C. Kentros

Characterization of phenotypic range in DYRK1A haploinsufficiency syndrome using standardized behavioral measures

W. Chung, Elizabeth Brooks, A. Ziegler, 2022, American journal of medical genetics. Part A.

Brain Abnormalities in Patients with Germline Variants in H3F3: Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors

E. Roeder, A. Vanderver, M. Tartaglia, 2022, American Journal of Neuroradiology.

Neurodevelopmental phenotypes associated with pathogenic variants in SLC6A1

W. Chung, Elizabeth Brooks, Haluk Kavus, 2021, Journal of Medical Genetics.

Availability of Services and Caregiver Burden: Supporting Individuals With Neurogenetic Conditions During the COVID-19 Pandemic

W. Chung, Jennifer Tjernagel, L. G. Snyder, 2021, Journal of child neurology.

COVID-19’s Impact on Genetics at One Medical Center in New York

W. Chung, R. Wapner, E. Griffin, 2020, Genetics in Medicine.