2016

David S. et al.
Multiple major disease-associated clones of Legionella pneumophila have emerged recently and independently
Genome Res. (2016) 26(11):1555-1564
doi:

Schartner V. et al.
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy
Acta Neuropathol. (2016) Dec 23
doi: 10.1007/s00401-016-1656-8

Mayjonade B. et al.
Extraction of high-molecular-weight genomic DNA for long-read sequencing of single molecules
BioTechniques. (2016) 61:203-205
doi: 10.2144/000114460

Hardies K. et al.
Loss of SYNJ1 dual phosphatase activity leads to early onset refractory seizures and progressive neurological decline
Brain. (2016) 139(Pt 9):2420-30
doi: 10.1093/brain/aww180

Le Provost, G. et al.
Implication of the suberin pathway in adaptation to waterlogging and hypertrophied lenticels formation in pedunculate oak (Quercus robur L.)
Tree Physiology. (2016) 36(11): p. 1330-1342
doi:

Leitwein M. et al.
Genome-wide nucleotide diversity of hatchery-reared Atlantic and Mediterranean strains of brown trout Salmo trutta compared to wild Mediterranean populations
J Fish Biol. (2016) 89:2717-2734
doi:

Prasad MK. et al.
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement
J Med Genet. 2016 53(2):98-110
doi: 10.1136/jmedgenet-2015-103302

Popova T. et al.
Ovarian Cancers Harboring Inactivating Mutations in CDK12 Display a Distinct Genomic Instability Pattern Characterized by Large Tandem Duplications
Cancer Res. (2016) 76(7):1882-91
doi: 10.1158/0008-5472.CAN-15-2128

Diodato A. et al.
Molecular signatures of neural connectivity in the olfactory cortex
Nat Commun. (2016) 7:12238
doi: 10.1038/ncomms12238

Caubit X. et al.
TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons
Nat Genet. (2016) 48:1359-69
doi: 10.1038/ng.3681