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SHAINE MORRIS to Male

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This is a "connection" page, showing publications SHAINE MORRIS has written about Male.
SHAINE MORRIS
Connection Strength
0.841
Male
  1. Mitral annular disjunction and its progression during childhood in Marfan syndrome. Eur Heart J Cardiovasc Imaging. 2024 Aug 26; 25(9):1306-1314.
    View in: PubMed
    Score: 0.039
  2. Evidence of cardiomyopathy associated with Marfan syndrome in children. Heart. 2024 Jun 17; 110(13):887-891.
    View in: PubMed
    Score: 0.039
  3. 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.
    View in: PubMed
    Score: 0.037
  4. Evaluating perinatal and neonatal outcomes among children with vascular Ehlers-Danlos syndrome. Genet Med. 2022 10; 24(10):2134-2143.
    View in: PubMed
    Score: 0.034
  5. Hospital Outcomes Among Infants With Interrupted Aortic Arch With Simple and Complex Associated Heart Defects. Am J Cardiol. 2022 03 01; 166:97-106.
    View in: PubMed
    Score: 0.033
  6. Congenital Heart Disease and Myelomeningocele in the Newborn: Prevalence and Mortality. Pediatr Cardiol. 2021 Jun; 42(5):1026-1032.
    View in: PubMed
    Score: 0.031
  7. Intraperitoneal bladder rupture in a young child with vascular Ehlers-Danlos syndrome. Am J Med Genet A. 2021 03; 185(3):841-844.
    View in: PubMed
    Score: 0.030
  8. Trends in Preterm Delivery among Singleton Gestations with Critical Congenital Heart Disease. J Pediatr. 2020 07; 222:28-34.e4.
    View in: PubMed
    Score: 0.029
  9. Trends in Infant Mortality After TAPVR Repair over 18?Years in Texas and Impact of Hospital Surgical Volume. Pediatr Cardiol. 2020 Jan; 41(1):77-87.
    View in: PubMed
    Score: 0.028
  10. Thoracic Aortic, Aortic Valve, and Mitral Valve Surgery in Pediatric and Young Adult Patients With Marfan Syndrome: Characteristics and Outcomes. Semin Thorac Cardiovasc Surg. 2019; 31(4):818-825.
    View in: PubMed
    Score: 0.027
  11. A population-based analysis of mortality in patients with Turner syndrome and hypoplastic left heart syndrome using the Texas Birth Defects Registry. Congenit Heart Dis. 2017 Jan; 12(1):105-112.
    View in: PubMed
    Score: 0.023
  12. Prenatal diagnosis, hospital characteristics, and mortality in transposition of the great arteries. Birth Defects Res A Clin Mol Teratol. 2016 Sep; 106(9):739-48.
    View in: PubMed
    Score: 0.022
  13. Thoracic aortic dissection and rupture in conotruncal cardiac defects: A population-based study. Int J Cardiol. 2015 Apr 01; 184:521-527.
    View in: PubMed
    Score: 0.020
  14. Prenatal diagnosis, birth location, surgical center, and neonatal mortality in infants with hypoplastic left heart syndrome. Circulation. 2014 Jan 21; 129(3):285-92.
    View in: PubMed
    Score: 0.019
  15. Aortic dissection in hospitalized children and young adults: a multiinstitutional study. Congenit Heart Dis. 2014 Jan-Feb; 9(1):54-62.
    View in: PubMed
    Score: 0.018
  16. 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.
    View in: PubMed
    Score: 0.018
  17. 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.
    View in: PubMed
    Score: 0.016
  18. 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.
    View in: PubMed
    Score: 0.010
  19. Mitral Annular Disjunction in Heritable Thoracic Aortic Disease: Insights From the Montalcino Aortic Consortium. J Am Heart Assoc. 2024 Nov 05; 13(21):e036274.
    View in: PubMed
    Score: 0.010
  20. Caught in the Act: A Detailed Analysis of Cardiac Event Monitoring in a Cohort of Pediatric and ACHD Patients. Pacing Clin Electrophysiol. 2024 Dec; 47(12):1593-1603.
    View in: PubMed
    Score: 0.010
  21. Non-coding cause of congenital heart defects: Abnormal RNA splicing with multiple isoforms as a mechanism for heterotaxy. HGG Adv. 2024 Oct 10; 5(4):100353.
    View in: PubMed
    Score: 0.010
  22. 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.
    View in: PubMed
    Score: 0.010
  23. Enhancing the Classification of Congenital Heart Defects for Outcome Association Studies in Birth Defects Registries. Birth Defects Res. 2024 Aug; 116(8):e2393.
    View in: PubMed
    Score: 0.010
  24. 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.
