CNRGH

Bruel AL. et al.
Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis.
Clin Genet. (2017) Feb. 91(2):333-338.
doi: 10.1111/cge.12794

Pivot X. et al.
Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort.
NPJ Breast Cancer (2017) Feb. 3:4.
doi: 10.1038/s41523-017-0005-y

Sefrioui D. et al.
Comparison of the quantification of KRAS mutations by digital PCR and E-ice-COLD-PCR in circulating-cell-free DNA from metastatic colorectal cancer patients.
Clin Chim Acta (2017) Feb. 465:1-4.
doi: 10.1016/j.cca.2016

Stoekle HC. et al.
Toward dynamic informed consent.
Med Sci. (Paris) (2017) Feb. 33(2):188-192.
doi: 10.1051/medsci/20173302015

Costantino F. et al.
A family-based genome-wide association study reveals an association of spondyloarthritis with MAPK14.
Ann Rheum Dis. (2017) Jan. 76(1):310-314.
doi: 10.1136/annrheumdis-2016-209449

Fleischer T. et al.
DNA methylation signature (SAM40) identifies subgroups of the Luminal A breast cancer samples with distinct survival.
Oncotarget (2017) Jan. 8(1):1074-1082.
doi: 10.18632/oncotarget.13718

Fogel O. et al.
Epigenetic changes in chronic inflammatory diseases.
Adv Protein Chem Struct Biol. (2017) 106:139-189.
doi: 10.1016/bs.apcsb.2016.09.003

Kaut O. et al.
Epigenome-wide DNA methylation analysis in siblings and monozygotic twins discordant for sporadic Parkinson's disease revealed different epigenetic patterns in peripheral blood mononuclear cells.
Neurogenetics (2017) Jan. 18(1):7-22.
doi: 10.1007/s10048-016-0497-x

Khalaf-Nazzal R. et al.
Early born neurons are abnormally positioned in the doublecortin knockout hippocampus.
Hum Mol Genet. (2017) Jan. 26(1):90-108.
doi: 10.1093/hmg/ddw370