SHAINE MORRIS to Cohort Studies
This is a "connection" page, showing publications SHAINE MORRIS has written about Cohort Studies.
Connection Strength
0.425
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Mitral annular disjunction and its progression during childhood in Marfan syndrome. Eur Heart J Cardiovasc Imaging. 2024 Aug 26; 25(9):1306-1314.
Score: 0.121
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Labyrinthine cor triatriatum sinister in fetal hypoplastic left heart syndrome is associated with poor outcomes. Prenat Diagn. 2024 06; 44(6-7):758-772.
Score: 0.117
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Impact of Socioeconomic Status, Race and Ethnicity, and Geography on Prenatal Detection of Hypoplastic Left Heart Syndrome and Transposition of the Great Arteries. Circulation. 2021 05 25; 143(21):2049-2060.
Score: 0.024
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Extracardiac Doppler indices predict perinatal mortality in fetuses with Ebstein anomaly and tricuspid valve dysplasia. Prenat Diagn. 2021 02; 41(3):332-340.
Score: 0.024
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Hospital outcomes for pediatric heart transplant recipients undergoing tracheostomy: A multi-institutional analysis. Pediatr Transplant. 2021 May; 25(3):e13904.
Score: 0.023
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Neurovascular findings in children and young adults with Loeys-Dietz syndromes: Informing recommendations for screening. J Neurol Sci. 2020 Feb 15; 409:116633.
Score: 0.022
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Association of Wolff-Parkinson-White With Left Ventricular Noncompaction Cardiomyopathy in Children. J Card Fail. 2019 Dec; 25(12):1004-1008.
Score: 0.022
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Copy Number Variants of Undetermined Significance Are Not Associated with Worse Clinical Outcomes in Hypoplastic Left Heart Syndrome. J Pediatr. 2018 11; 202:206-211.e2.
Score: 0.020
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Associations of Age and Sex With Marfan Phenotype: The National Heart, Lung, and Blood Institute GenTAC (Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions) Registry. Circ Cardiovasc Genet. 2017 Jun; 10(3).
Score: 0.018
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A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20. Hum Mol Genet. 2016 06 01; 25(11):2331-2341.
Score: 0.017
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Disrupted nitric oxide signaling due to GUCY1A3 mutations increases risk for moyamoya disease, achalasia and hypertension. Clin Genet. 2016 10; 90(4):351-60.
Score: 0.017