Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome

Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

Trilochan Sahoo, Daniela del Gaudio, Jennifer R. German et al. · Nature Genetics · 2008 · 664 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

Jérôme Cavaillé, Karin Buiting, Martin Kiefmann et al. · Proceedings of the National Academy of Sciences · 2000 · 597 citations

Life Sciences, Genetics, Molecular Biology +12

Recommendations for the Diagnosis and Management of Prader-Willi Syndrome

Anthony P. Goldstone, Anthony Holland, B. P. Hauffa et al. · The Journal of Clinical Endocrinology & Metabolism · 2008 · 516 citations · Full text

Medicine, Neurology, Psychiatry +5

Long Noncoding RNAs with snoRNA Ends

Qing-Fei Yin, Li Yang, Yang Zhang et al. · Molecular Cell · 2012 · 437 citations · Full text

Life Sciences, Genetics, Molecular Biology +5

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism

Adam J. de Smith, Carolin Purmann, Robin Walters et al. · Human Molecular Genetics · 2009 · 355 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15