Publications
Xavière Lornage et al.
Clinical, histological, and genetic characterization of PYROXD1-related myopathy
Acta Neuropathologica Communications 2019, vol. 7, issue 1
doi: 10.1186/s40478-019-0781-8
Yaiza M. Castillo et al.
Assessing the viral content of uncultured picoeukaryotes in the global‐ocean by single cell genomics
Molecular Ecology 2019, vol. 28, issue 18
doi: 10.1111/mec.15210
Roberta Ragazzini et al.
EZHIP constrains Polycomb Repressive Complex 2 activity in germ cells
Nature Communications 2019, vol. 10, issue 1
doi: 10.1038/s41467-019-11800-x
Gilles Morin et al.
Tubular aggregate myopathy and Stormorken syndrome: Mutation spectrum and genotype/phenotype correlation
Human Mutation 2019, vol. 41, issue 1
doi: 10.1002/humu.23899
Qiaowei Pan et al.
Identification of the master sex determining gene in Northern pike (Esox lucius) reveals restricted sex chromosome differentiation
PLOS Genetics 2019, vol. 15, issue 8
doi: 10.1371/journal.pgen.1008013
François Legoux et al.
Molecular mechanisms of lineage decisions in metabolite-specific T cells
Nature Immunology 2019, vol. 20, issue 9
doi: 10.1038/s41590-019-0465-3
Nadège Bidan et al.
Transcriptomic Analysis of Breast Cancer Stem Cells and Development of a pALDH1A1:mNeptune Reporter System for Live Tracking
PROTEOMICS 2019, vol. 19, issue 21-22
doi: 10.1002/pmic.201800454
N. Alcala et al.
Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids
Nature Communications 2019, vol. 10, issue 1
doi: 10.1038/s41467-019-11276-9
Fabienne Levi-Acobas et al.
Compatibility of 5-ethynyl-2′F-ANA UTP with in vitro selection for the generation of base-modified, nuclease resistant aptamers
Organic & Biomolecular Chemistry 2019, vol. 17, issue 35
doi: 10.1039/c9ob01515a
Sara Lindström et al.
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism
Blood 2019, vol. 134, issue 19
doi: 10.1182/blood.2019000435
Mickaël Canouil et al.
NACHO: an R package for quality control of NanoString nCounter data
Bioinformatics 2019
doi: 10.1093/bioinformatics/btz647
Chris Balak et al.
Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation
The American Journal of Human Genetics 2019, vol. 105, issue 3
doi: 10.1016/j.ajhg.2019.07.010
Laura Moreno Leon et al.
The nuclear hypoxia-regulated NLUCAT1 long non-coding RNA contributes to an aggressive phenotype in lung adenocarcinoma through regulation of oxidative stress
Oncogene 2019, vol. 38, issue 46
doi: 10.1038/s41388-019-0935-y
Joris Deelen et al.
A meta-analysis of genome-wide association studies identifies multiple longevity genes
Nature Communications 2019, vol. 10, issue 1
doi: 10.1038/s41467-019-11558-2
Simon Durand et al.
ALK mutation dynamics and clonal evolution in a neuroblastoma model exhibiting two ALK mutations
Oncotarget 2019, vol. 10, issue 48
doi: 10.18632/oncotarget.27119
Julie Piccand et al.
Rfx6 promotes the differentiation of peptide-secreting enteroendocrine cells while repressing genetic programs controlling serotonin production
Molecular Metabolism 2019, vol. 29
doi: 10.1016/j.molmet.2019.08.007
Moïra Rossitto et al.
In utero exposure to acetaminophen and ibuprofen leads to intergenerational accelerated reproductive aging in female mice
Communications Biology 2019, vol. 2, issue 1
doi: 10.1038/s42003-019-0552-x
Thibault Leroy et al.
Adaptive introgression as a driver of local adaptation to climate in European white oaks
New Phytologist 2019
doi: 10.1111/nph.16095
Suzanne V. Saenko et al.
Unravelling the genes forming the wing pattern supergene in the polymorphic butterfly Heliconius numata
EvoDevo 2019, vol. 10, issue 1
doi: 10.1186/s13227-019-0129-2
Luc Cabel et al.
Abstract 2298: Monitoring of circulating tumor DNA in non metastatic gastric cancer
Clinical Research (Excluding Clinical Trials) 2019
doi: 10.1158/1538-7445.am2019-2298
Catherine Branger et al.
Specialization of small non-conjugative plasmids in Escherichia coli according to their family types
Microbial Genomics 2019, vol. 5, issue 9
doi: 10.1099/mgen.0.000281
François Lecoquierre et al.
Confirmation and further delineation of the SMG9‐deficiency syndrome, a rare and severe developmental disorder
American Journal of Medical Genetics Part A 2019, vol. 179, issue 11
doi: 10.1002/ajmg.a.61317
Ana Uzquiano et al.
Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary Cilia
Cell Reports 2019, vol. 28, issue 6
doi: 10.1016/j.celrep.2019.06.096
Fatou K. Ndiaye et al.
The expression of genes in top obesity-associated loci is enriched in insula and substantia nigra brain regions involved in addiction and reward
International Journal of Obesity 2019, vol. 44, issue 2
doi: 10.1038/s41366-019-0428-7
Julien Jarroux et al.
HOTAIR promotes an epithelial-to-mesenchymal transition through relocation of the histone demethylase Lsd1
2019
doi: 10.1101/724948
Camille d’Humières et al.
A simple, reproducible and cost-effective procedure to analyse gut phageome: from phage isolation to bioinformatic approach
Scientific Reports 2019, vol. 9, issue 1
doi: 10.1038/s41598-019-47656-w
Tiziana La Bella et al.
Adeno-associated virus in the liver: natural history and consequences in tumour development
Gut 2019, vol. 69, issue 4
doi: 10.1136/gutjnl-2019-318281
Mariam Raliou et al.
Subclinical endometritis in dairy cattle is associated with distinct mRNA expression patterns in blood and endometrium
PLOS ONE 2019, vol. 14, issue 8
doi: 10.1371/journal.pone.0220244
Diana Chapeton-Montes et al.
The population structure of Clostridium tetani deduced from its pan-genome
Scientific Reports 2019, vol. 9, issue 1
doi: 10.1038/s41598-019-47551-4
Caroline Hoffmann et al.
Pdl1 and icosl discriminate human secretory and helper dendritic cells
2019
doi: 10.1101/721563