日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Case Report: Expanding the diagnostic spectrum of non-invasive prenatal testing to structural chromosomal abnormalities

病例报告:将无创产前检测的诊断范围扩展到结构性染色体异常

Kim, Jong Chul; Kim, Hyunjin; Jang, HeeYeon; Go, Minyeon; Park, Ji Eun; Ryu, Chang Soo; Chin, Mi Uk; Kim, Eun Hye; Lee, Young Jin; Shim, Sung Han; Cha, Dong Hyun

Prognostic Associations and Functional Implications of Angiogenesis-Related miRNA Variants in Ischemic Stroke

缺血性卒中中血管生成相关miRNA变异的预后关联和功能意义

Ryu, Chang Soo; Lee, Kee-Ook; Ko, Eun Ju; Park, Hyeon Woo; Lee, Jae Hyun; Kim, Ok Joon; Kim, Nam Keun

Genetic Association of PCSK5 and MUC2 Gene Polymorphisms with Recurrent Pregnancy Loss (RPL)

PCSK5和MUC2基因多态性与复发性流产(RPL)的遗传关联

Ryu, Chang Soo; Kim, Ji Hyang; Ko, Eun Ju; Park, Hyeon Woo; Lee, Jae Hyun; Shin, Ji Eun; Kim, Young Ran; Ahn, Eun Hee; Kim, Nam Keun

Association Study of SPARCL1 Gene Polymorphisms in Ischemic Stroke

SPARCL1基因多态性与缺血性卒中关联研究

Kwak, Seong Shin; Lee, Ki Ook; Ryu, Chang Soo; Ko, Eun Ju; Park, Hyeon Woo; Lee, Jae Hyun; Kim, Ok Joon; Kim, Nam Keun

Discovery of Pathogenic Variants Associated with Idiopathic Recurrent Pregnancy Loss Using Whole-Exome Sequencing

利用全外显子组测序发现与特发性复发性流产相关的致病变异

Lee, Jeong Yong; Moon, JaeWoo; Hu, Hae-Jin; Ryu, Chang Soo; Ko, Eun Ju; Ahn, Eun Hee; Kim, Young Ran; Kim, Ji Hyang; Kim, Nam Keun

Genetic Associations of Plasminogen Activator Inhibitor-1-Related miRNA Variants with Coronary Artery Disease.

纤溶酶原激活物抑制剂-1相关miRNA变异与冠状动脉疾病的遗传关联

Ha Yong Hyun, Sung Jung Hoon, Ryu Chang Soo, Ko Eun Ju, Park Hyeon Woo, Park Han Sung, Kim Ok Joon, Kim In Jai, Kim Nam Keun

Association of Polymorphisms in FSHR, ESR1, and BMP15 with Primary Ovarian Insufficiency and Meta-Analysis

FSHR、ESR1 和 BMP15 多态性与原发性卵巢功能不全的关联及荟萃分析

Lee, Jeong Yong; Kim, Young Ran; Ko, Eun Ju; Ryu, Chang Soo; Kwack, KyuBum; Na, Eun Duc; Shin, Ji Eun; Kim, Ji Hyang; Ahn, Eun Hee; Kim, Nam Keun

Association of Thymidylate Synthase (TS) Gene Polymorphisms with Incidence and Prognosis of Coronary Artery Disease

胸苷酸合成酶(TS)基因多态性与冠状动脉疾病的发生率和预后的关系

Kim, Jung Oh; Ryu, Chang Soo; Lee, Jeong Yong; Ko, Eun Ju; Ha, Yong Hyun; Sung, Jung Hoon; Hwang, Tae Sun; Kim, In Jai; Kim, Nam Keun

Genetic variants of MUC4 are associated with susceptibility to and mortality of colorectal cancer and exhibit synergistic effects with LDL-C levels

MUC4基因变异与结直肠癌的易感性和死亡率相关,并与低密度脂蛋白胆固醇(LDL-C)水平表现出协同效应。

Kwon, Min Jung; Lee, Jeong Yong; Kim, Eo Jin; Ko, Eun Ju; Ryu, Chang Soo; Cho, Hye Jung; Jun, Hak Hoon; Kim, Jong Woo; Kim, Nam Keun

Association of Polymorphisms in FSHR, INHA, ESR1, and BMP15 with Recurrent Implantation Failure

FSHR、INHA、ESR1 和 BMP15 多态性与复发性着床失败的相关性

Ko, Eun-Ju; Shin, Ji-Eun; Lee, Jung-Yong; Ryu, Chang-Soo; Hwang, Ji-Young; Kim, Young-Ran; Ahn, Eun-Hee; Kim, Ji-Hyang; Kim, Nam-Keun