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Nayoung K. D. Kim
Nayoung K. D. Kim
Samsung Genome Institute, Samsung Medical Center
Verified email at samsung.com
Title
Cited by
Cited by
Year
Introducing the bacterial ‘chromid’: not a chromosome, not a plasmid
PW Harrison, RPJ Lower, NKD Kim, JPW Young
Trends in microbiology 18 (4), 141-148, 2010
4112010
Pharmacogenomic landscape of patient-derived tumor cells informs precision oncology therapy
JK Lee, Z Liu, JK Sa, S Shin, J Wang, M Bordyuh, HJ Cho, O Elliott, T Chu, ...
Nature genetics 50 (10), 1399-1411, 2018
1712018
Tumor genomic profiling guides patients with metastatic gastric cancer to targeted treatment: the VIKTORY umbrella trial
J Lee, ST Kim, K Kim, H Lee, I Kozarewa, PGS Mortimer, JI Odegaard, ...
Cancer discovery 9 (10), 1388-1405, 2019
1702019
Prevalence and detection of low-allele-fraction variants in clinical cancer samples
HT Shin, YL Choi, JW Yun, NKD Kim, SY Kim, HJ Jeon, JY Nam, C Lee, ...
Nature communications 8 (1), 1377, 2017
1662017
Characterization of background noise in capture-based targeted sequencing data
G Park, JK Park, SH Shin, HJ Jeon, NKD Kim, YJ Kim, HT Shin, E Lee, ...
Genome biology 18, 1-13, 2017
622017
Four distinct immune microenvironment subtypes in gastric adenocarcinoma with special reference to microsatellite instability
J Cho, YH Chang, YJ Heo, S Kim, NKD Kim, JO Park, WK Kang, J Lee, ...
ESMO open 3 (3), e000326, 2018
602018
Patient-derived cell models as preclinical tools for genome-directed targeted therapy
JY Lee, SY Kim, C Park, NKD Kim, J Jang, K Park, JH Yi, M Hong, T Ahn, ...
Oncotarget 6 (28), 25619, 2015
562015
Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population
NKD Kim, AR Kim, KT Park, SY Kim, MY Kim, JY Nam, SJ Woo, SH Oh, ...
Genetics in Medicine, 2015
532015
Dysregulated Wnt signalling and recurrent mutations of the tumour suppressor RNF43 in early gastric carcinogenesis
BH Min, J Hwang, NKD Kim, G Park, SY Kang, S Ahn, S Ahn, SY Ha, ...
The Journal of pathology 240 (3), 304-314, 2016
522016
Evaluation of somatic copy number estimation tools for whole-exome sequencing data
JY Nam, NKD Kim, SC Kim, JG Joung, R Xi, S Lee, PJ Park, WY Park
Briefings in bioinformatics 17 (2), 185-192, 2016
512016
Atypical hemolytic uremic syndrome: Korean pediatric series
JM Lee, YS Park, JH Lee, SJ Park, JI Shin, YH Park, KH Yoo, MH Cho, ...
Pediatrics International, 2014
512014
ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathy
KH Han, DY Oh, S Lee, C Lee, JH Han, MY Kim, HR Park, MK Park, ...
Scientific reports 7 (1), 16504, 2017
502017
Bridging genomics and phenomics of gastric carcinoma
J Cho, S Ahn, DS Son, NKD Kim, KW Lee, S Kim, J Lee, SH Park, JO Park, ...
International journal of cancer 145 (9), 2407-2417, 2019
472019
Design and implementation of the hepatorenal fibrocystic disease core center clinical database: a centralized resource for characterizing autosomal recessive polycystic kidney …
B Alzarka, H Morizono, JW Bollman, D Kim, LM Guay-Woodford
Frontiers in pediatrics 5, 80, 2017
412017
Good laboratory standards for clinical next-generation sequencing cancer panel tests
J Kim, WY Park, NKD Kim, SJ Jang, SM Chun, CO Sung, J Choi, YH Ko, ...
Journal of pathology and translational medicine 51 (3), 191, 2017
402017
Phase II study of a triplet regimen of S-1 combined with irinotecan and oxaliplatin in patients with metastatic gastric cancer: clinical and pharmacogenetic results
SR Park, SY Kong, J Rhee, YI Park, KW Ryu, JH Lee, YW Kim, IJ Choi, ...
Annals of oncology 22 (4), 890-896, 2011
402011
Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans
BJ Kim, AR Kim, C Lee, SY Kim, NKD Kim, MY Chang, J Rhee, MH Park, ...
PLoS One 11 (10), e0165680, 2016
362016
Targeted exome sequencing resolves allelic and the genetic heterogeneity in the genetic diagnosis of nephronophthisis-related ciliopathy
HG Kang, HK Lee, YH Ahn, JG Joung, J Nam, NKD Kim, JM Ko, MH Cho, ...
Experimental & molecular medicine 48 (8), e251-e251, 2016
352016
Genetic study in Korean pediatric patients with steroid-resistant nephrotic syndrome or focal segmental glomerulosclerosis
E Park, C Lee, NKD Kim, YH Ahn, YS Park, JH Lee, SH Kim, MH Cho, ...
Journal of clinical medicine 9 (6), 2013, 2020
332020
BGN mutations in X-linked spondyloepimetaphyseal dysplasia
SY Cho, JS Bae, NKD Kim, F Forzano, KM Girisha, C Baldo, F Faravelli, ...
The American Journal of Human Genetics 98 (6), 1243-1248, 2016
332016
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