Harvard Catalyst Profiles

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Paula Goldenberg, M.D.


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.
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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. Lines MA, Goldenberg P, Wong A, Srivastava S, Bayat A, Hove H, Karstensen HG, Anyane-Yeboa K, Liao J, Jiang N, May A, Guzman E, Morleo M, D'Arrigo S, Ciaccio C, Pantaleoni C, Castello R, McKee S, Ong J, Zibdeh-Lough H, Tran-Mau-Them F, Gerasimenko A, Heron D, Keren B, Margot H, de Sainte Agathe JM, Burglen L, Voets T, Vriens J, Innes AM, Dyment DA. Phenotypic spectrum of the recurrent TRPM3 p.(Val837Met) substitution in seven individuals with global developmental delay and hypotonia. Am J Med Genet A. 2022 Feb 10. PMID: 35146895.
    Citations:    Fields:    
  2. Wu F, Goldenberg PC, Mukai S. Bilateral anterior segment dysgenesis and peripheral avascular retina with tractional retinal detachment in an infant with multiple congenital anomalies-hypotony-seizures syndrome 3. Ophthalmic Genet. 2021 06; 42(3):334-337. PMID: 33620284.
    Citations: 1     Fields:    Translation:Humans
  3. Patel KR, Partain M, Ryan DP, Hersh C, Goldenberg P, Hartnick CJ. Carotid artery mobilization prior to pharyngeal flap inset for patients with 22q11.2 deletion syndrome. Int J Pediatr Otorhinolaryngol. 2021 Feb; 141:110573. PMID: 33359933.
    Citations:    Fields:    Translation:Humans
  4. Shikany AR, Landis BJ, Parrott A, Miller EM, Coyan A, Walters L, Hinton RB, Goldenberg P, Ware SM. A Comprehensive Clinical Genetics Approach to Critical Congenital Heart Disease in Infancy. J Pediatr. 2020 12; 227:231-238.e14. PMID: 32717230.
    Citations: 3     Fields:    Translation:Humans
  5. Lin AE, Santoro S, High FA, Goldenberg P, Gutmark-Little I. Congenital heart defects associated with aneuploidy syndromes: New insights into familiar associations. Am J Med Genet C Semin Med Genet. 2020 03; 184(1):53-63. PMID: 31868316.
    Citations: 3     Fields:    Translation:Humans
  6. Greenberg M, Caloway C, Hersh C, Ryan D, Goldenberg P, Hartnick C. Pharyngeal flap using carotid artery mobilization in 22q11.2 deletion syndrome with velopharyngeal insufficiency. Int J Pediatr Otorhinolaryngol. 2019 May; 120:130-133. PMID: 30784809.
    Citations:    Fields:    Translation:Humans
  7. Levin MD, Saitta SC, Gripp KW, Wenger TL, Ganesh J, Kalish JM, Epstein MR, Smith R, Czosek RJ, Ware SM, Goldenberg P, Myers A, Chatfield KC, Gillespie MJ, Zackai EH, Lin AE. Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients. Am J Med Genet A. 2018 08; 176(8):1711-1722. PMID: 30055033.
    Citations: 4     Fields:    Translation:Humans
  8. Goldenberg P. An Update on Common Chromosome Microdeletion and Microduplication Syndromes. Pediatr Ann. 2018 May 01; 47(5):e198-e203. PMID: 29750287.
    Citations: 16     Fields:    Translation:HumansCells
  9. Hickey CL, Sherman JC, Goldenberg P, Kritzer A, Caruso P, Schmahmann JD, Colvin MK. Cerebellar cognitive affective syndrome: insights from Joubert syndrome. Cerebellum Ataxias. 2018; 5:5. PMID: 29568536.
    Citations: 3     
  10. Goldenberg PC, Adler BJ, Parrott A, Anixt J, Mason K, Phillips J, Cooper DS, Ware SM, Marino BS. High burden of genetic conditions diagnosed in a cardiac neurodevelopmental clinic. Cardiol Young. 2017 Apr; 27(3):459-466. PMID: 27641144.
