Publications:

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Association of Inherited Genetic Factors With Drug-Induced Hepatic Damage Among Children With Acute Lymphoblastic Leukemia.

Jama Network Open

Yang, Wenjian W; Karol, Seth E SE; Hoshitsuki, Keito K; Lee, Shawn S; Larsen, Eric C EC; Winick, Naomi N; Carroll, William L WL; Loh, Mignon L ML; Raetz, Elizabeth A EA; Hunger, Stephen P SP; Winter, Stuart S SS; Dunsmore, Kimberly P KP; Devidas, Meenakshi M; Relling, Mary V MV; Yang, Jun J JJ

Publication Date: 2022-12-01

Variant appearance in text: rs6547692

PubMed Link: 36580335

Variant Present in the following documents:

• jamanetwopen-e2248803-s001.pdf

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Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes.

Communications Biology

Lee, Chia-Jung CJ; Chen, Ting-Huei TH; Lim, Aylwin Ming Wee AMW; Chang, Chien-Ching CC; Sie, Jia-Jyun JJ; Chen, Pei-Lung PL; Chang, Su-Wei SW; Wu, Shang-Jung SJ; Hsu, Chia-Lin CL; Hsieh, Ai-Ru AR; Yang, Wei-Shiung WS; Fann, Cathy S J CSJ

Publication Date: 2022-11-03

Variant appearance in text: rs6547692

PubMed Link: 36329257

Variant Present in the following documents:

• Main text
• 42003_2022_Article_4168.pdf
• 42003_2022_4168_MOESM1_ESM.pdf

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Additive genetic effect of GCKR, G6PC2, and SLC30A8 variants on fasting glucose levels and risk of type 2 diabetes.

Plos One

Chen, Guanjie G; Shriner, Daniel D; Zhang, Jianhua J; Zhou, Jie J; Adikaram, Poorni P; Doumatey, Ayo P AP; Bentley, Amy R AR; Adeyemo, Adebowale A; Rotimi, Charles N CN

Publication Date: 2022

Variant appearance in text: rs6547692

PubMed Link: 35657990

Variant Present in the following documents:

• pone.0269378.s010.xlsx, sheet 1

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Pleiotropic Effects of Common and Rare GCKR Exonic Mutations on Cardiometabolic Traits.

Genes

Yeh, Kuan-Hung KH; Hsu, Lung-An LA; Teng, Ming-Sheng MS; Wu, Semon S; Chou, Hsin-Hua HH; Ko, Yu-Lin YL

Publication Date: 2022-03-10

Variant appearance in text: rs6547692

PubMed Link: 35328045

Variant Present in the following documents:

• genes-13-00491.pdf

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Genetic variants associated with inflammatory bowel disease and gut graft-versus-host disease.

Blood Advances

Martin, Paul J PJ; Storer, Barry E BE; Levine, David M DM; Hansen, John A JA

Publication Date: 2021-11-09

Variant appearance in text: rs6547692

PubMed Link: 34535014

Variant Present in the following documents:

• Main text
• advancesADV2021004959.pdf

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Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology.

Nature Communications

Chen, Vincent L VL; Du, Xiaomeng X; Chen, Yanhua Y; Kuppa, Annapurna A; Handelman, Samuel K SK; Vohnoutka, Rishel B RB; Peyser, Patricia A PA; Palmer, Nicholette D ND; Bielak, Lawrence F LF; Halligan, Brian B; Speliotes, Elizabeth K EK

Publication Date: 2021-02-05

Variant appearance in text: rs6547692

PubMed Link: 33547301

Variant Present in the following documents:

• 41467_2020_20870_MOESM1_ESM.pdf

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Understanding the genetic architecture of the metabolically unhealthy normal weight and metabolically healthy obese phenotypes in a Korean population.

Scientific Reports

Park, Jae-Min JM; Park, Da-Hyun DH; Song, Youhyun Y; Kim, Jung Oh JO; Choi, Ja-Eun JE; Kwon, Yu-Jin YJ; Kim, Seong-Jin SJ; Lee, Ji-Won JW; Hong, Kyung-Won KW

Publication Date: 2021-01-26

Variant appearance in text: rs6547692

PubMed Link: 33500527

Variant Present in the following documents:

• Main text
• 41598_2021_Article_81940.pdf

View BVdb publication page

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Genetics of 35 blood and urine biomarkers in the UK Biobank.

