LAURA ESTELA RIBA RAMIREZ



DATOS GENERALES NOMBRAMIENTOS
Nombre completo   LAURA ESTELA RIBA RAMIREZ
Máximo nivel de estudios   MAESTRÍA
Antigüedad académica en la UNAM   18 años, 9 meses, 0 días

Último  TECNICO ACADEMICO TITULAR C TC Definitivo
Instituto de Investigaciones Biomédicas
ESTIMULOS, PROGRAMAS, PREMIOS Y RECONOCIMIENTOS
* SNI I - 2015

INFORMACIÓN DE PUBLICACIONES
Firmas  
Riba L. Riba, L Riba-Ramírez L.
ID's SCOPUS  
55993654200 6701409590 55441132000
Áreas de conocimiento  
Cardiac & cardiovascular systems Endocrinology & metabolism Endocrinology and metabolism Genetics & heredity Genetics and heredity
Hematology Medicine, general and internal Medicine, research & experimental Multidisciplinary sciences Pediatrics
Peripheral vascular disease Rheumatology Scie jcr Cardiology and Cardiovascular Medicine Chemistry (miscellaneous)
Endocrinology, Diabetes and Metabolism Genetics Genetics (clinical) Medicine (miscellaneous) Multidisciplinary
Nutrition and Dietetics Pharmacology (medical)
Coautorías con entidades de la UNAM  
  • Instituto de Investigaciones Biomédicas
  • Instituto de Biotecnología
  • Facultad de Ciencias
  • Facultad de Química
Revistas en las que ha publicado  (31):
  1. AM J MED GENET, (1997)
  2. AMERICAN JOURNAL OF HUMAN GENETICS, Estados Unidos America (2007)
  3. ANNALS OF HUMAN GENETICS, Estados Unidos America (2004)
  4. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, Estados Unidos America (2005, 2009, 2010, 2011)
  5. ARTHRITIS AND RHEUMATISM, Estados Unidos America (2010, 2012, 2013)
  6. Atherosclerosis, Irlanda (2011)
  7. BMC MEDICAL GENOMICS, Reino Unido (2012)
  8. CIRCULATION RESEARCH, Estados Unidos America (2003)
  9. CIRCULATION-CARDIOVASCULAR GENETICS, Estados Unidos America (2010)
  10. CURRENT OPINION IN LIPIDOLOGY, Reino Unido (2009)
  11. Diabetes, Estados Unidos America (2012)
  12. DIABETIC MEDICINE, Estados Unidos America (2006)
  13. Diabetologia, Estados Unidos America (2009)
  14. GACETA MEDICA DE MEXICO, México (2005)
  15. Gene, Países Bajos (1985, 1988)
  16. Genetica, Países Bajos (2005)
  17. GENOME RES, (1996)
  18. HUMAN GENETICS, Estados Unidos America (1998, 2005)
  19. HUMAN MOLECULAR GENETICS, Reino Unido (1993)
  20. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, Estados Unidos America (2014)
  21. JOURNAL OF CLINICAL INVESTIGATION, Estados Unidos America (2011)
  22. JOURNAL OF MEDICAL GENETICS, Reino Unido (1998, 2013)
  23. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, Alemania (2003)
  24. Journal of the Pancreas, Italia (2005)
  25. MAMMALIAN GENOME, Estados Unidos America (1996)
  26. Nature, Reino Unido (2012, 2014)
  27. NATURE COMMUNICATIONS, Reino Unido (2014)
  28. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, Estados Unidos America (1995, 2014)
  29. Revista Mexicana de Ciencias Farmaceuticas, México (2001)
  30. Science, Estados Unidos America (1991)
  31. SOMAT CELL MOLEC GEN, (1991)


Documentos indexados (WoS y Scopus)

