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Christina H. Frater

Observed name: Christina H Frater
Institution: Stanford University
ORCID: 0009-0005-2182-8207
Observed ORCID: 0009-0005-2182-8207
OpenAlex ID: A5032992133
Delineating the epilepsy phenotype of NGLY1 deficiency
2022 · Rebecca J. Levy, Christina H. Frater, et al. · Journal of Inherited Metabolic Disease · 21
NGLY1 deficiency: a prospective natural history study
2023 · Sandra Tong, Pamela Ventola, et al. · Human Molecular Genetics · 13
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Ocular features of NGLY1 deficiency from a prospective longitudinal cohort
2024 · Christina H. Frater, Maura R.Z. Ruzhnikov, et al. · Journal of American Association for Pediatric Ophthalmology and Strabismus · 6
P457: Characterization of a balanced translocation disrupting SOX9: Implications for campomelic dysplasia
2025 · Aisha Rekab, Christina Frater, et al. · Genetics in Medicine Open
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Works count: 3
Citation count: 40
H-index: 3
I10-index: 2
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