Publications:

Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass.

Nature Communications

Khurshid, Shaan S; Lazarte, Julieta J; Pirruccello, James P JP; Weng, Lu-Chen LC; Choi, Seung Hoan SH; Hall, Amelia W AW; Wang, Xin X; Friedman, Samuel F SF; Nauffal, Victor V; Biddinger, Kiran J KJ; Aragam, Krishna G KG; Batra, Puneet P; Ho, Jennifer E JE; Philippakis, Anthony A AA; Ellinor, Patrick T PT; Lubitz, Steven A SA

Publication Date: 2023-03-21

Variant appearance in text: rs199501

PubMed Link: 36944631

Variant Present in the following documents:

• Main text
• 41467_2023_Article_37173.pdf
• 41467_2023_37173_MOESM2_ESM.pdf
• 41467_2023_37173_MOESM1_ESM.pdf

View BVdb publication page

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: rs199501

PubMed Link: 32879140

Variant Present in the following documents:

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

View BVdb publication page

A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank.

Nature Communications

Shen, Xueyi X; Howard, David M DM; Adams, Mark J MJ; Hill, W David WD; Clarke, Toni-Kim TK; , ; Deary, Ian J IJ; Whalley, Heather C HC; McIntosh, Andrew M AM

Publication Date: 2020-05-08

Variant appearance in text: rs199501

PubMed Link: 32385265

Variant Present in the following documents:

• 41467_2020_16022_MOESM17_ESM.pdf

View BVdb publication page

Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate.

Human Molecular Genetics

Chiquet, Brett T BT; Blanton, Susan H SH; Burt, Amber A; Ma, Deqiong D; Stal, Samuel S; Mulliken, John B JB; Hecht, Jacqueline T JT

Publication Date: 2008-07-15

Variant appearance in text: rs199501

PubMed Link: 18413325

Variant Present in the following documents:

• Main text

View BVdb publication page