Sajan, S.A., Gradisch, R., …, Jayakar, A., et al (2024). Multi-center implementation of rapid whole genome sequencing provides additional evidence of its utility in the pediatric inpatient setting.
Frontier Pediatrics,
12(), 1349519.
View in Pubmed
Sajan, S.A., Gradisch, R., …, Jayakar, A., et al (2024). De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities, and epilepsy.
European Journal of Human Genetics,
32(8), 912-919.
Uppal, P., Smith, J., ..., Jayakar, A., et al (2023). Glial Fibrillary Acidic Protein (GFAP) Astrocytopathy: An Emerging Cause of Meningoencephalomyelitis in Children and Adolescents.
Journal of child neurology,
8(13-14), 659-664.
View in Pubmed
Harrar, D.B., Benedetti, G.M., Jayakar, A., et al (2022). Pediatric Acute Stroke Protocols in the United States and Canada.
The Journal of pediatrics,
242(), 220-227.e7.
View in Pubmed
Farias-Moeller, R., Jayakar, A., Guerriero, R.M., et al
(2022). Pediatric Critical Care Neurologists in the United States and Canada: A Survey of Clinical Practice Experience.
Journal of child neurology,
37(4), 288-297.
View in Pubmed
Kirschen, M.P., LaRovere, K., Jayakar, A., et al
(2022). A Survey of Neuromonitoring Practices in North American Pediatric Intensive Care Units.
Pediatric neurology,
126(), 125-130.
View in Pubmed
Diaby, V., Babcock, A., Jayakar, A., et al
(2022). Real-world economic evaluation of prospective rapid whole-genome sequencing compared to a matched retrospective cohort of critically ill pediatric patients in the United States.
The pharmacogenomics journal,
22(4), 223-229.
View in Pubmed
Scala, M., Wortmann, S.B., Jayakar, A., et al
(2022). Clinico-radiological features, molecular spectrum, and identification of prognostic factors in developmental and epileptic encephalopathy due to inosine triphosphate pyrophosphatase (ITPase) deficiency.
Human mutation,
43(3), 403-419.
View in Pubmed