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Spontaneous Coronary Artery Dissection: Current State of the Science: A Scientific Statement From the American Heart Association

Circulation (New York, N.Y.), 2018-05, Vol.137 (19), p.e523-e557

2018

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mtPGS: Leverage multiple correlated traits for accurate polygenic score construction

American journal of human genetics, 2023-10, Vol.110 (10), p.1673-1689

2023

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Letter to the Editor Regarding Lavanya et al. A patient with a novel pathogenic variant in COL5A1 exhibiting prominent vascular and cardiac features

American journal of medical genetics. Part A, 2022-09, Vol.188 (9), p.2832-2833

2022

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Canadian spontaneous coronary artery dissection cohort study: in-hospital and 30-day outcomes

European heart journal, 2019-04, Vol.40 (15), p.1188-1197

2019

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From Atherosclerosis to Spontaneous Coronary Artery Dissection: Defining a Clinical and Genetic Risk Spectrum for Myocardial Infarction

Current atherosclerosis reports, 2024-07, Vol.26 (7), p.331-340

2024

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Differences in Demographics and Outcomes Between Men and Women With Spontaneous Coronary Artery Dissection

JACC. Cardiovascular interventions, 2022-10, Vol.15 (20), p.2052-2061

2022

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The in vivo endothelial cell translatome is highly heterogeneous across vascular beds

Proceedings of the National Academy of Sciences - PNAS, 2019-11, Vol.116 (47), p.23618-23624

2019

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FMD and SCAD: Sex-Biased Arterial Diseases With Clinical and Genetic Pleiotropy

Circulation research, 2021-06, Vol.128 (12), p.1958-1972

2021

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Sex-specific genetic architecture of blood pressure

Nature medicine, 2024-03, Vol.30 (3), p.818

2024

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SARS-CoV-2 Spike Protein S1-Mediated Endothelial Injury and Pro-Inflammatory State Is Amplified by Dihydrotestosterone and Prevented by Mineralocorticoid Antagonism

Viruses, 2021-11, Vol.13 (11), p.2209

2021

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Advancements in the Genetics of Spontaneous Coronary Artery Dissection

Current cardiology reports, 2023-12, Vol.25 (12), p.1735-1743

2023

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IFN-γ and TNF-α synergism may provide a link between psoriasis and inflammatory atherogenesis

Scientific reports, 2017-10, Vol.7 (1), p.13831-11, Article 13831

2017

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Canadian Spontaneous Coronary Artery Dissection Cohort Study: 3-Year Outcomes

Journal of the American College of Cardiology, 2022-10, Vol.80 (17), p.1585-1597

2022

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Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve

Nature communications, 2017-05, Vol.8 (1), p.15481-10, Article 15481

2017

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Lysyl oxidase interactions with transforming growth factor‐β during angiogenesis are mediated by endothelin 1

The FASEB journal, 2021-09, Vol.35 (9), p.e21824-n/a

2021

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Histologic and morphologic character of pediatric renal artery occlusive disease

Journal of vascular surgery, 2021-01, Vol.73 (1), p.161-171

2021

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Histologic and morphologic character of pediatric abdominal aortic developmental coarctation and hypoplasia

Journal of vascular surgery, 2022-08, Vol.76 (2), p.556-563.e4

2022

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Imputation of Exome Sequence Variants into Population-Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project

American journal of human genetics, 2012-11, Vol.91 (5), p.794-808

2012

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Placental transcriptome analysis of hypertensive pregnancies identifies distinct gene expression profiles of preeclampsia superimposed on chronic hypertension

BMC medical genomics, 2023-05, Vol.16 (1), p.91-91, Article 91

2023

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Loss-of-Function Mutations in YY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like Vascular Disease

American journal of human genetics, 2017-01, Vol.100 (1), p.21-30

2017

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Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease

Nature genetics, 2017-12, Vol.49 (12), p.1722

2017

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Spontaneous Coronary Artery Dissection: Current State of the Science: A Scientific Statement From the American Heart Association

mtPGS: Leverage multiple correlated traits for accurate polygenic score construction

PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance

Letter to the Editor Regarding Lavanya et al. A patient with a novel pathogenic variant in COL5A1 exhibiting prominent vascular and cardiac features

First international consensus on the diagnosis and management of fibromuscular dysplasia

Canadian spontaneous coronary artery dissection cohort study: in-hospital and 30-day outcomes

From Atherosclerosis to Spontaneous Coronary Artery Dissection: Defining a Clinical and Genetic Risk Spectrum for Myocardial Infarction

Differences in Demographics and Outcomes Between Men and Women With Spontaneous Coronary Artery Dissection

The in vivo endothelial cell translatome is highly heterogeneous across vascular beds

FMD and SCAD: Sex-Biased Arterial Diseases With Clinical and Genetic Pleiotropy

Sex-specific genetic architecture of blood pressure

SARS-CoV-2 Spike Protein S1-Mediated Endothelial Injury and Pro-Inflammatory State Is Amplified by Dihydrotestosterone and Prevented by Mineralocorticoid Antagonism

Advancements in the Genetics of Spontaneous Coronary Artery Dissection

IFN-γ and TNF-α synergism may provide a link between psoriasis and inflammatory atherogenesis

Canadian Spontaneous Coronary Artery Dissection Cohort Study: 3-Year Outcomes

Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve

Lysyl oxidase interactions with transforming growth factor‐β during angiogenesis are mediated by endothelin 1

Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk

Histologic and morphologic character of pediatric renal artery occlusive disease

Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia

Histologic and morphologic character of pediatric abdominal aortic developmental coarctation and hypoplasia

Imputation of Exome Sequence Variants into Population-Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project

Placental transcriptome analysis of hypertensive pregnancies identifies distinct gene expression profiles of preeclampsia superimposed on chronic hypertension

Loss-of-Function Mutations in YY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like Vascular Disease

Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease

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