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Anne Fulton, MD
Ophthalmologist, Department of Ophthalmology
Professor, Harvard Medical School
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Anne Fulton, MD
Ophthalmologist, Department of Ophthalmology
Professor, Harvard Medical School
Medical Services
Languages
English
Education
Undergraduate School
Radcliffe College
1962
Cambridge
MA
Medical School
Tufts University School of Medicine
1996
Boston
MA
Internship
Grady Memorial Hospital
1967
New Haven
CT
Residency
Yale University School of Medicine
1976
New Haven
CT
Media
Caregiver Profile
Meet Dr. Anne Fulton
Certifications
American Board of Ophthalmology (General)
Professional History
Dr. Fulton serves as an expert for the Department of Ophthalmology for Boston Children's Hospital Precision Medicine Service. For more information about the Precision Medicine Service please visit bostonchildrens.org/precisionmed.
Publications
Timing of Retinopathy of Prematurity Diagnosis and Treatment in Micro-Premature and Nano-Premature Infants During Inpatient Screening. View Abstract
Quantifying the Progression of Stargardt Disease in Double-Null ABCA4 Carriers Using Fundus Autofluorescence Imaging. View Abstract
Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study. View Abstract
Advancing Insights into Pediatric Macular Diseases: A Comprehensive Review. View Abstract
Evaluating the Utility of Initial Examinations in Retinopathy of Prematurity: Proposal of FIRST-ROP Algorithm for a Medium-Risk Cohort. View Abstract
HBS1L deficiency causes retinal dystrophy in a child and in a mouse model associated with defective development of photoreceptor cells. View Abstract
Validation of the "TWO-ROP" Algorithm at a Multi-Neonatal Intensive Care Unit Tertiary Referral Center. View Abstract
The Surviving, Not Thriving, Photoreceptors in Patients with ABCA4 Stargardt Disease. View Abstract
Refractive errors in patients with Bardet Biedl syndrome. View Abstract
Vision Loss and Difficulty Walking in a Pediatric Sexual Assault Victim. View Abstract
KEARNS-SAYRE SYNDROME MASQUERADING AS MYASTHENIA GRAVIS. View Abstract
Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules. View Abstract
Characteristics of Eyes With CRB1-Associated EOSRD/LCA: Age-Related Changes. View Abstract
Genetic deficiency of ribosomal rescue factor HBS1L causes retinal dystrophy associated with Pelota and EDF1 depletion. View Abstract
A Simplified Model of Activation and Deactivation of Human Rod Phototransduction-An Electroretinographic Study. View Abstract
The Development of Retinal Function and Refractive Error in Children With Retinopathy of Prematurity. View Abstract
Do the retinal abnormalities in X-linked juvenile retinoschisis include impaired phototransduction? View Abstract
Non-Rigid Registration for High-Resolution Retinal Imaging. View Abstract
Electroretinographic Responses in Retinopathy of Prematurity Treated Using Intravitreal Bevacizumab or Laser. View Abstract
Microcephaly and chorioretinopathy associated with TUBGCP4: a case report and a review of the literature. View Abstract
Modelling eye lengths and refractions in the periphery. View Abstract
Insights into the genotype-phenotype relationship of ocular manifestations in Kabuki syndrome. View Abstract
Can Nerve Growth Factor (NGF) Be a Treatment Option for Pediatric Eye Diseases? View Abstract
Membrane Frizzled-Related Protein-Related Disease Mimicking Idiopathic Intracranial Hypertension. View Abstract
The relation of the multifocal electroretinographic response to macular layer volume. View Abstract
Longitudinal Change of Refractive Error in Retinopathy of Prematurity Treated With Intravitreal Bevacizumab or Laser Photocoagulation. View Abstract
The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences. View Abstract
Evaluation of the Relationship Between Preferential Looking Testing and Visual Evoked Potentials as a Biomarker of Cerebral Visual Impairment. View Abstract
Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRD. View Abstract
Fundus Pigmentary Whorls in a Patient With Mosaicism for Tetrasomy 3q. View Abstract
Cerebral visual impairment in CDKL5 deficiency disorder: vision as an outcome measure. View Abstract
Artificial Intelligence (AI) Applications for Age-Related Macular Degeneration (AMD) and Other Retinal Dystrophies. View Abstract
