SHAINE MORRIS

TitleAssociate Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Pediatrics
Address6621 FANNIN
Houston, TX 77030
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    Collapse Biography 
    Collapse education and training
    Stanford University, Stanford, CABS06/1998Biological Sciences
    Univ. of Texas Southwestern Medical School, Dallas, TXMD05/2002Medicine
    Boston Combined Residency Program, Boston, MA06/2005Pediatrics
    Boston Combined Residency Program, Boston, MA06/2006Chief Residency, Pediatrics
    Texas Children's Hospital and Baylor College of Medicine, Houston, TX06/2009Pediatric Cardiology
    Boston Children's Hospital, Boston, MA06/2010Advanced Cardiovascular Imaging
    Harvard School of Public Health, Boston, MAMPH11/2012Clinical Effectiveness
    Collapse awards and honors
    2004Medical Student Teaching Award , Children’s Hospital Boston/Harvard Medical Student Education Committee
    2012Dan McNamara Teaching Award for Outstanding Faculty Educator , Texas Children's Hospital
    2017Dan McNamara Teaching Award for Outstanding Faculty Educator, Texas Children's Hospital
    2015Invited Lectureship: Niland Lecture, for promising junior faculty in Pediatric Cardiology, C.S. Mott Children's Hospital, University of Michigan
    2016Fellow of the American Heart Association
    2018Norton Rose Fulbright Award in Teaching and Mentoring, Baylor College of Medicine

    Collapse Overview 
    Collapse overview
    Clinical interests: Pediatric Aortic Dissection, Marfan Syndrome, Turner Syndrome, Loeys-Dietz Syndrome, Familial Thoracic Aortic aneurysm and Dissection, Bicuspid Aortic Valve, Aortic Dilation
    Fetal Cardiology, Hypoplastic Left Heart Syndrome, Outcomes in Congenital Heart Disease, Population Research, Epidemiology

    Collapse Research 
    Collapse research activities and funding
    R21HL121630     (MORRIS, SHAINE ALAINE)Jul 11, 2014 - Jun 30, 2017
    NIH
    A Biomarker to Predict Cardiovascular Events in Patients with Aortic Dilation
    Role: Principal Investigator

    K23HL127266     (MORRIS, SHAINE ALAINE)Apr 1, 2015 - Mar 31, 2021
    NIH
    Evaluation of an Imaging Biomarker in Children and Young Adults with Aortopathy
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Holmes KW, Markwardt S, Eagle KA, Devereux RB, Weinsaft JW, Asch FM, LeMaire SA, Maslen CL, Song HK, Milewicz DM, Prakash SK, Guo D, Morris SA, Pyeritz RE, Milewski RC, Ravekes WJ, Dietz HC, Shohet RV, Silberbach M, Roman MJ. Cardiovascular Outcomes in Aortopathy: GenTAC Registry of Genetically Triggered Aortic Aneurysms and Related Conditions. J Am Coll Cardiol. 2022 05 31; 79(21):2069-2081. PMID: 35618343.
      Citations:    Fields:    Translation:Humans
    2. Lynn MM, Salemi JL, Meath CJ, Dolgner SJ, Morris SA, Sexson Tejtel SK, Lopez KN. Lesion-specific mortality due to congenital heart disease in U.S. adults from 1999 to 2017. Birth Defects Res. 2022 May 20. PMID: 35593518.
      Citations:    Fields:    
    3. Venardos A, Colquitt J, Morris SA. Fetal growth of left-sided structures and postnatal surgical outcome in borderline left heart varies by cardiac phenotype. Ultrasound Obstet Gynecol. 2022 05; 59(5):642-650. PMID: 33998097.
      Citations:    Fields:    Translation:Humans
    4. Zarate YA, Morris SA, Blackshare A, Algaze CA, Connor BS, Kim AJ, Yutzey KE, Miller EM, Weaver KN, Collins RT. A clinical scoring system for early onset (neonatal) Marfan syndrome. Genet Med. 2022 Apr 13. PMID: 35420547.
      Citations:    Fields:    
    5. Cox KL, Morris SA, Tacy T, Long J, Becker J, Schoppe L, Zhang J, Maskatia SA. Impact of Maternal Hyperoxygenation on Myocardial Deformation and Loading Conditions in Fetuses with and without Left Heart Hypoplasia. J Am Soc Echocardiogr. 2022 Mar 25. PMID: 35346806.
      Citations:    Fields:    
    6. Prablek MA, LoPresti M, Bertot B, Morris SA, Bauer D, Lam S, Ravindra V. Evaluation of cervical spine pathology in children with Loeys-Dietz syndrome. Surg Neurol Int. 2022; 13:96. PMID: 35399906.
      Citations:    
    7. Alali A, Acosta S, Ahmed M, Spinner J, Akcan-Arikan A, Morris SA, Jain PN. Postoperative physiological parameters associated with severe acute kidney injury after pediatric heart transplant. Pediatr Transplant. 2022 Mar 13; e14267. PMID: 35279933.
      Citations:    Fields:    
    8. Lopez KN, Morris SA. Cracking the Administrative Database Code to Risk Stratify Congenital Heart Disease Surgery. J Am Coll Cardiol. 2022 02 08; 79(5):479-481. PMID: 35115104.
      Citations:    Fields:    Translation:Humans
    9. Colquitt JL, Loar RW, Bolin EH, Ezon DS, Heinle JS, Morris SA. Left heart hypoplasia in the fetus: Echocardiographic predictors of outcome. Prenat Diagn. 2022 04; 42(4):447-460. PMID: 35040508.
      Citations:    Fields:    Translation:Humans
    10. Meester JAN, Peeters S, Van Den Heuvel L, Vandeweyer G, Fransen E, Cappella E, Dietz HC, Forbus G, Gelb BD, Goldmuntz E, Hoskoppal A, Landstrom AP, Lee T, Mital S, Morris S, Olson AK, Renard M, Roden DM, Singh MN, Selamet Tierney ES, Tretter JT, Van Driest SL, Willing M, Verstraeten A, Van Laer L, Lacro RV, Loeys BL. Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort. Genet Med. 2022 05; 24(5):1045-1053. PMID: 35058154.
