Detalhe da pesquisa
1.
The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type V.
BMC Musculoskelet Disord
; 15: 107, 2014 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-24674092
2.
Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.
PLoS Genet
; 7(4): e1001372, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21533022
3.
Association of variants at 1q32 and STAT3 with ankylosing spondylitis suggests genetic overlap with Crohn's disease.
PLoS Genet
; 6(12): e1001195, 2010 Dec 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-21152001
4.
Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21.
Hum Genet
; 129(1): 51-8, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20976470
5.
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci.
Nat Genet
; 45(7): 730-8, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23749187
6.
Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.
Nat Genet
; 42(2): 123-7, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20062062