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American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.European Journal of Epidemiology|May 9, 2020
Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthoodYan Zheng, Tao Huang, Tiange Wang, et al.Nature|January 18, 2023
FinnGen provides genetic insights from a well-phenotyped isolated populationMitja I Kurki, Juha Karjalainen, Priit Palta, et al.American Journal of Human Genetics|February 14, 2012
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes lociRicha Saxena, Clara C Elbers, Yiran Guo, et al.Pageof 8