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Frontiers in Genetics|February 21, 2022
Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic LociTiffany R Bellomo, William P Bone, Brian Y Chen, et al.
Nature Medicine|August 22, 2017
A human APOC3 missense variant and monoclonal antibody accelerate apoC-III clearance and lower triglyceride-rich lipoprotein levelsSumeet A Khetarpal, Xuemei Zeng, John S Millar, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 2017
A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I MutationIram Hussain, Nivedita Patni, Masako Ueda, et al.
European Urology|May 28, 2023
Germline Exome Sequencing for Men with Testicular Germ Cell Tumor Reveals Coding Defects in Chromosomal Segregation and Protein-targeting GenesLouise C Pyle, Jung Kim, Jonathan Bradfield, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 28, 2020
Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease-Brief ReportAeron M Small, Jennifer E Huffman, Derek Klarin, et al.
Circulation Research|September 23, 2016
GlycA Is a Novel Biomarker of Inflammation and Subclinical Cardiovascular Disease in PsoriasisAditya A Joshi, Joseph B Lerman, Tsion M Aberra, et al.
European Heart Journal|December 6, 2013
Higher plasma CXCL12 levels predict incident myocardial infarction and death in chronic kidney disease: findings from the Chronic Renal Insufficiency Cohort studyNehal N Mehta, Gregory J Matthews, Parasuram Krishnamoorthy, et al.
Scientific Reports|June 3, 2021
Association of the transthyretin variant V122I with polyneuropathy among individuals of African ancestryMargaret M Parker, Scott M Damrauer, Catherine Tcheandjieu, et al.
Circulation|April 3, 2020
Reduced Apolipoprotein M and Adverse Outcomes Across the Spectrum of Human Heart FailureJulio A Chirinos, Lei Zhao, Yi Jia, et al.
Circulation. Genomic and Precision Medicine|September 1, 2020
Heterozygous ABCG5 Gene Deficiency and Risk of Coronary Artery DiseaseAkihiro Nomura, Connor A Emdin, Hong Hee Won, et al.
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