Detalhe da pesquisa
1.
Human Adaptive Immunity Rescues an Inborn Error of Innate Immunity.
Cell
; 168(5): 789-800.e10, 2017 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-28235196
2.
An ACT1 mutation selectively abolishes interleukin-17 responses in humans with chronic mucocutaneous candidiasis.
Immunity
; 39(4): 676-86, 2013 Oct 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-24120361
3.
Genome-Wide Association Study for Alcohol-Related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1.
Gastroenterology
; 159(4): 1276-1289.e7, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32561361
4.
The severity of the pathogen-induced acute sickness response is affected by polymorphisms in genes of the NLRP3 inflammasome pathway.
Brain Behav Immun
; 93: 186-193, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33434563
5.
Exploring the interactions between the human and viral genomes.
Hum Genet
; 139(6-7): 777-781, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31729546
6.
Impact of Interferon Lambda 4 Genotype on Interferon-Stimulated Gene Expression During Direct-Acting Antiviral Therapy for Hepatitis C.
Hepatology
; 68(3): 859-871, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29534310
7.
Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage.
Proc Natl Acad Sci U S A
; 113(24): 6713-8, 2016 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-27247391
8.
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections.
N Engl J Med
; 372(25): 2409-22, 2015 Jun 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-26083206
9.
Exome and genome sequencing for inborn errors of immunity.
J Allergy Clin Immunol
; 138(4): 957-969, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27720020
10.
Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species-induced meningoencephalitis, colitis, or both.
J Allergy Clin Immunol
; 135(6): 1558-68.e2, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25702837
11.
Inherited CARD9 deficiency in 2 unrelated patients with invasive Exophiala infection.
J Infect Dis
; 211(8): 1241-50, 2015 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25057046
12.
Mycobacterium simiae infection in two unrelated patients with different forms of inherited IFN-γR2 deficiency.
J Clin Immunol
; 34(8): 904-9, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25135595
13.
EVER2 deficiency is associated with mild T-cell abnormalities.
J Clin Immunol
; 33(1): 14-21, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22903682
14.
Utility of a buccal swab point-of-care test for the IFNL4 genotype in the era of direct acting antivirals for hepatitis C virus.
PLoS One
; 18(1): e0280551, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36689413
15.
Interferon lambda 4 variant rs12979860 is not associated with RAV NS5A Y93H in hepatitis C virus genotype 3a.
Hepatology
; 64(4): 1377-8, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26945900
16.
Refined association of melanoma differentiation-associated gene 5 variants with spontaneous hepatitis C virus clearance in Egypt.
Hepatology
; 63(3): 1059-61, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26105514
17.
Comprehensive Comparative Analysis of Standard Validated, Genetic, and Novel Biomarkers to Enhance Prognostic Risk-Stratification in Patients With Hepatitis C Virus Cirrhosis.
Clin Transl Gastroenterol
; 13(3): e00462, 2022 02 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35142723
18.
The rs429358 Locus in Apolipoprotein E Is Associated With Hepatocellular Carcinoma in Patients With Cirrhosis.
Hepatol Commun
; 6(5): 1213-1226, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34958182
19.
Using host genetics to infer the global spread and evolutionary history of HCV subtype 3a.
Virus Evol
; 7(2): veab065, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34532064
20.
Viral genome wide association study identifies novel hepatitis C virus polymorphisms associated with sofosbuvir treatment failure.
Nat Commun
; 12(1): 6105, 2021 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34671027