D. Cho

发表

Neonatal Screening Tests for Inherited Metabolic Disorders using Tandem Mass Spectrometry: Experience of a Clinical Laboratory in Korea

Eun Jung Park, S. Cho, D. Seo, 2015 .

Evaluating the results of the Momguard noninvasive prenatal test

Jihun Kim, D. Seo, D. Cho, 2015 .

Genetic Polymorphisms of Selected DNA Repair Genes, Estrogen and Progesterone Receptor Status, and Breast Cancer Risk

D. Noh, Q. Wei, D. Kang, 2005, Clinical Cancer Research.

Usefulness of the Prostate Health Index in Predicting the Presence and Aggressiveness of Prostate Cancer Among Korean Men

H. Kim, Jae-Yoon Kim, L. Sung, 2021 .

Development of HLA-A, -B and -DR Typing Method Using Next-Generation Sequencing

S. Y. Kim, D. Seo, Hyun Ju Lee, 2018, The Korean Journal of Blood Transfusion.

A Novel COMP Gene Mutation in a Korean Kindred with Multiple Epiphyseal Dysplasia

Hyon J. Kim, J. Ko, Kyu-sung Kwack, 2009 .

BRCA1 and BRCA2 germline mutations in Korean patients with sporadic breast cancer

S. Ahn, Jun Suk Kim, Yeul-Hong Kim, 2004, Human mutation.

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

W. Han, D. Noh, S. Ahn, 2007, Cancer letters.

PHEX Gene Mutations and Genotype-Phenotype Analysis of Korean Patients with Hypophosphatemic Rickets

Hae-Ryong Song, J. Yang, H. Yoon, 2007, Journal of Korean medical science.

Genetic Polymorphism of FLG in Korean Ichthyosis Vulgaris Patients.

Mi-Kyung Lee, Y. Yoon, Kapsok Li, 2011, Annals of dermatology.

Large genomic rearrangement of BRCA1 and BRCA2 genes in familial breast cancer patients in Korea

H. Park, S. Ahn, B. Son, 2014, Familial Cancer.

MHC II immunogenicity shapes the neoepitope landscape in human tumors

J. Choi, Suhwan Chang, Hyungjoo Kim, 2023, Nature Genetics.

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

S. Ahn, B. Son, B. Haffty, 2008, Breast Cancer Research and Treatment.

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

S. Ahn, B. Son, B. Haffty, 2010, Breast Cancer Research and Treatment.

Prevalence of BRCA1 and BRCA2 Mutations in Korean Breast Cancer Patients

S. Ahn, B. Son, B. Ko, 2004, Journal of Korean medical science.

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

Dong Yeon Lee, C. Chung, M. Park, 2008, Journal of Human Genetics.

Analysis of BRIP1 Variants among Korean Patients with BRCA1/2 Mutation-Negative High-Risk Breast Cancer

J. Lee, S. Kim, S. Nam, 2016, Cancer research and treatment : official journal of Korean Cancer Association.

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

S. Ahn, Sung-Won Kim, B. Son, 2012, Breast Cancer Research and Treatment.

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

J. Lee, S. Kim, S. Nam, 2016, Breast Cancer Research and Treatment.

Frequency of the CHEK2 1100delC Mutation in Korean Women with Early Onset Breast Cancer

B. Haffty, D. Choi, D. Cho, 2008 .

Prospective clinical evaluation of Momguard non-invasive prenatal test in 1011 Korean high-risk pregnant women

Mi-Young Lee, H. Won, H. Ryu, 2019, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Exome sequencing in a breast cancer family without BRCA mutation

J. Noh, D. Choi, S. Huh, 2015, Radiation oncology journal.

Performance of Momguard, a new non-invasive prenatal testing protocol developed in Korea

Mi-Young Lee, H. Won, Jihun Kim, 2015, Obstetrics & gynecology science.

Clinical Study of Non-Invasive Prenatal Testing Using Next-Generation Sequencing

S. Y. Kim, Jihun Kim, S. Cho, 2015 .

1053 Heterozygous germline mutations in MRE11 among korean patients with high-risk breast cancer negative for BRCA1/2 mutation

Hyung Joon Kim, D. Cho, J. Hue, 2015 .

Heterozygous germline mutations in NBS1 among Korean patients with high-risk breast cancer negative for BRCA1/2 mutation

J. Lee, Sung-Won Kim, Sue-Kyung Park, 2015, Familial Cancer.

Germline Genetic Alterations in Intraductal Papillary Neoplasms Associated with Extrapancreatic Tumors

Jin‐Young Jang, Sun-Whe Kim, Y. Ahn, 2009 .