# Título del documento Autores Año Rista Fuente Citas WoS Citas Scopus
1Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in MexicoCoautor: Riba, L, Abboud, HE, Aguilar-Delfin, I, Aguilar-Salinas, CA, et al.2014NatureWoS-id: 000330648100039
Scopus-id: 2-s2.0-84893716900
319372
2Association of a low-frequency variant in HNF1A with type 2 diabetes in a latino population the SIGMA Type 2 Diabetes ConsortiumCoautor: Riba, L, Estrada, K, Aukrust, I, Bjorkhaug, L, et al.2014JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATIONWoS-id: 000336972600022
Scopus-id: 2-s2.0-84902185032
176181
3Amerindian-specific regions under positive selection harbour new lipid variants in LatinosCoautor: Riba L., Ko A., Cantor R.M., Weissglas-Volkov D., et al.2014NATURE COMMUNICATIONSWoS-id: 000338835400001
Scopus-id: 2-s2.0-84901949893
6570
4Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetesCoautor: Riba L., Majithia A.R., Flannick J., Shahinian P., et al.2014PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICAWoS-id: 000341625600043
Scopus-id: 2-s2.0-84907013152
130134
5Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid lociCoautor: Riba, L, Weissglas-Volkov, D, Aguilar-Salinas, CA, Nikkola, E, et al.2013JOURNAL OF MEDICAL GENETICSWoS-id: 000317563800004
Scopus-id: 2-s2.0-84878849984
9495
6Rheumatoid arthritis in latin americans enriched for amerindian ancestry is associated with loci in chromosomes 1, 12, and 13, and the HLA Class II regionCoautor: Riba, L, Herraez, DL, Martinez-Bueno, M, de la Torre, IG, et al.2013ARTHRITIS AND RHEUMATISMWoS-id: 000319740600007
Scopus-id: 2-s2.0-84878560466
2835
7Reconstructing Native American population historyCoautor: Riba L., Reich D., Patterson N., Campbell D., et al.2012NatureWoS-id: 000307501000040
Scopus-id: 2-s2.0-84865120805
515547
8Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populationsCoautor: Riba L., Sánchez E., Rasmussen A., Acevedo-Vasquez E., et al.2012ARTHRITIS AND RHEUMATISMWoS-id: 000310544500022
Scopus-id: 2-s2.0-84868092719
5862
9Erratum: 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.2012NatureWoS-id: 000310774300052
Scopus-id: 2-s2.0-84868618389
01
10Contribution of Common Genetic Variation to the Risk of Type 2 Diabetes in the Mexican Mestizo PopulationCoautor: Riba L., Gamboa-Meléndez M.A., Huerta-Chagoya A., Moreno-Macías H., et al.2012DiabetesWoS-id: 000312041700039
Scopus-id: 2-s2.0-84870311448
7588
11Adipose Co-expression networks across Finns and Mexicans identify novel triglyceride-associated genesCoautor: Riba L., Haas B.E., Horvath S., Pietilainen, KH, et al.2012BMC MEDICAL GENOMICSWoS-id: 000313566500001
Scopus-id: 2-s2.0-84870461579
3132
12Evidence of How rs7575840 Influences Apolipoprotein B-Containing Lipid ParticlesCoautor: Riba L., Haas B.E., Weissglas-Volkov D., Aguilar-Salinas C.A., et al.2011ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGYWoS-id: 000289720800037
Scopus-id: 2-s2.0-79955624738
1212
13The non-synonymous Arg230Cys variant (R230C) of the ATP-binding cassette transporter A1 is associated with low HDL cholesterol concentrations in Mexican adults: A population basCoautor: Riba L., Aguilar-Salinas C.A., Canizales-Quinteros S., Rojas-Martínez R., et al.2011AtherosclerosisWoS-id: 000290205800023
Scopus-id: 2-s2.0-79955528671
2323
14The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humansCoautor: Riba L., Weissglas-Volkov D., Calkin A.C., Tusie-Luna T., et al.2011JOURNAL OF CLINICAL INVESTIGATIONWoS-id: 000293495500017
Scopus-id: 2-s2.0-79960985140
4851
15Identification of Two Common Variants Contributing to Serum Apolipoprotein B Levels in MexicansCoautor: Riba L., Weissglas-Volkov D., Plaisier C.L., Huertas-Vazquez A., et al.2010ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGYWoS-id: 000273799900036
