Maxime Rotival researcher
Rotival, Maxime, 1984-...
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
VIAF ID: 285510642 ( Personal )
Permalink: http://viaf.org/viaf/285510642
Preferred Forms
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100 0 _
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Maxime Rotival
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researcher
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100 1 _
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Rotival, Maxime
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1984-..
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100 1 _
‡a
Rotival, Maxime,
‡d
1984-...
4xx's: Alternate Name Forms (1)
Works
| Title | Sources |
|---|---|
| Approches intégrées du génome et du transcriptome dans les maladies complexes humaines |
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| Association between serum trans-monounsaturated fatty acids and breast cancer risk in the E3N-EPIC Study |
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| 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 |
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| Characterising the genetic basis of immune response variation to identify causal mechanisms underlying disease susceptibility |
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| The choice of the filtering method in microarrays affects the inference regarding dosage compensation of the active X-chromosome |
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| Comprehensive exploration of the effects of miRNA SNPs on monocyte gene expression |
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| Correlation between serum phospholipid fatty acids and dietary intakes assessed a few years earlier. |
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| Defining the genetic and evolutionary architecture of alternative splicing in response to infection |
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| The epigenomic landscape of African rainforest hunter-gatherers and farmers |
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| Ethnicity-Specific Skeletal Muscle Transcriptional Signatures and Their Relevance to Insulin Resistance in Singapore |
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| Exploring the genetic basis of human population differences in DNA methylation and their causal impact on immune gene regulation |
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| Genetic Adaptation and Neandertal Admixture Shaped the Immune System of Human Populations |
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| Genetic analysis of the cardiac methylome at single nucleotide resolution in a model of human cardiovascular disease |
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| Genetic influences on brain gene expression in rats selected for tameness and aggression |
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| A genetic variant controls interferon-β gene expression in human myeloid cells by preventing C/EBP-β binding on a conserved enhancer |
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| Genetics and beyond--the transcriptome of human monocytes and disease susceptibility |
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| Genome sequencing reveals loci under artificial selection that underlie disease phenotypes in the laboratory rat |
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| Genome-wide analysis of differential RNA editing in epilepsy. |
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| Graphical modeling of gene expression in monocytes suggests molecular mechanisms explaining increased atherosclerosis in smokers |
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| Identification de biomarqueurs de la réponse au traitement antipsychotique chez des patients avec un premier épisode psychotique |
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| Identification of biomarkers to predict antipsychotic treatment response in patients with a first episode of schizophrenia. |
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| Identification of Ceruloplasmin as a Gene that Affects Susceptibility to Glomerulonephritis Through Macrophage Function. |
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| Identification of protein complexes that bind to histone H3 combinatorial modifications using super-SILAC and weighted correlation network analysis |
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| Impact and Evolutionary Determinants of Neanderthal Introgression on Transcriptional and Post-Transcriptional Regulation |
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| Influence of sex and genetic variability on expression of X-linked genes in human monocytes. |
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| Integrated approaches of genome and transcriptome in the study of human complex diseases. |
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| Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans |
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| Integrating phosphoproteome and transcriptome reveals new determinants of macrophage multinucleation. |
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| Kcnn4 is a regulator of macrophage multinucleation in bone homeostasis and inflammatory disease |
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| Leveraging gene co-expression networks to pinpoint the regulation of complex traits and disease, with a focus on cardiovascular traits |
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| Multi-tissue analysis of co-expression networks by higher-order generalized singular value decomposition identifies functionally coherent transcriptional modules |
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| Statistical colocalization of monocyte gene expression and genetic risk variants for type 1 diabetes |
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| Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease. |
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| Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus |
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| A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk |
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| Wars2 is a determinant of angiogenesis. |
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| WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling |
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