Challenges and opportunities for precision medicine in neurodevelopmental disorders

por Chen, George T., Geschwind, Daniel H.
Publicado 2022

Human in vitro models for understanding mechanisms of autism spectrum disorder

por Gordon, Aaron, Geschwind, Daniel H.
Publicado 2020

Out FOXing Parkinson Disease: Where Development Meets Neurodegeneration

por Wexler, Eric M, Geschwind, Daniel H
Publicado 2007

Autism genetics: searching for specificity and convergence

por Berg, Jamee M, Geschwind, Daniel H
Publicado 2012

Recurrence rates provide evidence for sex-differential, familial genetic liability for autism spectrum disorders in multiplex families and twins

por Werling, Donna M, Geschwind, Daniel H
Publicado 2015

Gene co-expression network analysis in human spinal cord highlights mechanisms underlying amyotrophic lateral sclerosis susceptibility

por Wang, Jerry C., Ramaswami, Gokul, Geschwind, Daniel H.
Publicado 2021

Neuronal protein interaction networks in autism spectrum disorder

por Bicks, Lucy K., Eyring, Katherine Wade, Geschwind, Daniel H.
Publicado 2023

Gene expression in human brain implicates sexually dimorphic pathways in autism spectrum disorders

por Werling, Donna M., Parikshak, Neelroop N., Geschwind, Daniel H.
Publicado 2016

Evolutionary conservation and divergence of the human brain transcriptome

por Pembroke, William G., Hartl, Christopher L., Geschwind, Daniel H.
Publicado 2021

Genome-wide, integrative analysis implicates microRNA dysregulation in autism spectrum disorder

por Wu, Ye E., Parikshak, Neelroop N., Belgard, T. Grant, Geschwind, Daniel H.
Publicado 2016

Cell Lineage and Regional Identity of Cultured Spinal Cord Neural Stem Cells and Comparison to Brain-Derived Neural Stem Cells

por Kelly, Theresa K., Karsten, Stanislav L., Geschwind, Daniel H., Kornblum, Harley I.
Publicado 2009

Correction: The Autism Related Protein Contactin-Associated Protein-Like 2 (CNTNAP2) Stabilizes New Spines: An In Vivo Mouse Study

por Gdalyahu, Amos, Lazaro, Maria, Penagarikano, Olga, Golshani, Peyman, Trachtenberg, Joshua T., Geschwind, Daniel H.
Publicado 2015

Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility

por Won, Hyejung, Huang, Jerry, Opland, Carli K., Hartl, Chris L., Geschwind, Daniel H.
Publicado 2019

Profiling allele specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage

por Lee, Changhoon, Kang, Eun Yong, Gandal, Michael J., Eskin, Eleazar, Geschwind, Daniel H.
Publicado 2019

Genes and pathways underlying regional and cell type changes in Alzheimer's disease

por Miller, Jeremy A, Woltjer, Randall L, Goodenbour, Jeff M, Horvath, Steve, Geschwind, Daniel H
Publicado 2013

Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder

por Werling, Donna M, Lowe, Jennifer K, Luo, Rui, Cantor, Rita M, Geschwind, Daniel H
Publicado 2014

VoICE: A semi-automated pipeline for standardizing vocal analysis across models

por Burkett, Zachary D., Day, Nancy F., Peñagarikano, Olga, Geschwind, Daniel H., White, Stephanie A.
Publicado 2015

Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree

por Peng, Minshi, Wamsley, Brie, Elkins, Andrew G, Geschwind, Daniel H, Wei, Yuting, Roeder, Kathryn
Publicado 2021

ASD Restricted and Repetitive Behaviors Associated at 17q21.33: Genes Prioritized by Expression in Fetal Brains

por Cantor, Rita M., Navarro, Linda, Won, Hyejung, Walker, Rebecca L., Lowe, Jennifer K., Geschwind, Daniel H.
Publicado 2017

Inducible and reversible phenotypes in a novel mouse model of Friedreich’s Ataxia

por Chandran, Vijayendran, Gao, Kun, Swarup, Vivek, Versano, Revital, Dong, Hongmei, Jordan, Maria C, Geschwind, Daniel H
Publicado 2017