Search Results - "Dunaway, Keith W"

Snord116-dependent diurnal rhythm of DNA methylation in mouse cortex by Coulson, Rochelle L., Yasui, Dag H., Dunaway, Keith W., Laufer, Benjamin I., Vogel Ciernia, Annie, Zhu, Yihui, Mordaunt, Charles E., Totah, Theresa S., LaSalle, Janine M.

“…Rhythmic oscillations of physiological processes depend on integrating the circadian clock and diurnal environment. DNA methylation is epigenetically…”
Get full text

Phosphorylation of Distinct Sites in MeCP2 Modifies Cofactor Associations and the Dynamics of Transcriptional Regulation by Gonzales, Michael L., Adams, Sarrita, Dunaway, Keith W., LaSalle, Janine M.

“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
Get full text

Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes by Mordaunt, Charles E, Jianu, Julia M, Laufer, Benjamin I, Zhu, Yihui, Hwang, Hyeyeon, Dunaway, Keith W, Bakulski, Kelly M, Feinberg, Jason I, Volk, Heather E, Lyall, Kristen, Croen, Lisa A, Newschaffer, Craig J, Ozonoff, Sally, Hertz-Picciotto, Irva, Fallin, M Daniele, Schmidt, Rebecca J, LaSalle, Janine M

“…Autism spectrum disorder (ASD) is a neurodevelopmental disorder with complex heritability and higher prevalence in males. The neonatal epigenome has the…”
Get full text

Cumulative Impact of Polychlorinated Biphenyl and Large Chromosomal Duplications on DNA Methylation, Chromatin, and Expression of Autism Candidate Genes by Dunaway, Keith W., Islam, M. Saharul, Coulson, Rochelle L., Lopez, S. Jesse, Vogel Ciernia, Annie, Chu, Roy G., Yasui, Dag H., Pessah, Isaac N., Lott, Paul, Mordaunt, Charles, Meguro-Horike, Makiko, Horike, Shin-ichi, Korf, Ian, LaSalle, Janine M.

“…Rare variants enriched for functions in chromatin regulation and neuronal synapses have been linked to autism. How chromatin and DNA methylation interact with…”
Get full text

A comparison of existing global DNA methylation assays to low-coverage whole-genome bisulfite sequencing for epidemiological studies by Crary-Dooley, Florence K., Tam, Mitchell E., Dunaway, Keith W., Hertz-Picciotto, Irva, Schmidt, Rebecca J., LaSalle, Janine M.

“…DNA methylation is an epigenetic mark at the interface of genetic and environmental factors relevant to human disease. Quantitative assessments of global DNA…”
Get full text

Experience-dependent neuroplasticity of the developing hypothalamus: integrative epigenomic approaches by Vogel Ciernia, Annie, Laufer, Benjamin I ., Dunaway, Keith W., Mordaunt, Charles E., Coulson, Rochelle L., Totah, Theresa S., Stolzenberg, Danielle S., Frahm, Jaime C., Singh-Taylor, Akanksha, Baram, Tallie Z., LaSalle, Janine M., Yasui, Dag H.

“…Augmented maternal care during the first postnatal week promotes life-long stress resilience and improved memory compared with the outcome of routine rearing…”
Get full text

MeCP2 modulates gene expression pathways in astrocytes by Yasui, Dag H, Xu, Huichun, Dunaway, Keith W, Lasalle, Janine M, Jin, Lee-Way, Maezawa, Izumi

“…Mutations in MECP2 encoding methyl-CpG-binding protein 2 (MeCP2) cause the X-linked neurodevelopmental disorder Rett syndrome. Rett syndrome patients exhibit…”
Get full text

Placental DNA methylation levels at CYP2E1 and IRS2 are associated with child outcome in a prospective autism study by Zhu, Yihui, Mordaunt, Charles E, Yasui, Dag H, Marathe, Ria, Coulson, Rochelle L, Dunaway, Keith W, Jianu, Julia M, Walker, Cheryl K, Ozonoff, Sally, Hertz-Picciotto, Irva, Schmidt, Rebecca J, LaSalle, Janine M

“…DNA methylation acts at the interface of genetic and environmental factors relevant for autism spectrum disorder (ASD). Placenta, normally discarded at birth,…”
Get full text

15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain by Yasui, Dag H., Scoles, Haley A., Horike, Shin-ichi, Meguro-Horike, Makiko, Dunaway, Keith W., Schroeder, Diane I., LaSalle, Janine M.

“…Copy number variations (CNVs) within human 15q11.2-13.3 show reduced penetrance and variable expressivity in a range of neurologic disorders. Therefore,…”
Get full text

Investigation of modifier genes within copy number variations in Rett syndrome by Artuso, Rosangela, Papa, Filomena T, Grillo, Elisa, Mucciolo, Mafalda, Yasui, Dag H, Dunaway, Keith W, Disciglio, Vittoria, Mencarelli, Maria A, Pollazzon, Marzia, Zappella, Michele, Hayek, Giuseppe, Mari, Francesca, Renieri, Alessandra, LaSalle, Janine M, Ariani, Francesca

Get full text

Investigation of modifier genes within copy number variations in Rett syndrome by Artuso, Rosangela, Papa, Filomena T, Grillo, Elisa, Mucciolo, Mafalda, Yasui, Dag H, Dunaway, Keith W, Disciglio, Vittoria, Mencarelli, Maria A, Pollazzon, Marzia, Zappella, Michele, Hayek, Giuseppe, Mari, Francesca, Renieri, Alessandra, Lasalle, Janine M, Ariani, Francesca

“…MECP2 mutations are responsible for two different phenotypes in females, classical Rett syndrome and the milder Zappella variant (Z-RTT). We investigated…”
Get full text

Erratum: Investigation of modifier genes within copy number variations in Rett syndrome by Artuso, Rosangela, Papa, Filomena T, Grillo, Elisa, Mucciolo, Mafalda, Yasui, Dag H, Dunaway, Keith W, Disciglio, Vittoria, Mencarelli, Maria A, Pollazzon, Marzia, Zappella, Michele, Hayek, Giuseppe, Mari, Francesca, Renieri, Alessandra, LaSalle, Janine M, Ariani, Francesca

“…Correction to: Journal of Human Genetics 2011, 56(7): 508–515; doi:10.1038/jhg.2011.50; published online 19 May 2011. After the publication of the article, the…”
Get full text