Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11–q13 by Stormy J. Chamberlain, Marc Lalande

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Prader-Willi syndrome: reflections on seminal studies and future therapies by Michael S. Chung, Maéva Langouët, Stormy J. Chamberlain, Gordon G. Carmichael

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Communication‐related assessments in an Angelman syndrome mouse model by Peter A. Perrino, Stormy J. Chamberlain, Inge‐Marie Eigsti, Roslyn Holly Fitch

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Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus. by Emily Y Smith, Christopher R Futtner, Stormy J Chamberlain, Karen A Johnstone, James L Resnick

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Disrupted neuronal maturation in Angelman syndrome-derived induced pluripotent stem cells by James J. Fink, Tiwanna M. Robinson, Noelle D. Germain, Carissa L. Sirois, Kaitlyn A. Bolduc, Amanda J. Ward, Frank Rigo, Stormy J. Chamberlain, Eric S. Levine

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A rare inherited 15q11.2-q13.1 interstitial duplication with maternal somatic mosaicism, renal carcinoma and autism by Nora Urraca, Nora Urraca, Brian Potter, Brian Potter, Rachel Hundley, Eniko Pivnick, Eniko Pivnick, Kathryn McVicar, Ronald Thibert, Chistopher Ledbetter, Reed Chamberlain, Leticia Miravalle, Carissa L. Sirois, Stormy J. Chamberlain, Lawrence T. Reiter, Lawrence T. Reiter

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