    View in: PubMed
    Score: 0.010
  25. Abnormal muscle mechanosignaling triggers cardiomyopathy in mice with Marfan syndrome. J Clin Invest. 2014 Mar; 124(3):1329-39.
    View in: PubMed
    Score: 0.009
  26. Natural history of TANGO2 deficiency disorder: Baseline assessment of 73 patients. Genet Med. 2023 04; 25(4):100352.
    View in: PubMed
    Score: 0.009
  27. 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.
    View in: PubMed
    Score: 0.008
  28. Hospital outcomes for pediatric heart transplant recipients undergoing tracheostomy: A multi-institutional analysis. Pediatr Transplant. 2021 May; 25(3):e13904.
    View in: PubMed
    Score: 0.008
  29. Risk Factors for Mortality and Circulatory Outcome Among Neonates Prenatally Diagnosed With Ebstein Anomaly or Tricuspid Valve Dysplasia: A Multicenter Study. J Am Heart Assoc. 2020 11 03; 9(21):e016684.
    View in: PubMed
    Score: 0.008
  30. 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.
    View in: PubMed
    Score: 0.007
  31. US Mortality Attributable to Congenital Heart Disease Across the Lifespan From 1999 Through 2017 Exposes Persistent Racial/Ethnic Disparities. Circulation. 2020 09 22; 142(12):1132-1147.
    View in: PubMed
    Score: 0.007
  32. Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome. J Pediatr. 2020 07; 222:213-220.e5.
    View in: PubMed
    Score: 0.007
  33. Necrotizing Enterocolitis and Associated Mortality in Neonates With Congenital Heart Disease: A Multi-Institutional Study. Pediatr Crit Care Med. 2020 03; 21(3):228-234.
    View in: PubMed
    Score: 0.007
  34. Neurovascular findings in children and young adults with Loeys-Dietz syndromes: Informing recommendations for screening. J Neurol Sci. 2020 Feb 15; 409:116633.
    View in: PubMed
    Score: 0.007
  35. Association of Wolff-Parkinson-White With Left Ventricular Noncompaction Cardiomyopathy in Children. J Card Fail. 2019 Dec; 25(12):1004-1008.
    View in: PubMed
    Score: 0.007
  36. Right Ventricle-Dependent Coronary Circulation: Location of Obstruction Is Associated With Survival. Ann Thorac Surg. 2020 05; 109(5):1480-1487.
    View in: PubMed
    Score: 0.007
  37. Improved 6 Minute Walk Distance and Brain-Type Natriuretic Peptide After Continuous-Flow Ventricular Assist Device Placement in Children. ASAIO J. 2019 Sep/Oct; 65(7):725-730.
    View in: PubMed
    Score: 0.007
  38. Impact of Treatment Modality on Vascular Function in Coarctation of the Aorta: The LOVE - COARCT Study. J Am Heart Assoc. 2019 04 02; 8(7):e011536.
    View in: PubMed
    Score: 0.007
  39. Cervical lymphatic malformations: Prenatal characteristics and ex utero intrapartum treatment. Prenat Diagn. 2019 03; 39(4):287-292.
    View in: PubMed
    Score: 0.007
  40. Serial Strain Analysis Identifies Hypoplastic Left Heart Syndrome Infants at Risk for Cardiac Morbidity and Mortality: A Pilot Study. J Am Soc Echocardiogr. 2019 05; 32(5):643-650.
    View in: PubMed
    Score: 0.007
  41. 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.
    View in: PubMed
    Score: 0.006
  42. Controversy About a High-Risk and Innovative Fetal Cardiac Intervention. Pediatrics. 2018 09; 142(3).
    View in: PubMed
    Score: 0.006
  43. Out-of-pocket medical expenses in severe CHD. Cardiol Young. 2018 Aug; 28(8):1014-1018.
    View in: PubMed
    Score: 0.006
  44. Characteristics and outcomes of children with ductal-dependent congenital heart disease and esophageal atresia/tracheoesophageal fistula: A multi-institutional analysis. Surgery. 2018 04; 163(4):847-853.
    View in: PubMed
    Score: 0.006
  45. 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.
    View in: PubMed
    Score: 0.006
  46. Fatal cardiac arrest in pediatric heart transplant recipients: Query of the UNOS database. Pediatr Transplant. 2018 02; 22(1).
    View in: PubMed
    Score: 0.006
  47. Heterotaxy syndrome and associated arrhythmias in pediatric patients. Heart Rhythm. 2018 04; 15(4):548-554.
    View in: PubMed
    Score: 0.006
  48. Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns. Genome Med. 2017 10 31; 9(1):95.
