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Elizabeth Goldmuntz, BA, MD

Elizabeth Goldmuntz, BA, MD

faculty photo
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
Office: 215-590-5820
Fax: 215-590-5454
Education:
B.A. (History)
Yale University, 1983.
M.D.
University of Pennsylvania School of Medicine, 1987.
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Selected Publications

Lin KY, Freedman JL, Ginsberg J, Goldmuntz E, Shaddy RE: Cardiac biomarkers are elevated in children during chemotherapy regardless of anthracycline status. Presented at the American Heart Association Scientific Sessions 2014, Chicago, IL Nov 2014.

Avitabile CM, Leonard MB, Zemel BS, Brodsky JL, Lee D, Dodds K, Hayden-Rush C, Whitehead KK, Goldmuntz E, Paridon SM, Rychik J, Goldberg DJ: Lean mass deficits, vitamin D status, and exercise capacity in children and young adults after Fontan palliation. Heart 100(21): 1702-7, Nov 2014 Notes: [PubMed - in process]

Natarajan SS, Glatz AC, Goldmuntz E, Cohen MS: Abnormal aortic wall properties in children with isolated bicuspid aortic valve. Presented at the American Heart Association Scientific Sessions 2014, Chicago, IL Nov 2014.

O'Byrne ML, Yang W, Mercer-Rosa L, Parnell AS, Oster ME, Levenbrown Y, Tanel RE, Goldmuntz E: 22q11.2 deletion syndrome is associated with increased perioperative events and more complicated postoperative course in infants undergoing infant operative correction of truncus arteriosus communis or interrupted aortic arch. J Thorac Cardiovasc Surg 148(4): 1597-605, Oct 2014.

Glessner J, Bick AG, Ito K, Homsy J, Rodriguez-Murillo L, Fromer M, Mazaika EJ, Vardarajan B, Italia MJ, Leipzig J, DePalma S, Golhar R, Sanders SJ, Yamrom B, Ronemus M, Iossifov I, Willsey AJ, State MW, Kaltman JR, White PS, Shen Y, Warburton D, Brueckner M, Seidman C, Goldmuntz E, Gelb BD, Lifton R, Seidman JG, Hakonarson H, Chung WK: Increased frequency of de novo copy number variations in congenital heart disease by integrative analysis of SNP array and exome sequence data. Circ Res 115(10): 884-96, Sept 2014.

Werner P, Paluru P, Simpson AM, Latney B, Iyer R, Brodeur GM, Goldmuntz E: Mutations in NTRK3 suggest a novel signaling pathway in human congenital heart disease. Hum Mutat Sep 2014 Notes: [Epub ahead of print]

Mitchell LE, Agopian AJ, Bhalla A, Glessner JT, Kim CE, Swartz MD, Hakonarson H, Goldmuntz E: Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations. Hum Mol Genet Aug 2014 Notes: [Epub ahead of print]

White PS, Xie HM, Werner P, Glessner J, Latney B, Hakonarson H, Goldmuntz E: Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions. Birth Defects Res A Clin Mol Teratol Jul 26 2014 Notes: [Epub ahead of print]

Peyvandi S, Ingall E, Woyciechowski S, Garbarini J, Mitchell LE, Goldmuntz E: Risk of congenital heart disease in relatives of probands with conotruncal cardiac defects: An evaluation of 1,620 families. Am J Med Genet A 164A(6): 1490-5, Jun 2014.

Agopian AJ, Mitchell LE, Glessner J, Bhalla AD, Sewda A, Hakonarson H, Goldmuntz E: Genome-wide association study identifies maternal and inherited candidate loci for conotruncal heart defects. Plos One 9(5): e96057, May 2014.

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Last updated: 11/24/2014
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