Gael Yvert, PhD - Publications

University of Lyon, Lyon, Auvergne-Rhône-Alpes, France 

34 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Chuffart F, Richard M, Jost D, Burny C, Duplus-Bottin H, Ohya Y, Yvert G. Exploiting Single-Cell Quantitative Data to Map Genetic Variants Having Probabilistic Effects. Plos Genetics. 12: e1006213. PMID 27479122 DOI: 10.1371/Journal.Pgen.1006213  0.36
2015 Filleton F, Chuffart F, Nagarajan M, Bottin-Duplus H, Yvert G. The complex pattern of epigenomic variation between natural yeast strains at single-nucleosome resolution. Epigenetics & Chromatin. 8: 26. PMID 26229551 DOI: 10.1186/S13072-015-0019-3  0.52
2015 Gasch AP, Yvert G. MEETING REPORT on Experimental Approaches to Evolution and Ecology Using Yeast & Other Model Systems. G3 (Bethesda, Md.). PMID 25908568 DOI: 10.1534/G3.115.018614  0.52
2014 Richard M, Yvert G. How does evolution tune biological noise? Frontiers in Genetics. 5: 374. PMID 25389435 DOI: 10.3389/fgene.2014.00374  0.52
2014 Vanoosthuyse V, Legros P, van der Sar SJ, Yvert G, Toda K, Le Bihan T, Watanabe Y, Hardwick K, Bernard P. CPF-associated phosphatase activity opposes condensin-mediated chromosome condensation. Plos Genetics. 10: e1004415. PMID 24945319 DOI: 10.1371/Journal.Pgen.1004415  0.52
2014 Chuffart F, Yvert G. MyLabStocks: a web-application to manage molecular biology materials. Yeast (Chichester, England). 31: 179-84. PMID 24643870 DOI: 10.1002/Yea.3008  0.52
2014 Yvert G. 'Particle genetics': treating every cell as unique. Trends in Genetics : Tig. 30: 49-56. PMID 24315431 DOI: 10.1016/J.Tig.2013.11.002  0.52
2013 Fehrmann S, Bottin-Duplus H, Leonidou A, Mollereau E, Barthelaix A, Wei W, Steinmetz LM, Yvert G. Natural sequence variants of yeast environmental sensors confer cell-to-cell expression variability. Molecular Systems Biology. 9: 695. PMID 24104478 DOI: 10.1038/Msb.2013.53  0.52
2013 Yvert G, Ohnuki S, Nogami S, Imanaga Y, Fehrmann S, Schacherer J, Ohya Y. Single-cell phenomics reveals intra-species variation of phenotypic noise in yeast. Bmc Systems Biology. 7: 54. PMID 23822767 DOI: 10.1186/1752-0509-7-54  0.52
2012 Abraham AL, Nagarajan M, Veyrieras JB, Bottin H, Steinmetz LM, Yvert G. Genetic modifiers of chromatin acetylation antagonize the reprogramming of epi-polymorphisms. Plos Genetics. 8: e1002958. PMID 23028365 DOI: 10.1371/Journal.Pgen.1002958  0.52
2012 Boitard L, Cottinet D, Kleinschmitt C, Bremond N, Baudry J, Yvert G, Bibette J. Monitoring single-cell bioenergetics via the coarsening of emulsion droplets. Proceedings of the National Academy of Sciences of the United States of America. 109: 7181-6. PMID 22538813 DOI: 10.1073/Pnas.1200894109  0.52
2011 Fehrmann S, Yvert G. Finding modulators of stochasticity levels by quantitative genetics. Methods in Molecular Biology (Clifton, N.J.). 734: 223-40. PMID 21468992 DOI: 10.1007/978-1-61779-086-7_11  0.52
2010 Nagarajan M, Veyrieras JB, de Dieuleveult M, Bottin H, Fehrmann S, Abraham AL, Croze S, Steinmetz LM, Gidrol X, Yvert G. Natural single-nucleosome epi-polymorphisms in yeast. Plos Genetics. 6: e1000913. PMID 20421933 DOI: 10.1371/Journal.Pgen.1000913  0.52
2010 Gallois A, Lachuer J, Yvert G, Wierinckx A, Brunet F, Rabourdin-Combe C, Delprat C, Jurdic P, Mazzorana M. Genome-wide expression analyses establish dendritic cells as a new osteoclast precursor able to generate bone-resorbing cells more efficiently than monocytes. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 25: 661-72. PMID 19775202 DOI: 10.1359/jbmr.090829  0.52
2008 Ansel J, Bottin H, Rodriguez-Beltran C, Damon C, Nagarajan M, Fehrmann S, François J, Yvert G. Cell-to-cell stochastic variation in gene expression is a complex genetic trait. Plos Genetics. 4: e1000049. PMID 18404214 DOI: 10.1371/Journal.Pgen.1000049  0.52
2007 Marullo P, Yvert G, Bely M, Aigle M, Dubourdieu D. Efficient use of DNA molecular markers to construct industrial yeast strains. Fems Yeast Research. 7: 1295-306. PMID 17888000 DOI: 10.1111/j.1567-1364.2007.00281.x  0.52
2007 Marullo P, Aigle M, Bely M, Masneuf-Pomarède I, Durrens P, Dubourdieu D, Yvert G. Single QTL mapping and nucleotide-level resolution of a physiologic trait in wine Saccharomyces cerevisiae strains. Fems Yeast Research. 7: 941-52. PMID 17537182 DOI: 10.1111/j.1567-1364.2007.00252.x  0.52