Scopus-id: 2-s2.0-75149145515
1313
16Investigation of Variants Identified in Caucasian Genome-Wide Association Studies for Plasma High-Density Lipoprotein Cholesterol and Triglycerides Levels in Mexican DyslipidemiCoautor: Riba L., Weissglas-Volkov D., Aguilar-Salinas C.A., Sinsheimer J.S., et al.2010CIRCULATION-CARDIOVASCULAR GENETICSWoS-id: 000275979700006
Scopus-id: 2-s2.0-77952533413
4141
17Genetically Determined Amerindian Ancestry Correlates With Increased Frequency of Risk Alleles for Systemic Lupus ErythematosusCoautor: Riba L., Sanchez E., Webb R.D., Rasmussen A., et al.2010ARTHRITIS AND RHEUMATISMWoS-id: 000285210200025
Scopus-id: 2-s2.0-78650065026
6066
18Galanin Preproprotein Is Associated With Elevated Plasma TriglyceridesCoautor: Riba L., Plaisier C.L., Kyttala, M, Weissglas-Volkov D., et al.2009ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGYWoS-id: 000261797200024
Scopus-id: 2-s2.0-58849095360
2424
19Hypoalphalipoproteinemia in populations of Native American ancestry: an opportunity to assess the interaction of genes and the environmentCoautor: Riba L., Aguilar-Salinas C.A., Canizales-Quinteros S., Rojas-Martfnez R., et al.2009CURRENT OPINION IN LIPIDOLOGYWoS-id: 000264956600002
Scopus-id: 2-s2.0-64549120714
2731
20Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetesCoautor: Riba L., Florez J.C., Price A.L., Campbell D., et al.2009DiabetologiaWoS-id: 000268006200010
Scopus-id: 2-s2.0-67650663161
6671
21A genomewide admixture map for latino populationsCoautor: Riba L., Price A.L., Patterson N., Yu F., et al.2007AMERICAN JOURNAL OF HUMAN GENETICSWoS-id: 000246553800003
Scopus-id: 2-s2.0-34250894969
218232
22HNF-1a G574S is a functional variant with decreased transactivation activityCoautor: Riba L., Navalón-García K., Mendoza-Alcantar L., Díaz-Vargas M.E., et al.2006DIABETIC MEDICINEWoS-id: 000243135700004
Scopus-id: 2-s2.0-33751253099
45
23A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemiaCoautor: Riba L., Canizales-Quinteros S., Aguilar-Salinas C.A., Huertas-Vázquez A., et al.2005HUMAN GENETICSWoS-id: 000226552200014
Scopus-id: 2-s2.0-19944430011
1616
24GENEHUNTER versus SimWalk2 in the context of an extended kindred and a qualitative trait locusCoautor: Riba L., Romero-Hidalgo S., Rodrigues E.R., Gutiérrez-Peña E., et al.2005GeneticaWoS-id: 000228542300004
Scopus-id: 2-s2.0-18144378086
23
25Familial combined hyperlipidemia in mexicans: Association with upstream transcription factor 1 and linkage on chromosome 16q24.1Coautor: Riba-Ramirez L., Huertas-Vazquez A., Aguilar-Salinas C., Lusis A.J., et al.2005ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGYWoS-id: 000231502500035
Scopus-id: 2-s2.0-24144435303
6165
26Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican familiesCoautor: Riba L., Domínguez-López A., Miliar-García Á., Segura-Kato Y.X., et al.2005Journal of the PancreasScopus-id: 2-s2.0-27644491272
022
27Identifying 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 eCoautor: Riba-Ramírez L., Canizales-Quinteros S., Huertas-Vázquez A., Monroy-Guzmán A., et al.2005GACETA MEDICA DE MEXICOScopus-id: 2-s2.0-20944438524
02
28Contribution of chromosome 1q21-q23 to familial combined hyperlipidemia in Mexican familiesCoautor: Riba L., Huertas-Vázquez A., del Rincón J.P., Canizales-Quinteros S., et al.2004ANNALS OF HUMAN GENETICSScopus-id: 2-s2.0-6444229534
1625
29Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemiaCoautor: Riba L., Canizales-Quinteros S., Aguilar-Salinas C.A., Reyes-Rodríguez E., et al.2003CIRCULATION RESEARCHWoS-id: 000181711300015
Scopus-id: 2-s2.0-0037459359
2832
30Steroid 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 protein2ᵒ autor: Riba L., Félix-López X., Ordóñez-Sánchez Ma.L., Ramírez-Jiménez S., et al.2003JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISMWoS-id: 000185343000010
