CNRGH

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

Charmet R. et al.
Association of impaired renal function with venous thrombosis: A genetic risk score approach.
Thromb Res. (2017) Oct. 158:102-107.
doi: 10.1016/j.thromres.2017.08.015

Bruel AL. et al.
Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes.
J Med Genet. (2017) Jun. 54(6):371-380.
doi: 10.1136/jmedgenet-2016-104436

Mobuchon L. et al.
A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus.
NPJ Genom Med. (2017) Mar. 2. pii: 5.
doi: 10.1038/s41525-017-0008-5

Garcia-Oliver E. et al.
Bdf1 bromodomains are essential for meiosis and the expression of meiotic-specific genes.
PLoS Genet. (2017) Jan. 13(1):e1006541.
doi: 10.1371/journal.pgen.1006541

Stéphanie Bauché et al.
Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea
The American Journal of Human Genetics 2016, vol. 99, issue 3
doi: 10.1016/j.ajhg.2016.06.033

Kilan Le Guennec et al.
ABCA7 rare variants and Alzheimer disease risk
Neurology 2016, vol. 86, issue 23
doi: 10.1212/wnl.0000000000002627