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profileGena Heidary, Ph.D., M.D.

TitleAssistant Professor of Ophthalmology
InstitutionBoston Children's Hospital
DepartmentOphthalmology
AddressChildrens Hospital
Ophthalmology, Fegan 4
300 Longwood Ave
Boston MA 02115
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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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  1. Heidary G. Neuro-Ophthalmic Manifestations of Pediatric Neurodegenerative Disease. J Neuroophthalmol. 2017 Sep; 37 Suppl 1:S4-S13. PMID: 28806344.
    View in: PubMed
  2. Peeler CE, Edmond JC, Hollander J, Alexander JK, Zurakowski D, Ullrich NJ, Manley PE, Heidary G. Visual and ocular motor outcomes in children with posterior fossa tumors. J AAPOS. 2017 Oct; 21(5):375-379. PMID: 28867398.
    View in: PubMed
  3. Heidary G. Introduction. Semin Pediatr Neurol. 2017 May; 24(2):81-82. PMID: 28941530.
    View in: PubMed
  4. Mouw KW, Yeap BY, Caruso P, Fay A, Misra M, Sethi RV, MacDonald SM, Chen YL, Tarbell NJ, Yock TI, Freitag SK, Munzenrider JE, Grabowski E, Katz M, Kuhlthau K, DeCastro D, Heidary G, Ciralsky J, Mukai S, Shih HA. Analysis of patient outcomes following proton radiation therapy for retinoblastoma. Adv Radiat Oncol. 2017 Jan-Mar; 2(1):44-52. PMID: 28607957.
    View in: PubMed
  5. Avery RA, Katowitz JA, Fisher MJ, Heidary G, Dombi E, Packer RJ, Widemann BC. Orbital/Periorbital Plexiform Neurofibromas in Children with Neurofibromatosis Type 1: Multidisciplinary Recommendations for Care. Ophthalmology. 2017 Jan; 124(1):123-132. PMID: 27817916.
    View in: PubMed
  6. Gilbert AL, Heidary G. Update on the evaluation of pediatric idiopathic intracranial hypertension. Curr Opin Ophthalmol. 2016 Nov; 27(6):493-497. PMID: 27585209.
    View in: PubMed
  7. Wong MM, Schneier AJ, Ledoux D, Heidary G. Neuroimaging Findings in Patients With Down Syndrome and Nystagmus. J Pediatr Ophthalmol Strabismus. 2016 Nov 01; 53(6):383. PMID: 27858949.
    View in: PubMed
  8. Gilbert AL, Koo EB, Heidary G. Evaluation and Management of Acute Acquired Comitant Esotropia in Children. Semin Ophthalmol. 2017; 32(1):8-13. PMID: 27726470.
    View in: PubMed
  9. Sheldon CA, Paley GL, Xiao R, Kesler A, Eyal O, Ko MW, Boisvert CJ, Avery RA, Salpietro V, Phillips PH, Heidary G, McCormack SE, Liu GT. Pediatric Idiopathic Intracranial Hypertension: Age, Gender, and Anthropometric Features at Diagnosis in a Large, Retrospective, Multisite Cohort. Ophthalmology. 2016 Nov; 123(11):2424-2431. PMID: 27692528.
    View in: PubMed
  10. Wan MJ, Ullrich NJ, Manley PE, Kieran MW, Goumnerova LC, Heidary G. Long-term visual outcomes of optic pathway gliomas in pediatric patients without neurofibromatosis type 1. J Neurooncol. 2016 Aug; 129(1):173-8. PMID: 27311725.
    View in: PubMed
  11. Merabet LB, Devaney KJ, Bauer CM, Panja A, Heidary G, Somers DC. Characterizing Visual Field Deficits in Cerebral/Cortical Visual Impairment (CVI) Using Combined Diffusion Based Imaging and Functional Retinotopic Mapping: A Case Study. Front Syst Neurosci. 2016; 10:13. PMID: 26941619; PMCID: PMC4766290.
