Anne B. Fulton

Pediatrics

300 Longwood Ave
Boston, MA 02115

Last Updated: 09/26/2026

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Found 93 publications

Structure-Function Correlation With Optical Coherence Tomography-Derived Macular Thickness and Macular Microperimetry in Children, Adolescents, and Young Adults With Sickle Cell Disease.

Structure-Function Correlation With Optical Coherence Tomography-Derived Macular Thickness and Macular Microperimetry in Children, Adolescents, and Young Adults With Sickle Cell Disease.

Journal: Journal of vitreoretinal diseases

Published: July 02, 2026

Absent cone function and stable ophthalmic features in a non-syndromic woman with pathogenic variants in CEP290.

Absent cone function and stable ophthalmic features in a non-syndromic woman with pathogenic variants in CEP290.

Journal: Ophthalmic genetics

Published: June 25, 2026

Clinical, in vitro, and in vivo evidence of WAPL as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder.

Clinical, in vitro, and in vivo evidence of WAPL as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder.

Journal: medRxiv : the preprint server for health sciences

Published: March 11, 2026

Clinical, in vitro, and in vivo evidence of WAPL as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder.

Clinical, in vitro, and in vivo evidence of WAPL as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder.

Journal: medRxiv : the preprint server for health sciences

Published: March 11, 2026

Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorder.

Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorder.

Journal: American journal of human genetics

Published: February 15, 2026

Vitreoretinal Abnormalities in Poretti-Boltshauser Syndrome: An Imaging Overview.

Vitreoretinal Abnormalities in Poretti-Boltshauser Syndrome: An Imaging Overview.

Journal: Ophthalmology. Retina

Published: December 05, 2025

Severe Posterior Retinopathy of Prematurity: A Matched Cohort Analysis.

Severe Posterior Retinopathy of Prematurity: A Matched Cohort Analysis.

Journal: Ophthalmology. Retina

Published: November 05, 2025

Peripapillary Scleral Deposits in Mucopolysaccharidosis Type II.

Peripapillary Scleral Deposits in Mucopolysaccharidosis Type II.

Journal: Ophthalmology

Published: October 09, 2025

Novel structural variant in CACNA1F causing congenital stationary night blindness identified with whole genome sequencing.

Novel structural variant in CACNA1F causing congenital stationary night blindness identified with whole genome sequencing.

Journal: Ophthalmic genetics

Published: July 31, 2025

Poretti-Boltshauser Syndrome: A Potential Pathognomonic "Wolfjaw" Pattern of Retinal Perfusion.

Poretti-Boltshauser Syndrome: A Potential Pathognomonic "Wolfjaw" Pattern of Retinal Perfusion.

Journal: Ophthalmic surgery, lasers & imaging retina

Published: July 25, 2025

Real-world outcomes of retinopathy of prematurity treated with primary laser versus primary anti-vascular endothelial growth factor and deferred laser.

Real-world outcomes of retinopathy of prematurity treated with primary laser versus primary anti-vascular endothelial growth factor and deferred laser.

Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus

Published: June 06, 2025

Timing of Retinopathy of Prematurity Diagnosis and Treatment in Micro-Premature and Nano-Premature Infants during Inpatient Screening.

Timing of Retinopathy of Prematurity Diagnosis and Treatment in Micro-Premature and Nano-Premature Infants during Inpatient Screening.

Journal: Ophthalmology. Retina

Published: March 30, 2025

Showing 1-12 of 93

Last Updated: 09/26/2026