2017

Dos Santos RS. et al.
dUTPase (DUT) is mutated in a novel monogenic syndrome with diabetes and bone marrow failure.
Diabetes (2017) Apr. 66(4):1086-1096.
doi: 10.2337/db16-0839

Fradin D. et al.
Genome-wide methylation analysis identifies specific epigenetic marks in severely obese children.
Sci Rep. (2017) Apr. 7:46311.
doi: 10.1038/srep46311

Mercati O. et al.
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders.
Mol Psychiatry (2017) Apr. 22(4):625-633.
doi: 10.1038/mp.2016.61

Potaczek DP. et al.
Epigenetics and allergy: from basic mechanisms to clinical applications.
Epigenomics (2017) Apr. 9(4):539-571.
doi: 10.2217/epi-2016-0162

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

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

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

Leroy T. et al.
Extensive recent secondary contacts between four European white oak species.
New Phytol. (2017) Apr. 214(2):865-878.
doi: 10.1111/nph.14413

Thomas C. et al.
Erratum to: Rapid transcriptional plasticity of duplicated gene clusters enables a clonally reproducing aphid to colonise diverse plant species.
Genome Biology (2017) Apr. 18 (1): 63.
doi: doi :10.1186/s13059-017-1202-6

Portoso M. et al.
PRC2 is dispensable for HOTAIR-mediated transcriptional repression.
EMBO J. (2017) Apr. 36(8):981-994.
doi: 10.15252/embj.201695335