Armand Valsesia
educated at: University of Lausanne
occupation: researcher
Articles 38
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A fully joint Bayesian quantitative trait locus mapping of human protein abundance in plasma
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Augmented mitochondrial energy metabolism is an early response to chronic glucose stress in human pancreatic beta cells
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Endogenous nicotinamide riboside metabolism protects against diet-induced liver damage
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Subcutaneous Adipose Tissue and Systemic Inflammation Are Associated With Peripheral but Not Hepatic Insulin Resistance in Humans
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Analysis of circulating angiopoietin-like protein 3 and genetic variants in lipid metabolism and liver health: the DiOGenes study.
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FADS1 genotype is distinguished by human subcutaneous adipose tissue fatty acids, but not inflammatory gene expression
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Obesity shows preserved plasma proteome in large independent clinical cohorts
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Plasma lipid profiling of tissue-specific insulin resistance in human obesity
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Plasma metabolites and lipids predict insulin sensitivity improvement in obese, nondiabetic individuals after a 2-phase dietary intervention
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Copy Number Variation
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Diet-resistant obesity is characterized by a distinct plasma proteomic signature and impaired muscle fiber metabolism.
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Protein quantitative trait locus study in obesity during weight-loss identifies a leptin regulator.
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Transcriptome profiling from adipose tissue during a low-calorie diet reveals predictors of weight and glycemic outcomes in obese, nondiabetic subjects.
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Molecular Biomarkers for Weight Control in Obese Individuals Subjected to a Multiphase Dietary Intervention.
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Multiple hot-deck imputation for network inference from RNA sequencing data.
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Sexual Dimorphism, Age, and Fat Mass Are Key Phenotypic Drivers of Proteomic Signatures.
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Network Analysis of Metabolite GWAS Hits: Implication of CPS1 and the Urea Cycle in Weight Maintenance
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Distinct lipid profiles predict improved glycemic control in obese, nondiabetic patients after a low-caloric diet intervention: the Diet, Obesity and Genes randomized trial
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Rational and design of an overfeeding protocol in constitutional thinness: Understanding the physiology, metabolism and genetic background of resistance to weight gain.
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GH deficiency status combined with GH receptor polymorphism affects response to GH in children
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Proteomic Biomarker Discovery in 1000 Human Plasma Samples with Mass Spectrometry.
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The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation
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The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome.
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Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity
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Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort
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Genome-wide meta-analysis of common variant differences between men and women
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Network-guided analysis of genes with altered somatic copy number and gene expression reveals pathways commonly perturbed in metastatic melanoma
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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
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Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma.
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Corrigendum: Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy
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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
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Origins and functional impact of copy number variation in the human genome
Human - wd:Q59521582