Author details

Full Name

Laura Riba

Affiliation

ORCID

Career Start Year

1985

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
28838971	A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 Diabetes.	Diabetes	2017
24886709	Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.	Nat Commun	2014
24915262	Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population.	JAMA	2014
23505323	Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.	J Med Genet	2013
23460240	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.		2013
23217153	Adipose co-expression networks across Finns and Mexicans identify novel triglyceride-associated genes.	BMC Med Genomics	2012
22886787	Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populations.	Arthritis Rheum	2012
22801491	Reconstructing Native American population history.	Nature	2012
22923468	Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population.		2012
21765216	The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans.	J Clin Invest	2011
21393584	Evidence of how rs7575840 influences apolipoprotein B-containing lipid particles.	Arterioscler Thromb Vasc Biol	2011
21315358	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 based nation wide study.	Atherosclerosis	2011
19965785	Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans.	Arterioscler Thromb Vasc Biol	2010
20848568	Genetically determined Amerindian ancestry correlates with increased frequency of risk alleles for systemic lupus erythematosus.	Arthritis Rheum	2010
20160193	Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples.	Circ Cardiovasc Genet	2010
18988886	Galanin preproprotein is associated with elevated plasma triglycerides.	Arterioscler Thromb Vasc Biol	2009
19526211	Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes.	Diabetologia	2009
19280764	Hypoalphalipoproteinemia in populations of Native American ancestry: an opportunity to assess the interaction of genes and the environment.	Current Opinion in Lipidology	2009
17503322	A genomewide admixture map for Latino populations.	Am J Hum Genet	2007
17116178	HNF-1alpha G574S is a functional variant with decreased transactivation activity.	Diabetic Medicine	2006
16314194	Genetic heterogeneity of autosomal dominant hypercholesterolemia in Mexico.	Archives of Medical Research	2006
15892459	[Identifying different susceptibility loci associated with early onset diabetes and cardiovascular disease in Mexican families].	Gaceta Medica de Mexico	2005
15883474	Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families.	Journal of the Pancreas (discontinued)	2005
15599766	A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemia.	Human Genetics	2005
15954494	GENEHUNTER versus SimWalk2 in the context of an extended kindred and a qualitative trait locus.	Genetica	2005
15469419	Contribution of chromosome 1q21-q23 to familial combined hyperlipidemia in Mexican families.	Annals of Human Genetics	2004
14513879	Steroid 21-hydroxylase (P450c21) naturally occurring mutants I172N, V281L and I236n/V237E/M239K exert a dominant negative effect on enzymatic activity when co-expressed with the wild-type protein.	Journal of Pediatric Endocrinology and Metabolism	2003
12609970	Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia.	Circ Res	2003
9580109	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.	Human Genetics	1998
9863599	Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease.	Journal of Medical Genetics	1998
9375718	Analysis of the glucokinase gene in Mexican families displaying early-onset non-insulin-dependent diabetes mellitus including MODY families.	American Journal of Medical Genetics	1997
8661719	Generation and mapping of Mus spretus strain-specific markers for rapid genomic scanning.	Mammalian Genome	1996
8723722	Toward the construction of integrated physical and genetic maps of the mouse genome using interspersed repetitive sequence PCR (IRS-PCR) genomics.	Genome Res	1996
7777502	Efficient high-resolution genetic mapping of mouse interspersed repetitive sequence PCR products, toward integrated genetic and physical mapping of the mouse genome.	Proc Natl Acad Sci U S A	1995
8499921	The isolation of cDNAs within the Huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA library.	Human Molecular Genetics	1993
1836279	Site-specific cleavage of human chromosome 4 mediated by triple-helix formation.	Science	1991
1837181	Generation and characterization of irradiation hybrids of human chromosome 4.	Somatic Cell and Molecular Genetics	1991
2465204	Identification of a functional promoter for the Escherichia coli gdhA gene and its regulation.	Gene	1988
3902576	Repetitive extragenic palindromic (REP) sequences in the Escherichia coli gdhA gene.	Gene	1985