Elizabeth Goldmuntz, BA, MD
Elizabeth Goldmuntz, BA, MD
Associate Professor of Pediatrics at the Children's Hospital of Philadelphia
Department: Pediatrics
Contact information
Abramson Research Center, 702A
Division of Cardiology
The Children's Hospital of Philadelphia
3615 Civic Center Boulevard
Philadelphia, PA 19104-4318
Division of Cardiology
The Children's Hospital of Philadelphia
3615 Civic Center Boulevard
Philadelphia, PA 19104-4318
Office: 215-590-5820
Fax: 215-590-5454
Fax: 215-590-5454
Email:
goldmuntz@email.chop.edu
goldmuntz@email.chop.edu
Publications
Education:
B.A. (History)
Yale University, 1983.
M.D.
University of Pennsylvania School of Medicine, 1987.
Permanent linkB.A. (History)
Yale University, 1983.
M.D.
University of Pennsylvania School of Medicine, 1987.
Selected Publications
John AS, Rychik J, Khan M, Yang W, Goldmuntz E.: 22q11.2 deletion syndrome as a risk factor for aortic root dilation in tetralogy of Fallot. Cardiol Young 10: 1-8, Apr 2013.D'Alessandro LC, Latney BC, Paluru PC, Goldmuntz E: The phenotypic spectrum of ZIC3 mutations includes isolated d-transposition of the great arteries and double outlet right ventricle. Am J Med Genet A 161(4): 792-802, Apr 2013.
Avitable C, Brodsky J, Leonard M, Dodds K, Hayden-Rush C, Goldmuntz E, Rychik J, Goldberg D.: Abnormalities in Bone Density, Bone Structure, and Muscle Cross-Sectional Area After Fontan Palliation. Presented at the ACC Scientific Session 2013, San Francisco, CA. March 2013.
Mercer-Rosa L, Fogel M, Paridon S, Rychik J, Tanel R, Yang R, Yang W, Zhao H, Goldmuntz E.: Variable Intermediate Outcome in Tetralogy of fallot is Explained in Part by 22q11.2 Deletion Status. Presented at the ACC Scientific Session 2013, San Francisco, CA. March 2013.
O’Byrne M, Mercer-Rosa L, Zhao H, Zhang X, Yang W, Tanel R, Marino B, Casedy A, Fogel M, Rychik J, Paridon S, Goldmuntz E.: Middle term outcomes in survivors of surgical correction of interrupted aortic arch. Presented at the ACC Scientific Session 2013, San Francisco, CA. March 2013.
D'Alessandro L, Werner P, Xie H, Hakonarson H, White P, Goldmuntz E: The pervalence of 16p12.1 microdeletion in patients with left-sided cardiac lesions. Congenit Heart Dis March 2013.
Peyvandi S, Ingall E, Woyciechowski S, Garbarini, Mitchell L, Goldmuntz E.: Risk of Congenital Heart Disease in Relatives of Probands with Contruncal Cardiac Defects: An Evaluation of 1622 Families. Presented at the ACC Scientific Session 2013, San Francisco, CA. March 2013.
Murray B, Wagle R, Amat-Alarcon N, Wilkens A, Stephens P, Zackai E H, Goldmuntz E, Calkins H, Deardorff M A, Judge D P: A family with a complex clinical presentation characterized by arrhythmogenic right ventricular dysplasia/cardiomyopathy and features of branchio-oculo-facial syndrome. Am J Med Genet A 161A(2): 371-6, Feb 2013 Notes: Epub 2013 Jan 10.
Breitbart RE, Brueckner M, Chung WK, Colan SD, Deanfield J, Gelb BD, Giardini A, Goldmuntz E, Hakonarson H, Kaltman JR, Kaski JP, Kim RW, Kline JK, Lifton RP, Lu M, Mercer-Rosa L, Mitchell LE, Newburger JW, Peter I, Porter GA, Roberts AE, Rosenberg ER, Sachidanandam R, Seiden HS, Seidman JG, Sleeper LA, Tennstedt SL, Warburton D, White PS, Williams IA, for the Pediatric Cardiac Genomics Consortium: The Congenital Heart Disease Genetic Network Study (CHD GENES): Rationale, design. and early results pediatric cardiac genomics consortium. Circ Res 112(4): 698-706, Feb 2013.
Mercer-Rosa L, Pinto N, Yang W, Tanel R, Goldmuntz E: 22q11.2 Deletion syndrome is associated with perioperative outcome in tetralogy of Fallot. J Thorac Cardiovasc Surg Jan 2013.