      Citations:    Fields:    Translation:Humans
    11. Milewicz DM, Braverman AC, De Backer J, Morris SA, Boileau C, Maumenee IH, Jondeau G, Evangelista A, Pyeritz RE. Publisher Correction: Marfan syndrome. Nat Rev Dis Primers. 2022 Jan 17; 8(1):3. PMID: 35039531.
      Citations:    Fields:    
    12. Qasim A, Dam T, Kim JJ, Valdes SO, Howard T, Diaz MA, Morris SA, Miyake CY. Trends in hospitalization and factors associated with in-hospital death among pediatric admissions with implantable cardioverter defibrillators. J Cardiovasc Electrophysiol. 2022 03; 33(3):502-509. PMID: 34967982.
      Citations:    Fields:    Translation:Humans
    13. Sanchez Mejia AA, Cambronero N, Dongarwar D, Salihu HM, Vigil-Mallette MA, Garcia BY, Morris SA. Hospital Outcomes Among Infants With Interrupted Aortic Arch With Simple and Complex Associated Heart Defects. Am J Cardiol. 2022 03 01; 166:97-106. PMID: 34973687.
      Citations:    Fields:    Translation:Humans
    14. Wilkes JK, Doan TT, Morris SA, Altman CA, Ayres NA, Schoppe L, Nguyen M, Pignatelli R, Furtun BY. Right Ventricular Global Longitudinal Strain in Fetuses with Hypoplastic Left Heart Syndrome Does Not Differ Between Those With and Without Genetic Conditions. Pediatr Cardiol. 2022 Mar; 43(3):655-664. PMID: 34812908.
      Citations:    Fields:    Translation:Humans
    15. Milewicz DM, Braverman AC, De Backer J, Morris SA, Boileau C, Maumenee IH, Jondeau G, Evangelista A, Pyeritz RE. Marfan syndrome. Nat Rev Dis Primers. 2021 09 02; 7(1):64. PMID: 34475413.
      Citations: 7     Fields:    Translation:Humans
    16. Fick TA, Scott DA, Lupo PJ, Weigand J, Morris SA. The frequency and efficacy of genetic testing in individuals with scimitar syndrome. Cardiol Young. 2022 Apr; 32(4):550-557. PMID: 34210367.
      Citations:    Fields:    Translation:Humans
    17. Chelliah A, Moon-Grady AJ, Peyvandi S, Chiu JS, Bost JE, Schidlow D, Carroll SJ, Davey B, Divanovic A, Hornberger L, Howley LW, Kavanaugh-McHugh A, Kovalchin JP, Levasseur SM, Lindblade CL, Morris SA, Ngwezi D, Pruetz JD, Puchalski MD, Rychik J, Samai C, Tacy TA, Tworetzky W, Vernon MM, Yeh J, Donofrio MT. Contemporary Outcomes in Tetralogy of Fallot With Absent Pulmonary Valve After Fetal Diagnosis. J Am Heart Assoc. 2021 06 15; 10(12):e019713. PMID: 34098741.
      Citations: 1     Fields:    Translation:Humans
    18. Krishnan A, Jacobs MB, Morris SA, Peyvandi S, Bhat AH, Chelliah A, Chiu JS, Cuneo BF, Freire G, Hornberger LK, Howley L, Husain N, Ikemba C, Kavanaugh-McHugh A, Kutty S, Lee C, Lopez KN, McBrien A, Michelfelder EC, Pinto NM, Schwartz R, Stern KWD, Taylor C, Thakur V, Tworetzky W, Wittlieb-Weber C, Woldu K, Donofrio MT. 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. PMID: 33993718.
      Citations:    Fields:    Translation:Humans
    19. Morris SA, Lopez KN. Deep learning for detecting congenital heart disease in the fetus. Nat Med. 2021 05; 27(5):764-765. PMID: 33990805.
      Citations: 1     Fields:    Translation:Humans
    20. Wilkes JK, Whitehead WE, Wang Y, Morris SA. Congenital Heart Disease and Myelomeningocele in the Newborn: Prevalence and Mortality. Pediatr Cardiol. 2021 Jun; 42(5):1026-1032. PMID: 33688980.
      Citations:    Fields:    Translation:Humans
    21. Fick TA, Morris SA, Tume SC, Stafford TD, Aagaard K, Schady D, Molossi S. Fulminant Enteroviral Myocarditis in a Newborn Accompanying Maternal SARS-CoV-2 Infection. World J Pediatr Congenit Heart Surg. 2021 09; 12(5):669-671. PMID: 33599545.
      Citations:    Fields:    Translation:HumansCellsPHPublic Health
    22. Wang S, Freud LR, Detterich J, Moon-Grady AJ, Donofrio MT, Jaeggi ET, Szwast AL, Morris SA, Kavanaugh-Mchugh A, Howley LW, van der Velde ME, Cuneo BF, Phoon CK, Tworetzky W, Pruetz JD. Extracardiac Doppler indices predict perinatal mortality in fetuses with Ebstein anomaly and tricuspid valve dysplasia. Prenat Diagn. 2021 02; 41(3):332-340. PMID: 33242215.
      Citations:    Fields:    Translation:Humans
    23. Nanduri R, Jones E, Miller-Hance W, Lewis AM, Morris SA. Intraperitoneal bladder rupture in a young child with vascular Ehlers-Danlos syndrome. Am J Med Genet A. 2021 03; 185(3):841-844. PMID: 33586854.
      Citations:    Fields:    Translation:Humans
    24. Freud LR, Wilkins-Haug LE, Beroukhim RS, LaFranchi T, Phoon CK, Glickstein JS, Cumbermack KM, Makhoul M, Morris SA, Sun HY, Ferrer Q, Pedra SR, Tworetzky W. Effect of In Utero Non-Steroidal Anti-Inflammatory Drug Therapy for Severe Ebstein Anomaly or Tricuspid Valve Dysplasia (NSAID Therapy for Fetal Ebstein anomaly). Am J Cardiol. 2021 02 15; 141:106-112. PMID: 33217351.