    Citations: 5     Fields:    Translation:Humans
  11. Parrott A, James J, Goldenberg P, Hinton RB, Miller E, Shikany A, Aylsworth AS, Kaiser-Rogers K, Ferns SJ, Lalani SR, Ware SM. Aortopathy in the 7q11.23 microduplication syndrome. Am J Med Genet A. 2015 Feb; 167A(2):363-70. PMID: 25428557.
    Citations: 11     Fields:    Translation:HumansCells
  12. Ryan TD, Gupta A, Gupta D, Goldenberg P, Taylor MD, Lorts A, Jefferies JL. Dilated cardiomyopathy in a 32-year-old woman with Russell-Silver syndrome. Cardiovasc Pathol. 2014 Jan-Feb; 23(1):21-7. PMID: 24075556.
    Citations: 3     Fields:    Translation:HumansCells
  13. Goldenberg PC, Calkins ME, Richard J, McDonald-McGinn D, Zackai E, Mitra N, Emanuel B, Devoto M, Borgmann-Winter K, Kohler C, Conroy CG, Gur RC, Gur RE. Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and at-risk for psychosis. Am J Med Genet B Neuropsychiatr Genet. 2012 Jan; 159B(1):87-93. PMID: 22170773.
    Citations: 23     Fields:    Translation:HumansCells
  14. Rezaie L, Khazaie H, Soleimani A, Schwebel DC. Self-immolation a predictable method of suicide: a comparison study of warning signs for suicide by self-immolation and by self-poisoning. Burns. 2011 Dec; 37(8):1419-26. PMID: 21570773.
    Citations: 2     Fields:    Translation:Humans
  15. Bassett AS, McDonald-McGinn DM, Devriendt K, Digilio MC, Goldenberg P, Habel A, Marino B, Oskarsdottir S, Philip N, Sullivan K, Swillen A, Vorstman J. Practical guidelines for managing patients with 22q11.2 deletion syndrome. J Pediatr. 2011 Aug; 159(2):332-9.e1. PMID: 21570089.
    Citations: 179     Fields:    Translation:HumansCells
  16. Kishnani PS, Goldenberg PC, DeArmey SL, Heller J, Benjamin D, Young S, Bali D, Smith SA, Li JS, Mandel H, Koeberl D, Rosenberg A, Chen YT. Cross-reactive immunologic material status affects treatment outcomes in Pompe disease infants. Mol Genet Metab. 2010 Jan; 99(1):26-33. PMID: 19775921.
    Citations: 160     Fields:    Translation:HumansCTClinical Trials
  17. Toriello HV, Goldenberg P. Evidence-based medicine and practice guidelines: application to genetics. Am J Med Genet C Semin Med Genet. 2009 Aug 15; 151C(3):235-40. PMID: 19621463.
    Citations: 5     Fields:    Translation:Humans
  18. Poss AF, Goldenberg PC, Rehder CW, Kearney HM, Melvin EC, Koeberl DD, McDonald MT. Clinical experience with array CGH: case presentations from nine months of practice. Am J Med Genet A. 2006 Oct 01; 140(19):2050-6. PMID: 16906557.
    Citations: 2     Fields:    Translation:Humans
  19. Calvert JF, Goldenberg PC, Schock C. Chronic hepatitis C infection in a rural Medicaid HMO. J Rural Health. 2005; 21(1):74-8. PMID: 15667013.
    Citations:    Fields:    Translation:Humans
  20. Goldenberg PC, Steiner RD, Merkens LS, Dunaway T, Egan RA, Zimmerman EA, Nesbit G, Robinson B, Kennaway NG. Remarkable improvement in adult Leigh syndrome with partial cytochrome c oxidase deficiency. Neurology. 2003 Mar 11; 60(5):865-8. PMID: 12629249.
    Citations: 10     Fields:    Translation:Humans
  21. Franco LJ, Mameri C, Pagliaro H, Iochida LC, Goldenberg P. [Diabetes as primary or associated cause of death in the state of São Paulo, Brazil, 1992]. Rev Saude Publica. 1998 Jun; 32(3):237-45. PMID: 9778858.
    Citations: 2     Fields:    Translation:Humans
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.