A novel missense mutation in the ACTG1 gene in a family with congenital autosomal dominant deafness: A case report

por Lee, Cha Gon, Jang, Jahyeon, Jin, Hyun-Seok
Publicado 2018

Interaction between ALDH2 rs671 and life habits affects the risk of hypertension in Koreans: A STROBE observational study

por Kim, Sung-Soo, Park, Sangjung, Jin, Hyun-Seok
Publicado 2021

Identification of Genetic Markers Linked to The Activity of Indoleamine 2,3-Dioxygenase and Kidney Function

por Kim, Hye-Rim, Jin, Hyun-Seok, Eom, Yong-Bin
Publicado 2023

MYLK and PTGS1 Genetic Variations Associated with Osteoporosis and Benign Breast Tumors in Korean Women

por Cho, Hye-Won, Jin, Hyun-Seok, Eom, Yong-Bin
Publicado 2021

Association of MACROD2 gene variants with obesity and physical activity in a Korean population

por Kim, Hye‐Rim, Jin, Hyun‐Seok, Eom, Yong‐Bin
Publicado 2021

A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans

por Cho, Hye-Won, Jin, Hyun-Seok, Eom, Yong-Bin
Publicado 2021

A Genome-Wide Association Study for Hypertensive Kidney Disease in Korean Men

por Kim, Hye-Rim, Jin, Hyun-Seok, Eom, Yong-Bin
Publicado 2021

Association between MANBA Gene Variants and Chronic Kidney Disease in a Korean Population

por Kim, Hye-Rim, Jin, Hyun-Seok, Eom, Yong-Bin
Publicado 2021

Metabolite Genome-Wide Association Study for Indoleamine 2,3-Dioxygenase Activity Associated with Chronic Kidney Disease

por Kim, Hye-Rim, Jin, Hyun-Seok, Eom, Yong-Bin
Publicado 2021

FGFRL1 and FGF genes are associated with height, hypertension, and osteoporosis

por Cho, Hye-Won, Jin, Hyun-Seok, Eom, Yong-Bin
Publicado 2022

Identifying Interactions between Dietary Sodium, Potassium, Sodium–Potassium Ratios, and FGF5 rs16998073 Variants and Their Associated Risk for Hypertension in Korean Adults

por Jeong, Hyeyun, Jin, Hyun-Seok, Kim, Sung-Soo, Shin, Dayeon
Publicado 2020

Association Analysis of Reactive Oxygen Species-Hypertension Genes Discovered by Literature Mining

por Lim, Ji Eun, Hong, Kyung-Won, Jin, Hyun-Seok, Oh, Bermseok
Publicado 2012

Dietary Protein and Fat Intake Affects Diabetes Risk with CDKAL1 Genetic Variants in Korean Adults

por Choi, Woo Jeong, Jin, Hyun-Seok, Kim, Sung-Soo, Shin, Dayeon
Publicado 2020

Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans

por Cho, Hye-Won, Ban, Hyo-Jeong, Jin, Hyun-Seok, Cha, Seongwon, Eom, Yong-Bin
Publicado 2023

Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies

por Jin, Hyun-Seok, Kim, Jeonhyun, Kwak, Woori, Jeong, Hyeonsoo, Lim, Gyu-Bin, Lee, Cha Gon
Publicado 2017

Correction: Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies

por Jin, Hyun-Seok, Kim, Jeonghyung, Kwak, Woori, Jeong, Hyeonsoo, Lim, Gyu-Bin, Lee, Cha Gon
Publicado 2017

Interactions with the MC4R rs17782313 variant, mental stress and energy intake and the risk of obesity in Genome Epidemiology Study

por Park, Sunmin, Daily, James W., Zhang, Xin, Jin, Hyun Seok, Lee, Hye Ja, Lee, Yong Hyun
Publicado 2016

Type 2 diabetes genetic association database manually curated for the study design and odds ratio

por Lim, Ji Eun, Hong, Kyung-Won, Jin, Hyun-Seok, Kim, Yang Seok, Park, Hun Kuk, Oh, Bermseok
Publicado 2010

Scopolin Attenuates Osteoporotic Bone Loss in Ovariectomized Mice

por Park, Eunkuk, Kim, Jeonghyun, Jin, Hyun-Seok, Choi, Chun Whan, Choi, Tae Hyun, Choi, Sangho, Huh, Dam, Jeong, Seon-Yong
Publicado 2020

Rapid detection of duplication/deletion of the PMP22 gene in patients with Charcot-Marie-Tooth disease Type 1A and hereditary neuropathy with liability to pressure palsy by real-ti...

por Kim, Sang-Wun, Lee, Kwang-Soo, Jin, Hyun-Seok, Lee, Tae-Mi, Koo, Soo Kyung, Lee, Yong-Jun, Jung, Sung-Chul
Publicado 2003