Detalhe da pesquisa
1.
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci.
Eur Heart J
; 2024 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38747976
2.
Flecainide Is Associated With a Lower Incidence of Arrhythmic Events in a Large Cohort of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia.
Circulation
; 148(25): 2029-2037, 2023 12 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37886885
3.
Familial multiple discoid fibromas is linked to a locus on chromosome 5 including the FNIP1 gene.
J Hum Genet
; 68(4): 273-279, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36599954
4.
Microglial cell response in α7 nicotinic acetylcholine receptor-deficient mice after systemic infection with Escherichia coli.
J Neuroinflammation
; 19(1): 94, 2022 Apr 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35413868
5.
Immunogenicity of a 5-dose pneumococcal vaccination schedule following allogeneic hematopoietic stem cell transplantation.
Am J Hematol
; 97(5): 592-602, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35147238
6.
Incidence and Risk Factors for Invasive Pneumococcal Disease and Community-acquired Pneumonia in Human Immunodeficiency Virus-Infected Individuals in a High-income Setting.
Clin Infect Dis
; 71(1): 41-50, 2020 06 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-31634398
7.
Red blood cell transfusion results in adhesion of neutrophils in human endotoxemia and in critically ill patients with sepsis.
Transfusion
; 60(2): 294-302, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31804732
8.
Predicting cardiac electrical response to sodium-channel blockade and Brugada syndrome using polygenic risk scores.
Eur Heart J
; 40(37): 3097-3107, 2019 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31504448
9.
Identification of genetic biomarkers for alloimmunization in sickle cell disease.
Br J Haematol
; 186(6): 887-899, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31168801
10.
Complement factor H contributes to mortality in humans and mice with bacterial meningitis.
J Neuroinflammation
; 16(1): 279, 2019 Dec 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-31883521
11.
Nonclassical FCGR2C haplotype is associated with protection from red blood cell alloimmunization in sickle cell disease.
Blood
; 130(19): 2121-2130, 2017 11 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28899854
12.
SNP rs688 within the low-density lipoprotein receptor (LDL-R) gene associates with HCV susceptibility.
Liver Int
; 39(3): 463-469, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30260075
13.
A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathy.
Eur Heart J
; 39(31): 2898-2907, 2018 08 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-29718149
14.
A comprehensive evaluation of the genetic architecture of sudden cardiac arrest.
Eur Heart J
; 39(44): 3961-3969, 2018 11 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30169657
15.
Phenotypic and clinical implications of variants in the dihydropyrimidine dehydrogenase gene.
Biochim Biophys Acta
; 1862(4): 754-762, 2016 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26804652
16.
Mannose-binding lectin-associated serine protease 2 (MASP-2) contributes to poor disease outcome in humans and mice with pneumococcal meningitis.
J Neuroinflammation
; 14(1): 2, 2017 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28086930
17.
Biomarkers to predict infection and infection-related complications during chemotherapy-induced neutropenia in acute myeloid leukaemia: a pilot study.
Br J Haematol
; 193(5): 1008-1012, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33829503
18.
Fc-gamma receptor polymorphisms differentially influence susceptibility to systemic lupus erythematosus and lupus nephritis.
Rheumatology (Oxford)
; 55(5): 939-48, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26748351
19.
A founder effect for p47(phox)Trp193Ter chronic granulomatous disease in Kavkazi Jews.
Blood Cells Mol Dis
; 55(4): 320-7, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26460255
20.
Dissection of a quantitative trait locus for PR interval duration identifies Tnni3k as a novel modulator of cardiac conduction.
PLoS Genet
; 8(12): e1003113, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23236294