2007 Nogami S, Ohya Y, Yvert G. Genetic complexity and quantitative trait loci mapping of yeast morphological traits. Plos Genetics. 3: e31. PMID 17319748 DOI: 10.1371/Journal.Pgen.0030031  0.52
2005 Ronald J, Akey JM, Whittle J, Smith EN, Yvert G, Kruglyak L. Simultaneous genotyping, gene-expression measurement, and detection of allele-specific expression with oligonucleotide arrays. Genome Research. 15: 284-91. PMID 15687292 DOI: 10.1101/Gr.2850605  0.52
2004 Helmlinger D, Abou-Sleymane G, Yvert G, Rousseau S, Weber C, Trottier Y, Mandel JL, Devys D. Disease progression despite early loss of polyglutamine protein expression in SCA7 mouse model. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 1881-7. PMID 14985428 DOI: 10.1523/JNEUROSCI.4407-03.2004  0.52
2003 Yvert G, Brem RB, Whittle J, Akey JM, Foss E, Smith EN, Mackelprang R, Kruglyak L. Trans-acting regulatory variation in Saccharomyces cerevisiae and the role of transcription factors. Nature Genetics. 35: 57-64. PMID 12897782 DOI: 10.1038/Ng1222  0.52
2002 Helmlinger D, Yvert G, Picaud S, Merienne K, Sahel J, Mandel JL, Devys D. Progressive retinal degeneration and dysfunction in R6 Huntington's disease mice. Human Molecular Genetics. 11: 3351-9. PMID 12471061 DOI: 10.1093/hmg/11.26.3351  0.52
2002 Takahashi J, Fujigasaki H, Zander C, El Hachimi KH, Stevanin G, Dürr A, Lebre AS, Yvert G, Trottier Y, de Thé H, Hauw JJ, Duyckaerts C, Brice A. Two populations of neuronal intranuclear inclusions in SCA7 differ in size and promyelocytic leukaemia protein content. Brain : a Journal of Neurology. 125: 1534-43. PMID 12077003 DOI: 10.1093/Brain/Awf154  0.52
2002 Brem RB, Yvert G, Clinton R, Kruglyak L. Genetic dissection of transcriptional regulation in budding yeast. Science (New York, N.Y.). 296: 752-5. PMID 11923494 DOI: 10.1126/Science.1069516  0.52
2001 Devys D, Yvert G, Lunkes A, Trottier Y, Mandel JL. Pathological mechanisms in polyglutamine expansion diseases. Advances in Experimental Medicine and Biology. 487: 199-210. PMID 11403159  0.52
2000 Cancel G, Duyckaerts C, Holmberg M, Zander C, Yvert G, Lebre AS, Ruberg M, Faucheux B, Agid Y, Hirsch E, Brice A. Distribution of ataxin-7 in normal human brain and retina. Brain : a Journal of Neurology. 123: 2519-30. PMID 11099453 DOI: 10.1093/Brain/123.12.2519  0.52
2000 Yvert G, Lindenberg KS, Picaud S, Landwehrmeyer GB, Sahel JA, Mandel JL. Expanded polyglutamines induce neurodegeneration and trans-neuronal alterations in cerebellum and retina of SCA7 transgenic mice. Human Molecular Genetics. 9: 2491-506. PMID 11030754 DOI: 10.1093/HMG/9.17.2491  0.52
2000 Lindenberg KS, Yvert G, Müller K, Landwehrmeyer GB. Expression analysis of ataxin-7 mRNA and protein in human brain: evidence for a widespread distribution and focal protein accumulation. Brain Pathology (Zurich, Switzerland). 10: 385-94. PMID 10885657  0.52
1999 Yvert G, Mandel JL. Variation on a trinucleotide theme. Nature Medicine. 5: 383-4. PMID 10202924 DOI: 10.1038/7381  0.52
1998 Wittekindt O, Jauch A, Burgert E, Schärer L, Holtgreve-Grez H, Yvert G, Imbert G, Zimmer J, Hoehe MR, Macher JP, Chiaroni P, van Calker D, Crocq MA, Morris-Rosendahl DJ. The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia. Neurogenetics. 1: 259-65. PMID 10732800  0.52
1998 Stevanin G, David G, Abbas N, Agid Y, Brice A, Yvert G. Ataxie cérébelleuse autosomîque dominante avec dystrophie maculaire progressive: Un modèle d'étude des maladies dues à une expansion de polyglutamine Medecine/Sciences. 14: 758-763.  0.52
1997 David G, Abbas N, Stevanin G, Dürr A, Yvert G, Cancel G, Weber C, Imbert G, Saudou F, Antoniou E, Drabkin H, Gemmill R, Giunti P, Benomar A, Wood N, et al. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. Nature Genetics. 17: 65-70. PMID 9288099 DOI: 10.1038/ng0997-65  0.52
1997 Cancel G, Dürr A, Didierjean O, Imbert G, Bürk K, Lezin A, Belal S, Benomar A, Abada-Bendib M, Vial C, Guimarães J, Chneiweiss H, Stevanin G, Yvert G, Abbas N, et al. Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families. Human Molecular Genetics. 6: 709-15. PMID 9158145 DOI: 10.1093/Hmg/6.5.709  0.52
1996 Imbert G, Saudou F, Yvert G, Devys D, Trottier Y, Garnier JM, Weber C, Mandel JL, Cancel G, Abbas N, Dürr A, Didierjean O, Stevanin G, Agid Y, Brice A. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats. Nature Genetics. 14: 285-91. PMID 8896557 DOI: 10.1038/ng1196-285  0.52
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