Optical Coherence Tomography Angiography in Prematurity. View Abstract
Genetic causes of nystagmus, foveal hypoplasia and subnormal visual acuity- other than albinism. View Abstract
Dark-adapted threshold and electroretinogram for diagnosis of Usher syndrome. View Abstract
Homozygous deletion of 21q22.2 in a patient with hypotonia, developmental delay, cortical visual impairment, and retinopathy. View Abstract
Carbonic anhydrase inhibition in X-linked retinoschisis: An eye on the photoreceptors. View Abstract
The Fovea in Retinopathy of Prematurity. View Abstract
Retinal Function in X-Linked Juvenile Retinoschisis. View Abstract
Extracting the ON and OFF contributions to the full-field photopic flash electroretinogram using summed growth curves. View Abstract
Impact of Obstructive Sleep Apnea on Optic Nerve Function in Patients With Craniosynostosis and Recurrent Intracranial Hypertension. View Abstract
Microperimetry in Three Inherited Retinal Disorders. View Abstract
The migraine eye: distinct rod-driven retinal pathways' response to dim light challenges the visual cortex hyperexcitability theory. View Abstract
Neurobiology of Photophobia. View Abstract
High prevalence of strabismic visual field expansion in pediatric homonymous hemianopia. View Abstract
Color-selective photophobia in ictal vs interictal migraineurs and in healthy controls. View Abstract
ISCEV guide to visual electrodiagnostic procedures. View Abstract
The importance of genetic testing as demonstrated by two cases of CACNA1F-associated retinal generation misdiagnosed as LCA. View Abstract
Increased Survival and Partly Preserved Cognition in a Patient With ACO2-Related Disease Secondary to a Novel Variant. View Abstract
Juvenile Macular Degenerations. View Abstract
Multifocal ERG Responses in Subjects With a History of Preterm Birth. View Abstract
Progressive retinal degeneration in a girl with Knobloch syndrome who presented with signs of ocular albinism. View Abstract
Available Evidence on Leber Congenital Amaurosis and Gene Therapy. View Abstract
The neural retina in retinopathy of prematurity. View Abstract
Reduced Left Lateralization of Language in Congenitally Blind Individuals. View Abstract
Retinal, visual, and refractive development in retinopathy of prematurity. View Abstract
Migraine photophobia originating in cone-driven retinal pathways. View Abstract
Increment Threshold Functions in Retinopathy of Prematurity. View Abstract
Expansion of phenotype and genotypic data in CRB2-related syndrome. View Abstract
Differentiation of murine models of "negative ERG" by single and repetitive light stimuli. View Abstract
Extrafoveal Cone Packing in Eyes With a History of Retinopathy of Prematurity. View Abstract
Eye growth in term- and preterm-born eyes modeled from magnetic resonance images. View Abstract
Vigabatrin can enhance electroretinographic responses in pigmented and albino rats. View Abstract
Temporal summation in children with a history of retinopathy of prematurity. View Abstract
Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing. View Abstract
Effect of retinopathy of prematurity on scotopic spatial summation. View Abstract
The rat with oxygen-induced retinopathy is myopic with low retinal dopamine. View Abstract
The hermansky-pudlak syndrome: clinical features and imperatives from an ophthalmic perspective. View Abstract
CRB1: one gene, many phenotypes. View Abstract
Introduction to the special issue: vision after premature birth. View Abstract
Photoreceptor and postreceptor responses in congenital stationary night blindness. View Abstract
Next-generation sequencing analysis of gene regulation in the rat model of retinopathy of prematurity. View Abstract
Alterations of the tunica vasculosa lentis in the rat model of retinopathy of prematurity. View Abstract
Multimodal adaptive optics retinal imager: design and performance. View Abstract
Electroretinographic (ERG) responses in pediatric patients using vigabatrin. View Abstract
Effect of carotenoid supplementation on plasma carotenoids, inflammation and visual development in preterm infants. View Abstract
Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndrome. View Abstract