Scopus-id: 2-s2.0-0141891454
56
31What 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.2001Revista Mexicana de Ciencias FarmaceuticasScopus-id: 2-s2.0-0035679691
00
32What 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.2001Revista Mexicana de Ciencias FarmaceuticasScopus-id: 2-s2.0-0035680190
00
33Molecular 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 mutationsCoautor: Riba L., Ordoñez-Sánchez M.L., Ramírez-Jiménez S., López-Gutierrez A.U., et al.1998HUMAN GENETICSWoS-id: 000072457500008
Scopus-id: 2-s2.0-2642651108
5258
34Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: Evidence of different genetic mechanisms involved in the production of the disease2ᵒ autor: Riba L., López-Gutiérrez A.U., Ordoñez-Sánchez M.L., Ramirez-Jiménez S., et al.1998JOURNAL OF MEDICAL GENETICSWoS-id: 000077266400010
Scopus-id: 2-s2.0-0031759339
2328
35Analysis of the glucokinase gene in Mexican families displaying early- onset non-insulin-dependent diabetes mellitus including MODY familiesCoautor: Riba L., Del Bosque-Plata L., Garcia-Garcia E., Ramirez-Jimenez S., et al.1997AM J MED GENETWoS-id: A1997YD48100003
Scopus-id: 2-s2.0-0030735219
67
36Generation and mapping of Mus spretus strain-specific markers for rapid genomic scanning2ᵒ autor: Riba L., Elango R., Housman D., Hunter K.1996MAMMALIAN GENOMEWoS-id: A1996UM12900003
Scopus-id: 2-s2.0-0030140565
1010
37Toward the construction of integrated physical and genetic maps of the mouse genome using interspersed repetitive sequence PCR (IRS-PCR) genomics2ᵒ autor: Riba L., Hunter K.W., Schalkwyk L., Clark M., et al.1996GENOME RESWoS-id: A1996UJ01400006
Scopus-id: 2-s2.0-19144368944
1314
38Efficient high-resolution genetic mapping of mouse interspersed repetitive sequence PCR products, toward integrated genetic and physical mapping of the mouse genomeCoautor: Riba L., Mccarthy L., Hunter K., Schalkwyk L., et al.1995PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICAWoS-id: A1995RB80400010
Scopus-id: 2-s2.0-0029051320
3131
39The isolation of cDNAs within the huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA libraryCoautor: Riba L., Snell R.G., Doucette-stamm L.A., Gillespie K.M., et al.1993HUMAN MOLECULAR GENETICSWoS-id: A1993KU13700018
Scopus-id: 2-s2.0-0027175814
1515
40Site-specific cleavage of human chromosome 4 mediated by triple-helix formationCoautor: Riba L., Strobel S.A., Doucette-Stamm L.A., Housman D.E., et al.1991ScienceWoS-id: A1991GV07300044
Scopus-id: 2-s2.0-0026348013
196195
41Generation and characterization of irradiation hybrids of human chromosome 42ᵒ autor: Riba L., Doucette-Stamm L.A., Handelin B., Difilippantonio M., et al.1991SOMAT CELL MOLEC GENWoS-id: A1991GZ55100006
Scopus-id: 2-s2.0-0026337905
1014
42Identification of a functional promoter for the Escherichia coli gdhA gene and its regulation1ᵉʳ autor: Riba L., Becerril B., Servín-González L., Valle F., et al.1988GeneWoS-id: A1988R610900001
Scopus-id: 2-s2.0-0024246277
1012
43Repetitive extragenic palindromic (REP) sequences in the Escherichia coli gdhA geneCoautor: Riba L., Becerril B., Valle F., Merino E., et al.1985GeneWoS-id: A1985ASP1800006
Scopus-id: 2-s2.0-0022251699
1718

Capítulos de libros (WoS y Scopus)

# Título del capítulo Título del libro Autores Alcance Año ISBN Fuente
1Strong association of socioeconomic status and genetic ancestry in latinos: Implications for admixture studies of type 2 diabetesStrong Association Of Socioeconomic Status And Genetic Ancestry In Latinos: Implications For Admixture Studies Of Type 2 DiabetesRiba, L., Tusié-Luna, M.T., Aguilar-Salinas, C.A., et al.Capítulo de un Libro20119781137001702Scopus-id: 2-s2.0-85014173285

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