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Hannah L. Scanga

Developing a pediatric ophthalmology telemedicine program in the COVID-19 crisis
2020 · Saloni Kapoor, Amgad Eldib, et al. · Journal of American Association for Pediatric Ophthalmology and Strabismus · 33
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Iris anomalies and the incidence ofACTA2mutation
2018 · Kenneth J Taubenslag, Hannah L Scanga, et al. · British Journal of Ophthalmology · 18
Carcinoma-associated retinopathy in a young teenager with immature teratoma of the ovary
2014 · Kiran Turaka, Daniel Kietz, et al. · Journal of American Association for Pediatric Ophthalmology and Strabismus · 17
Congenital primary aphakia
2022 · Julia Ernst, Anagha Medsinge, et al. · Journal of American Association for Pediatric Ophthalmology and Strabismus · 16
Coenzyme Q10 in the Treatment of Corneal Edema in Kearns-Sayre
2016 · Jocelyn Kim, Anagha Medsinge, et al. · Cornea · 16
Somatic KRAS mutation affecting codon 146 in linear sebaceous nevus syndrome
2021 · Saloni Kapoor, Hannah L. Scanga, et al. · American Journal of Medical Genetics Part A · 15
A proposal for an updated staging system for LCHADD retinopathy
2024 · Nida Wongchaisuwat, Melanie B. Gillingham, et al. · Ophthalmic Genetics · 14
Early diagnosis and treatment by newborn screening ( NBS ) or family history is associated with improved visual outcomes for long‐chain 3‐hydroxyacylCoA dehydrogenase deficiency ( LCHADD ) chorioretinopathy
2024 · Melanie B. Gillingham, Dongseok Choi, et al. · Journal of Inherited Metabolic Disease · 9
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Clinical and imaging characteristics of posterior column ataxia with retinitis pigmentosa with a specific FLVCR1 mutation
2018 · Jennifer Lee, Hannah L. Scanga, et al. · Ophthalmic Genetics · 9
Case series: Pyramidal cataracts, intact irides and nystagmus from three novel PAX6 mutations
2018 · Bharesh K. Chauhan, Anagha Medsinge, et al. · American Journal of Ophthalmology Case Reports · 8
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Isolated Sagittal Synostosis in a Boy with Craniofrontonasal Dysplasia and a Novel EFNB1 Mutation
2015 · Bharesh K. Chauhan, Jacqueline M. Hoover, et al. · Plastic & Reconstructive Surgery Global Open · 8
Genetics and Ocular Disorders
2014 · Hannah L. Scanga, Ken K. Nischal · Pediatric Clinics of North America · 8
Plasma Metabolomics, Lipidomics, and Acylcarnitines Are Associated With Vision and Genotype but Not With Dietary Intake in Long‐Chain 3‐Hydroxyacyl‐ CoA Dehydrogenase Deficiency ( LCHADD )
2025 · Hak Chung, Dongseok Choi, et al. · Journal of Inherited Metabolic Disease · 7
Variable phenotype of secondary congenital corneal opacities associated with microphthalmia with linear skin defects syndrome
2022 · Elena Franco, Hannah L. Scanga, et al. · American Journal of Medical Genetics Part A · 7
Macular atrophy in JAG1- related Alagille syndrome: a case series
2021 · Manuel Paez-Escamilla, Hannah L. Scanga, et al. · Ophthalmic Genetics · 7
Variable Phenotype of Congenital Corneal Opacities in Biallelic CYP1B1 Pathogenic Variants
2023 · Elena Franco, Meghal Gagrani, et al. · Cornea · 6
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Congenital corneal staphyloma in 8q21.11 microdeletion syndrome
2022 · Elena Franco, Hannah L. Scanga, et al. · Ophthalmic Genetics · 6
Novel clinical presentation of a CRX rod-cone dystrophy
2021 · Luis Alonso Gonzalez-Gonzalez, Hannah Scanga, et al. · BMJ Case Reports · 6
Improved visual function with dietary intervention in a child with lipemia retinalis
2014 · Valeria Fu, Hannah L. Scanga, et al. · Journal of American Association for Pediatric Ophthalmology and Strabismus · 5
Personalized pediatric ophthalmology: a case report
2019 · Lillian K. To, Parth R. Shah, et al. · Journal of American Association for Pediatric Ophthalmology and Strabismus · 4
Tectonic Corneal Transplant in the Management of Congenital Anterior Staphyloma
2025 · Rita Rodrigues, Hannah Scanga, et al. · Cornea · 3
Recurrent retinal detachment in Stickler Syndrome
2024 · Timothy H. Chen, Marjan Imani Fooladi, et al. · Eye · 3
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Thygeson’s superficial punctate keratitis in children
2023 · Meghal Gagrani, Elizabeth A. Conner, et al. · Eye · 3
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ADAMTSL4‐related ectopia lentis: A case of pseudodominance with an asymptomatic parent
2022 · Hannah L. Scanga, Ken K. Nischal · American Journal of Medical Genetics Part A · 3
NYX-related Congenital Stationary Night Blindness in Two Siblings due to Probable Maternal Germline Mosaicism
2021 · H. l. Scanga, A. Liasis, et al. · Ophthalmic Genetics · 3
Works count: 51
Citation count: 245
H-index: 9
I10-index: 7
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