      Citations:    Fields:    Translation:Humans
    25. Spinner JA, Denfield SW, Puri K, Morris SA, Costello JM, Moffett BS, Wang Y, Shekerdemian LS, Tunuguntla HP, Price JF, Heinle JS, Adachi I, Dreyer WJ, Cabrera AG. Hospital outcomes for pediatric heart transplant recipients undergoing tracheostomy: A multi-institutional analysis. Pediatr Transplant. 2021 May; 25(3):e13904. PMID: 33179431.
      Citations:    Fields:    Translation:Humans
    26. Freud LR, McElhinney DB, Kalish BT, Escobar-Diaz MC, Komarlu R, Puchalski MD, Jaeggi ET, Szwast AL, Freire G, Levasseur SM, Kavanaugh-McHugh A, Michelfelder EC, Moon-Grady AJ, Donofrio MT, Howley LW, Selamet Tierney ES, Cuneo BF, Morris SA, Pruetz JD, van der Velde ME, Kovalchin JP, Ikemba CM, Vernon MM, Samai C, Satou GM, Gotteiner NL, Phoon CK, Silverman NH, Tworetzky W. 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. PMID: 33076749.
      Citations: 4     Fields:    Translation:Humans
    27. Pinto NM, Morris SA, Moon-Grady AJ, Donofrio MT. Prenatal cardiac care: Goals, priorities & gaps in knowledge in fetal cardiovascular disease: Perspectives of the Fetal Heart Society. Prog Pediatr Cardiol. 2020 Dec; 59:101312. PMID: 33100800.
      Citations: 2     
    28. Baskin SM, Morris SA, Vara A, Hecht JT, Farach LS. 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. PMID: 32935439.
      Citations:    Fields:    Translation:Humans
    29. Lopez KN, Morris SA, Sexson Tejtel SK, Espaillat A, Salemi JL. 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. PMID: 32795094.
      Citations: 18     Fields:    Translation:Humans
    30. Hogan WJ, Grinenco S, Armstrong A, Devlieger R, Dangel J, Ferrer Q, Frommelt M, Galindo A, Gardiner H, Gelehrter S, Herberg U, Howley L, Jaeggi E, Miranda J, Morris SA, Oepkes D, Pedra S, Peterson R, Sholler G, Simpson J, Strainic J, Vigneswarran TV, Wacker-Gussmann A, Moon-Grady AJ. Fetal Cardiac Intervention for Pulmonary Atresia with Intact Ventricular Septum: International Fetal Cardiac Intervention Registry. Fetal Diagn Ther. 2020 Jul 07; 1-9. PMID: 32634804.
      Citations: 2     Fields:    
    31. Dhillon GS, Ghanayem NS, Broda CR, Lalani SR, Mery CM, Shekerdemian LS, Staffa SJ, Morris SA. An Analysis of Hospital Mortality After Cardiac Operations in Children With Down Syndrome. Semin Thorac Cardiovasc Surg. 2020 Winter; 32(4):947-957. PMID: 32621963.
      Citations:    Fields:    Translation:Humans
    32. Van Driest SL, Sleeper LA, Gelb BD, Morris SA, Dietz HC, Forbus GA, Goldmuntz E, Hoskoppal A, James J, Lee TM, Levine JC, Li JS, Loeys BL, Markham LW, Meester JAN, Mital S, Mosley JD, Olson AK, Renard M, Shaffer CM, Sharkey A, Young L, Lacro RV, Roden DM. Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome. J Pediatr. 2020 07; 222:213-220.e5. PMID: 32586526.
      Citations:    Fields:    Translation:Humans
    33. Castellanos DA, Lopez KN, Salemi JL, Shamshirsaz AA, Wang Y, Morris SA. Trends in Preterm Delivery among Singleton Gestations with Critical Congenital Heart Disease. J Pediatr. 2020 07; 222:28-34.e4. PMID: 32586534.
      Citations: 1     Fields:    Translation:Humans
    34. Swanson TM, Patel A, Baxter AJ, Morris SA, Maskatia SA, Lantos JD. Pediatric Cardiology Specialist's Opinions Toward the Acceptability of Comfort Care for Congenital Heart Disease. Pediatr Cardiol. 2020 Aug; 41(6):1160-1165. PMID: 32419096.
      Citations:    Fields:    Translation:Humans
    35. Patel ND, Nageotte S, Ing FF, Armstrong AK, Chmait R, Detterich JA, Galindo A, Gardiner H, Grinenco S, Herberg U, Jaeggi E, Morris SA, Oepkes D, Simpson JM, Moon-Grady A, Pruetz JD. Procedural, pregnancy, and short-term outcomes after fetal aortic valvuloplasty. Catheter Cardiovasc Interv. 2020 09 01; 96(3):626-632. PMID: 32216096.
      Citations: 1     Fields:    Translation:Humans
    36. Howard TS, Niu MC, Morris SA, Valdes SO, Follansbee CW, Pignatelli RH, Miyake CY, Wang Y, Kim JJ. Right Ventricular Pacing After Ventricular Septal Defect Closure Is Associated With Development of Cardiac Dysfunction. JACC Clin Electrophysiol. 2020 03; 6(3):348-350. PMID: 32192687.
      Citations:    Fields:    Translation:Humans
    37. Spinner JA, Morris SA, Nandi D, Costarino AT, Marino BS, Rossano JW, Shamszad P. 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. PMID: 31568264.
      Citations: 11     Fields:    Translation:Humans
    38. Sage L, Russo ML, Byers PH, Demasi J, Morris SA, Puryear LN, Fulton DS, Shalhub S. Setting a research agenda for vascular Ehlers-Danlos syndrome using a patient and stakeholder engagement model. J Vasc Surg. 2020 10; 72(4):1436-1444.e2. PMID: 32115322.