Nature Genetics

Sinnott-Armstrong, Nasa N; Tanigawa, Yosuke Y; Amar, David D; Mars, Nina N; Benner, Christian C; Aguirre, Matthew M; Venkataraman, Guhan Ram GR; Wainberg, Michael M; Ollila, Hanna M HM; Kiiskinen, Tuomo T; Havulinna, Aki S AS; Pirruccello, James P JP; Qian, Junyang J; Shcherbina, Anna A; , ; Rodriguez, Fatima F; Assimes, Themistocles L TL; Agarwala, Vineeta V; Tibshirani, Robert R; Hastie, Trevor T; Ripatti, Samuli S; Pritchard, Jonathan K JK; Daly, Mark J MJ; Rivas, Manuel A MA

Publication Date: 2021-02

Variant appearance in text: GCKR: 1422+3854G>A; rs6547692

PubMed Link: 33462484

Variant Present in the following documents:

• NIHMS1651539-supplement-2.xlsx, sheet 21

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Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight

Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL

Publication Date: 2020-09-03

Variant appearance in text: rs6547692

PubMed Link: 32879140

Variant Present in the following documents:

• jciinsight-5-136477-s105.xlsx, sheet 5

View BVdb publication page

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Phenotypic and Genetic Characterization of Lower LDL Cholesterol and Increased Type 2 Diabetes Risk in the UK Biobank.

Diabetes

Klimentidis, Yann C YC; Arora, Amit A; Newell, Michelle M; Zhou, Jin J; Ordovas, Jose M JM; Renquist, Benjamin J BJ; Wood, Alexis C AC

Publication Date: 2020-10

Variant appearance in text: rs6547692

PubMed Link: 32493714

Variant Present in the following documents:

• Main text
• db191134.pdf

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Multiple Membrane Transporters and Some Immune Regulatory Genes are Major Genetic Factors to Gout.

The Open Rheumatology Journal

Zhu, Weifeng W; Deng, Yan Y; Zhou, Xiaodong X

Publication Date: 2018

Variant appearance in text: rs6547692

PubMed Link: 30123371

Variant Present in the following documents:

• Main text
• TORJ-12-94.pdf

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Replication of Gout/Urate Concentrations GWAS Susceptibility Loci Associated with Gout in a Han Chinese Population.

Scientific Reports

Li, Zhiqiang Z; Zhou, Zhaowei Z; Hou, Xu X; Lu, Dajiang D; Yuan, Xuan X; Lu, Jie J; Wang, Can C; Han, Lin L; Cui, Lingling L; Liu, Zhen Z; Chen, Jianhua J; Cheng, Xiaoyu X; Zhang, Keke K; Ji, Jue J; Jia, Zhaotong Z; Ma, Lidan L; Xin, Ying Y; Liu, Tian T; Yu, Qing Q; Ren, Wei W; Wang, Xuefeng X; Li, Xinde X; Mi, Qing-Sheng QS; Shi, Yongyong Y; Li, Changgui C

Publication Date: 2017-06-22

Variant appearance in text: rs6547692

PubMed Link: 28642574

Variant Present in the following documents:

• Main text
• 41598_2017_Article_4127.pdf

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Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes.

Annals Of The Rheumatic Diseases

Matsuo, Hirotaka H; Yamamoto, Ken K; Nakaoka, Hirofumi H; Nakayama, Akiyoshi A; Sakiyama, Masayuki M; Chiba, Toshinori T; Takahashi, Atsushi A; Nakamura, Takahiro T; Nakashima, Hiroshi H; Takada, Yuzo Y; Danjoh, Inaho I; Shimizu, Seiko S; Abe, Junko J; Kawamura, Yusuke Y; Terashige, Sho S; Ogata, Hiraku H; Tatsukawa, Seishiro S; Yin, Guang G; Okada, Rieko R; Morita, Emi E; Naito, Mariko M; Tokumasu, Atsumi A; Onoue, Hiroyuki H; Iwaya, Keiichi K; Ito, Toshimitsu T; Takada, Tappei T; Inoue, Katsuhisa K; Kato, Yukio Y; Nakamura, Yukio Y; Sakurai, Yutaka Y; Suzuki, Hiroshi H; Kanai, Yoshikatsu Y; Hosoya, Tatsuo T; Hamajima, Nobuyuki N; Inoue, Ituro I; Kubo, Michiaki M; Ichida, Kimiyoshi K; Ooyama, Hiroshi H; Shimizu, Toru T; Shinomiya, Nariyoshi N

Publication Date: 2016-04

Variant appearance in text: rs6547692

PubMed Link: 25646370

Variant Present in the following documents:

• annrheumdis-2014-206191-s1.pdf

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