Amanda Sandoval Karamian

13PUBLICATIONS
35CO-AUTHORS
Infant and child healthEpigenetics (incl. genome methylation and epigenomics)Major global burdens of diseaseNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)
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Publications (13)

|Aug 08, 2026
Management of Infantile Epileptic Spasms Syndrome: A survey of US pediatric hospitals.

|Jul 16, 2026
Heterozygous RNF13 Truncating Variants Are Associated With Developmental and Epileptic Encephalopathy.

|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.

|Aug 26, 2025
Investigating the frequency of unreported cases and laboratory correspondence practices for variants of uncertain significance in pediatric epilepsy.

Tatum Vilaboy, Kristen Wong, Martin Tristani-Firouzi

|Dec 16, 2024
Development of a model to predict electroencephalographic seizures in neonates with hypoxic ischemic encephalopathy treated with therapeutic hypothermia.

Shavonne L Massey, Amanda G Sandoval Karamian, Mark P Fitzgerald

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Frequent Collaborators

3 joint publications

Mark P Fitzgerald

3 joint publications

Shavonne L Massey

2 joint publications

Nicholas S Abend

1 joint publications

Q-Z Yang