Publications:

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: rs42398

PubMed Link: 32879140

Variant Present in the following documents:

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

View BVdb publication page

Comparative and Functional Genomic Resource for Mechanistic Studies of Human Blood Pressure-Associated Single Nucleotide Polymorphisms.

Hypertension (Dallas, Tex. : 1979)

Mishra, Manoj K MK; Liang, Eugene Y EY; Geurts, Aron M AM; Auer, Paul W L PWL; Liu, Pengyuan P; Rao, Sridhar S; Greene, Andrew S AS; Liang, Mingyu M; Liu, Yong Y

Publication Date: 2020-03

Variant appearance in text: rs42398

PubMed Link: 31902252

Variant Present in the following documents:

• Main text

View BVdb publication page

Gene Variation of Endoplasmic Reticulum Aminopeptidases 1 and 2, and Risk of Blood Pressure Progression and Incident Hypertension among 17,255 Initially Healthy Women.

International Journal Of Genomics

Zee, Robert Y L RYL; Rivera, Alicia A; Inostroza, Yaritza Y; Ridker, Paul M PM; Chasman, Daniel I DI; Romero, Jose R JR

Publication Date: 2018

Variant appearance in text: rs42398

PubMed Link: 29850473

Variant Present in the following documents:

• Main text
• IJG2018-2308585.pdf

View BVdb publication page

Identification of QTL genes for BMD variation using both linkage and gene-based association approaches.

Human Genetics

Li, Gloria Hoi-Yee GH; Cheung, Ching-Lung CL; Xiao, Su-Mei SM; Lau, Kam-Shing KS; Gao, Yi Y; Bow, Cora H CH; Huang, Qing-Yang QY; Sham, Pak-Chung PC; Kung, Annie Wai-Chee AW

Publication Date: 2011-10

Variant appearance in text: rs42398

PubMed Link: 21424381

Variant Present in the following documents:

• Main text
• 439_2011_Article_972.pdf

View BVdb publication page

SNPs in CAST are associated with Parkinson disease: a confirmation study.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics

Allen, Andrew S AS; Satten, Glen A GA

Publication Date: 2010-06-05

Variant appearance in text: rs42398

PubMed Link: 20127884

Variant Present in the following documents:

• Main text

View BVdb publication page