CNRGH

Nicolas G. et al.
Brain calcifications and PCDH12 variants.
Neurol Genet. (2017) Jul. 3(4):e166.
doi: 10.1212/NXG.0000000000000166

Bruel AL. et al.
Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes.
J Med Genet. (2017) Jun. 54(6):371-380.
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Louveau B. et al.
Clinical value of early detection of circulating tumour DNA-BRAFV600mut in patients with metastatic melanoma treated with a BRAF inhibitor.
ESMO Open. (2017) Jun. 2(2):e000173.
doi: 10.1136/esmoopen-2017-000173

Mauger F. et al.
COLD-PCR technologies in the area of personalized medicine: Methodology and Applications.
Mol Diagn Ther. (2017) Jun. 21(3):269-283.
doi: 10.1007/s40291-016-0254-8

Saultier P. et al.
Macrothrombocytopenia and dense granule deficiency associated with FLI1 variants: ultrastructural and pathogenic features.
Haematologica (2017) Jun. 102(6):1006-1016.
doi: 10.3324/haematol.2016.153577

Scelo G. et al.
Genome-wide association study identifies multiple risk loci for renal cell carcinoma.
Nat Commun. (2017) Jun. 8:15724.
doi: 10.1038/ncomms15724

Simioni M. et al.
Genomic investigation of balanced chromosomal rearrangements in patients with abnormal phenotypes.
Mol Syndromol. (2017) Jun. 8(4):187-194.
doi: 10.1159/000477084

Contrepois K. et al.
Histone variant H2A.J accumulates in senescent cells and promotes inflammatory gene expression.
Nat Commun. (2017) May. 8:14995.
doi: 10.1038/ncomms14995

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.
doi: 10.1038/nnano.2016.260