      Citations:    Fields:    Translation:Humans
    39. Loar RW, Pignatelli RH, Morris SA, Colquitt JL, Feagin DK, Denfield SW, Tunuguntla HP. Left Atrial Strain Correlates with Elevated Filling Pressures in Pediatric Heart Transplantation Recipients. J Am Soc Echocardiogr. 2020 04; 33(4):504-511.e1. PMID: 31987750.
      Citations: 2     Fields:    Translation:Humans
    40. LoPresti MA, Ghali MZ, Srinivasan VM, Morris SA, Kralik SF, Chiou K, Du RY, Lam S. Neurovascular findings in children and young adults with Loeys-Dietz syndromes: Informing recommendations for screening. J Neurol Sci. 2020 Feb 15; 409:116633. PMID: 31862516.
      Citations: 1     Fields:    Translation:HumansPHPublic Health
    41. von Kodolitsch Y, Demolder A, Girdauskas E, Kaemmerer H, Kornhuber K, Muino Mosquera L, Morris S, Neptune E, Pyeritz R, Rand-Hendriksen S, Rahman A, Riise N, Robert L, Staufenbiel I, Szöcs K, Vanem TT, Linke SJ, Vogler M, Yetman A, De Backer J. Features of Marfan syndrome not listed in the Ghent nosology - the dark side of the disease. Expert Rev Cardiovasc Ther. 2019 Dec; 17(12):883-915. PMID: 31829751.
      Citations: 12     Fields:    Translation:Humans
    42. Lahiri S, Wang Y, Caldarone CA, Morris SA. 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. PMID: 31758210.
      Citations: 1     Fields:    Translation:Humans
    43. Morris SA, Ghanayem NS. Patient With Poor Prognosis, Family Wishes to Pursue All Options, Care Team Cannot Reach Consensus. Ann Thorac Surg. 2019 11; 108(5):1284-1286. PMID: 31653290.
      Citations:    Fields:    Translation:Humans
    44. Howard TS, Valdes SO, Hope KD, Morris SA, Landstrom AP, Schneider AE, Miyake CY, Denfield SW, Pignatelli RH, Wang Y, Kim JJ. Association of Wolff-Parkinson-White With Left Ventricular Noncompaction Cardiomyopathy in Children. J Card Fail. 2019 Dec; 25(12):1004-1008. PMID: 31626950.
      Citations: 4     Fields:    Translation:Humans
    45. Spigel ZA, Qureshi AM, Morris SA, Mery CM, Sexson-Tejtel SK, Zea-Vera R, Binsalamah ZM, Imamura M, Heinle JS, Adachi I. Right Ventricle-Dependent Coronary Circulation: Location of Obstruction Is Associated With Survival. Ann Thorac Surg. 2020 05; 109(5):1480-1487. PMID: 31580859.
      Citations:    Fields:    Translation:Humans
    46. Goldberg JF, Schlosser RS, Walrath JG, Morris SA, Elias BA, Price JF, Cabrera AG, Denfield SW, Dreyer WJ, Wang Y, Adachi I, Jeewa A. 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. PMID: 30161035.
      Citations:    Fields:    Translation:Humans
    47. Knadler JJ, LeMaire S, McKenzie ED, Moffett B, Morris SA. 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. PMID: 31233783.
      Citations: 1     Fields:    Translation:Humans
    48. Martins JD, Zachariah J, Selamet Tierney ES, Truong U, Morris SA, Kutty S, de Ferranti SD, Guarino M, Thomas B, Oliveira D, Marinho A, António M, Gauvreau K, Jalles N, Geva T, Carmo MM, Prakash A. 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. PMID: 30929556.
      Citations: 7     Fields:    Translation:Humans
    49. Shamshirsaz AA, Stewart KA, Erfani H, Nassr AA, Sundgren NC, Mehollin-Ray AR, Morris SA, Espinoza J, Sanz Cortes M, Cassady C, Lee TC, Castro EC, Olutoye OA, Mehta DK, Cass D, Olutoye OO, Belfort MA. Cervical lymphatic malformations: Prenatal characteristics and ex utero intrapartum treatment. Prenat Diagn. 2019 03; 39(4):287-292. PMID: 30707444.
      Citations: 3     Fields:    Translation:Humans
    50. Castellanos DA, McKenzie ED, Morris SA. Fetal and postnatal echocardiographic imaging of transposition of the great arteries with the aortic valve posterior to the pulmonary valve. Echocardiography. 2019 May; 36(5):1005-1008. PMID: 30801777.
      Citations:    Fields:    Translation:Humans
    51. Colquitt JL, Loar RW, Morris SA, Feagin DK, Sami S, Pignatelli RH. 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. PMID: 30803862.
      Citations: 7     Fields:    Translation:Humans
    52. Corbitt H, Morris SA, Gravholt CH, Mortensen KH, Tippner-Hedges R, Silberbach M, Maslen CL. TIMP3 and TIMP1 are risk genes for bicuspid aortic valve and aortopathy in Turner syndrome. PLoS Genet. 2018 10; 14(10):e1007692. PMID: 30281655.
      Citations: 12     Fields:    Translation:HumansCells
    53. Edwards LA, Lara DA, Sanz Cortes M, Hunter JV, Andreas S, Nguyen MJ, Schoppe LJ, Zhang J, Smith EM, Maskatia SA, Sexson-Tejtel SK, Lopez KN, Lawrence EJ, Wang Y, Challman M, Ayres NA, Altman CA, Aagaard K, Becker JA, Morris SA. Chronic Maternal Hyperoxygenation and Effect on Cerebral and Placental Vasoregulation and Neurodevelopment in Fetuses with Left Heart Hypoplasia. Fetal Diagn Ther. 2019; 46(1):45-57. PMID: 30223262.
