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Showing results 1 to 19 of 19

Issue DateTitle / Author(s) / CitationFileAltmetrics
2008-11
A genome-wide Asian genetic map and ethnic comparison: The GENDISCAN study
view fileDOI
2008-11
A genome-wide Asian genetic map and ethnic comparison: the GENDISCAN study
view fileDOI
2009-04
Higher mitochondrial DNA copy number is associated with lower prevalence of microalbuminuria

Lee, Jung Eun; Park, Hansoo; Ju, Young Seok; Kwak, Minhye; Oh, Ha Young; Seo, Jeong-Sun; Kim, Jong-Il

EXPERIMENTAL AND MOLECULAR MEDICINE; Vol.41 4; 253-258

view fileDOI
2010
The first Irish genome and ways of improving sequence accuracy
view fileDOI
2010-05
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing
DOI
2010-08
Reference-unbiased copy number variant analysis using CGH microarrays
view fileDOI
2010-09
Gene Mapping Study of Constitutive Skin Color in a Genetically Isolated Population
DOI
2012-12
Comprehensive genomic analyses associate UGT8 variants with musical ability in a Mongolian population
DOI
2013
A family-based association study after genome-wide linkage analysis identified two genetic loci for renal function in a Mongolian population
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2017-09
Clonal History and Genetic Predictors of Transformation Into Small-Cell Carcinomas From Lung Adenocarcinomas
DOI
2018-04
Alterations in the Rho pathway contribute to Epstein-Barr virus-induced lymphomagenesis in immunosuppressed environments
DOI
2020-03
Germline gain-of-function mutation of STAT1 rescued by somatic mosaicism in immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like disorder
DOI
2020-03
PRMT1 is required for the maintenance of mature β-cell identity
DOI
2021-10
Severe protein C deficiency in a newborn caused by a homozygous pathogenic variant in the PROC gene: a case report
view fileDOI
2021-11
Acquired Resistance to Third-Generation EGFR Tyrosine Kinase Inhibitors in Patients With De Novo EGFR(T790M)-Mutant NSCLC
DOI
2022-05
Heterogeneous genetic landscape of congenital neutropenia in Korean patients revealed by whole exome sequencing: genetic, phenotypic and histologic correlations
DOI
2022-06
Patient-derived organoids as a preclinical platform for precision medicine in colorectal cancer
DOI
2024-08
Mitochondrial DNA mosaicism in normal human somatic cells
DOI
2024-09
Resistance mechanisms of EGFR tyrosine kinase inhibitors, in EGFR exon 20 insertion-mutant lung cancer
DOI
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