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Xiaoguang (Victor) Zhen
Ahmet Asan, Ph.D.
Katherine Stalnaker
Kate graduated from American University in 2016 with a BA in Psychology. In 2020 she graduated from Rutgers University with her MS in Biomedical Science with a concentration in Neuroscience. Her thesis was on glucose sensing in the brain and the relationship to feeding behavior. Kate has worked in...
Vladimir Tkachev
Vladimir graduated from the University of New Hampshire in the spring of 2022 with a major in Neuroscience and Behavior and a minor in Biomedical Sciences. During his undergraduate years, Vladimir conducted research in the Neurobiology lab of Dr. Arturo Andrade and Immunology lab of Dr. Sherine...
Sean P Moran, Ph.D.
Sean Moran is a neuropharmacologist with a strong passion for translational neuroscience research who earned his PhD from Vanderbilt University under the mentorship of P. Jeffrey Conn. During his graduate training at the Vanderbilt Center for Neuroscience Drug Discovery, Sean utilized molecular...
Heterozygous deletion of the autism-associated gene CHD8 impairs synaptic function through widespread changes in gene expression and chromatin compaction
Shi, Xi. 2021. “Heterozygous Deletion of the Autism-Associated Gene CHD8 Impairs Synaptic Function through Widespread Changes in Gene Expression and Chromatin Compaction”. American Journal of Human Genetics.
Mouse mutants in schizophrenia risk genes GRIN2A and AKAP11 show EEG abnormalities in common with schizophrenia patients
Herzog, Linnea E. 2023. “Mouse Mutants in Schizophrenia Risk Genes GRIN2A and AKAP11 Show EEG Abnormalities in Common With Schizophrenia Patients”. Translational Psychiatry.
IntelliSleepScorer, a software package with a graphic user interface for automated sleep stage scoring in mice based on a light gradient boosting machine algorithm.
Dylan Mercado
Dylan joined the Broad Summer Scholars Program eager to explore how tiny changes in DNA can ripple outward to affect brain function and health. At the Stanley Center, he worked on understanding the functional effects of missense mutations in the CACNA1A gene, which encodes the CaV2.1 calcium channel...