Weissenbach, Jean
Centre National de la Recherche Scientifique · Commissariat à l'Énergie Atomique et aux Énergies Alternatives · Génomique Métabolique du Genoscope · Genoscope · Université d'Évry Val-d'Essonne
16 papers on CoChatORCID 0000-0001-6564-0840
Most cited papers
- Verified
Initial sequencing and analysis of the human genome
International Human Genome Sequencing Consortium, Whitehead Institute for Biomedical Research, C. F. G. R., Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., et al. (2001) · Nature
Genomics and Phylogenetic StudiesGenetic Associations and Epidemiology
Cited by 24,216
- Verified
A human gut microbial gene catalogue established by metagenomic sequencing
MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature
Gut microbiota and healthGenomics and Phylogenetic Studies
Cited by 11,624
- Verified
Enterotypes of the human gut microbiome
MetaHIT Consortium (additional members), Arumugam, M., Raes, J., Pelletier, E., Le Paslier, D., Yamada, T., Mende, D. R., Fernandes, G. R., Tap, J., Bruls, T., et al. (2011) · Nature
Gut microbiota and healthOral microbiology and periodontitis research
Cited by 7,548
- Verified
Richness of human gut microbiome correlates with metabolic markers
Le Chatelier, E., Nielsen, T., Qin, J., Prifti, E., Hildebrand, F., Falony, G., Almeida, M., Arumugam, M., Batto, J.-M., Kennedy, S., et al. (2013) · Nature
Gut microbiota and healthAdipokines, Inflammation, and Metabolic Diseases
Cited by 4,662
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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
- Verified
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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Dietary intervention impact on gut microbial gene richness
Cotillard, A., Kennedy, S. P., Kong, L. C., Prifti, E., Pons, N., Le Chatelier, E., Almeida, M., Quinquis, B., Levenez, F., Galleron, N., et al. (2013) · Nature
Gut microbiota and healthAdipokines, Inflammation, and Metabolic Diseases
Cited by 1,832
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Genome evolution in yeasts
Dujon, B., Sherman, D., Fischer, G., Durrens, P., Casaregola, S., Lafontaine, I., de Montigny, J., Marck, C., Neuvéglise, C., Talla, E., et al. (2004) · Nature
Fungal and yeast genetics researchYeasts and Rust Fungi Studies
Cited by 1,623
- Verified
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 holistic approach to marine eco-systems biology
Karsenti, E., Acinas, S. G., Bork, P., Bowler, C., De Vargas, C., Raes, J., Sullivan, M., Arendt, D., Benzoni, F., Claverie, J.-M., et al. (2011) · PLoS Biology
Marine Plankton and BiogeochemistryMicrobial Community Ecology and Physiology
Cited by 477
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The Xist RNA Gene Evolved in Eutherians by Pseudogenization of a Protein-Coding Gene
Duret, L., Chureau, C., Samain, S., Weissenbach, J., & Avner, P. (2006) · Science
Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesChromosomal and Genetic Variations
Cited by 418
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Mutant WD-repeat protein in triple-A syndrome
Tullio-Pelet, A., Salomon, R., Hadj-Rabia, S., Mugnier, C., de Laet, M.-H., Chaouachi, B., Bakiri, F., Brottier, P., Cattolico, L., Penet, C., et al. (2000) · Nature Genetics
Adrenal Hormones and DisordersGenomics and Rare Diseases
Cited by 312
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Plasticity of animal genome architecture unmasked by rapid evolution of a pelagic tunicate
Denoeud, F., Henriet, S., Mungpakdee, S., Aury, J.-M., Da Silva, C., Brinkmann, H., Mikhaleva, J., Olsen, L. C., Jubin, C., Cañestro, C., et al. (2010) · Science
Chromosomal and Genetic VariationsGenomics and Phylogenetic Studies
Cited by 285
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Vertebrate-Type Intron-Rich Genes in the Marine Annelid Platynereis dumerilii
Raible, F., Tessmar-Raible, K., Osoegawa, K., Wincker, P., Jubin, C., Balavoine, G., Ferrier, D., Benes, V., de Jong, P., Weissenbach, J., et al. (2005) · Science
Chromosomal and Genetic VariationsGenomics and Phylogenetic Studies
Cited by 257
- Verified
A fourth locus for autosomal dominant hypercholesterolemia maps at 16q22.1
The French Research Network on ADH, Marques-Pinheiro, A., Marduel, M., Rabès, J.-P., Devillers, M., Villéger, L., Allard, D., Weissenbach, J., Guerin, M., Zair, Y., et al. (2010) · European Journal of Human Genetics
Lipoproteins and Cardiovascular HealthGenetic Associations and Epidemiology
Cited by 38
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