TY  - JOUR 
AU  - Borghini, L.
AU  - Png, E.
AU  - Binder, A.
AU  - Wright, V. J.
AU  - Pinnock, E.
AU  - de Groot, R.
AU  - Hazelzet, J.
AU  - Emonts, M.
AU  - Van der Flier, M.
AU  - Schlapbach, L. J.
AU  - Anderson, S.
AU  - Secka, F.
AU  - Salas, A.
AU  - Fink, C.
AU  - Carrol, E. D.
AU  - Pollard, A. J.
AU  - Coin, L. J.
AU  - Kuijpers, T. W.
AU  - Martinón Torres, Federico
AU  - Zenz, W.
AU  - Levin, M.
AU  - Hibberd, M. L.
AU  - Davila, S.
PY  - 2019
SN  - 2045-2322
UR  - http://hdl.handle.net/20.500.11940/15380
AB  - Non-coding genetic variants play an important role in driving susceptibility to complex diseases but their characterization remains challenging. Here, we employed a novel approach to interrogate the genetic risk of such polymorphisms in a more...
LA  - eng
KW  - Humans
KW  - Genetic Association Studies
KW  - Meningococcal Infections
KW  - Phenotype
KW  - High-Throughput Nucleotide Sequencing
KW  - Hypopharyngeal Neoplasms
KW  - Case-Control Studies
KW  - Genomics
KW  - Genetic Predisposition to Disease
KW  - Neisseria meningitidis
KW  - Cohort Studies
TI  - Identification of regulatory variants associated with genetic susceptibility to meningococcal disease
DO  - 10.1038/s41598-019-43292-6
T2  - Scientific Reports
M2  - 6966
KW  - CHUS
KW  - IDIS
VL  - 9
ER  -