Detalhe da pesquisa
1.
Positional cloning of a novel gene influencing asthma from chromosome 2q14.
Nat Genet
; 35(3): 258-63, 2003 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-14566338
2.
Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17.
PLoS Genet
; 2(5): e72, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16710446
3.
Targeted mutagenesis of the Hira gene results in gastrulation defects and patterning abnormalities of mesoendodermal derivatives prior to early embryonic lethality.
Mol Cell Biol
; 22(7): 2318-28, 2002 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-11884616
4.
The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysis.
Ann Intern Med
; 145(4): 255-64, 2006 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16908916
5.
Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS study.
PLoS Med
; 3(4): e90, 2006 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-16475872
6.
Single-point haplotype scores telomeric to human leukocyte antigen-C give a high susceptibility major histocompatibility complex haplotype for psoriasis in a Caucasian population.
J Invest Dermatol
; 124(3): 545-52, 2005 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15737195
7.
Association of the TSHR gene with Graves' disease: the first disease specific locus.
Eur J Hum Genet
; 13(11): 1223-30, 2005 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-16106256
8.
Fine mapping of the IBD1 locus did not identify Crohn disease-associated NOD2 variants: implications for complex disease genetics.
Am J Med Genet
; 111(3): 253-9, 2002 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12210321
9.
Differential genetic effects of ESR1 gene polymorphisms on osteoporosis outcomes.
JAMA
; 292(17): 2105-14, 2004 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-15523071
10.
LPIN2 is associated with type 2 diabetes, glucose metabolism, and body composition.
Diabetes
; 56(12): 3020-6, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17804763
11.
Association between a complex insertion/deletion polymorphism in NOD1 (CARD4) and susceptibility to inflammatory bowel disease.
Hum Mol Genet
; 14(10): 1245-50, 2005 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-15790594
12.
Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26.
Am J Hum Genet
; 77(3): 365-76, 2005 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16080113
13.
Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF(-kappa)B transcription factors.
Hum Mol Genet
; 11(11): 1281-9, 2002 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12019209
14.
The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants.
Hum Mol Genet
; 12(20): 2569-75, 2003 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12928481