CNRGH
Simandi Z. et al.
RXR heterodimers orchestrate transcriptional control of neurogenesis and cell fate specification.
Mol Cell Endocrinol. (2017) Aug. pii: S0303-7207(17)30413-6.
doi: 10.1016/j.mce.2017.07.033
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
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
Letouze E. et al.
Mutational signatures reveal the dynamic interplay of risk factors and cellular processes during liver tumorigenesis.
Nat Commun. (2017) Nov. 8(1):1315.
doi: 10.1038/s41467-017-01358-x
Bellenguez C. et al.
Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls.
Neurobiol. Aging (2017) Jul. pii: S0197-4580(17)30232-4.
doi: 10.1016/j.neurobiolaging.2017.07.001
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
Mercier S. et al.
Expanding the spectrum of congenital myopathy linked to recessive mutations in SCN4A.
Neurology (2017) Jan. 88(4):414-416.
doi: 10.1212/WNL.0000000000003535
Machiela MJ. et al.
Genetic variants related to longer telomere length are associated with increased risk of Renal Cell Carcinoma.
Europ. Urol. (2017) Nov. 72 (5): 747-754
doi: 10.1016/j.eururo.2017.07.015
Czimmerer Z. et al.
Extensive and functional overlap of the STAT6 and RXR cistromes in the active enhancer repertoire of human CD14+ monocyte derived differentiating macrophages.
Mol Cell Endocrinol. (2017) Jul. pii: S0303-7207(17)30414-8.
doi: 10.1016/j.mce.2017.07.034
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