Lee H, Fernandes M, Lee J, Merino J, Kwak S
Diabetologia. 2025; .
PMID: 40088285
DOI: 10.1007/s00125-025-06403-9.
Moura S, Nasciben L, Ramirez A, Coombs L, Rivero J, Van Booven D
Alzheimers Dement. 2025; 21(2):e70031.
PMID: 40008916
PMC: 11863361.
DOI: 10.1002/alz.70031.
Giugni F, Berry J, Khera A, Shah A, de Lemos J
Circulation. 2024; 150(21):1720-1731.
PMID: 39556656
PMC: 11575940.
DOI: 10.1161/CIRCULATIONAHA.124.070081.
Mitsis A, Khattab E, Christodoulou E, Myrianthopoulos K, Myrianthefs M, Tzikas S
J Clin Med. 2024; 13(21).
PMID: 39518492
PMC: 11545949.
DOI: 10.3390/jcm13216352.
Carreras-Torres R, Galvan-Femenia I, Farre X, Cortes B, Diez-Obrero V, Carreras A
Genome Med. 2024; 16(1):122.
PMID: 39449064
PMC: 11515386.
DOI: 10.1186/s13073-024-01397-2.
Analyses of GWAS signal using GRIN identify additional genes contributing to suicidal behavior.
Sullivan K, Lane M, Cashman M, Miller J, Pavicic M, Walker A
Commun Biol. 2024; 7(1):1360.
PMID: 39433874
PMC: 11494055.
DOI: 10.1038/s42003-024-06943-7.
Exposure to Air Pollutants and Myocardial Infarction Incidence: A UK Biobank Study Exploring Gene-Environment Interaction.
Ma Y, Li D, Cui F, Wang J, Tang L, Yang Y
Environ Health Perspect. 2024; 132(10):107002.
PMID: 39388260
PMC: 11466320.
DOI: 10.1289/EHP14291.
The association between index-year, average, and variability of the triglyceride-glucose index with health outcomes: more than a decade of follow-up in Tehran lipid and glucose study.
Molavizadeh D, Cheraghloo N, Tohidi M, Azizi F, Hadaegh F
Cardiovasc Diabetol. 2024; 23(1):321.
PMID: 39217401
PMC: 11365227.
DOI: 10.1186/s12933-024-02387-9.
Genetic Backgrounds Associated With Stent Thrombosis: A Pilot Study From a Percutaneous Coronary Intervention Registry.
Shoji S, Sawano M, Inohara T, Hiraide T, Ueda I, Suzuki M
JACC Adv. 2024; 2(1):100172.
PMID: 38939036
PMC: 11198226.
DOI: 10.1016/j.jacadv.2022.100172.
Exome sequence analysis identifies rare coding variants associated with a machine learning-based marker for coronary artery disease.
Petrazzini B, Forrest I, Rocheleau G, Vy H, Marquez-Luna C, Duffy A
Nat Genet. 2024; 56(7):1412-1419.
PMID: 38862854
PMC: 11781350.
DOI: 10.1038/s41588-024-01791-x.
MSGene: a multistate model using genetic risk and the electronic health record applied to lifetime risk of coronary artery disease.
Urbut S, Yeung M, Khurshid S, Cho S, Schuermans A, German J
Nat Commun. 2024; 15(1):4884.
PMID: 38849421
PMC: 11161589.
DOI: 10.1038/s41467-024-49296-9.
Genetic Architecture and Clinical Outcomes of Combined Lipid Disturbances.
Gilliland T, Dron J, Selvaraj M, Trinder M, Paruchuri K, Urbut S
Circ Res. 2024; 135(2):265-276.
PMID: 38828614
PMC: 11223949.
DOI: 10.1161/CIRCRESAHA.123.323973.
Convergence of coronary artery disease genes onto endothelial cell programs.
Schnitzler G, Kang H, Fang S, Angom R, Lee-Kim V, Ma X
Nature. 2024; 626(8000):799-807.
PMID: 38326615
PMC: 10921916.
DOI: 10.1038/s41586-024-07022-x.
CCDC92 promotes podocyte injury by regulating PA28α/ABCA1/cholesterol efflux axis in type 2 diabetic mice.
Zuo F, Liu Z, Wang M, Du J, Ding P, Zhang H
Acta Pharmacol Sin. 2024; 45(5):1019-1031.
PMID: 38228909
PMC: 11053164.
DOI: 10.1038/s41401-023-01213-4.
Protein interaction networks in the vasculature prioritize genes and pathways underlying coronary artery disease.
Zhu Q, Hsu Y, Lassen F, MacDonald B, Stead S, Malolepsza E
Commun Biol. 2024; 7(1):87.
PMID: 38216744
PMC: 10786878.
DOI: 10.1038/s42003-023-05705-1.
Somatic and Germline Variants and Coronary Heart Disease in a Chinese Population.
Zhao K, Shen X, Liu H, Lin Z, Li J, Chen S
JAMA Cardiol. 2024; 9(3):233-242.
PMID: 38198131
PMC: 10782380.
DOI: 10.1001/jamacardio.2023.5095.
Genome-wide association studies on coronary artery disease: A systematic review and implications for populations of different ancestries.
Silva S, Nitsch D, Fatumo S
PLoS One. 2023; 18(11):e0294341.
PMID: 38019802
PMC: 10686512.
DOI: 10.1371/journal.pone.0294341.
Vascular dysfunction caused by loss of Brn-3b/POU4F2 transcription factor in aortic vascular smooth muscle cells is linked to deregulation of calcium signalling pathways.
Yogendran V, Mele L, Prysyazhna O, Budhram-Mahadeo V
Cell Death Dis. 2023; 14(11):770.
PMID: 38007517
PMC: 10676411.
DOI: 10.1038/s41419-023-06306-w.
MSGene: Derivation and validation of a multistate model for lifetime risk of coronary artery disease using genetic risk and the electronic health record.
Urbut S, Yeung M, Khurshid S, Cho S, Schuermans A, German J
medRxiv. 2023; .
PMID: 37986972
PMC: 10659503.
DOI: 10.1101/2023.11.08.23298229.
Evolution of the search for a common mechanism of congenital risk of coronary heart disease and type 2 diabetes mellitus in the chromosomal locus 9p21.3.
Benberin V, Karabaeva R, Kulmyrzaeva N, Bigarinova R, Vochshenkova T
Medicine (Baltimore). 2023; 102(41):e35074.
PMID: 37832109
PMC: 10578751.
DOI: 10.1097/MD.0000000000035074.