Detalhe da pesquisa
1.
Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling.
Hum Mol Genet
; 26(21): 4301-4313, 2017 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28973304
2.
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.
N Engl J Med
; 374(12): 1134-44, 2016 03 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-26934567
3.
No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study.
PLoS Genet
; 12(10): e1006343, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27792727
4.
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies.
J Med Genet
; 54(9): 598-606, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28756411
5.
A haplotype block downstream of plasminogen is associated with chronic and aggressive periodontitis.
J Clin Periodontol
; 44(10): 962-970, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28548211
6.
Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma.
Commun Biol
; 2: 89, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30854481