera L, Liceaga-Fuentes AE, Campos-Perez FJ, Lopez-Contreras BE, Tusie-Luna T, Del Rio-Navarro BE, Aguilar-Salinas CA, Canizales-Quinteros S. PCSK1 rs6232 is associated with childhood and adult class III obesity in the Mexican population.. PLoS One. 2012; 7(6):e39037.

Romero-Hidalgo S, Villarreal-Molina T, Gonzalez-Barrios JA, Canizales-Quinteros S, Rodriguez-Arellano ME, Yanez-Velazco LB, Bernal-Alcantara DA, Villa AR, Antuna-Puente B, Acuna-Alonzo V, Merino-Garcia JL, Moreno-Sandoval HN, Carnevale A. Carbohydrate intake modulates the effect of the ABCA1-R230C variant on HDL cholesterol concentrations in premenopausal women. J Nutr. 2012 Feb; 142(2):278-83.

Rojano-Mejia D, Coral-Vazquez RM, Espinosa LC, Romero-Hidalgo S, Lopez-Medina G, Garcia Mdel C, Coronel A, Ibarra R, Canto P. TNFRSF11B gene haplotype and its association with bone mineral density variations in postmenopausal Mexican-Mestizo women. Maturitas. 2012 Jan; 71(1):49-54.

Flores-Dorantes T, Arellano-Campos O, Posadas-Sanchez R, Villarreal-Molina T, Medina-Urrutia A, Romero-Hidalgo S, Yescas-Gomez P, Perez-Mendez O, Jorge-Galarza E, Tusie-Luna T, Villalobos-Comparan M, Jacobo-Albavera L, Villamil-Ramirez H, Lopez-Contreras BE, Aguilar-Salinas CA, Posadas-Romero C, Canizales-Quinteros S. Association of R230C ABCA1 gene variant with low HDL-C levels and abnormal HDL subclass distribution in Mexican school-aged children. Clin Chim Acta. 2010 Sep 6; 411(17-18):1214-7.

Acuna-Alonzo V, Flores-Dorantes T, Kruit JK, Villarreal-Molina T, Arellano-Campos O, Hunemeier T, Moreno-Estrada A, Ortiz-Lopez MG, Villamil-Ramirez H, Leon-Mimila P, Villalobos-Comparan M, Jacobo-Albavera L, Ramirez-Jimenez S, Sikora M, Zhang LH, Pape TD, Granados-Silvestre Mde A, Montufar-Robles I, Tito-Alvarez AM, Zurita-Salinas C, Bustos-Arriaga J, Cedillo-Barron L, Gomez-Trejo C, Barquera-Lozano R, Vieira-Filho JP, Granados J, Romero-Hidalgo S, Huertas-Vazquez A, Gonzalez-Martin A, Gorostiza A, Bonatto SL, Rodriguez-Cruz M, Wang L, Tusie-Luna T, Aguilar-Salinas CA, Lisker R, Moises RS, Menjivar M, Salzano FM, Knowler WC, Bortolini MC, Hayden MR, Baier LJ, Canizales-Quinteros S. A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans. Hum Mol Genet. 2010 Jul 15; 19(14):2877-85.

Jimenez-Morales S, Velazquez-Cruz R, Ramirez-Bello J, Bonilla-Gonzalez E, Romero-Hidalgo S, Escamilla-Guerrero G, Cuevas F, Espinosa-Rosales F, Martinez-Aguilar NE, Gomez-Vera J, Baca V, Orozco L. Tumor necrosis factor-alpha is a common genetic risk factor for asthma, juvenile rheumatoid arthritis, and systemic lupus erythematosus in a Mexican pediatric population. Hum Immunol. 2009 Apr; 70(4):251-6.