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Frequency of pathogenic germline mutation in CHEK2, PALB2, MRE11, and RAD50 in patients at high risk for hereditary breast cancer

Breast cancer research and treatment, 2017-01, Vol.161 (1), p.95-102

2017

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Gene essentiality for tumour growth influences neoantigen‐directed immunoediting

Clinical and translational medicine, 2022-01, Vol.12 (1), p.e714-n/a

2022

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Colorimetric SNP Genotyping Based on Allele-Specific PCR by Using a Thiol-Labeled Primer

Chembiochem : a European journal of chemical biology, 2011-06, Vol.12 (9), p.1387-1390

2011

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MHC II immunogenicity shapes the neoepitope landscape in human tumors

Nature genetics, 2023-02, Vol.55 (2), p.221-231

2023

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The c.3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease)

Journal of human genetics, 2008-10, Vol.53 (10), p.947-949

2008

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Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer

Breast cancer research and treatment, 2012-08, Vol.134 (3), p.1315-1326

2012

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Mismatch DNA-specific enzymatic cleavage employed in a new method for the electrochemical detection of genetic mutations

Chemical communications (Cambridge, England), 2009-01 (28), p.4230-4232

2009

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BRCA1 and BRCA2 germline mutations in Korean breast cancer patients at high risk of carrying mutations

Cancer letters, 2007-01, Vol.245 (1), p.90-95

2007

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The CHEK2 1100delC mutation is not present in Korean patients with breast cancer cases tested for BRCA1 and BRCA2 mutation

Breast cancer research and treatment, 2008-12, Vol.112 (3), p.569-573

2008

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Microarray-based detection of Korean-specific BRCA1 mutations

Analytical and bioanalytical chemistry, 2008-05, Vol.391 (1), p.405-413

2008

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PALB2 mutations 1592delT and 229delT are not present in Korean breast cancer patients negative for BRCA1 and BRCA2 mutations

Breast cancer research and treatment, 2010-07, Vol.122 (1), p.303-306

2010

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PHEX gene mutations and genotype-phenotype analysis of Korean patients with hypophosphatemic rickets

Journal of Korean Medical Science, 2007, 22(6), , pp.981-986

2007

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Genetic Polymorphism of FLG in Korean Ichthyosis Vulgaris Patients

Annals of Dermatology, 2011, 23(2), , pp.170-176

2011

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Genomic and transcriptomic profiles associated with response to eribulin and nivolumab combination in HER-2-negative metastatic breast cancer

Cancer Immunology, Immunotherapy : CII, 2024-08, Vol.73 (10), p.197, Article 197

2024

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Electrochemical detection of DNA mutations on a PNA-modified electrode utilizing a single-stranded DNA specific endonuclease

Chemical communications (Cambridge, England), 2011-06, Vol.47 (23), p.6611-6613

2011

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Genetic Polymorphism of FLG in Korean Ichthyosis Vulgaris Patients

Annals of dermatology, 2011-05, Vol.23 (2), p.170-176

2011

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A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease

PloS one, 2014-10, Vol.9 (10), p.e110292-e110292

2014

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Mutational analysis of KRAS, BRAF, and TP53 genes of ovarian serous carcinomas in Korean women

Yonsei Medical Journal, 2009, 50(2), , pp.266-272

2009

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Minke whale genome and aquatic adaptation in cetaceans

Nature genetics, 2014-01, Vol.46 (1), p.88-92

2014

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Frequency of pathogenic germline mutation in CHEK2, PALB2, MRE11, and RAD50 in patients at high risk for hereditary breast cancer

Gene essentiality for tumour growth influences neoantigen‐directed immunoediting

Colorimetric SNP Genotyping Based on Allele-Specific PCR by Using a Thiol-Labeled Primer

MHC II immunogenicity shapes the neoepitope landscape in human tumors

The c.3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease)

Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer

Mismatch DNA-specific enzymatic cleavage employed in a new method for the electrochemical detection of genetic mutations

BRCA1 and BRCA2 germline mutations in Korean breast cancer patients at high risk of carrying mutations

The CHEK2 1100delC mutation is not present in Korean patients with breast cancer cases tested for BRCA1 and BRCA2 mutation

Microarray-based detection of Korean-specific BRCA1 mutations

PALB2 mutations 1592delT and 229delT are not present in Korean breast cancer patients negative for BRCA1 and BRCA2 mutations

PHEX gene mutations and genotype-phenotype analysis of Korean patients with hypophosphatemic rickets

Genetic Polymorphism of FLG in Korean Ichthyosis Vulgaris Patients

Genomic and transcriptomic profiles associated with response to eribulin and nivolumab combination in HER-2-negative metastatic breast cancer

Electrochemical detection of DNA mutations on a PNA-modified electrode utilizing a single-stranded DNA specific endonuclease

Genetic Polymorphism of FLG in Korean Ichthyosis Vulgaris Patients

A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease

Mutational analysis of KRAS, BRAF, and TP53 genes of ovarian serous carcinomas in Korean women

Minke whale genome and aquatic adaptation in cetaceans

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