Long-term effects of retinopathy of prematurity (ROP) on rod and rod-driven function. View Abstract
Cone ERG responses in patients with Smith-Lemli-Opitz Syndrome (SLOS). View Abstract
Visual cycle modulation in neurovascular retinopathy. View Abstract
Deactivation of the rod response in retinopathy of prematurity. View Abstract
Editorial for special issue: rat models of ROP. View Abstract
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial. View Abstract
The anatomy of the rat eye with oxygen-induced retinopathy. View Abstract
The neurovascular retina in retinopathy of prematurity. View Abstract
Visual fields in young children treated with vigabatrin. View Abstract
Development of rod function in term born and former preterm subjects. View Abstract
The neurovascular relation in oxygen-induced retinopathy. View Abstract
ISCEV Standard for full-field clinical electroretinography (2008 update). View Abstract
Rod and rod-driven function in achromatopsia and blue cone monochromatism. View Abstract
Synergistic interaction of the OCA2 and OCA3 genes in a family. View Abstract
Multifocal ERG responses in infants. View Abstract
Retinal degenerative and hypoxic ischemic disease. View Abstract
The cone electroretinogram in retinopathy of prematurity. View Abstract
Foveal fine structure in retinopathy of prematurity: an adaptive optics Fourier domain optical coherence tomography study. View Abstract
The oscillatory potentials of the dark-adapted electroretinogram in retinopathy of prematurity. View Abstract
Effects of desferoxamine on retinal and visual function. View Abstract
Development of scotopic visual thresholds in retinopathy of prematurity. View Abstract
The genetics and ocular findings of Alagille syndrome. View Abstract
Rod photoreceptor function predicts blood vessel abnormality in retinopathy of prematurity. View Abstract
Retinal degeneration in children: dark adapted visual threshold and arteriolar diameter. View Abstract
Development of the electroretinographic oscillatory potentials in normal and ROP rats. View Abstract
Pediatric clinical visual electrophysiology: a survey of actual practice. View Abstract
The retinal vasculature and function of the neural retina in a rat model of retinopathy of prematurity. View Abstract
Proceedings of the Third International Symposium on Retinopathy of Prematurity: an update on ROP from the lab to the nursery (November 2003, Anaheim, California). View Abstract
Multifocal ERG in subjects with a history of retinopathy of prematurity. View Abstract
X-linked creatine transporter defect: a report on two unrelated boys with a severe clinical phenotype. View Abstract
Diagnosis of plus disease in retinopathy of prematurity using Retinal Image multiScale Analysis. View Abstract
Development of the cone ERG in infants. View Abstract
Development of visual acuity in children with cerebral visual impairment. View Abstract
Maculopathy and retinal degeneration in cobalamin C methylmalonic aciduria and homocystinuria. View Abstract
Early ametropia and rod photoreceptor function in retinopathy of prematurity. View Abstract
ERG oscillatory potentials in infants. View Abstract
Recovery of the rod photoresponse in infants. View Abstract
Comparison of ERGs recorded with skin and corneal-contact electrodes in normal children and adults. View Abstract
Recovery of the rod photoresponse in infant rats. View Abstract
Rod photoreceptor responses in children with Smith-Lemli-Opitz syndrome. View Abstract
Development of ERG responses: the ISCEV rod, maximal and cone responses in normal subjects. View Abstract
Effects of telazol and nembutal on retinal responses. View Abstract
Retinal function in carriers of Bardet-Biedl syndrome. View Abstract
Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1). View Abstract
Rod photoreceptor function in children with mitochondrial disorders. View Abstract
Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome. View Abstract
Fundus photography for measurement of macular pigment density distribution in children. View Abstract
Background adaptation in a rat model of retinopathy of prematurity. View Abstract
Novel frameshift mutations in CRX associated with Leber congenital amaurosis. View Abstract
Cycloplegic refractions in healthy children aged 1 through 48 months. View Abstract
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2). View Abstract
