SHAINE MORRIS to Adult
This is a "connection" page, showing publications SHAINE MORRIS has written about Adult.
Connection Strength
0.733
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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: 0.054
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Vertebral Tortuosity Is Associated With Increased Rate of Cardiovascular Events in Vascular Ehlers-Danlos Syndrome. J Am Heart Assoc. 2023 10 03; 12(19):e029518.
Score: 0.053
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Evaluating Variation in the Cardiac Management of Children with Hereditary Thoracic Aortic Disease in the United States. Pediatr Cardiol. 2024 Jan; 45(1):133-142.
Score: 0.053
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Aortic tortuosity in Turner syndrome is associated with larger ascending aorta. Int J Cardiovasc Imaging. 2022 Nov; 38(11):2479-2490.
Score: 0.048
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Intraperitoneal bladder rupture in a young child with vascular Ehlers-Danlos syndrome. Am J Med Genet A. 2021 03; 185(3):841-844.
Score: 0.043
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Idiopathic congenital right atrial dilation: Fetal presentation. J Clin Ultrasound. 2018 Oct; 46(8):553-554.
Score: 0.036
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Thoracic aortic dissection and rupture in conotruncal cardiac defects: A population-based study. Int J Cardiol. 2015 Apr 01; 184:521-527.
Score: 0.029
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Prenatal diagnosis, birth location, surgical center, and neonatal mortality in infants with hypoplastic left heart syndrome. Circulation. 2014 Jan 21; 129(3):285-92.
Score: 0.026
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Aortic dissection in hospitalized children and young adults: a multiinstitutional study. Congenit Heart Dis. 2014 Jan-Feb; 9(1):54-62.
Score: 0.026
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Impact of obesity on ventricular size and function in children, adolescents and adults with Tetralogy of Fallot after initial repair. Am J Cardiol. 2013 Aug 15; 112(4):594-8.
Score: 0.026
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Increased vertebral artery tortuosity index is associated with adverse outcomes in children and young adults with connective tissue disorders. Circulation. 2011 Jul 26; 124(4):388-96.
Score: 0.023
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Aortic and arterial manifestations and clinical features in TGFB3-related heritable thoracic aortic disease: results from the Montalcino Aortic Consortium. J Med Genet. 2025 Jan 27; 62(2):82-88.
Score: 0.014
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Mitral Annular Disjunction in Heritable Thoracic Aortic Disease: Insights From the Montalcino Aortic Consortium. J Am Heart Assoc. 2024 Nov 05; 13(21):e036274.
Score: 0.014
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Caught in the Act: A Detailed Analysis of Cardiac Event Monitoring in a Cohort of Pediatric and ACHD Patients. Pacing Clin Electrophysiol. 2024 12; 47(12):1593-1603.
Score: 0.014
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Whole-exome sequencing uncovers the genetic complexity of bicuspid aortic valve in families with early-onset complications. Am J Hum Genet. 2024 Oct 03; 111(10):2219-2231.
Score: 0.014
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Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016-2023). Am J Med Genet A. 2024 Oct; 194(10):e63638.
Score: 0.014
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Abnormal muscle mechanosignaling triggers cardiomyopathy in mice with Marfan syndrome. J Clin Invest. 2014 Mar; 124(3):1329-39.
Score: 0.014
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Fetal Diagnosis of Supravalvular Aortic Stenosis and Pulmonary Stenosis in a Family with Non-Syndromic Elastin Mutation. Pediatr Cardiol. 2024 Jun; 45(5):1154-1156.
Score: 0.013
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Abnormal Left Ventricular Strain Correlates with Left Ventricular Dysfunction but not Aortic Pathology in Marfan Syndrome in Children. Pediatr Cardiol. 2023 Oct; 44(7):1536-1545.
Score: 0.013
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Atypical infiltrates on endomyocardial biopsy are associated with adverse outcomes in pediatric heart transplantation. J Heart Lung Transplant. 2023 12; 42(12):1743-1752.
