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Alana C. Cecchi

University of Texas Health Science Center at Houston

15

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214

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Aortic root dilatation and dilated cardiomyopathy in an adult with Tatton-Brown-Rahman syndrome

2021 American Journal of Medical Genetics Part A
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Association of de novo RNF213 Variants with Childhood Onset Moyamoya Disease and Diffuse Occlusive Vasculopathy.

2021 Neurology
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Update on the genetic risk for thoracic aortic aneurysms and acute aortic dissections: implications for clinical care.

2021 Journal of Cardiovascular Surgery
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Sex Differences in Proximal Thoracic Aortic Disease Pathology: A Call to Action

2021 American Journal of Clinical Pathology
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Abstract 53: Missense Pathogenic Variants in ANO1 Predispose to Moyamoya Disease

2020 Stroke
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Abstract 140: Heterozygous Missense Mutations in PLEKHO2 Predispose to Thoracic Aortic Aneurysms and Dissections

2019 Arteriosclerosis, Thrombosis, and Vascular Biology
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Molecular diagnosis in vascular Ehlers-Danlos syndrome predicts pattern of arterial involvement and outcomes

2014 Journal of Vascular Surgery
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Missense mutations in FBN1 exons 41 and 42 cause Weill–Marchesani syndrome with thoracic aortic disease and Marfan syndrome

2013 American Journal of Medical Genetics Part A
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Citations (28)