The rod photoreceptors in retinopathy of prematurity: an electroretinographic study. View Abstract
Mutations in the CRB1 gene cause Leber congenital amaurosis. View Abstract
Cortical visual impairment in infants and children. View Abstract
Rod-mediated increment threshold functions in infants. View Abstract
The development of scotopic sensitivity. View Abstract
Background adaptation in children with a history of mild retinopathy of prematurity. View Abstract
The rhodopsin content of human eyes. View Abstract
The course of maturation of rod-mediated visual thresholds in infants. View Abstract
Rod photoreceptor maturation does not vary with retinal eccentricity in mammalian retina. View Abstract
Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome) [correction of (Hennansky-Pudlak)]. View Abstract
Rod photoreceptors in infant rats with a history of oxygen exposure. View Abstract
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. View Abstract
Rod and rod mediated function in patients with beta-thalassemia major. View Abstract
Central retinal vein occlusion in a young child with cyanotic heart disease. View Abstract
Dark-adapted thresholds in children with histories of mild retinopathy of prematurity. View Abstract
Rhodopsin in immature rod outer segments. View Abstract
Vision in Leber congenital amaurosis. View Abstract
Photoreceptor function in infants and children with a history of mild retinopathy of prematurity. View Abstract
Effect of prior oxygen exposure on the electroretinographic responses of infant rats. View Abstract
The effects of acetazolamide on the electroretinographic responses in rats. View Abstract
The development of the rod photoresponse from dark-adapted rats. View Abstract
The course of myopia in children with mild retinopathy of prematurity. View Abstract
Dark-adapted thresholds at 10- and 30-deg eccentricities in 10-week-old infants. View Abstract
The VEP thresholds for full-field stimuli in dark-adapted infants. View Abstract
Electroretinogram responses and refractive errors in patients with a history of retinopathy prematurity. View Abstract
Scotopic optokinetic nystagmus thresholds in 10-week-old infants. View Abstract
Scotopic center surround organization in 10-week-old infants. View Abstract
Clinical physiology of heritable photoreceptor diseases. View Abstract
Natural course of visual functions in the Bardet-Biedl syndrome. View Abstract
The rod sensitivity of dark adapted human infants. View Abstract
Screening preschool children to detect visual and ocular disorders. View Abstract
Effects of halothane on children's electroretinograms. View Abstract
The effect of light adaptation on scotopic spatial summation in 10-week-old infants. View Abstract
Albinism. View Abstract
The quantity of rhodopsin in young human eyes. View Abstract
Visual development of infants with severe ocular disorders. View Abstract
Delayed visual maturation. View Abstract
Dark adapted thresholds in young RCS rats. View Abstract
Temporal summation in dark-adapted 10-week old infants. View Abstract
Electroretinographic assessment of background adaptation in 10-week-old human infants. View Abstract
The quantity of rhodopsin in human eyes. View Abstract
Hyperopia in complicated Leber's congenital amaurosis. View Abstract
Dark adaptation in hyperprolactinemic women. View Abstract
Electrophysiologic testing techniques for children. View Abstract
Psychophysical estimates of ocular media density of human infants. View Abstract
Visual acuities and dark-adapted thresholds of children with Bardet-Biedl syndrome. View Abstract
Visual fields of young children. View Abstract
The development of scotopic retinal function in human infants. View Abstract
Visual fields of infants assessed with a new perimetric technique. View Abstract
Scotopic stimulus/response relations of the B-wave of the electroretinogram. View Abstract
The relation of rhodopsin and scotopic retinal sensitivity in sector retinitis pigmentosa. View Abstract
Optokinetic nystagmus thresholds of dark-adapted RCS rats. View Abstract
Esotropic children with amblyopia: effects of patching on acuity. View Abstract
Special diagnostic and therapeutic modalities in pediatric ophthalmology. View Abstract
