Publications
Lescot, M. et al.
Reverse transcriptase genes are highly abundant and transcriptionally active in marine plankton assemblages
Isme Journal. (2016) 10(5): p. 1134-1146
doi:10.1038/ismej.2015.192
Flegontova, O. et al.
Extreme Diversity of Diplonemid Eukaryotes in the Ocean
Current Biology. (2016) 26(22): p. 3060-3065
doi:10.1016/j.cub.2016.09.031
Farrant, G.K. et al.
Delineating ecologically significant taxonomic units from global patterns of marine picocyanobacteria
Proc Nat Acad Sci U.S.A. (2016) 113(24): p. E3365-E3374
doi:10.1073/pnas.1524865113
Gallouet AS. et al.
Macrophage production and activation are dependent on TRIM33
Oncotarget. (2016) 8(3):5111-5122
doi: 10.18632/oncotarget.13872
Holmes, A. et al.
Mechanistic signatures of HPV insertions in cervical carcinomas
Npj Genomic Medicine. (2016) 16004
doi: 10.1038/npjgenmed.2016.4
Tabet R. et al.
Fragile X Mental Retardation Protein (FMRP) controls diacylglycerol kinase activity in neurons
Proc Natl Acad Sci USA. (2016) 113(26):E3619-28
doi: 10.1073/pnas.1522631113
Demais V. et al.
Reversal of Pathologic Lipid Accumulation in NPC1-Deficient Neurons by Drug-Promoted Release of LAMP1-Coated Lamellar Inclusions
J Neurosci. (2016) 36: 8012-25
doi: 10.1523/JNEUROSCI.0900-16.2016
Hardies K. et al.
Loss of SYNJ1 dual phosphatase activity leads to early onset refractory seizures and progressive neurological decline
Brain. (2016) 139(Pt 9):2420-30
doi: 10.1093/brain/aww180
Haas G. et al.
Identification of factors involved in target RNA-directed microRNA degradation
Nucleic Acids Res. (2016) 44(6):2873-87
doi: 10.1093/nar/gkw040
Renaud M. et al.
Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia
J Neurol. (2016) 263(8):1552-8
doi: 10.1007/s00415-016-8167-3
Guarani V. et al.
QIL1 mutation causes MICOS disassembly and early onset fatal mitochondrial encephalopathy with liver disease
Elife. (2016) 5. pii: e17163
doi: 10.7554
Schaefer E. et al.
Identification of a novel mutation confirms the implication of IFT172 (BBS20) in Bardet-Biedl syndrome
J Hum Genet. (2016) 61(5):447-50
doi: 10.1038/jhg.2015.162