Charles Schwartz

16PUBLICATIONS
85CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene mappingNeurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)Neurogenetics
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Publications (16)

|Aug 04, 2026
Abidi Syndrome and Another Family With X-Linked Intellectual Disability Have TAF1 Variants and Reduced Phosphorylation of RNA Polymerase II Associated Protein 74.

|Jul 31, 2026
An improved Sms p.Gly56Ser model of Snyder-Robinson syndrome reveals phenotypic parallels with clinical features.

|Dec 18, 2025
Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative Review.

Elizabeth A VanSickle, Sara M Sarasua, Tracy Lowe

|Feb 08, 2024
Personal journeys to and in human genetics and dysmorphology.

Charles E Schwartz, Arthur S Aylsworth, Judith Allanson

|Jul 14, 2023
Defining the 3'Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome.

David E Godler, Yoshimi Inaba, Minh Q Bui

|Mar 30, 2023
Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability.

Yu-Ri Lee, Mervyn G Thomas, Arkaprava Roychaudhury

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Frequent Collaborators

6 joint publications

Roger E Stevenson

3 joint publications

Jozef Gecz

3 joint publications

Tao Wang

3 joint publications

Jennifer Kerkhof