1 | Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico | Coautor: Riba, L, Abboud, HE, Aguilar-Delfin, I, Aguilar-Salinas, CA, et al. | 2014 | Nature | WoS-id: 000330648100039 Scopus-id: 2-s2.0-84893716900
| 319 | 380 |
2 | Association of a low-frequency variant in HNF1A with type 2 diabetes in a latino population the SIGMA Type 2 Diabetes Consortium | Coautor: Riba, L, Estrada, K, Aukrust, I, Bjorkhaug, L, et al. | 2014 | JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | WoS-id: 000336972600022 Scopus-id: 2-s2.0-84902185032
| 184 | 191 |
3 | Amerindian-specific regions under positive selection harbour new lipid variants in Latinos | Coautor: Riba L., Ko A., Cantor R.M., Weissglas-Volkov D., et al. | 2014 | NATURE COMMUNICATIONS | WoS-id: 000338835400001 Scopus-id: 2-s2.0-84901949893
| 71 | 73 |
4 | Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes | Coautor: Riba L., Majithia A.R., Flannick J., Shahinian P., et al. | 2014 | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | WoS-id: 000341625600043 Scopus-id: 2-s2.0-84907013152
| 130 | 136 |
5 | Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci | Coautor: Riba, L, Weissglas-Volkov, D, Aguilar-Salinas, CA, Nikkola, E, et al. | 2013 | JOURNAL OF MEDICAL GENETICS | WoS-id: 000317563800004 Scopus-id: 2-s2.0-84878849984
| 97 | 97 |
6 | Rheumatoid arthritis in latin americans enriched for amerindian ancestry is associated with loci in chromosomes 1, 12, and 13, and the HLA Class II region | Coautor: Riba, L, Herraez, DL, Martinez-Bueno, M, de la Torre, IG, et al. | 2013 | ARTHRITIS AND RHEUMATISM | WoS-id: 000319740600007 Scopus-id: 2-s2.0-84878560466
| 32 | 36 |
7 | Reconstructing Native American population history | Coautor: Riba L., Reich D., Patterson N., Campbell D., et al. | 2012 | Nature | WoS-id: 000307501000040 Scopus-id: 2-s2.0-84865120805
| 526 | 562 |
8 | Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populations | Coautor: Riba L., Sánchez E., Rasmussen A., Acevedo-Vasquez E., et al. | 2012 | ARTHRITIS AND RHEUMATISM | WoS-id: 000310544500022 Scopus-id: 2-s2.0-84868092719
| 61 | 66 |
9 | Erratum: Reconstructing Native American population history (Nature (2012) 488 (370-374) DOI:10.1038/nature11258) | Coautor: Riba L., Reich D., Patterson N., Campbell D., et al. | 2012 | Nature | WoS-id: 000310774300052 Scopus-id: 2-s2.0-84868618389
| 0 | 1 |
10 | Contribution of Common Genetic Variation to the Risk of Type 2 Diabetes in the Mexican Mestizo Population | Coautor: Riba L., Gamboa-Meléndez M.A., Huerta-Chagoya A., Moreno-Macías H., et al. | 2012 | Diabetes | WoS-id: 000312041700039 Scopus-id: 2-s2.0-84870311448
| 80 | 89 |
11 | Adipose Co-expression networks across Finns and Mexicans identify novel triglyceride-associated genes | Coautor: Riba L., Haas B.E., Horvath S., Pietilainen, KH, et al. | 2012 | BMC MEDICAL GENOMICS | WoS-id: 000313566500001 Scopus-id: 2-s2.0-84870461579
| 31 | 32 |
12 | Evidence of How rs7575840 Influences Apolipoprotein B-Containing Lipid Particles | Coautor: Riba L., Haas B.E., Weissglas-Volkov D., Aguilar-Salinas C.A., et al. | 2011 | ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY | WoS-id: 000289720800037 Scopus-id: 2-s2.0-79955624738
| 12 | 12 |
13 | The non-synonymous Arg230Cys variant (R230C) of the ATP-binding cassette transporter A1 is associated with low HDL cholesterol concentrations in Mexican adults: A population bas | Coautor: Riba L., Aguilar-Salinas C.A., Canizales-Quinteros S., Rojas-Martínez R., et al. | 2011 | Atherosclerosis | WoS-id: 000290205800023 Scopus-id: 2-s2.0-79955528671
| 23 | 23 |
14 | The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans | Coautor: Riba L., Weissglas-Volkov D., Calkin A.C., Tusie-Luna T., et al. | 2011 | JOURNAL OF CLINICAL INVESTIGATION | WoS-id: 000293495500017 Scopus-id: 2-s2.0-79960985140
| 48 | 53 |
15 | Identification of Two Common Variants Contributing to Serum Apolipoprotein B Levels in Mexicans | Coautor: Riba L., Weissglas-Volkov D., Plaisier C.L., Huertas-Vazquez A., et al. | 2010 | ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY | WoS-id: 000273799900036 Scopus-id: 2-s2.0-75149145515
