Abidemi A. Adegbola

Redefining the MED13L syndrome

Steven P. Angus, T. Wienker, A. Chess, 2015, European Journal of Human Genetics.

Disruption of CTNND2, encoding delta-catenin, causes a penetrant attention deficit disorder and myopia

A. Wynshaw-Boris, E. Nikkola, J. Picker, 2020, HGG advances.

A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype

Michael L. Gonzales, A. Chess, J. LaSalle, 2008, Human Genetics.

Rede fi ning the MED 13 L syndrome

Steven P. Angus, T. Wienker, A. Chess, 2015 .

PTPN4 germline variants result in aberrant neurodevelopment and growth

R. Płoski, A. Wynshaw-Boris, L. Escobar, 2021, HGG advances.

A novel mutation in JARID1C/SMCX in a patient with autism spectrum disorder (ASD)

Hanlin Gao, S. Sommer, M. Browning, 2008, American journal of medical genetics. Part A.

Concise Review: Induced Pluripotent Stem Cell Models for Neuropsychiatric Diseases

A. Wynshaw-Boris, Abidemi A. Adegbola, Meixiang Zhang, 2017, Stem cells translational medicine.

Monoallelic expression of the human FOXP2 speech gene

A. Chess, D. Hafler, E. Bradshaw, 2014, Proceedings of the National Academy of Sciences.

Function of Rhodopsin in Temperature Discrimination in Drosophila

A. Chess, C. Montell, Junjie Luo, 2011, Science.