Detalhe da pesquisa
1.
Prevalence of Mutations in Mendelian Stroke Genes in Early Onset Stroke Patients.
Ann Neurol
; 93(4): 768-782, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36541592
2.
Asian-specific 3'UTR variant in CDKN2B associated with risk of pituitary adenoma.
Mol Biol Rep
; 49(11): 10339-10346, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36097105
3.
A non-synonymous variant rs12614 of complement factor B associated with risk of chronic hepatitis B in a Korean population.
BMC Med Genet
; 21(1): 241, 2020 12 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33334325
4.
Identification of additional EHMT2 variant associated with the risk of chronic hepatitis B by GWAS follow-up study.
Genes Immun
; 20(1): 1-9, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29238036
5.
Reply to "Clinical Relevance of Genetic Variants in Juvenile Stroke Patients: A Plea for a Precise Classification".
Ann Neurol
; 94(3): 609, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37463060
6.
A PHLDB1 variant associated with the nonfunctional pituitary adenoma.
J Neurooncol
; 142(2): 223-229, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30868356
7.
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
Hum Mol Genet
; 25(23): 5265-5275, 2016 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27702942
8.
Genetic association of complement component 2 variants with chronic hepatitis B in a Korean population.
Liver Int
; 38(9): 1576-1582, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29283494
9.
Genetic diversity and divergence among Korean cattle breeds assessed using a BovineHD single-nucleotide polymorphism chip.
Asian-Australas J Anim Sci
; 31(11): 1691-1699, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30056676
10.
Gene profile of fibroblasts identify relation of CCL8 with idiopathic pulmonary fibrosis.
Respir Res
; 18(1): 3, 2017 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28057004
11.
MCM7 polymorphisms associated with the AML relapse and overall survival.
Ann Hematol
; 96(1): 93-98, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27837251
12.
Identification of novel OCT4 genetic variant associated with the risk of chronic hepatitis B in a Korean population.
Liver Int
; 37(3): 354-361, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27596359
13.
Sotos syndrome associated with Hirschsprung's disease: a new case and exome-sequencing analysis.
Pediatr Res
; 82(1): 87-92, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28399120
14.
Potential association between ITPKC genetic variations and Hirschsprung disease.
Mol Biol Rep
; 44(3): 307-313, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28664405
15.
Genetic variants of the gasdermin B gene associated with the development of aspirin-exacerbated respiratory diseases.
Allergy Asthma Proc
; 38(1): 4-12, 2017 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28052796
16.
RNA-Seq for Gene Expression Profiling of Human Necrotizing Enterocolitis: a Pilot Study.
J Korean Med Sci
; 32(5): 817-824, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28378556
17.
Genome-wide association study with the risk of schizophrenia in a Korean population.
Am J Med Genet B Neuropsychiatr Genet
; 171B(2): 257-65, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26531332
18.
A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.
Hum Mol Genet
; 22(20): 4233-8, 2013 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23760081
19.
Association of VARS2-SFTA2 polymorphisms with the risk of chronic hepatitis B in a Korean population.
Liver Int
; 35(8): 1934-40, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25404243
20.
Functional Study of Haplotypes in UGT1A1 Promoter to Find a Novel Genetic Variant Leading to Reduced Gene Expression.
Ther Drug Monit
; 37(3): 369-74, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25478904