| 13 | 13 |
16 | Investigation of Variants Identified in Caucasian Genome-Wide Association Studies for Plasma High-Density Lipoprotein Cholesterol and Triglycerides Levels in Mexican Dyslipidemi | Coautor: Riba L., Weissglas-Volkov D., Aguilar-Salinas C.A., Sinsheimer J.S., et al. | 2010 | CIRCULATION-CARDIOVASCULAR GENETICS | WoS-id: 000275979700006 Scopus-id: 2-s2.0-77952533413
| 43 | 43 |
17 | Genetically Determined Amerindian Ancestry Correlates With Increased Frequency of Risk Alleles for Systemic Lupus Erythematosus | Coautor: Riba L., Sanchez E., Webb R.D., Rasmussen A., et al. | 2010 | ARTHRITIS AND RHEUMATISM | WoS-id: 000285210200025 Scopus-id: 2-s2.0-78650065026
| 61 | 67 |
18 | Galanin Preproprotein Is Associated With Elevated Plasma Triglycerides | Coautor: Riba L., Plaisier C.L., Kyttala, M, Weissglas-Volkov D., et al. | 2009 | ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY | WoS-id: 000261797200024 Scopus-id: 2-s2.0-58849095360
| 26 | 24 |
19 | Hypoalphalipoproteinemia in populations of Native American ancestry: an opportunity to assess the interaction of genes and the environment | Coautor: Riba L., Aguilar-Salinas C.A., Canizales-Quinteros S., Rojas-Martfnez R., et al. | 2009 | CURRENT OPINION IN LIPIDOLOGY | WoS-id: 000264956600002 Scopus-id: 2-s2.0-64549120714
| 28 | 31 |
20 | Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes | Coautor: Riba L., Florez J.C., Price A.L., Campbell D., et al. | 2009 | Diabetologia | WoS-id: 000268006200010 Scopus-id: 2-s2.0-67650663161
| 69 | 72 |
21 | A genomewide admixture map for latino populations | Coautor: Riba L., Price A.L., Patterson N., Yu F., et al. | 2007 | AMERICAN JOURNAL OF HUMAN GENETICS | WoS-id: 000246553800003 Scopus-id: 2-s2.0-34250894969
| 224 | 235 |
22 | HNF-1a G574S is a functional variant with decreased transactivation activity | Coautor: Riba L., Navalón-García K., Mendoza-Alcantar L., Díaz-Vargas M.E., et al. | 2006 | DIABETIC MEDICINE | WoS-id: 000243135700004 Scopus-id: 2-s2.0-33751253099
| 4 | 5 |
23 | A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemia | Coautor: Riba L., Canizales-Quinteros S., Aguilar-Salinas C.A., Huertas-Vázquez A., et al. | 2005 | HUMAN GENETICS | WoS-id: 000226552200014 Scopus-id: 2-s2.0-19944430011
| 16 | 16 |
24 | GENEHUNTER versus SimWalk2 in the context of an extended kindred and a qualitative trait locus | Coautor: Riba L., Romero-Hidalgo S., Rodrigues E.R., Gutiérrez-Peña E., et al. | 2005 | Genetica | WoS-id: 000228542300004 Scopus-id: 2-s2.0-18144378086
| 2 | 3 |
25 | Familial combined hyperlipidemia in mexicans: Association with upstream transcription factor 1 and linkage on chromosome 16q24.1 | Coautor: Riba-Ramirez L., Huertas-Vazquez A., Aguilar-Salinas C., Lusis A.J., et al. | 2005 | ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY | WoS-id: 000231502500035 Scopus-id: 2-s2.0-24144435303
| 61 | 65 |
26 | Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families | Coautor: Riba L., Domínguez-López A., Miliar-García Á., Segura-Kato Y.X., et al. | 2005 | Journal of the Pancreas | Scopus-id: 2-s2.0-27644491272
| 0 | 22 |
27 | Identifying different susceptibility loci associated with early onset diabetes and cardiovascular disease in Mexican families [Identificación de distintos loci de susceptibilidad relacionados al desarrollo de diabetes de inicio temprano y e | Coautor: Riba-Ramírez L., Canizales-Quinteros S., Huertas-Vázquez A., Monroy-Guzmán A., et al. | 2005 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-20944438524
| 0 | 2 |
28 | Contribution of chromosome 1q21-q23 to familial combined hyperlipidemia in Mexican families | Coautor: Riba L., Huertas-Vázquez A., del Rincón J.P., Canizales-Quinteros S., et al. | 2004 | ANNALS OF HUMAN GENETICS | Scopus-id: 2-s2.0-6444229534
| 16 | 25 |
29 | Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia | Coautor: Riba L., Canizales-Quinteros S., Aguilar-Salinas C.A., Reyes-Rodríguez E., et al. | 2003 | CIRCULATION RESEARCH | WoS-id: 000181711300015 Scopus-id: 2-s2.0-0037459359
| 29 | 32 |
