Mary C. Whitman

Pediatrics

300 Longwood Ave
Boston, MA 02115

Last Updated: 09/26/2026

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Found 47 publications

Genomic Copy Number Variants Associated With Strabismus and Amblyopia in the All of Us Research Program.

Genomic Copy Number Variants Associated With Strabismus and Amblyopia in the All of Us Research Program.

Journal: Investigative ophthalmology & visual science

Published: July 07, 2026

Genome-Wide and Rare Variant Association Studies of Amblyopia in Admixed American and African Ancestry Groups.

Genome-Wide and Rare Variant Association Studies of Amblyopia in Admixed American and African Ancestry Groups.

Journal: Ophthalmology

Published: May 29, 2026

Prevalence of Strabismus and Decreased Stereopsis in Parents of Children with Strabismus.

Prevalence of Strabismus and Decreased Stereopsis in Parents of Children with Strabismus.

Journal: Ophthalmology

Published: February 27, 2026

Rare and Common Genomic Copy Number Variants Associated with Strabismus and Amblyopia in the All of Us Research Program.

Rare and Common Genomic Copy Number Variants Associated with Strabismus and Amblyopia in the All of Us Research Program.

Journal: medRxiv : the preprint server for health sciences

Published: November 24, 2025

Update on Congenital Cranial Dysinnervation Disorders (CCDDs).

Update on Congenital Cranial Dysinnervation Disorders (CCDDs).

Journal: International ophthalmology clinics

Published: September 30, 2025

Amblyopia and adult health: a comprehensive analysis of long-term systemic, sensory and mental health comorbidities in a national cohort.

Amblyopia and adult health: a comprehensive analysis of long-term systemic, sensory and mental health comorbidities in a national cohort.

Journal: The British journal of ophthalmology

Published: September 23, 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

Disrupted Motor Neuron and Neuromuscular Junction Development in an Albino Mice Model of Infantile Nystagmus.

Disrupted Motor Neuron and Neuromuscular Junction Development in an Albino Mice Model of Infantile Nystagmus.

Journal: Investigative ophthalmology & visual science

Published: July 10, 2025

Gene Identification for Ocular Congenital Cranial Motor Neuron Disorders Using Human Sequencing, Zebrafish Screening, and Protein Binding Microarrays.

Gene Identification for Ocular Congenital Cranial Motor Neuron Disorders Using Human Sequencing, Zebrafish Screening, and Protein Binding Microarrays.

Journal: Investigative ophthalmology & visual science

Published: March 31, 2025

Genome-Wide Association Study and Rare Variant Association Studies of Strabismus in the All of Us Research Program.

Genome-Wide Association Study and Rare Variant Association Studies of Strabismus in the All of Us Research Program.

Journal: Ophthalmology science

Published: February 05, 2025

Chromosome 4 Duplication Associated with Strabismus Leads to Gene Expression Changes in iPSC-Derived Cortical Neurons.

Chromosome 4 Duplication Associated with Strabismus Leads to Gene Expression Changes in iPSC-Derived Cortical Neurons.

Journal: Genes

Published: December 18, 2024

Genome-Wide and Rare Variant Association Studies of Amblyopia in the All of Us Research Program.

Genome-Wide and Rare Variant Association Studies of Amblyopia in the All of Us Research Program.

Journal: Ophthalmology

Published: November 11, 2024

Showing 1-12 of 47

Last Updated: 09/26/2026