CELF4 c.286+7074T>C

Variant ID: 18-35138245-A-G

NM_020180.3(CELF4):c.286+7074T>C

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Shared Genetics and Causality Between Decaffeinated Coffee Consumption and Neuropsychiatric Diseases: A Large-Scale Genome-Wide Cross-Trait Analysis and Mendelian Randomization Analysis.

Frontiers In Psychiatry
Yin, Bian B; Wang, Xinpei X; Huang, Tao T; Jia, Jinzhu J
Publication Date: 2022

Variant appearance in text: rs12967855
PubMed Link: 35898629
Variant Present in the following documents:
  • Main text
  • fpsyt-13-910432.pdf
View BVdb publication page



Major depression disorder may causally associate with the increased breast cancer risk: Evidence from two-sample mendelian randomization analyses.

Cancer Medicine
Ren, Qian Q; Luo, Fangxiu F; Ge, Sheng S; Chen, Peizhan P
Publication Date: 2022-07-19

Variant appearance in text: rs12967855
PubMed Link: 35852181
Variant Present in the following documents:
  • Main text
View BVdb publication page



Depression and Osteoporosis: A Mendelian Randomization Study.

Calcified Tissue International
He, Bin B; Lyu, Qiong Q; Yin, Lifeng L; Zhang, Muzi M; Quan, Zhengxue Z; Ou, Yunsheng Y
Publication Date: 2021-12

Variant appearance in text: rs12967855
PubMed Link: 34259888
Variant Present in the following documents:
  • Main text
  • 223_2021_Article_886.pdf
View BVdb publication page



Smoking and heart failure: a Mendelian randomization and mediation analysis.

Esc Heart Failure
Lu, Yunlong Y; Xu, Zhouming Z; Georgakis, Marios K MK; Wang, Zhen Z; Lin, Hefeng H; Zheng, Liangrong L
Publication Date: 2021-06

Variant appearance in text: rs12967855
PubMed Link: 33656795
Variant Present in the following documents:
  • EHF2-8-1954-s001.pdf
View BVdb publication page



Lifetime Smoking and Asthma: A Mendelian Randomization Study.

Frontiers In Genetics
Shen, Ming M; Liu, Xin X; Li, Guoqi G; Li, Zhun Z; Zhou, Hongyu H
Publication Date: 2020

Variant appearance in text: rs12967855
PubMed Link: 32903690
Variant Present in the following documents:
  • Main text
  • fgene-11-00769.pdf
View BVdb publication page