The relation of rhodopsin and scotopic sensitivity in choroideremia. View Abstract
Oscillatory potentials of visually inattentive children. View Abstract
Foveal cone pigments and sensitivity in young patients with Usher's syndrome. View Abstract
Intramuscular vitamin E repletion in children with chronic cholestasis. View Abstract
Concurrence of congenital ocular motor apraxia and other motor problems: an expanded syndrome. View Abstract
The relationship of retinal sensitivity and rhodopsin in human infants. View Abstract
"Self-screening" of rhodopsin in rod outer segments. View Abstract
Pupillary changes during dark adaptation in human infants. View Abstract
Assessment of acuity of amblyopic subjects using face, grating, and recognition stimuli. View Abstract
Background adaptation in human infants. View Abstract
Electroretinography: application to clinical studies of infants. View Abstract
Assessment of young amblyopes. Array vs. single picture acuities. View Abstract
Retinal degenerations and brain abnormalities in infants and young children. View Abstract
Visual acuity of infants and children with retinal degenerations. View Abstract
Preferential looking grating acuities of infants at risk of amblyopia. View Abstract
Grating and recognition acuities of pediatric patients. View Abstract
Assessment of acuity in human infants using face and grating stimuli. View Abstract
The relation of retinal sensitivity and rhodopsin in developing rat retina. View Abstract
Retinal degeneration in vitamin B12 disorder associated with methylmalonic aciduria and sulfur amino acid abnormalities. View Abstract
Cycloplegic refractions of infants and young children: the axis of astigmatism. View Abstract
Retinal sensitivity and adaptation in pediatric patients. View Abstract
Preferential looking acuity of pediatric patients with developmental disabilities. View Abstract
Background adaptation in RCS rats. View Abstract
Preferential looking vision testing: application to evaluation of high-risk, prematurely born infants and children. View Abstract
Preferential looking acuity obtained with a staircase procedure in pediatric patients. View Abstract
Scotopic thresholds and plasma retinol in cystic fibrosis. View Abstract
The relation of myopia and astigmatism in developing eyes. View Abstract
Dark-adapted sensitivity, rhodopsin content, and background adaptation in pcd/pcd mice. View Abstract
Development of the outer plexiform layer in albino rats. View Abstract
Retinal degeneration in the delayed amelanotic (DAM) chicken: an electroretinographic study. View Abstract
Behavioral measurement of background adaptation in infants. View Abstract
Cycloplegic refractions of premature infants. View Abstract
Cone pigments in acute posterior multifocal placoid pigment epitheliopathy. View Abstract
Measuring visual acuity in infants. View Abstract
Cycloplegic refractions in infants and young children. View Abstract
Increased incidence of choroidal malignant melanoma occurring in a single population of chemical workers. View Abstract
Background adaptation in developing rat retina: an electroretinographic study. View Abstract
Retinal anomalies in trisomy 18. View Abstract
Epidemikological investigation of increased incidence of choroidal melanoma in a single population of chemical workers. View Abstract
Infant vision testing by a behavioral method. View Abstract
A behavioral method for efficient screening of visual acuity in young infants. II. Clinical application. View Abstract
Human retinal dysplasia. View Abstract
Human albinism. Light and electron microscopy study. View Abstract
Rod ERG of the mudpuppy: effect of dim red backgrounds. View Abstract
The human rod ERG: correlation with psychophysical responses in light and dark adaptation. View Abstract
Ocular findings in triploidy. View Abstract
Spontaneous anophthalmia and microphthalmia in white-tailed deer. View Abstract
Comparative ophthalmic pathology. View Abstract
Active giant cell arteritis with cerebral involvement. Findings following four years of corticosteroid therapy. View Abstract
Gastrointestinal sarcoidosis diagnosed by conjunctival biopsy. View Abstract
Dark adaptation and the rate of pigment regeneration. View Abstract
Dark adaptation: free opsin or regeneration rate? View Abstract
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