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
Velasco G et al.
Comparative methylome analysis of ICF patients identifies heterochromatin loci that require ZBTB24, CDCA7 and HELLS for their methylated state
Human Molecular Genetics 2018 27(14)
doi: 10.1093/hmg/ddy130
Ulff-Møller CJ et al.
Twin DNA Methylation Profiling Reveals Flare-Dependent Interferon Signature and B Cell Promoter Hypermethylation in Systemic Lupus Erythematosus
Arthritis & Rheumatology 2018 70(6)
doi: 10.1002/art.40422
Tost J et al.
A translational perspective on epigenetics in allergic diseases
Journal of Allergy and Clinical Immunology 2018 142(3)
doi: 10.1016/j.jaci.2018.07.009
Tost J et al.
Epigenetic plasticity of eosinophils and other immune cell subsets in childhood asthma
The Lancet Respiratory Medicine 2018 6(5)
doi: 10.1016/s2213-2600(18)30051-1
Stoeklé HC et al.
La propriété des données génétiques
Médecine/Sciences 2018 34(12)
doi: 10.1051/medsci/2018291
Stoeklé HC et al.
Artificial intelligence in internal medicine: Between science and pseudoscience
European Journal of Internal Medicine 2018 51
doi: 10.1016/j.ejim.2018.01.027
Stengel B et al.
Risk profile, quality of life and care of patients with moderate and advanced CKD: The French CKD-REIN Cohort Study
Nephrology Dialysis Transplantation 2018 34(2)
doi: 10.1093/ndt/gfy058
Song MA et al.
Methylation of imprinted IGF2 regions is associated with total, visceral, and hepatic adiposity in postmenopausal women
Epigenetics 2018 13(8)
doi: 10.1080/15592294.2018.1518100
Singh V et al.
Computational Systems Biology Approach for the Study of Rheumatoid Arthritis: From a Molecular Map to a Dynamical Model
Genomics and Computational Biology 2017 4(1)
doi: 10.18547/gcb.2018.vol4.iss1.e100050
Simandi Z et al.
RXR heterodimers orchestrate transcriptional control of neurogenesis and cell fate specification
Molecular and Cellular Endocrinology 2018 471 .
doi: 10.1016/j.mce.2017.07.033
Robinson CM et al.
Consequences of VHL Loss on Global DNA Methylome
Scientific Reports 2018 8(1)
doi: 10.1038/s41598-018-21524-5
Pierron D et al.
Strong selection during the last millennium for African ancestry in the admixed population of Madagascar
Nature Communications 2018 9(1)
doi: 10.1038/s41467-018-03342-5
Perron G et al.
A General Framework for Interrogation of mRNA Stability Programs Identifies RNA-Binding Proteins that Govern Cancer Transcriptomes
Cell Reports 2018 23(6)
doi: 10.1016/j.celrep.2018.04.031
Mauger F et al.
Enrichment of methylated molecules using enhanced-ice-co-amplification at lower denaturation temperature-PCR (E-ice-COLD-PCR) for the sensitive detection of disease-related hypermethylation.
Epigenomics 2018 10(5)
doi: 10.2217/epi-2017-0166
Mary L et al.
Disease-causing variants in TCF4 are a frequent cause of intellectual disability: lessons from large-scale sequencing approaches in diagnosis
European Journal of Human Genetics 2018 26(7)
doi: 10.1038/s41431-018-0096-4
Magalhães M et al.
Dynamic changes of DNA methylation and lung disease in cystic fibrosis: lessons from a monogenic disease
Epigenomics 2018 10(8)
doi: 10.2217/epi-2018-0005
Lornage X et al.
Novel SPEG Mutations in Congenital Myopathy without Centralized Nuclei
Journal of Neuromuscular Diseases 2018 5(2)
doi: 10.3233/JND-170265
Lønning PE et al.
White Blood Cell BRCA1 Promoter Methylation Status and Ovarian Cancer Risk
Annals of Internal Medicine 2018 168(5)
doi: 10.7326/M17-0101
Le Guennec K et al.
Biallelic Loss of Function of SORL1 in an Early Onset Alzheimer’s Disease Patient
Journal of Alzheimers Disease 2018 62(2)
doi: 10.3233/jad-170981
Laugel-Haushalter V et al.
Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning
Frontiers in Physiology 2018 9
doi: 10.3389/fphys.2018.01329