      Citations: 5     Fields:    Translation:Humans
    54. Martins JD, Zachariah J, Selamet Tierney ES, Truong U, Morris SA, Kutty S, de Ferranti SD, Rhodes J, Antonio M, Guarino M, Thomas B, Oliveira D, Gauvreau K, Jalles N, Geva T, Carmo M, Prakash A. Rationale and design of Long-term Outcomes and Vascular Evaluation after Successful Coarctation of the Aorta Treatment study. Ann Pediatr Cardiol. 2018 Sep-Dec; 11(3):282-296. PMID: 30271019.
      Citations: 2     
    55. Dailey-Schwartz AL, Tadros HJ, Azamian MS, Lalani SR, Morris SA, Allen HD, Kim JJ, Landstrom AP. 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. PMID: 30172441.
      Citations: 1     Fields:    Translation:Humans
    56. Edwards LA, Justino H, Morris SA, Rychik J, Feudtner C, Lantos JD. Controversy About a High-Risk and Innovative Fetal Cardiac Intervention. Pediatrics. 2018 09; 142(3). PMID: 30097527.
      Citations: 1     Fields:    Translation:Humans
    57. Buffie AW, Belfort MA, Shamshirsaz AA, Justino H, Qureshi AM, Ayres NA, Morris SA, Espinoza J. Two- and Four-dimensional Ultrasonography of an Interatrial Stent in a Fetus With Hypoplastic Left Heart Syndrome. J Ultrasound Med. 2019 Feb; 38(2):549-551. PMID: 30058144.
      Citations:    Fields:    Translation:Humans
    58. Elhoff JJ, McHugh KE, Buckley JR, Morris SA, Simpson KN, Scheurer MA. Out-of-pocket medical expenses in severe CHD. Cardiol Young. 2018 Aug; 28(8):1014-1018. PMID: 29923476.
      Citations: 1     Fields:    Translation:Humans
    59. Russo ML, Sukhavasi N, Mathur V, Morris SA. Obstetric Management of Loeys-Dietz Syndrome. Obstet Gynecol. 2018 06; 131(6):1080-1084. PMID: 29742657.
      Citations: 2     Fields:    Translation:Humans
    60. Aggarwal V, Castellanos D, Becker JA, Edwards LA, Morris SA. Idiopathic congenital right atrial dilation: Fetal presentation. J Clin Ultrasound. 2018 Oct; 46(8):553-554. PMID: 29701295.
      Citations:    Fields:    Translation:Humans
    61. Puri K, Morris SA, Mery CM, Wang Y, Moffett BS, Heinle JS, Rodriguez JR, Shekerdemian LS, Cabrera AG. 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. PMID: 29325785.
      Citations: 1     Fields:    Translation:Humans
    62. Regalado ES, Mellor-Crummey L, De Backer J, Braverman AC, Ades L, Benedict S, Bradley TJ, Brickner ME, Chatfield KC, Child A, Feist C, Holmes KW, Iannucci G, Lorenz B, Mark P, Morisaki T, Morisaki H, Morris SA, Mitchell AL, Ostergaard JR, Richer J, Sallee D, Shalhub S, Tekin M, Estrera A, Musolino P, Yetman A, Pyeritz R, Milewicz DM. 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. PMID: 29300374.
      Citations: 11     Fields:    Translation:Humans
    63. Corbitt H, Maslen C, Prakash S, Morris SA, Silberbach M. 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. PMID: 29243875.
      Citations: 1     Fields:    Translation:Humans
    64. Loar RW, Denfield SW, Morris SA, Tunuguntla HP, Cabrera AG, Price JF, Zhang W, Hosek K, Kim JJ, Dreyer WJ, Jeewa A. Fatal cardiac arrest in pediatric heart transplant recipients: Query of the UNOS database. Pediatr Transplant. 2018 02; 22(1). PMID: 29226563.
      Citations:    Fields:    Translation:Humans
    65. Niu MC, Dickerson HA, Moore JA, de la Uz C, Valdés SO, Kim JJ, Bard DE, Morris SA, Miyake CY. Heterotaxy syndrome and associated arrhythmias in pediatric patients. Heart Rhythm. 2018 04; 15(4):548-554. PMID: 29154821.
      Citations: 3     Fields:    Translation:Humans
    66. Edwards LA, Masand P, Morris SA. Atypical Circular Shunt and Diffuse Emphysema in a Fetus with Double-Outlet Right Ventricle and Absent Pulmonary Valve. CASE: Cardiovascular Imaging Case Reports. 2017; 1(6):237–241. View Publication.
    67. Li AH, Hanchard NA, Furthner D, Fernbach S, Azamian M, Nicosia A, Rosenfeld J, Muzny D, D'Alessandro LCA, Morris S, Jhangiani S, Parekh DR, Franklin WJ, Lewin M, Towbin JA, Penny DJ, Fraser CD, Martin JF, Eng C, Lupski JR, Gibbs RA, Boerwinkle E, Belmont JW. 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. PMID: 29089047.
      Citations: 17     Fields:    Translation:Humans
    68. Maskatia SA, Cabrera AG, Morris SA, Altman CA. The pediatric echocardiography Boot Camp: Four-year experience and impact on clinical performance. Echocardiography. 2017 Oct; 34(10):1486-1494. PMID: 28980410.
      Citations: 2     Fields:    Translation:Humans
    69. Edwards LA, Masand P, Morris SA. Atypical Circular Shunt and Diffuse Emphysema in a Fetus with Double-Outlet Right Ventricle and Absent Pulmonary Valve. CASE (Phila). 2017 Dec; 1(6):237-241. PMID: 30062290.
      Citations:    
    70. Jantzen DW, Moon-Grady AJ, Morris SA, Armstrong AK, Berg C, Dangel J, Fifer CG, Frommelt M, Gembruch U, Herberg U, Jaeggi E, Kontopoulos EV, Marshall AC, Miller O, Oberhoffer R, Oepkes D, Pedra CA, Pedra SR, Peralta F, Quintero RA, Ryan G, Gelehrter SK. Hypoplastic Left Heart Syndrome With Intact or Restrictive Atrial Septum: A Report From the International Fetal Cardiac Intervention Registry. Circulation. 2017 10 03; 136(14):1346-1349. PMID: 28864444.
