Archives Publications
Grüning B et al.
Bioconda: sustainable and comprehensive software distribution for the life sciences
Nature Methods 2018 15(7)
doi: 10.1038/s41592-018-0046-7
Quartier A et al.
Genes and Pathways Regulated by Androgens in Human Neural Cells, Potential Candidates for the Male Excess in Autism Spectrum Disorder
Biological Psychiatry 2018 84(4)
doi: 10.1016/j.biopsych.2018.01.002
Rabineau M et al.
Chromatin de-condensation by switching substrate elasticity
Scientific Reports 2018 8(1)
doi: 10.1038/s41598-018-31023-2
Soustre-Gacougnolle I et al.
Responses to climatic and pathogen threats differ in biodynamic and conventional vines
Scientific Reports 2018 8(1)
doi: 10.1038/s41598-018-35305-7
Brucato N et al.
The Comoros Show the Earliest Austronesian Gene Flow into the Swahili Corridor
The American Journal of Human Genetics 2018 102(1)
doi: 10.1016/j.ajhg.2017.11.011
Yauy K et al.
B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation
Genetics in Medicine 2017 20(2)
doi: 10.1038/gim.2017.109
Weber A et al.
Epigenome-wide DNA methylation profiling in Progressive Supranuclear Palsy reveals major changes at DLX1
Nature Communications 2018 9(1)
doi: 10.1038/s41467-018-05325-y
Wang-Renault SF et al.
Deregulation of microRNA expression in purified T and B lymphocytes from patients with primary Sjögren's syndrome
Annals of the Rheumatic Diseases 2017 77(1)
doi: 10.1136/annrheumdis-2017-211417
Vulin A et al.
Severe PATCHED1 Deficiency in Cancer-Prone Gorlin Patient Cells Results in Intrinsic Radiosensitivity
International Journal of Radiation Oncology*Biology*Physics 2018 102(2)
doi: 10.1016/j.ijrobp.2018.05.057
Vuillaume ML et al.
Whole genome sequencing identifies a de novo 2.1?Mb balanced paracentric inversion disrupting FOXP1 and leading to severe intellectual disability
Clinica Chimica Acta 2018 485
doi: 10.1016/j.cca.2018.06.048