Mary C Whitman

8PUBLICATIONS
53CO-AUTHORS
Neurology and neuromuscular diseasesPsychology of ageingGene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Infant and child health
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Publications (8)

|Mar 23, 2026
Update on Congenital Cranial Dysinnervation Disorders (CCDDs).

Kathleen Aufderheide, Mary C Whitman

|Jan 27, 2026
Amblyopia and adult health: a comprehensive analysis of long-term systemic, sensory and mental health comorbidities in a national cohort.

Kyoung A Viola Lee, Carsten Langholm, Trevor Lin

|Nov 24, 2025
Rare and Common Genomic Copy Number Variants Associated with Strabismus and Amblyopia in the All of Us Research Program.

Kyoung A Viola Lee, Mary C Whitman

|Feb 13, 2025
Strabismus in Genetic Syndromes: A Review.

Seyda Kilic, Jillian Bove, Bethany Nahri So

|Jan 25, 2025
Chromosome 4 Duplication Associated with Strabismus Leads to Gene Expression Changes in iPSC-Derived Cortical Neurons.

Mayra Martinez-Sanchez, William Skarnes, Ashish Jain

|Jun 29, 2023
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.

Alan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb

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Frequent Collaborators

2 joint publications

Caroline D Robson

2 joint publications

Kyoung A Viola Lee

2 joint publications

Wai-Man Chan

2 joint publications

Elizabeth C Engle