      Citations: 11     Fields:    Translation:Humans
    71. Krepp JM, Roman MJ, Devereux RB, Bruce A, Prakash SK, Morris SA, Milewicz DM, Holmes KW, Ravekes W, Shohet RV, Pyeritz RE, Maslen CL, Kroner BL, Eagle KA, Preiss L, Asch FM. 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. PMID: 28805011.
      Citations: 3     Fields:    Translation:Humans
    72. Nassr AA, Shazly SA, Morris SA, Ayres N, Espinoza J, Erfani H, Olutoye OA, Sexson SK, Olutoye OO, Fraser CD, Belfort MA, Shamshirsaz AA. Prenatal management of fetal intrapericardial teratoma: a systematic review. Prenat Diagn. 2017 Sep; 37(9):849-863. PMID: 28695637.
      Citations: 1     Fields:    Translation:Humans
    73. Roman MJ, Pugh NL, Devereux RB, Eagle KA, Holmes K, LeMaire SA, Milewski RK, Morris SA, Prakash SK, Pyeritz RE, Ravekes WJ, Shohet RV, Song HK, Asch FM. 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. PMID: 28802510.
      Citations: 10     Fields:    Translation:Humans
    74. Hanchard NA, Umana LA, D'Alessandro L, Azamian M, Poopola M, Morris SA, Fernbach S, Lalani SR, Towbin JA, Zender GA, Fitzgerald-Butt S, Garg V, Bowman J, Zapata G, Hernandez P, Arrington CB, Furthner D, Prakash SK, Bowles NE, McBride KL, Belmont JW. 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. PMID: 28653806.
      Citations: 5     Fields:    Translation:Humans
    75. Roman MJ, Devereux RB, Preiss LR, Asch FM, Eagle KA, Holmes KW, LeMaire SA, Maslen CL, Milewicz DM, Morris SA, Prakash SK, Pyeritz RE, Ravekes WJ, Shohet RV, Song HK, Weinsaft JW. 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). PMID: 28600386.
      Citations: 24     Fields:    Translation:Humans
    76. Burrage LC, Guillerman RP, Das S, Singh S, Schady DA, Morris SA, Walkiewicz M, Schecter MG, Heinle JS, Lotze TE, Lalani SR, Mallory GB. Lung Transplantation for FLNA-Associated Progressive Lung Disease. J Pediatr. 2017 07; 186:118-123.e6. PMID: 28457522.
      Citations: 7     Fields:    Translation:HumansCells
    77. Colquitt JL, Jeewa A, Morris SA, Sexson Tejtel K, Dreyer WJ, Denfield SW, Pignatelli RH. Diminished Global Longitudinal Strain Predicts Late Allograft Failure in Pediatric Heart Transplant Recipients. JACC Cardiovasc Imaging. 2017 12; 10(12):1529-1531. PMID: 28330655.
      Citations: 3     Fields:    Translation:Humans
    78. Quick AP, Landstrom AP, Wang Q, Beavers DL, Reynolds JO, Barreto-Torres G, Tran V, Showell J, Philippen LE, Morris SA, Skapura D, Bos JM, Pedersen SE, Pautler RG, Ackerman MJ, Wehrens XH. Novel junctophilin-2 mutation A405S is associated with basal septal hypertrophy and diastolic dysfunction. JACC Basic Transl Sci. 2017 Feb; 2(1):56-67. PMID: 28393127.
      Citations: 15     
    79. Jeewa A, Morris SA, Dreyer WJ, Adachi I, Denfield SW, McKenzie ED. Visual Diagnosis: A Child with Presumed Reactive Airway Disease, Pectus Carinatum, and Aortic Root Dilation. Pediatr Rev. 2017 Jan; 38(1):e1-e5. PMID: 28044041.
      Citations:    Fields:    Translation:Humans
    80. Jondeau G, Ropers J, Regalado E, Braverman A, Evangelista A, Teixedo G, De Backer J, Muiño-Mosquera L, Naudion S, Zordan C, Morisaki T, Morisaki H, Von Kodolitsch Y, Dupuis-Girod S, Morris SA, Jeremy R, Odent S, Adès LC, Bakshi M, Holman K, LeMaire S, Milleron O, Langeois M, Spentchian M, Aubart M, Boileau C, Pyeritz R, Milewicz DM. 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. PMID: 27879313.
      Citations: 35     Fields:    Translation:Humans
    81. Mery CM, Nieto RM, De León LE, Morris SA, Zhang W, Colquitt JL, Adachi I, Kane LC, Heinle JS, McKenzie ED, Fraser CD. 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. PMID: 27717424.
      Citations: 1     Fields:    Translation:Humans
    82. Lara DA, Ethen MK, Canfield MA, Nembhard WN, Morris SA. 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. PMID: 27685952.
      Citations: 7     Fields:    Translation:Humans
    83. Lara DA, Morris SA, Maskatia SA, Challman M, Nguyen M, Feagin DK, Schoppe L, Zhang J, Bhatt A, Sexson-Tejtel SK, Lopez KN, Lawrence EJ, Andreas S, Wang Y, Belfort MA, Ruano R, Ayres NA, Altman CA, Aagaard KM, Becker J. 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. PMID: 26700848.
      Citations: 7     Fields:    Translation:Humans
    84. Horne D, Morris SA, Colquitt JL, Molossi SM, McKenzie ED. Incidental Finding of Right Coronary Artery to Pulmonary Artery Fistula During Surgical Repair of Aortic Arch Atresia in Turner Syndrome. World J Pediatr Congenit Heart Surg. 2017 09; 8(5):646-649. PMID: 27549732.
      Citations: 1     Fields:    Translation:Humans
    85. Roman MJ, Pugh NL, Hendershot TP, Devereux RB, Dietz H, Holmes K, Eagle KA, LeMaire SA, Milewicz DM, Morris SA, Pyeritz RE, Ravekes WJ, Shohet RV, Silberbach M. 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). PMID: 27515814.
