Richard Smith

Assistant Professor

Northwestern University Feinberg School of Medicine

United States

Research Interests

Explore related searches

Professors in United States

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

Richard Smith is an Assistant Professor at Northwestern University Feinberg School of Medicine in the United States. His research focuses on epilepsy, brain development, and neuropsychiatric disorders, as evidenced by his recent publications on gene therapy for childhood epilepsy, transcriptional regulation in neural specification, and the genetic underpinnings of developmental delays and psychotic disorders in children. He is dedicated to advancing understanding in the fields of neurogenetics and neurodevelopmental disorders.

Articles (10)

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2022

Year:

2021

Year:

Assistant Professor

Boston Children's Hospital

UNITED STATES

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Richard Smith

Research Interests

Explore related searches

Contact this professor

About

Articles (10)

Analysis of DNA from brain tissue on stereo-EEG electrodes reveals mosaic epilepsy-related variants

Conserved transcriptional regulation by BRN1 and BRN2 in neocortical progenitors drives mammalian neural specification and neocortical expansion

Gene therapy for targeting a prenatally enriched potassium channel associated with severe childhood epilepsy and premature death.

PRDM16 co-operates with LHX2 to shape the human brain.

Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants

Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria.

Loss of non-motor kinesin KIF26A causes congenital brain malformations via dysregulated neuronal migration and axonal growth as well as apoptosis

Early role for a Na + ,K + -ATPase ( ATP1A3 ) in brain development

RCL1 copy number variants are associated with a range of neuropsychiatric phenotypes.

A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features.

Collaborators (6)

Genevieve Stein-O'Brien

Xuyu Qian

Janet Song

BYOUNG-IL BAE

Alan Beggs

Catherine Brownstein

Make your next move.