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A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT projectThe SIB Swiss Institute of Bioinformatics' resources: focus on curated databasesA genome-wide association study of the Protein C anticoagulant pathwayGenome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosisA new gene-based association test for genome-wide association studiesA comparison of discrete versus continuous environment in a variance components-based linkage analysis of the COGA data.Searching for master regulators of transcription in a human gene expression data set.Smoothing of the bivariate LOD score for non-normal quantitative traits.Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32.Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels.Genetic interactions affecting human gene expression identified by variance association mapping.Heritability of thromboxane A2 and prostaglandin E2 biosynthetic machinery in a Spanish population.Gene expression changes with age in skin, adipose tissue, blood and brain.Cis and trans effects of human genomic variants on gene expression.C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies.Sex-specific regulation of mitochondrial DNA levels: genome-wide linkage analysis to identify quantitative trait lociGene age predicts the strength of purifying selection acting on gene expression variation in humansIdentification of antithrombin-modulating genes. Role of LARGE, a gene encoding a bifunctional glycosyltransferase, in the secretion of proteins?Quantitative variability of 342 plasma proteins in a human twin population.Four variants in transferrin and HFE genes as potential markers of iron deficiency anaemia risk: an association study in menstruating women.Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicingCirculating Proteomic Signatures of Chronological Age.A sequence variation scan of the coagulation factor VIII (FVIII) structural gene and associations with plasma FVIII activity levels.Cigarette smoking reduces DNA methylation levels at multiple genomic loci but the effect is partially reversible upon cessation.Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins.Inference and quantification of peptidoforms in large sample cohorts by SWATH-MS.Sex-biased genetic effects on gene regulation in humans.Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.Fast and efficient QTL mapper for thousands of molecular phenotypes.Passive and active DNA methylation and the interplay with genetic variation in gene regulationA genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levelsMapping cis- and trans-regulatory effects across multiple tissues in twins.Identification of a novel quantitative trait nucleotype related to iron status in a calcium channel gene.Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elements.Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study.Genome-wide linkage analysis for identifying quantitative trait loci involved in the regulation of lipoprotein a (Lpa) levels.A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease.solarius: an R interface to SOLAR for variance component analysis in pedigrees.Summary of Genetic Analysis Workshop 15: Group 9 linkage analysis of the CEPH expression data.Genetic correlation between plasma levels of C4BP isoforms containing beta chains and susceptibility to thrombosis.
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հետազոտող
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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Alfonso Buil
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P106
P21
P31
P496
0000-0002-3097-1014