  12. Wan MJ, Adebona O, Benson LA, Gorman MP, Heidary G. Reply: To PMID 24907434. Am J Ophthalmol. 2015 Jan; 159(1):211. PMID: 25488651.
    View in: PubMed
  13. Dagi LR, Tiedemann LM, Heidary G, Robson CD, Hall AM, Zurakowski D. Using spectral-domain optical coherence tomography to detect optic neuropathy in patients with craniosynostosis. J AAPOS. 2014 Dec; 18(6):543-9. PMID: 25498464.
    View in: PubMed
  14. Heidary G. Congenital optic nerve anomalies and hereditary optic neuropathies. J Pediatr Genet. 2014 Dec; 3(4):271-80. PMID: 27625883; PMCID: PMC5020999.
  15. Bauer CM, Heidary G, Koo BB, Killiany RJ, Bex P, Merabet LB. Abnormal white matter tractography of visual pathways detected by high-angular-resolution diffusion imaging (HARDI) corresponds to visual dysfunction in cortical/cerebral visual impairment. J AAPOS. 2014 Aug; 18(4):398-401. PMID: 25087644; PMCID: PMC4150820.
  16. Wan MJ, Adebona O, Benson LA, Gorman MP, Heidary G. Visual outcomes in pediatric optic neuritis. Am J Ophthalmol. 2014 Sep; 158(3):503-7.e2. PMID: 24907434.
    View in: PubMed
  17. Heidary G, Calderwood L, Cox GF, Robson CD, Teot LA, Mullon J, Anselm I. Optic atrophy and a Leigh-like syndrome due to mutations in the c12orf65 gene: report of a novel mutation and review of the literature. J Neuroophthalmol. 2014 Mar; 34(1):39-43. PMID: 24284555.
    View in: PubMed
  18. Ellika S, Robson CD, Heidary G, Paldino MJ. Morning glory disc anomaly: characteristic MR imaging findings. AJNR Am J Neuroradiol. 2013 Oct; 34(10):2010-4. PMID: 23660287.
    View in: PubMed
  19. Schneier AJ, Heidary G, Ledoux DM. Optic nerve appearance in patients with Down syndrome. J Pediatr Ophthalmol Strabismus. 2013 Jan-Feb; 50(1):60. PMID: 23343090.
    View in: PubMed
  20. Young MP, Heidary G, VanderVeen DK. Relationship between the timing of cataract surgery and development of nystagmus in patients with bilateral infantile cataracts. J AAPOS. 2012 Dec; 16(6):554-7. PMID: 23237753.
    View in: PubMed
  21. Heidary G, Rizzo JF. Use of optical coherence tomography to evaluate papilledema and pseudopapilledema. Semin Ophthalmol. 2010 Sep-Nov; 25(5-6):198-205. PMID: 21091000.
    View in: PubMed
  22. Heidary G, Vanderveen D, Smith LE. Retinopathy of prematurity: current concepts in molecular pathogenesis. Semin Ophthalmol. 2009 Mar-Apr; 24(2):77-81. PMID: 19373690; PMCID: PMC4019928.
  23. Heidary G, Engle EC, Hunter DG. Congenital fibrosis of the extraocular muscles. Semin Ophthalmol. 2008 Jan-Feb; 23(1):3-8. PMID: 18214786.
    View in: PubMed
  24. Heidary G, Ying GS, Maguire MG, Young TL. The association of astigmatism and spherical refractive error in a high myopia cohort. Optom Vis Sci. 2005 Apr; 82(4):244-7. PMID: 15829852.
    View in: PubMed
  25. Heidary G, Fortini ME. Identification and characterization of the Drosophila tau homolog. Mech Dev. 2001 Oct; 108(1-2):171-8. PMID: 11578871.
    View in: PubMed
  26. Heidary G, Hampton LL, Schanen NC, Rivkin MJ, Darras BT, Battey J, Francke U. Exclusion of the gastrin-releasing peptide receptor (GRPR) locus as a candidate gene for Rett syndrome. Am J Med Genet. 1998 Jun 30; 78(2):173-5. PMID: 9674911.
    View in: PubMed
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