Vincent Laudet

This study identifies a conserved post-embryonic gene network in teleost fish that is responsive to thyroid hormone and ecological variation, showing how it evolves through gene copy number changes.

This study shows that social context in clownfish affects growth, feeding behavior, aggression, and gene expression, reinforcing social role differentiation during hierarchy formation.

This study characterizes structural variation across 16 clownfish species, identifying extensive SVs and clarifying inversion events on chromosomes 18 and 9.

This study uses whole genome re-sequencing to reveal deep divergence within the Amphiprion clarkii species complex, identifying five lineages and challenging the taxonomic status of A. tricinctus.

This study identifies novel, host-specific Symbiodiniaceae strains in giant sea anemones using phylotranscriptomics, revealing hidden diversity and cophylogenetic relationships.

The paper investigates whether color polymorphism in the saddleback clownfish represents intraspecific variation or multiple species using genomic and image data.

This study examines the relationship between pigmentation pattern diversity, species richness, and geography in coral reef fishes, finding a positive correlation and evidence of rapid phenotypic diversification.

This study identifies the thyroid hormone (TH) precursor protein in the ascidian Styela clava, demonstrating endogenous TH synthesis and evolutionary conservation of the TG protein function.

RadarOmics provides a visualization tool for multidimensional omics data, revealing coordinated molecular responses across biological processes in ecological, evolutionary, and developmental studies.

This study identifies convergent substitutions in teleost fish genomes and shows they are associated with intermediate pleiotropy, enabling adaptive variation during ecological shifts.

The paper identifies a gene involved in pigment cell communication that governs color pattern formation in zebrafish and anemonefish.

The paper uses landscape transcriptomics to show urbanization in coastal habitats leads to inflammation and immune gene expression changes in fish, resembling overfed lab conditions.

This study shows that social environment influences the timing of color pattern changes in anemonefish juveniles through gene expression and apoptosis mechanisms.

The paper identifies conserved transcriptional programs in adult bilaterian guts across species, revealing how embryonic AP patterning relates to adult gut organization.

The paper presents a manually curated gene list for teleost fish transcriptomics to improve pathway reconstruction accuracy in non-model organisms.

This paper investigates how chlorpyrifos exposure disrupts thyroid hormone signaling and metamorphosis in clownfish larvae, showing impaired white band formation and body shape changes, with TH treatment reversing some effects.

The paper identifies BMP and Agouti signaling pathways that drive the transdifferentiation of melanophores to leucophores in zebrafish fins.

This paper investigates how anemonefish avoid triggering sea anemone nematocysts by reducing sialic acid levels in their mucus, suggesting a Trojan horse mechanism for symbiosis.

The paper presents the first genome assembly of a Pomacentrid fish, Chrysiptera cyanea, using long-read sequencing, providing a resource for studying evolutionary adaptations and environmental monitoring.

This study investigates how thyroid hormones regulate metamorphosis in clownfish by coordinating color vision changes and metabolic shifts, revealing their integrative role in life cycle transitions.

This paper presents a high-quality chromosome-scale genome assembly of the yellowtail clownfish Amphiprion clarkii and identifies a potential link between erbb3b gene copy number and melanism polymorphism.

This paper presents a high-quality chromosome-scale genome assembly for the false clownfish, along with gene annotations and comparative genomic analysis revealing lineage-specific elements.

The paper models Edar expression dynamics to reveal hidden patterning processes in tooth signaling centers, showing a two-step activation and erasure mechanism.