      Citations: 12     Fields:    Translation:Humans
    86. Ezon DS, Ayres NA, Altman CA, Denfield SW, Morris SA, Maskatia SA. Echocardiographic Parameters and Outcomes in Primary Fetal Cardiomyopathy. J Ultrasound Med. 2016 Sep; 35(9):1949-55. PMID: 27466259.
      Citations:    Fields:    Translation:Humans
    87. Lara DA, Fixler DE, Ethen MK, Canfield MA, Nembhard WN, Morris SA. 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. PMID: 27296724.
      Citations: 8     Fields:    Translation:Humans
    88. Weinsaft JW, Devereux RB, Preiss LR, Feher A, Roman MJ, Basson CT, Geevarghese A, Ravekes W, Dietz HC, Holmes K, Habashi J, Pyeritz RE, Bavaria J, Milewski K, LeMaire SA, Morris S, Milewicz DM, Prakash S, Maslen C, Song HK, Silberbach GM, Shohet RV, McDonnell N, Hendershot T, Eagle KA, Asch FM. 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. PMID: 27282895.
      Citations: 23     Fields:    Translation:Humans
    89. Hanchard NA, Swaminathan S, Bucasas K, Furthner D, Fernbach S, Azamian MS, Wang X, Lewin M, Towbin JA, D'Alessandro LC, Morris SA, Dreyer W, Denfield S, Ayres NA, Franklin WJ, Justino H, Lantin-Hermoso MR, Ocampo EC, Santos AB, Parekh D, Moodie D, Jeewa A, Lawrence E, Allen HD, Penny DJ, Fraser CD, Lupski JR, Popoola M, Wadhwa L, Brook JD, Bu'Lock FA, Bhattacharya S, Lalani SR, Zender GA, Fitzgerald-Butt SM, Bowman J, Corsmeier D, White P, Lecerf K, Zapata G, Hernandez P, Goodship JA, Garg V, Keavney BD, Leal SM, Cordell HJ, Belmont JW, McBride KL. 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. PMID: 26965164.
      Citations: 17     Fields:    Translation:HumansCells
    90. Wallace S, Guo DC, Regalado E, Mellor-Crummey L, Bamshad M, Nickerson DA, Dauser R, Hanchard N, Marom R, Martin E, Berka V, Sharina I, Ganesan V, Saunders D, Morris SA, Milewicz DM. Disrupted nitric oxide signaling due to GUCY1A3 mutations increases risk for moyamoya disease, achalasia and hypertension. Clin Genet. 2016 10; 90(4):351-60. PMID: 26777256.
      Citations: 26     Fields:    Translation:HumansAnimalsCells
    91. Asch FM, Yuriditsky E, Prakash SK, Roman MJ, Weinsaft JW, Weissman G, Weigold WG, Morris SA, Ravekes WJ, Holmes KW, Silberbach M, Milewski RK, Kroner BL, Whitworth R, Eagle KA, Devereux RB, Weissman NJ. 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. PMID: 26897684.
      Citations: 20     Fields:    Translation:Humans
    92. Prakash A, Adlakha H, Rabideau N, Hass CJ, Morris SA, Geva T, Gauvreau K, Singh MN, Lacro RV. 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. PMID: 26884630.
      Citations:    Fields:    Translation:Humans
    93. Colquitt JL, Morris SA, Denfield SW, Fraser CD, Wang Y, Kyle WB. Survival in Children With Down Syndrome Undergoing Single-Ventricle Palliation. Ann Thorac Surg. 2016 May; 101(5):1834-41. PMID: 26867706.
      Citations: 6     Fields:    Translation:Humans
    94. Niu MC, Morris SA, Krenek M, DE LA Uz CM, Pedroza C, Miyake CY, Kim JJ, Valdés SO. 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. PMID: 27074776.
      Citations: 1     Fields:    Translation:Humans
    95. Morris SA. Arterial tortuosity in genetic arteriopathies. Curr Opin Cardiol. 2015 Nov; 30(6):587-93. PMID: 26398550.
      Citations: 18     Fields:    Translation:Humans
    96. Moffett BS, Garrison JM, Hang A, Morris SA, Tsang R, Dinh K, Griffiths P, Bronicki R, Checchia PA. Prostaglandin Availability and Association with Outcomes for Infants with Congenital Heart Disease. Pediatr Cardiol. 2016 Feb; 37(2):338-44. PMID: 26499357.
      Citations: 1     Fields:    Translation:Humans
    97. Moon-Grady AJ, Morris SA, Belfort M, Chmait R, Dangel J, Devlieger R, Emery S, Frommelt M, Galindo A, Gelehrter S, Gembruch U, Grinenco S, Habli M, Herberg U, Jaeggi E, Kilby M, Kontopoulos E, Marantz P, Miller O, Otaño L, Pedra C, Pedra S, Pruetz J, Quintero R, Ryan G, Sharland G, Simpson J, Vlastos E, Tworetzky W, Wilkins-Haug L, Oepkes D. International Fetal Cardiac Intervention Registry: A Worldwide Collaborative Description and Preliminary Outcomes. J Am Coll Cardiol. 2015 Jul 28; 66(4):388-99. PMID: 26205597.
      Citations: 25     Fields:    Translation:Humans
    98. Prakash A, Adlakha H, Rabideau N, Hass CJ, Morris SA, Geva T, Gauvreau K, Singh MN, Lacro RV. 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. PMID: 26115544.
      Citations: 19     Fields:    Translation:Humans
    99. Freud LR, Escobar-Diaz MC, Kalish BT, Komarlu R, Puchalski MD, Jaeggi ET, Szwast AL, Freire G, Levasseur SM, Kavanaugh-McHugh A, Michelfelder EC, Moon-Grady AJ, Donofrio MT, Howley LW, Tierney ES, Cuneo BF, Morris SA, Pruetz JD, van der Velde ME, Kovalchin JP, Ikemba CM, Vernon MM, Samai C, Satou GM, Gotteiner NL, Phoon CK, Silverman NH, McElhinney DB, Tworetzky W. 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. PMID: 26059011.
