Search details
1.
Evaluation of low-pass genome sequencing in polygenic risk score calculation for Parkinson's disease.
Hum Genomics
; 15(1): 58, 2021 08 28.
Article
in English
| MEDLINE | ID: mdl-34454617
2.
Whole genome sequencing reveals a frameshift mutation and a large deletion in YY1AP1 in a girl with a panvascular artery disease.
Hum Genomics
; 15(1): 28, 2021 05 10.
Article
in English
| MEDLINE | ID: mdl-33971976
3.
De novo assembly and phasing of a Korean human genome.
Nature
; 538(7624): 243-247, 2016 Oct 13.
Article
in English
| MEDLINE | ID: mdl-27706134
4.
Legacy Data Confound Genomics Studies.
Mol Biol Evol
; 37(1): 2-10, 2020 Jan 01.
Article
in English
| MEDLINE | ID: mdl-31504792
5.
Divergent reprogramming routes lead to alternative stem-cell states.
Nature
; 516(7530): 192-7, 2014 Dec 11.
Article
in English
| MEDLINE | ID: mdl-25503232
6.
Genome-wide characterization of the routes to pluripotency.
Nature
; 516(7530): 198-206, 2014 Dec 11.
Article
in English
| MEDLINE | ID: mdl-25503233
7.
Virus Isolation from the First Patient with SARS-CoV-2 in Korea.
J Korean Med Sci
; 35(7): e84, 2020 Feb 24.
Article
in English
| MEDLINE | ID: mdl-32080990
8.
Prevalence and oncologic outcomes of BRCA 1/2 mutations in unselected triple-negative breast cancer patients in Korea.
Breast Cancer Res Treat
; 173(2): 385-395, 2019 Jan.
Article
in English
| MEDLINE | ID: mdl-30350268
9.
Comprehensive Analysis of the Transcriptional and Mutational Landscape of Follicular and Papillary Thyroid Cancers.
PLoS Genet
; 12(8): e1006239, 2016 08.
Article
in English
| MEDLINE | ID: mdl-27494611
10.
LYL1 gene amplification predicts poor survival of patients with uterine corpus endometrial carcinoma: analysis of the Cancer genome atlas data.
BMC Cancer
; 18(1): 494, 2018 05 02.
Article
in English
| MEDLINE | ID: mdl-29716549
11.
Genomic landscape of ovarian clear cell carcinoma via whole exome sequencing.
Gynecol Oncol
; 148(2): 375-382, 2018 02.
Article
in English
| MEDLINE | ID: mdl-29233531
12.
Development of a common platform for the noninvasive prenatal diagnosis of X-linked diseases.
Prenat Diagn
; 38(11): 835-840, 2018 10.
Article
in English
| MEDLINE | ID: mdl-30048567
13.
Prognostic effects of TERT promoter mutations are enhanced by coexistence with BRAF or RAS mutations and strengthen the risk prediction by the ATA or TNM staging system in differentiated thyroid cancer patients.
Cancer
; 122(9): 1370-9, 2016 05 01.
Article
in English
| MEDLINE | ID: mdl-26969876
14.
Corrigendum: Divergent reprogramming routes lead to alternative stem-cell states.
Nature
; 523(7562): 626, 2015 Jul 30.
Article
in English
| MEDLINE | ID: mdl-26083751
15.
Corrigendum: Genome-wide characterization of the routes to pluripotency.
Nature
; 523(7562): 626, 2015 Jul 30.
Article
in English
| MEDLINE | ID: mdl-26083747
16.
A transforming KIF5B and RET gene fusion in lung adenocarcinoma revealed from whole-genome and transcriptome sequencing.
Genome Res
; 22(3): 436-45, 2012 Mar.
Article
in English
| MEDLINE | ID: mdl-22194472
17.
The transcriptional landscape and mutational profile of lung adenocarcinoma.
Genome Res
; 22(11): 2109-19, 2012 Nov.
Article
in English
| MEDLINE | ID: mdl-22975805
18.
Noninvasive prenatal diagnosis of duchenne muscular dystrophy: comprehensive genetic diagnosis in carrier, proband, and fetus.
Clin Chem
; 61(6): 829-37, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-25847990
19.
A highly annotated whole-genome sequence of a Korean individual.
Nature
; 460(7258): 1011-5, 2009 Aug 20.
Article
in English
| MEDLINE | ID: mdl-19587683
20.
A public resource facilitating clinical use of genomes.
Proc Natl Acad Sci U S A
; 109(30): 11920-7, 2012 Jul 24.
Article
in English
| MEDLINE | ID: mdl-22797899