CNRGH

Schartner V. et al.
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy.
Acta Neuropathol. (2017) Apr. 133(4):517-533.
doi: 10.1007/s00401-016-1656-8

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

Tronik-Le Roux D. et al.
Novel landscape of HLA-G isoforms expressed in clear cell renal cell carcinoma patients.
Mol Oncol. (2017) Nov. 11(11):1561-1578.
doi: 10.1002/1878-0261

Engel M. et al.
Influence of lung CT changes in chronic obstructive pulmonary disease (COPD) on the human lung microbiome.
PLoS One (2017) Jul. 12(7):e0180859.
doi: 10.1371/journal.pone.0180859

Suchon P. et al.
Protein S Heerlen mutation heterozygosity is associated with venous thrombosis risk.
Sci Rep. (2017) Apr. 7:45507.
doi: 10.1038/srep45507

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

Abath Neto O. et al.
Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients.
Neuromuscul Disord. (2017) Nov. 27(11):975-985.
doi: 10.1016/j.nmd.2017.05.016

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

Tost J. et al.
Epigenetics of the immune system and alterations in inflammation and autoimmunity Foreword.
Epigenomics (2017) Apr. 9(4):371-373.
doi: 10.2217/epi-2017-0026

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