Vincent Plagnol, Ph.D.
Affiliations: | 2006 | University of Southern California, Los Angeles, CA, United States |
Area:
Mathematics, GeneticsGoogle:
"Vincent Plagnol"Parents
Sign in to add mentor| Simon Tavare | grad student | 2006 | USC | |
| (Ancestral inference from molecular and paleontological data.) | ||||
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Publications
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| Jarvis S, Birsa N, Secrier M, et al. (2020) A Comparison of Low Read Depth QuantSeq 3' Sequencing to Total RNA-Seq in FUS Mutant Mice. Frontiers in Genetics. 11: 562445 |
| Humphrey J, Birsa N, Milioto C, et al. (2020) FUS ALS-causative mutations impair FUS autoregulation and splicing factor networks through intron retention. Nucleic Acids Research |
| Papapietro O, Chandra A, Eletto D, et al. (2020) Topoisomerase 2β mutation impairs early B cell development. Blood |
| Göös H, Fogarty CL, Sahu B, et al. (2019) Gain-of-function CEBPE mutation causes non-canonical autoinflammatory inflammasomopathy. The Journal of Allergy and Clinical Immunology |
| Neves JF, Doffinger R, Barcena-Morales G, et al. (2018) Novel Mutation in a Patient With APLAID and Cutis Laxa. Frontiers in Immunology. 9: 2863 |
| Sivakumar P, De Giorgio F, Ule AM, et al. (2018) TDP-43 mutations increase HNRNP A1-7B through gain of splicing function. Brain : a Journal of Neurology |
| Cuchet-Lourenço D, Eletto D, Wu C, et al. (2018) Biallelic mutations in humans cause severe immunodeficiency, arthritis, and intestinal inflammation. Science (New York, N.Y.) |
| Rivas MA, Avila BE, Koskela J, et al. (2018) Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. Plos Genetics. 14: e1007329 |
| Fratta P, Sivakumar P, Humphrey J, et al. (2018) Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis. The Embo Journal |
| Bochukova EG, Lawler K, Croizier S, et al. (2018) A Transcriptomic Signature of the Hypothalamic Response to Fasting and BDNF Deficiency in Prader-Willi Syndrome. Cell Reports. 22: 3401-3408 |