Mark P Fitzgerald

16PUBLICATIONS
126CO-AUTHORS
Clinical social work practiceMajor global burdens of diseaseNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Cell and nuclear division
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Publications (16)

|Oct 06, 2026
Establishing consensus diagnostic criteria for ring chromosome 20 syndrome: A modified electronic Delphi consensus study.

|Jun 22, 2026
Racial, Ethnic, and Socioeconomic Associations with Outcomes in Neonatal Hypoxic Ischemic Encephalopathy: A Retrospective Cohort Study.

|May 23, 2026
White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy.

|Mar 08, 2026
Genetic testing for familial epilepsies: Diagnostic yield and genetic findings.

Colin A Ellis, Juliette Copeland, Isabella Velez

|Oct 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function.

Reza Asadollahi, Aisha Ahmad, Paranchai Boonsawat

|Jul 18, 2025
Mosaic Ring 20 Syndrome: A Meta-Analysis.

Sarah Woodson, William D James, Rudolf Roth

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Frequent Collaborators

6 joint publications

Nicholas S Abend

5 joint publications

Ingo Helbig

4 joint publications

Shavonne L Massey

3 joint publications

Amanda G Sandoval Karamian