Driscoll, Daniel J.

Prader-Willi syndrome

Cassidy, S. B., Schwartz, S., Miller, J. L., & Driscoll, D. J. (2012) · Genetics in Medicine

Genetic Syndromes and ImprintingGenomic variations and chromosomal abnormalities

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A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader–Willi syndrome critical region

Jong, M. T. C., Gray, T. A., Ji, Y., Glenn, C. C., Saitoh, S., Driscoll, D. J., & Nicholls, R. D. (1999) · Human Molecular Genetics

Genetic Syndromes and ImprintingGenomics and Chromatin Dynamics

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Enhanced activation of reward mediating prefrontal regions in response to food stimuli in Prader-Willi syndrome

Miller, J. L., James, G. A., Goldstone, A. P., Couch, J. A., He, G., Driscoll, D. J., & Liu, Y. (2007) · Journal of Neurology, Neurosurgery & Psychiatry

Regulation of Appetite and ObesityGenetic Syndromes and Imprinting

Cited by 119

Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader–Willi syndrome genetic region

Jong, M. T. C., Carey, A. H., Caldwell, K. A., Lau, M. H., Handel, M. A., Driscoll, D. J., Stewart, C. L., Rinchik, E. M., & Nicholls, R. D. (1999) · Human Molecular Genetics

Genetic Syndromes and ImprintingGenomics and Chromatin Dynamics

Cited by 112

Intracranial abnormalities detected by three‐dimensional magnetic resonance imaging in Prader–Willi syndrome

Miller, J. L., Couch, J. A., Schmalfuss, I., He, G., Liu, Y., & Driscoll, D. J. (2007) · American Journal of Medical Genetics Part A

Genetic Syndromes and ImprintingGenomic variations and chromosomal abnormalities

Cited by 95

Repetitive behavior profiles: consistency across autism spectrum disorder cohorts and divergence from Prader–Willi syndrome

Flores, C. G., Valcante, G., Guter, S., Zaytoun, A., Wray, E., Bell, L., Jacob, S., Lewis, M. H., Driscoll, D. J., Cook, E. H., et al. (2011) · Journal of Neurodevelopmental Disorders

Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues

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