Archives Publications
Stéphanie Guey et al.
Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians
European Journal of Human Genetics 2017, vol. 25, issue 8
doi: 10.1038/ejhg.2017.92
Alain Meyer et al.
IFN-β-induced reactive oxygen species and mitochondrial damage contribute to muscle impairment and inflammation maintenance in dermatomyositis
Acta Neuropathologica 2017, vol. 134, issue 4
doi: 10.1007/s00401-017-1731-9
Pierre-Antoine Juge et al.
Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis
European Respiratory Journal 2017, vol. 49, issue 5
doi: 10.1183/13993003.02314-2016
Kopylova E. et al.
Deciphering metatranscriptomic data.
Methods in molecular biology (Clifton, NJ), (2015) 1269:279-291.
doi: 10.1007/978-1-4939-2291-8_17
Prasad MK et al.
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement.
J Med Genet. Epub 2015 Oct 26.
doi: 10.1136/jmedgenet-2015-103302
Crottès D.et al.
SIGMAR1 Regulates Membrane Electrical Activity in Response to Extracellular Matrix Stimulation to Drive Cancer Cell Invasiveness.
Cancer Res. 76(3):607-18.
doi: 10.1158/0008-5472.CAN-15-1465
Portal MM. et al.
TARDIS, a targeted RNA directional sequencing method for rare RNA discovery.
Nat Protoc. (2015) (12):1915-38.
doi: 10.1038/nprot.2015.120
Mirzaa GM et al.
Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study.
Lancet Neurol. (2015)
doi: 10.1016/S1474-4422(15)00278-1
Chevalier B et al.
miR-34/449 control apical actin network formation during multicilio genesis through small GTPase pathways.
Nat Commun. (2015)
doi: 10.1038/ncomms9386
Grünewald TGP. et al.
Chimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatellite.
Nature Genetics (2015)
doi: 10.1038/ng.3363