CNRGH

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COLD-PCR technologies in the area of personalized medicine: Methodology and Applications.
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Saultier P. et al.
Macrothrombocytopenia and dense granule deficiency associated with FLI1 variants: ultrastructural and pathogenic features.
Haematologica (2017) Jun. 102(6):1006-1016.
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Scelo G. et al.
Genome-wide association study identifies multiple risk loci for renal cell carcinoma.
Nat Commun. (2017) Jun. 8:15724.
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Simioni M. et al.
Genomic investigation of balanced chromosomal rearrangements in patients with abnormal phenotypes.
Mol Syndromol. (2017) Jun. 8(4):187-194.
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Contrepois K. et al.
Histone variant H2A.J accumulates in senescent cells and promotes inflammatory gene expression.
Nat Commun. (2017) May. 8:14995.
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Hautefort A. et al.
Pulmonary endothelial cell DNA methylation signature in pulmonary arterial hypertension.
Oncotarget (2017) May. 8(32):52995-53016.
doi: 10.18632/oncotarget.18031

Haziza S. et al.
Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factors.
Nat Nanotechnol. (2017) May. 12(4):322-328.
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Fradin D. et al.
Genome-wide methylation analysis identifies specific epigenetic marks in severely obese children.
Sci Rep. (2017) Apr. 7:46311.
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