Author

Ayat Asleh

Observed name: Ayat N. Asleh

Institutions: Johns Hopkins University, Johns Hopkins Medicine

Observed institutions: Mayo Clinic, Johns Hopkins University, Johns Hopkins Medicine

OpenAlex ID: A5020760285

IQSEC2 mutation associated with epilepsy, intellectual disability, and autism results in hyperexcitability of patient-derived neurons and deficient synaptic transmission

2021 · Boris Brant, Tchelet Stern, et al. · Molecular Psychiatry · 46

Haptoglobin Phenotype Is Associated With High-Density Lipoprotein–Bound Hemoglobin Content and Coronary Endothelial Dysfunction in Patients With Mild Nonobstructive Coronary Artery Disease

2019 · Rabea Asleh, Andrew P. Levy, et al. · Arteriosclerosis Thrombosis and Vascular Biology · 38

Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly

2023 · Margaux Serey-Gaut, Marisol Cortes, et al. · The American Journal of Human Genetics · 6

Works count: 3

Citation count: 90

H-index: 3

I10-index: 2