Patrick Ellinor
Affiliations: | Cardiovascular Research Center | Massachuestts General Hospital |
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Parents
Sign in to add mentor| Richard W. Tsien | grad student | 1995 | Stanford (Neurotree) | |
| (Structural and functional analysis of voltage dependent calcium channels) | ||||
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Publications
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| Lin AE, Bapat AC, Xiao L, et al. (2024) Clonal Hematopoiesis of Indeterminate Potential With Loss of Enhances Risk for Atrial Fibrillation Through Inflammasome Activation. Circulation |
| Raghavan A, Pirruccello JP, Ellinor PT, et al. (2023) Using Genomics to Identify Novel Therapeutic Targets for Aortic Disease. Arteriosclerosis, Thrombosis, and Vascular Biology |
| Arduini A, Fleming SJ, Xiao L, et al. (2023) Transcriptional profile of the rat cardiovascular system at single cell resolution. Biorxiv : the Preprint Server For Biology |
| Schuermans A, Vlasschaert C, Nauffal V, et al. (2023) Clonal haematopoiesis of indeterminate potential predicts incident cardiac arrhythmias. European Heart Journal |
| Wang Y, Selvaraj MS, Li X, et al. (2023) Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study. American Journal of Human Genetics. 110: 1704-1717 |
| Rämö JT, Kany S, Hou CR, et al. (2023) The Cardiovascular Impact and Genetics of Pericardial Adiposity. Medrxiv : the Preprint Server For Health Sciences |
| Jameson HS, Hanley A, Hill MC, et al. (2023) Loss of the Atrial Fibrillation-Related Gene, , Results in Atrial Dilation and Arrhythmias. Circulation Research |
| Wang Y, Selvaraj MS, Li X, et al. (2023) Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study. Medrxiv : the Preprint Server For Health Sciences |
| Einson J, Glinos D, Boerwinkle E, et al. (2023) Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants. Genetics |
| Klarin D, Devineni P, Sendamarai AK, et al. (2023) Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program. Nature Genetics |