ME-Class2 reveals context dependent regulatory roles for 5-hydroxymethylcytosine

por Schlosberg, Christopher E, Wu, Dennis Y, Gabel, Harrison W, Edwards, John R
Publicado 2019

NSD1 deposits histone H3 lysine 36 dimethylation to pattern non-CG DNA methylation in neurons

por Hamagami, Nicole, Wu, Dennis Y., Clemens, Adam W., Nettles, Sabin A., Gabel, Harrison W.
Publicado 2023

The chromatin remodeling enzyme Chd4 regulates genome architecture in the mouse brain

por Goodman, Jared V., Yamada, Tomoko, Yang, Yue, Kong, Lingchun, Wu, Dennis Y., Zhao, Guoyan, Gabel, Harrison W., Bonni, Azad
Publicado 2020

Towards a comprehensive regulatory map of Mammalian Genomes

por Gonçalves, Tássia Mangetti, Stewart, Casey L, Baxley, Samantha D, Xu, Jason, Li, Daofeng, Gabel, Harrison W, Wang, Ting, Avraham, Oshri, Zhao, Guoyan
Publicado 2023

LONGO: an R package for interactive gene length dependent analysis for neuronal identity

por McCoy, Matthew J, Paul, Alexander J, Victor, Matheus B, Richner, Michelle, Gabel, Harrison W, Gong, Haijun, Yoo, Andrew S, Ahn, Tae-Hyuk
Publicado 2018

Disruption of DNA methylation-dependent long gene repression in Rett syndrome

por Gabel, Harrison W., Kinde, Benyam Z., Stroud, Hume, Gilbert, Caitlin S., Harmin, David A., Kastan, Nathaniel R., Hemberg, Martin, Ebert, Daniel H., Greenberg, Michael E.
Publicado 2015

Small RNA pathway genes identified by patterns of phylogenetic conservation and divergence

por Tabach, Yuval, Billi, Allison C., Hayes, Gabriel D., Newman, Martin A., Zuk, Or, Gabel, Harrison, Kamath, Ravi, Yacoby, Keren, Chapman, Brad, Garcia, Susana M., Borowsky, Mark, Kim, John K., Ruvkun, Gary
Publicado 2012

CHARGE syndrome protein CHD7 regulates epigenomic activation of enhancers in granule cell precursors and gyrification of the cerebellum

por Reddy, Naveen C., Majidi, Shahriyar P., Kong, Lingchun, Nemera, Mati, Ferguson, Cole J., Moore, Michael, Goncalves, Tassia M., Liu, Hai-Kun, Fitzpatrick, James A. J., Zhao, Guoyan, Yamada, Tomoko, Bonni, Azad, Gabel, Harrison W.
Publicado 2021

DNMT3A Haploinsufficiency Results in Behavioral Deficits and Global Epigenomic Dysregulation Shared across Neurodevelopmental Disorders

por Christian, Diana L., Wu, Dennis Y., Martin, Jenna R., Moore, J. Russell, Liu, Yiran R., Clemens, Adam W., Nettles, Sabin A., Kirkland, Nicole M., Papouin, Thomas, Hill, Cheryl A., Wozniak, David F., Dougherty, Joseph D., Gabel, Harrison W.
Publicado 2020

Distinct disease mutations in DNMT3A result in a spectrum of behavioral, epigenetic, and transcriptional deficits

por Beard, Diana C., Zhang, Xiyun, Wu, Dennis Y., Martin, Jenna R., Hamagami, Nicole, Swift, Raylynn G., McCullough, Katherine B., Ge, Xia, Bell-Hensley, Austin, Zheng, Hongjun, Lawrence, Austin B., Hill, Cheryl A., Papouin, Thomas, McAlinden, Audrey, Garbow, Joel R., Dougherty, Joseph D., Maloney, Susan E., Gabel, Harrison W.
Publicado 2023

Functional and epigenetic phenotypes of humans and mice with DNMT3A Overgrowth Syndrome

por Smith, Amanda M., LaValle, Taylor A., Shinawi, Marwan, Ramakrishnan, Sai M., Abel, Haley J., Hill, Cheryl A., Kirkland, Nicole M., Rettig, Michael P., Helton, Nichole M., Heath, Sharon E., Ferraro, Francesca, Chen, David Y., Adak, Sangeeta, Semenkovich, Clay F., Christian, Diana L., Martin, Jenna R., Gabel, Harrison W., Miller, Christopher A., Ley, Timothy J.
Publicado 2021