Score: 0.013
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Lesion-specific mortality due to congenital heart disease in U.S. adults from 1999 to 2017. Birth Defects Res. 2022 08 01; 114(13):725-745.
Score: 0.012
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The first reported case of Loeys-Dietz syndrome in a patient with biallelic SMAD3 variants. Am J Med Genet A. 2020 11; 182(11):2755-2760.
Score: 0.011
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Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome. J Pediatr. 2020 07; 222:213-220.e5.
Score: 0.011
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The influence of an Urgent Care Center on the frequency of ED visits in an urban hospital setting. Am J Emerg Med. 2000 Mar; 18(2):123-5.
Score: 0.010
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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: 0.010
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Thulium laser-assisted atrial septal stent placement: first use in fetal hypoplastic left heart syndrome and intact atrial septum. Ultrasound Obstet Gynecol. 2019 Mar; 53(3):417-418.
Score: 0.010
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Cervical lymphatic malformations: Prenatal characteristics and ex utero intrapartum treatment. Prenat Diagn. 2019 03; 39(4):287-292.
Score: 0.010
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Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations. Genet Med. 2018 10; 20(10):1206-1215.
Score: 0.009
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Allometric considerations when assessing aortic aneurysms in Turner syndrome: Implications for activity recommendations and medical decision-making. Am J Med Genet A. 2018 Feb; 176(2):277-282.
Score: 0.009
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Bicuspid and unicuspid aortic valves: Different phenotypes of the same disease? Insight from the GenTAC Registry. Congenit Heart Dis. 2017 Dec; 12(6):740-745.
Score: 0.009
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Aortic Dilatation Associated With Bicuspid Aortic Valve: Relation to Sex, Hemodynamics, and Valve Morphology (the National Heart Lung and Blood Institute-Sponsored National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions). Am J Cardiol. 2017 Oct 01; 120(7):1171-1175.
Score: 0.009
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Assessment of large copy number variants in patients with apparently isolated congenital left-sided cardiac lesions reveals clinically relevant genomic events. Am J Med Genet A. 2017 Aug; 173(8):2176-2188.
Score: 0.009
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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: 0.008
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Aortic Complications Associated With Pregnancy in Marfan Syndrome: The NHLBI National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC). J Am Heart Assoc. 2016 08 11; 5(8).
Score: 0.008
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Echocardiographic Parameters and Outcomes in Primary Fetal Cardiomyopathy. J Ultrasound Med. 2016 Sep; 35(9):1949-55.
Score: 0.008
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Aortic Dissection in Patients With Genetically Mediated Aneurysms: Incidence and Predictors in the GenTAC Registry. J Am Coll Cardiol. 2016 06 14; 67(23):2744-2754.
Score: 0.008
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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: 0.008
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The Need for Standardized Methods for Measuring the Aorta: Multimodality Core Lab Experience From the GenTAC Registry. JACC Cardiovasc Imaging. 2016 Mar; 9(3):219-26.
Score: 0.008
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Segmental Aortic Stiffness in Children and Young Adults With Connective Tissue Disorders: Relationships With Age, Aortic Size, Rate of Dilation, and Surgical Root Replacement. Circulation. 2015 Aug 18; 132(7):595-602.
Score: 0.007
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Outcomes and Predictors of Perinatal Mortality in Fetuses With Ebstein Anomaly or Tricuspid Valve Dysplasia in the Current Era: A Multicenter Study. Circulation. 2015 Aug 11; 132(6):481-9.
Score: 0.007
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Low incidence of arrhythmias in the right ventricular infundibulum sparing approach to tetralogy of Fallot repair. Pediatr Cardiol. 2014 Feb; 35(2):261-9.
Score: 0.007
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Reforming procedural skills training for pediatric residents: a randomized, interventional trial. Pediatrics. 2009 Aug; 124(2):610-9.
Score: 0.005
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Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q. Am J Med Genet. 1999 Aug 27; 85(5):455-62.
Score: 0.002