Publications:

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Integrative proteogenomic characterization of early esophageal cancer.

Nature Communications

Li, Lingling L; Jiang, Dongxian D; Zhang, Qiao Q; Liu, Hui H; Xu, Fujiang F; Guo, Chunmei C; Qin, Zhaoyu Z; Wang, Haixing H; Feng, Jinwen J; Liu, Yang Y; Chen, Weijie W; Zhang, Xue X; Bai, Lin L; Tian, Sha S; Tan, Subei S; Xu, Chen C; Song, Qi Q; Liu, Yalan Y; Zhong, Yunshi Y; Chen, Tianyin T; Zhou, Pinghong P; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C

Publication Date: 2023-03-25

Variant appearance in text: rs3825017

PubMed Link: 36966136

Variant Present in the following documents:

• 41467_2023_37440_MOESM4_ESM.xlsx, sheet 2

View BVdb publication page

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The impact of an URAT1 polymorphism on the losartan treatment of hypertension and hyperuricemia.

Journal Of Clinical Laboratory Analysis

Wu, Liting L; Fan, Yingchao Y; Wang, Yuan Y; Li, Zhumeng Z; Mao, Delong D; Zhuang, Wenfang W

Publication Date: 2021-10

Variant appearance in text: rs3825017

PubMed Link: 34498315

Variant Present in the following documents:

• Main text
• JCLA-35-e23949.pdf

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Urate Transporters in the Kidney: What Clinicians Need to Know.

Electrolyte & Blood Pressure : E & Bp

Chung, Sungjin S; Kim, Gheun-Ho GH

Publication Date: 2021-06

Variant appearance in text: rs3825017

PubMed Link: 34290818

Variant Present in the following documents:

• Main text
• ebp-19-1.pdf

View BVdb publication page

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Cohort profile: the Ewha Birth and Growth Study.

Epidemiology And Health

Lee, Hye Ah HA; Park, Bohyun B; Min, Jungwon J; Choi, Eun Jeong EJ; Kim, Ui Jeong UJ; Park, Hyun Jin HJ; Park, Eun Ae EA; Cho, Su Jin SJ; Kim, Hae Soon HS; Lee, Hwayoung H; Kim, Young Ju YJ; Hong, Young Sun YS; Kim, Eui-Jung EJ; Ha, Eun Hee EH; Park, Hyesook H

Publication Date: 2021

Variant appearance in text: rs3825017

PubMed Link: 33677859

Variant Present in the following documents:

• Main text
• epih-43-e2021016.pdf

View BVdb publication page

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Regulation of organic anion transporters: Role in physiology, pathophysiology, and drug elimination.

Pharmacology & Therapeutics

Zhang, Jinghui J; Wang, Haoxun H; Fan, Yunzhou Y; Yu, Zhou Z; You, Guofeng G

Publication Date: 2021-01

Variant appearance in text: rs3825017

PubMed Link: 32758646

Variant Present in the following documents:

• Main text

View BVdb publication page

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Contribution of Rare Variants of the SLC22A12 Gene to the Missing Heritability of Serum Urate Levels.

Genetics

Misawa, Kazuharu K; Hasegawa, Takanori T; Mishima, Eikan E; Jutabha, Promsuk P; Ouchi, Motoshi M; Kojima, Kaname K; Kawai, Yosuke Y; Matsuo, Masafumi M; Anzai, Naohiko N; Nagasaki, Masao M

Publication Date: 2020-04

Variant appearance in text: rs3825017

PubMed Link: 32005656

Variant Present in the following documents:

• 1079.pdf

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Multiple genetic mutations caused by NKX6.3 depletion contribute to gastric tumorigenesis.

Scientific Reports

Yoon, Jung Hwan JH; Kim, Olga O; Eun, Jung Woo JW; Choi, Sung Sook SS; Ashktorab, Hassan H; Smoot, Duane T DT; Nam, Suk Woo SW; Park, Won Sang WS

Publication Date: 2018-12-04

Variant appearance in text: rs3825017

PubMed Link: 30514953

Variant Present in the following documents:

• 41598_2018_35733_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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Long-term effects of the SLC2A9 G844A and SLC22A12 C246T variants on serum uric acid concentrations in children.

Bmc Pediatrics

Lee, Hye Ah HA; Park, Bo Hyun BH; Park, Eun Ae EA; Cho, Su Jin SJ; Kim, Hae Soon HS; Park, Hyesook H

Publication Date: 2018-09-06

Variant appearance in text: rs3825017

PubMed Link: 30189835

Variant Present in the following documents:

• Main text
• 12887_2018_Article_1272.pdf

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Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation

Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H

Publication Date: 2017

Variant appearance in text: rs3825017

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

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