Detalhe da pesquisa
1.
Cell Specific eQTL Analysis without Sorting Cells.
PLoS Genet
; 11(5): e1005223, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25955312
2.
Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant.
Hum Mol Genet
; 23(9): 2481-9, 2014 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24334606
3.
Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA.
PLoS Genet
; 7(8): e1002197, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21829388
4.
Common and different genetic background for rheumatoid arthritis and coeliac disease.
Hum Mol Genet
; 18(21): 4195-203, 2009 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19648290
5.
Gene expression analysis in predicting the effectiveness of insect venom immunotherapy.
J Allergy Clin Immunol
; 125(5): 1092-7, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20334904
6.
Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac disease.
Eur J Hum Genet
; 28(3): 313-323, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31591516
7.
PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations.
Hum Mutat
; 29(7): 939-47, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18435454
8.
A locus at 7p14.3 predisposes to refractory celiac disease progression from celiac disease.
Eur J Gastroenterol Hepatol
; 30(8): 828-837, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29787419
9.
Identification of a novel PROS1 c.1113T-->GG frameshift mutation in a family with mixed type I/type III protein S deficiency.
Haematologica
; 91(8): 1151-2, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16885060
10.
Serum lipid levels, body mass index, and their role in coronary artery calcification: a polygenic analysis.
Circ Cardiovasc Genet
; 8(2): 327-33, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25577604
11.
Susceptibility to chronic mucus hypersecretion, a genome wide association study.
PLoS One
; 9(4): e91621, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24714607
12.
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.
Nat Genet
; 43(12): 1193-201, 2011 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-22057235
13.
Understanding human immune function using the resources from the Human Functional Genomics Project.
Nat Med
; 22(8): 831-3, 2016 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27490433
14.
Correction: Susceptibility to chronic mucus hypersecretion, a genome wide association study.
PLoS One
; 10(5): e0129524, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26024482
15.
Multiple common variants for celiac disease influencing immune gene expression.
Nat Genet
; 42(4): 295-302, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20190752
16.
HLA-A*02 is associated with a reduced risk and HLA-A*01 with an increased risk of developing EBV+ Hodgkin lymphoma.
Blood
; 110(9): 3310-5, 2007 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17630352