      Citations: 19     Fields:    Translation:Humans
    100. Maskatia SA, Morris SA, Spinner JA, Krishnamurthy R, Altman CA. 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. PMID: 25916551.
      Citations: 3     Fields:    Translation:Humans
    101. Frischhertz BP, Shamszad P, Pedroza C, Milewicz DM, Morris SA. Thoracic aortic dissection and rupture in conotruncal cardiac defects: A population-based study. Int J Cardiol. 2015 Apr 01; 184:521-527. PMID: 25767008.
      Citations: 6     Fields:    Translation:Humans
    102. Krishnamurthy R, Pednekar A, Atweh LA, Vogelius E, Chu ZD, Zhang W, Maskatia S, Masand P, Morris SA, Krishnamurthy R, Muthupillai R. Clinical validation of free breathing respiratory triggered retrospectively cardiac gated cine balanced steady-state free precession cardiovascular magnetic resonance in sedated children. J Cardiovasc Magn Reson. 2015 Jan 14; 17(1):1. PMID: 25589308.
      Citations: 16     Fields:    Translation:Humans
    103. Reinstein E, Morris SA, Rimoin DL, Robertson SP, Lacro RV. Arterial tortuosity in patients with Filamin A- associated vascular aneurysms. Am J Med Genet A. 2014 Nov; 164A(11):2961-3. PMID: 25124759.
      Citations: 2     Fields:    Translation:HumansCells
    104. Cook JR, Carta L, Bénard L, Chemaly ER, Chiu E, Rao SK, Hampton TG, Yurchenco P, Costa KD, Hajjar RJ, Ramirez F. Abnormal muscle mechanosignaling triggers cardiomyopathy in mice with Marfan syndrome. J Clin Invest. 2014 Mar; 124(3):1329-39. PMID: 24531548.
      Citations: 61     Fields:    Translation:HumansAnimalsCells
    105. Ezon DS, Khan MS, Adachi I, Jeewa A, Morris SA, Nagy CZ, Morales DL, Heinle JS. 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. PMID: 24342901.
      Citations: 6     Fields:    Translation:Humans
    106. Morris SA, Ethen MK, Penny DJ, Canfield MA, Minard CG, Fixler DE, Nembhard WN. Prenatal diagnosis, birth location, surgical center, and neonatal mortality in infants with hypoplastic left heart syndrome. Circulation. 2014 Jan 21; 129(3):285-92. PMID: 24135071.
      Citations: 37     Fields:    Translation:Humans
    107. Niu MC, Morris SA, Morales DL, Fraser CD, Kim JJ. Low incidence of arrhythmias in the right ventricular infundibulum sparing approach to tetralogy of Fallot repair. Pediatr Cardiol. 2014 Feb; 35(2):261-9. PMID: 23921493.
      Citations: 1     Fields:    Translation:Humans
    108. Maskatia SA, Altman CA, Morris SA, Cabrera AG. The echocardiography "boot camp": a novel approach in pediatric cardiovascular imaging education. J Am Soc Echocardiogr. 2013 Oct; 26(10):1187-1192. PMID: 23860091.
      Citations: 5     Fields:    Translation:Humans
    109. Shamszad P, Barnes JN, Morris SA. Aortic dissection in hospitalized children and young adults: a multiinstitutional study. Congenit Heart Dis. 2014 Jan-Feb; 9(1):54-62. PMID: 23682693.
      Citations: 3     Fields:    Translation:Humans
    110. Maskatia SA, Spinner JA, Nutting AC, Slesnick TC, Krishnamurthy R, Morris SA. 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. PMID: 23677064.
      Citations: 7     Fields:    Translation:Humans
    111. Lawrence EJ, Nguyen K, Morris SA, Hollinger I, Graham DA, Jenkins KJ, Bodian C, Lin HM, Gelb BD, Mittnacht AJ. Economic and safety implications of introducing fast tracking in congenital heart surgery. Circ Cardiovasc Qual Outcomes. 2013 Mar 01; 6(2):201-7. PMID: 23443672.
      Citations: 10     Fields:    Translation:Humans
    112. Maskatia SA, Spinner JA, Morris SA, Petit CJ, Krishnamurthy R, Nutting AC. 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. PMID: 23411101.
      Citations: 3     Fields:    Translation:Humans
    113. Morris SA, Orbach DB, Geva T, Singh MN, Gauvreau K, Lacro RV. 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. PMID: 21730308.
      Citations: 51     Fields:    Translation:Humans
    114. Gaies MG, Morris SA, Hafler JP, Graham DA, Capraro AJ, Zhou J, Landrigan CP, Sandora TJ. Reforming procedural skills training for pediatric residents: a randomized, interventional trial. Pediatrics. 2009 Aug; 124(2):610-9. PMID: 19651582.
      Citations: 24     Fields:    Translation:Humans
    115. Morris SA, Bernstein HH. Immunizations, neonatal jaundice, and animal-induced injuries. Curr Opin Pediatr. 2004 Aug; 16(4):450-60. PMID: 15273509.
      Citations: 1     Fields:    Translation:HumansAnimalsPHPublic Health
    116. Villanueva MP, Aiyer AR, Muller S, Pletcher MT, Liu X, Emanuel B, Srivastava D, Reeves RH. Genetic and comparative mapping of genes dysregulated in mouse hearts lacking the Hand2 transcription factor gene. Genomics. 2002 Dec; 80(6):593-600. PMID: 12504851.
      Citations: 2     Fields:    Translation:HumansAnimalsCells
    117. Cody JD, Ghidoni PD, DuPont BR, Hale DE, Hilsenbeck SG, Stratton RF, Hoffman DS, Muller S, Schaub RL, Leach RJ, Kaye CI. Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q. Am J Med Genet. 1999 Aug 27; 85(5):455-62. PMID: 10405442.
      Citations: 38     Fields:    Translation:HumansCells
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