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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

Mlynarski EE, Xie M, Taylor D, Sheridan MB, Guo T, Racedo SE, McDonald-McGinn DM, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, Philip N, Simon TJ, Roberts AE, Piotrowicz M, Bearden CE, Eliez S, Gothelf D, Coleman K, Kates WR, Devoto M, Zackai E, Heine-Suñer D, Goldmuntz E, Bassett AS, Morrow BE, Emanuel BS; International Chromosome 22q11.2 Consortium: Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome. Hum Genet 135(3): 273-85, Mar 2016.

Werner P, Latney B, Deardorff MA, Goldmuntz E: MESP1 mutations in patients with congenital heart defects. Hum Mutat 37(3): 308-14, Mar 2016.

Bhatt SM, Cassedy A, Marino B, Goldmuntz E, Mercer-Rosa L: 199-Quality of life is diminished in patients with tetralogy of Fallot with mild residual disease: a comparison of tetralogy of Fallot and isolated valvar pulmonary stenosis. Presented at the ACC Scientific Sessions 2016, Chicago, IL March 2016.

Li Y, Yagi H, Onuoha EO, Damerla RR, Francis R, Furutani Y, Tariq M, King SM, Hendricks G, Cui C, Saydmohammed M, Lee DM, Zahid M, Sami I, Leatherbury L,Pazour GJ, Ware SM, Nakanishi T, Goldmuntz E, Tsang M, Lo CW: DNAH6 and its interactions with PCD genes in heterotaxy and primary ciliary dyskinesia. PLoS Genet 12(2), Feb 2016.

Ahrens-Nicklas1 RC, Khan S, Garbarini J, Woyciechowski S, D’Alessandro S, Zackai EH, Deardorff MA, Goldmuntz E: Utility of genetic evaluation in infants with congenital heart defects admitted to the cardiac intensive care unit. Am J Med Genet 2016 Notes: "in press"

McKean D, Homsy J, Wakimoto H, Patel N, Gorham J, DePalma S, Ware K, Zaidi S, Ma W, Patel N, Lifton R, Chung W, Kim R, Shen Y, Brueckner M, Goldmuntz E, Sharp A, Seidman C, Gelb B, Seidman J : Loss of RNA expression and allele-specific expression associated with congenital heart disease. Nature 2016 Notes: "in press"

Kim Y, Londono C, Slap G, Goldmuntz E: Adult congenital heart disease: the ongoing need for physician counseling about heredity and contraceptive options. Cardiol Young 2016 Notes: Accepted CTY-16-Feb-053.R1.

Homsy J, Zaidi S, Shen Y, Ware JS, Samocha KE, Karczewski KJ, DePalma SR, McKean D, Wakimoto H, Gorham J, Jin SC, Deanfield J, Giardini A, Porter GA Jr, Kim R, Bilguvar K, López-Giráldez F, Tikhonova I, Mane S, Romano-Adesman A, Qi H, Vardarajan B, Ma L, Daly M, Roberts AE, Russell MW, Mital S, Newburger JW, Gaynor JW, Breitbart RE, Iossifov I, Ronemus M, Sanders SJ, Kaltman JR, Seidman JG, Brueckner M, Gelb BD, Goldmuntz E, Lifton RP, Seidman CE, Chung WK: De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies. Science 350(6265): 1262-6, Dec 2015.

Fogel MA, Pawlowski T, Keller MS, Cohen MS, Goldmuntz E, Diaz L, Li C, Whitehead KK, Harrisa MA: The cardiovascular effects of obesity on ventricular function and mass in patients after tetralogy of Fallot repair. J Pediatr 167(2): 325-330, Aug 2015.

Avitabile CM, Goldberg DJ, Zemel BS, Brodsky JL, Dodds K, Hayden-Rush C, Whitehead KK, Goldmuntz E, Rychik J, Leonard MB: Deficits in bone density and structure in children and young adults following Fontan palliation. Bone 77: 12-6, Aug 2015.

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Last updated: 08/04/2016
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