Publications Grand Projet
Michel Azizi et al.
Emerging Drug Classes and Their Potential Use in Hypertension
Hypertension 2019, vol. 74, issue 5
doi: 10.1161/hypertensionaha.119.12676
Jonathan Kreplak et al.
A reference genome for pea provides insight into legume genome evolution
Nature Genetics 2019, vol. 51, issue 9
doi: 10.1038/s41588-019-0480-1
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
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
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
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
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
Andrés Berardo et al.
HNRNPDL-related muscular dystrophy: expanding the clinical, morphological and MRI phenotypes
Journal of Neurology 2019, vol. 266, issue 10
doi: 10.1007/s00415-019-09437-3
Thibault Leroy et al.
Massive postglacial gene flow between European white oaks uncovered genes underlying species barriers
New Phytologist 2019
doi: 10.1111/nph.16039
Thibault Leroy et al.
Oak symbolism in the light of genomics
New Phytologist 2019, vol. 226, issue 4
doi: 10.1111/nph.15987
Marion Dupouy et al.
Two large reciprocal translocations characterized in the disease resistance-rich burmannica genetic group of Musa acuminata
Annals of Botany 2019, vol. 124, issue 2
doi: 10.1093/aob/mcz078
Mathias Lorieux et al.
NOISYmputer: genotype imputation in bi-parental populations for noisy low-coverage next-generation sequencing data
2019
doi: 10.1101/658237
Cubry P et al.
The Rise and Fall of African Rice Cultivation Revealed by Analysis of 246 New Genomes
Current Biology 2018 28(14)
doi: 10.1016/j.cub.2018.05.066
Deveau P et al.
QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction
Bioinformatics 2018 34(11)
doi: 10.1093/bioinformatics/bty016
Ávila-Polo R et al.
Loss of Sarcomeric Scaffolding as a Common Baseline Histopathologic Lesion in Titin-Related Myopathies
Journal of Neuropathology & Experimental Neurology 2018 77(12)
doi: 10.1093/jnen/nly095
Bayard Q et al.
Cyclin A2/E1 activation defines a hepatocellular carcinoma subclass with a rearrangement signature of replication stress
Nature Communications 2018 9(1)
doi: 10.1038/s41467-018-07552-9
Peter J et al.
Genome evolution across 1,011 Saccharomyces cerevisiae isolates
Nature 2018 556(7701)
doi: 10.1038/s41586-018-0030-5
Manzano-Marín A et al.
A Freeloader? The Highly Eroded Yet Large Genome of the Serratia symbiotica Symbiont of Cinara strobi
Genome Biology and Evolution 2018 10(9)
doi: 10.1093/gbe/evy173
Karimi B et al.
Biogeography of soil bacteria and archaea across France
Science Advances 2018 4(7)
doi: 10.1126/sciadv.aat1808
Böhm J et al.
Novel ASCC1 mutations causing prenatal-onset muscle weakness with arthrogryposis and congenital bone fractures
Journal of Medical Genetics 2018, vol. 56, issu 9
doi: 10.1136/jmedgenet-2018-105390
Dutreux F et al.
De novo assembly and annotation of three Leptosphaeria genomes using Oxford Nanopore MinION sequencing
Scientific Data 2018 5
doi: DOI:10.1038/sdata.2018.235
Girard E et al.
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing
International Journal of Cancer 2018 144(8)
doi: 10.1002/ijc.31921
Khan W et al.
MACARON: a python framework to identify and re-annotate multi-base affected codons in whole genome/exome sequence data
Bioinformatics 2018 34(19)
doi: 10.1093/bioinformatics/bty382
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
Chicard M et al.
Whole-Exome Sequencing of Cell-Free DNA Reveals Temporo-spatial Heterogeneity and Identifies Treatment-Resistant Clones in Neuroblastoma
Clinical Cancer Research 2017 24(4)
doi: 10.1158/1078-0432.CCR-17-1586
Angela Bellini et al.
Study of chromatin remodeling genes implicates SMARCA4 as a putative player in oncogenesis in neuroblastoma
International Journal of Cancer 2019, vol. 145, issue 10
doi: 10.1002/ijc.32361
Emmanuelle Boscher et al.
Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer’s Disease
Journal of Alzheimer's Disease 2019, vol. 68, issue 3
doi: 10.3233/jad-180940
Battle Karimi et al.
Biogeography of Soil Bacterial Networks along a Gradient of Cropping Intensity
Scientific Reports 2019, vol. 9, issue 1
doi: 10.1038/s41598-019-40422-y
Xavière Lornage et al.
ACTN2 mutations cause “Multiple structured Core Disease” (MsCD)
Acta Neuropathologica 2019, vol. 137, issue 3
doi: 10.1007/s00401-019-01963-8
Julie Ferreira de Carvalho et al.
Cytonuclear interactions remain stable during allopolyploid evolution despite repeated whole‐genome duplications in Brassica
The Plant Journal 2019, vol. 98, issue 3
doi: 10.1111/tpj.14228