TY  - JOUR
AU  - Borghini, Lisa
AU  - Png, Eileen
AU  - Binder, Alexander
AU  - Wright, Victoria J
AU  - Pinnock, Ellie
AU  - de Groot, Ronald
AU  - Hazelzet, Jan
AU  - Emonts, Marieke
AU  - Van der Flier, Michiel
AU  - Schlapbach, Luregn J
AU  - Anderson, Suzanne
AU  - Secka, Fatou
AU  - Salas, Antonio
AU  - Fink, Colin
AU  - Carrol, Enitan D
AU  - Pollard, Andrew J
AU  - Coin, Lachlan J
AU  - Kuijpers, Taco W
AU  - Martinon-Torres, Federico
AU  - Zenz, Werner
AU  - Levin, Michael
AU  - Hibberd, Martin L
AU  - Davila, Sonia
AU  - EUCLIDS consortium
PY  - 2019
DO  - 10.1038/s41598-019-43292-6
UR  - https://hdl.handle.net/10668/24612
T2  - Scientific reports
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  - en
KW  - Case-Control Studies
KW  - Cohort Studies
KW  - Genetic Association Studies
KW  - Genetic Predisposition to Disease
KW  - Genomics
KW  - High-Throughput Nucleotide Sequencing
KW  - Humans
KW  - Hypopharyngeal Neoplasms
KW  - Meningococcal Infections
KW  - Neisseria meningitidis
KW  - Phenotype
KW  - Polymorphism, Single Nucleotide
KW  - Regulatory Sequences, Nucleic Acid
KW  - Tumor Cells, Cultured
TI  - Identification of regulatory variants associated with genetic susceptibility to meningococcal disease.
TY  - research article
VL  - 9
ER  -