CNRGH
Cerino M. et al.
Genetic characterization of a French cohort of GNE-mutation negative inclusion body myopathy patients with exome sequencing.
Muscle Nerve (2017) Nov. 56(5):993-997.
doi: 10.1002/mus.25638
Pierron D. et al.
Genomic landscape of human diversity across Madagascar.
Proc Natl Acad Sci U S A (2017) Aug. 114(32):E6498-E6506.
doi: 10.1073/pnas
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
Stoekle HC. et al.
Toward dynamic informed consent.
Med Sci. (Paris) (2017) Feb. 33(2):188-192.
doi: 10.1051/medsci/20173302015
Fleischer T. et al.
DNA methylation at enhancers identifies distinct breast cancer lineages.
Nat Commun. (2017) Nov. 8(1):1379.
doi: 10.1038/s41467-017-00510-x
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