Cruaud, Corinne
Centre National de la Recherche Scientifique · Commissariat à l'Énergie Atomique et aux Énergies Alternatives · Université Paris-Saclay · Génomique Métabolique du Genoscope · Genoscope · Université d'Évry Val-d'Essonne
9 papers on CoChatORCID 0000-0002-4752-7278
Most cited papers
- Verified
Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
Abifadel, M., Varret, M., Rabès, J.-P., Allard, D., Ouguerram, K., Devillers, M., Cruaud, C., Benjannet, S., Wickham, L., Erlich, D., et al. (2003) · Nature Genetics
Lipoproteins and Cardiovascular HealthLipid metabolism and disorders
Cited by 2,985
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Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
Joutel, A., Corpechot, C., Ducros, A., Vahedi, K., Chabriat, H., Mouton, P., Alamowitch, S., Domenga, V., Cécillion, M., Maréchal, E., et al. (1996) · Nature
Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments
Cited by 2,068
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Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype
Jaillon, O., Aury, J.-M., Brunet, F., Petit, J.-L., Stange-Thomann, N., Mauceli, E., Bouneau, L., Fischer, C., Ozouf-Costaz, C., Bernot, A., et al. (2004) · Nature
Chromosomal and Genetic VariationsGenome Rearrangement Algorithms
Cited by 1,966
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Genome evolution across 1,011 Saccharomyces cerevisiae isolates
Peter, J., De Chiara, M., Friedrich, A., Yue, J.-X., Pflieger, D., Bergström, A., Sigwalt, A., Barre, B., Freel, K., Llored, A., et al. (2018) · Nature
Fungal and yeast genetics researchYeasts and Rust Fungi Studies
Cited by 1,117
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Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients
Joutel, A., Vahedi, K., Corpechot, C., Troesch, A., Chabriat, H., Vayssière, C., Cruaud, C., Maciazek, J., Weissenbach, J., Bousser, M.-G., et al. (1997) · The Lancet
Cerebrovascular and genetic disordersGenetic Neurodegenerative Diseases
Cited by 682
- Verified
A Role for RNAi in the Selective Correction of DNA Methylation Defects
Teixeira, F. K., Heredia, F., Sarazin, A., Roudier, F., Boccara, M., Ciaudo, C., Cruaud, C., Poulain, J., Berdasco, M., Fraga, M. F., et al. (2009) · Science
Epigenetics and DNA MethylationPlant Molecular Biology Research
Cited by 358
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SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome
Hanchate, N. K., Giacobini, P., Lhuillier, P., Parkash, J., Espy, C., Fouveaut, C., Leroy, C., Baron, S., Campagne, C., Vanacker, C., et al. (2012) · PLoS Genetics
Hypothalamic control of reproductive hormonesOlfactory and Sensory Function Studies
Cited by 217
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Functional repertoire convergence of distantly related eukaryotic plankton lineages abundant in the sunlit ocean
Delmont, T. O., Gaia, M., Hinsinger, D. D., Frémont, P., Vanni, C., Fernandez-Guerra, A., Eren, A. M., Kourlaiev, A., d'Agata, L., Clayssen, Q., et al. (2022) · Cell Genomics
Protist diversity and phylogenyGenomics and Phylogenetic Studies
Cited by 173
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The rise and fall of African rice cultivation revealed by analysis of 246 new genomes
Cubry, P., Tranchant-Dubreuil, C., Thuillet, A.-C., Monat, C., Ndjiondjop, M.-N., Labadie, K., Cruaud, C., Engelen, S., Scarcelli, N., Rhoné, B., et al. (2018) · Current Biology
Genetic Mapping and Diversity in Plants and AnimalsGenetic diversity and population structure
Cited by 142
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