RNAs of the human chromsome 15q11-q13 imprinted region

Por Chamberlain, Stormy J.
Publicado em 2012

Prader-Willi, Angelman, and 15q11-q13 duplication syndromes

Por Kalsner, Louisa, Chamberlain, Stormy J.
Publicado no Pediatr Clin North Am (2015)

Angelman Syndrome, a Genomic Imprinting Disorder of the Brain

Por Chamberlain, Stormy J., Lalande, Marc
Publicado no J Neurosci (2010)

Polycomb Repressive Complex 2 is dispensable for maintenance of embryonic stem cell pluripotency

Por Chamberlain, Stormy J., Yee, Della, Magnuson, Terry
Publicado em 2008

Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders

Por LaSalle, Janine M, Reiter, Lawrence T, Chamberlain, Stormy J
Publicado no Epigenomics (2015)

RBFOX1 and RBFOX2 are dispensable in iPSCs and iPSC-derived neurons and do not contribute to neural-specific paternal UBE3A silencing

Por Chen, Pin-Fang, Hsiao, Jack S., Sirois, Carissa L., Chamberlain, Stormy J.
Publicado no Sci Rep (2016)

Neuronal chromatin dynamics of imprinting in development and disease

Por Leung, Karen N., Chamberlain, Stormy J., Lalande, Marc, LaSalle, Janine M.
Publicado em 2011

Transcription Is Required to Establish Maternal Imprinting at the Prader-Willi Syndrome and Angelman Syndrome Locus

Por Smith, Emily Y., Futtner, Christopher R., Chamberlain, Stormy J., Johnstone, Karen A., Resnick, James L.
Publicado em 2011

Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader–Willi syndromes

Por Chamberlain, Stormy J., Chen, Pin-Fang, Ng, Khong Y., Bourgois-Rocha, Fany, Lemtiri-Chlieh, Fouad, Levine, Eric S., Lalande, Marc
Publicado em 2010

A bipartite boundary element restricts UBE3A imprinting to mature neurons

Por Hsiao, Jack S., Germain, Noelle D., Wilderman, Andrea, Stoddard, Christopher, Wojenski, Luke A., Villafano, Geno J., Core, Leighton, Cotney, Justin, Chamberlain, Stormy J.
Publicado no Proc Natl Acad Sci U S A (2019)

Imprinted expression of UBE3A in non-neuronal cells from a Prader–Willi syndrome patient with an atypical deletion

Por Martins-Taylor, Kristen, Hsiao, Jack S., Chen, Pin-Fang, Glatt-Deeley, Heather, De Smith, Adam J., Blakemore, Alexandra I.F., Lalande, Marc, Chamberlain, Stormy J.
Publicado em 2014

Disrupted neuronal maturation in Angelman syndrome-derived induced pluripotent stem cells

Por Fink, James J., Robinson, Tiwanna M., Germain, Noelle D., Sirois, Carissa L., Bolduc, Kaitlyn A., Ward, Amanda J., Rigo, Frank, Chamberlain, Stormy J., Levine, Eric S.
Publicado no Nat Commun (2017)

Topoisomerases facilitate transcription of long genes linked to autism

Por King, Ian F., Yandava, Chandri N., Mabb, Angela M., Hsiao, Jack S., Huang, Hsien-Sung, Pearson, Brandon L., Calabrese, J. Mauro, Starmer, Joshua, Parker, Joel S., Magnuson, Terry, Chamberlain, Stormy J., Philpot, Benjamin D., Zylka, Mark J.
Publicado em 2013

Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1

Por Germain, Noelle D, Chen, Pin-Fang, Plocik, Alex M, Glatt-Deeley, Heather, Brown, Judith, Fink, James J, Bolduc, Kaitlyn A, Robinson, Tiwanna M, Levine, Eric S, Reiter, Lawrence T, Graveley, Brenton R, Lalande, Marc, Chamberlain, Stormy J
Publicado no Mol Autism (2014)

Subtelomeric hotspots of aberrant 5-hydroxymethylcytosine-mediated epigenetic modifications during reprogramming to pluripotency

Por Wang, Tao, Wu, Hao, Li, Yujing, Szulwach, Keith E., Lin, Li, Li, Xuekun, Chen, I-Ping, Goldlust, Ian S., Chamberlain, Stormy J., Dodd, Ann, Gong, He, Ananiev, Gene, Han, Ji Woong, Yoon, Young-sup, Rudd, M. Katharine, Yu, Miao, Song, Chun-Xiao, He, Chuan, Chang, Qiang, Warren, Stephen T., Jin, Peng
Publicado em 2013