Publications 2016

Paban V. et al.
Omics analysis of mouse brain models of human diseases
Gene. (2016)
doi: 10.1016/j.gene.2016.11.022

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

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:

Roux, S. et al.
Ecogenomics and potential biogeochemical impacts of globally abundant ocean viruses
Nature. (2016) 537(7622): p. 689-693
doi:

Popa A. et al.
Pateamine A-sensitive ribosome profiling reveals the scope of translation in mouse embryonic stem cells
BMC Genomics. (2016) Jan 14.17(1):52
doi: 10.1186/s12864-016-2384-0

Bronnec V. et al.
Draft Genome Sequence of Campylobacter jejuni Bf, an Atypical Strain Able To Grow under Aerobiosis
Genome Announc. (2016) Apr 7.4(2).
doi: 10.1128/genomeA.00058-16

Narbonne-Reveau K. et al.
Neural stem cell-encoded temporal patterning delineates an early window of malignant susceptibility in Drosophila
Elife. (2016) 5: e13463
doi: 10.7554/eLife.13463

Beclin C. et al.
miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition
Sci Rep. (2016) 6:35729
doi: 10.1038/srep35729

Ji B. et al.
The chimeric nature of the genomes of marine magnetotactic coccoid-ovoid bacteria defines a novel group of Proteobacteria
Environ Microbiol. (2016) Nov 30
doi: 10.1111/1462-2920.13637

Venton G. et al.
Natural killer cells in acute myeloid leukemia patients: from phenotype to transcriptomic analysis
mmunologic research. (2016)
doi: 10.1007/s12026-016-8848-0

Santamaría Nuñez G.et al.
Lurbinectedin Specifically Triggers the Degradation of Phosphorylated RNA Polymerase II and the Formation of DNA Breaks in Cancer Cells
Mol Cancer Ther. (2016) 15(10):2399-2412
doi:

Flegontova, O. et al.
Extreme Diversity of Diplonemid Eukaryotes in the Ocean
Current Biology. (2016) 26(22): p. 3060-3065
doi:

Vanhove, A.S. et al.
Copper homeostasis at the host vibrio interface: lessons from intracellular vibrio transcriptomics
Environmental Microbiology. (2016) 18(3): p. 875-888
doi:

Lavergne A. et al.
Identification of lymphocytic choriomeningitis mammarenavirus in house mouse (Mus musculus, Rodentia) in French Guiana
Infect Genet Evol. (2016) 37:225-30
doi: 10.1016/j.meegid.2015.11.023

Roquis D. et al.
Frequency and mitotic heritability of epimutations in Schistosoma mansoni
Mol Ecol. (2016) 25:1741-58
doi: 10.1111/mec.13555

Gargaun E. et al.
EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome
J Neurol. (2016) 263(7):1456-8
doi: 10.1007/s00415-016-8153-9

Remenant B. et al.
Draft Genome Sequence of Carnobacterium divergens V41, a Bacteriocin-Producing Strain
Genome Announc. (2016) 4(5)
doi: 10.1128/genomeA.01109-16

Arguel MJ. et al.
A cost effective 5' selective single cell transcriptome profiling approach with improved UMI design
Nucleic Acids Res. (2016) Dec 9. pii: gkw1242
doi:

Landel V. et al.
Vitamin D interacts with Esr1 and Igf1 to regulate molecular pathways relevant to Alzheimer's disease
Molecular Neurodegeneration. (2016)
doi: 10.1186/s13024-016-0087-2

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

Forster, D. et al.
Benthic protists: the under-charted majority
Fems Microbiology Ecology. (2016) 92(8)
doi:

Vannier, T. et al.
Survey of the green picoalga Bathycoccus genomes in the global ocean
Scientific Reports. (2016) 6: p. e37900
doi:

Guillem Rigaill et al.
Synthetic data sets for the identification of key ingredients for RNA-seq differential analysis
Briefings in Bioinformatics 2016
doi: 10.1093/bib/bbw092

Stéphanie Bauché et al.
Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea
The American Journal of Human Genetics 2016, vol. 99, issue 3
doi: 10.1016/j.ajhg.2016.06.033

Kilan Le Guennec et al.
ABCA7 rare variants and Alzheimer disease risk
Neurology 2016, vol. 86, issue 23
doi: 10.1212/wnl.0000000000002627