    View in: PubMed
    Score: 0.006
  49. 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.
    View in: PubMed
    Score: 0.006
  50. Prenatal management of fetal intrapericardial teratoma: a systematic review. Prenat Diagn. 2017 Sep; 37(9):849-863.
    View in: PubMed
    Score: 0.006
  51. 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.
    View in: PubMed
    Score: 0.006
  52. 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.
    View in: PubMed
    Score: 0.006
  53. 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).
    View in: PubMed
    Score: 0.006
  54. Diminished Global Longitudinal Strain Predicts?Late Allograft Failure in Pediatric?Heart Transplant Recipients. JACC Cardiovasc Imaging. 2017 12; 10(12):1529-1531.
    View in: PubMed
    Score: 0.006
  55. International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium). Circ Cardiovasc Genet. 2016 Dec; 9(6):548-558.
    View in: PubMed
    Score: 0.006
  56. The Role of Echocardiography and Intracardiac Exploration in the Evaluation of Candidacy for Biventricular Repair in Patients With Borderline Left Heart Structures. Ann Thorac Surg. 2017 Mar; 103(3):853-861.
    View in: PubMed
    Score: 0.006
  57. Pilot study of chronic maternal hyperoxygenation and effect on aortic and mitral valve annular dimensions in fetuses with left heart hypoplasia. Ultrasound Obstet Gynecol. 2016 Sep; 48(3):365-72.
    View in: PubMed
    Score: 0.006
  58. 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.
    View in: PubMed
    Score: 0.006
  59. 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.
    View in: PubMed
    Score: 0.005
  60. Disrupted nitric oxide signaling due to GUCY1A3 mutations increases risk for moyamoya disease, achalasia and hypertension. Clin Genet. 2016 10; 90(4):351-60.
    View in: PubMed
    Score: 0.005
  61. 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.
    View in: PubMed
    Score: 0.005
  62. Response to Letters Regarding Article "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. 2016 Feb 16; 133(7):e405.
    View in: PubMed
    Score: 0.005
  63. Survival in Children With Down Syndrome Undergoing Single-Ventricle Palliation. Ann Thorac Surg. 2016 May; 101(5):1834-41.
    View in: PubMed
    Score: 0.005
  64. Reassessing Risk Factors in Pediatric Patients With Pacemakers Implanted for Atrioventricular Block: The Impact of Nonsustained Ventricular Tachycardia. J Cardiovasc Electrophysiol. 2016 Apr; 27(4):471-9.
    View in: PubMed
    Score: 0.005
  65. Prostaglandin Availability and Association with Outcomes for Infants with Congenital Heart Disease. Pediatr Cardiol. 2016 Feb; 37(2):338-44.
    View in: PubMed
    Score: 0.005
  66. 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.
    View in: PubMed
    Score: 0.005
  67. 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.
    View in: PubMed
    Score: 0.005
  68. Echocardiographic Parameters of Right Ventricular Diastolic Function in Repaired Tetralogy of Fallot Are Associated with Important Findings on Magnetic Resonance Imaging. Congenit Heart Dis. 2015 May-Jun; 10(3):E113-22.
    View in: PubMed
    Score: 0.005
  69. Pediatric ventricular assist device use as a bridge to transplantation does not affect long-term quality of life. J Thorac Cardiovasc Surg. 2014 Apr; 147(4):1334-43.
    View in: PubMed
    Score: 0.005
  70. Low incidence of arrhythmias in the right ventricular infundibulum sparing approach to tetralogy of Fallot repair. Pediatr Cardiol. 2014 Feb; 35(2):261-9.
    View in: PubMed
    Score: 0.005
  71. Economic and safety implications of introducing fast tracking in congenital heart surgery. Circ Cardiovasc Qual Outcomes. 2013 Mar 01; 6(2):201-7.
    View in: PubMed
    Score: 0.004
  72. Effect of branch pulmonary artery stenosis on right ventricular volume overload in patients with tetralogy of fallot after initial surgical repair. Am J Cardiol. 2013 May 01; 111(9):1355-60.
    View in: PubMed
    Score: 0.004
  73. Verapamil ameliorates clinical, pathologic and biochemical manifestations of experimental chagasic cardiomyopathy in mice. J Am Coll Cardiol. 1989 Sep; 14(3):782-9.
    View in: PubMed
    Score: 0.003
  74. Reforming procedural skills training for pediatric residents: a randomized, interventional trial. Pediatrics. 2009 Aug; 124(2):610-9.
    View in: PubMed
    Score: 0.003
  75. Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q. Am J Med Genet. 1999 Aug 27; 85(5):455-62.
    View in: PubMed
    Score: 0.002
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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.