30 | Steroid 21-hydroxylase (P450c21) naturally occuring mutants I172N, v281L and I236N/V237E/M239K exert a dominant negative effect on enzymatic activity when co-expressed with the wild-type protein | 2ᵒ autor: Riba L., Félix-López X., Ordóñez-Sánchez Ma.L., Ramírez-Jiménez S., et al. | 2003 | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | WoS-id: 000185343000010 Scopus-id: 2-s2.0-0141891454
| 6 | 7 |
31 | What do you know about...Gene therapy? [Qué sabe usted acerca de...Terapia génica?] | Coautor: Riba L., López Gutiérrez A.U., Canizales Quinteros S., Del Muro Delgado R., et al. | 2001 | Revista Mexicana de Ciencias Farmaceuticas | Scopus-id: 2-s2.0-0035679691
| 0 | 0 |
32 | What do you know about... gene therapy? [Qué sabe usted acerca de... terapia génica?] | Coautor: Riba L., López G. A.U., Canizales Q. S., Del Muro D. R., et al. | 2001 | Revista Mexicana de Ciencias Farmaceuticas | Scopus-id: 2-s2.0-0035680190
| 0 | 0 |
33 | Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population: Identification of possible new mutations and high prevalence of apparent germ-line mutations | Coautor: Riba L., Ordoñez-Sánchez M.L., Ramírez-Jiménez S., López-Gutierrez A.U., et al. | 1998 | HUMAN GENETICS | WoS-id: 000072457500008 Scopus-id: 2-s2.0-2642651108
| 52 | 59 |
34 | Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: Evidence of different genetic mechanisms involved in the production of the disease | 2ᵒ autor: Riba L., López-Gutiérrez A.U., Ordoñez-Sánchez M.L., Ramirez-Jiménez S., et al. | 1998 | JOURNAL OF MEDICAL GENETICS | WoS-id: 000077266400010 Scopus-id: 2-s2.0-0031759339
| 23 | 28 |
35 | Analysis of the glucokinase gene in Mexican families displaying early- onset non-insulin-dependent diabetes mellitus including MODY families | Coautor: Riba L., Del Bosque-Plata L., Garcia-Garcia E., Ramirez-Jimenez S., et al. | 1997 | AM J MED GENET | WoS-id: A1997YD48100003 Scopus-id: 2-s2.0-0030735219
| 6 | 7 |
36 | Generation and mapping of Mus spretus strain-specific markers for rapid genomic scanning | 2ᵒ autor: Riba L., Elango R., Housman D., Hunter K. | 1996 | MAMMALIAN GENOME | WoS-id: A1996UM12900003 Scopus-id: 2-s2.0-0030140565
| 10 | 10 |
37 | Toward the construction of integrated physical and genetic maps of the mouse genome using interspersed repetitive sequence PCR (IRS-PCR) genomics | 2ᵒ autor: Riba L., Hunter K.W., Schalkwyk L., Clark M., et al. | 1996 | GENOME RES | WoS-id: A1996UJ01400006 Scopus-id: 2-s2.0-19144368944
| 13 | 14 |
38 | Efficient high-resolution genetic mapping of mouse interspersed repetitive sequence PCR products, toward integrated genetic and physical mapping of the mouse genome | Coautor: Riba L., Mccarthy L., Hunter K., Schalkwyk L., et al. | 1995 | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | WoS-id: A1995RB80400010 Scopus-id: 2-s2.0-0029051320
| 31 | 31 |
39 | The isolation of cDNAs within the huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA library | Coautor: Riba L., Snell R.G., Doucette-stamm L.A., Gillespie K.M., et al. | 1993 | HUMAN MOLECULAR GENETICS | WoS-id: A1993KU13700018 Scopus-id: 2-s2.0-0027175814
| 15 | 15 |
40 | Site-specific cleavage of human chromosome 4 mediated by triple-helix formation | Coautor: Riba L., Strobel S.A., Doucette-Stamm L.A., Housman D.E., et al. | 1991 | Science | WoS-id: A1991GV07300044 Scopus-id: 2-s2.0-0026348013
| 196 | 195 |
41 | Generation and characterization of irradiation hybrids of human chromosome 4 | 2ᵒ autor: Riba L., Doucette-Stamm L.A., Handelin B., Difilippantonio M., et al. | 1991 | SOMAT CELL MOLEC GEN | WoS-id: A1991GZ55100006 Scopus-id: 2-s2.0-0026337905
| 10 | 14 |
42 | Identification of a functional promoter for the Escherichia coli gdhA gene and its regulation | 1ᵉʳ autor: Riba L., Becerril B., Servín-González L., Valle F., et al. | 1988 | Gene | WoS-id: A1988R610900001 Scopus-id: 2-s2.0-0024246277
| 11 | 12 |
43 | Repetitive extragenic palindromic (REP) sequences in the Escherichia coli gdhA gene | Coautor: Riba L., Becerril B., Valle F., Merino E., et al. | 1985 | Gene | WoS-id: A1985ASP1800006 Scopus-id: 2-s2.0-0022251699
| 18 | 19 |