Circadian abnormalities in mouse models of smith-magenis syndrome: Evidence for involvement ofRAI1

Smith-Magenis Syndrome Results in Disruption of CLOCK Gene Transcription and Reveals an Integral Role for RAI1 in the Maintenance of Circadian Rhythmicity

(2012) Stephen R. Williams et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits

(2012) Melanie Lacaria et al.   HUMAN MOLECULAR GENETICS

A Duplication CNV That Conveys Traits Reciprocal to Metabolic Syndrome and Protects against Diet-Induced Obesity in Mice and Men

(2012) Melanie Lacaria et al.   PLoS Genetics

Abnormal circadian rhythm of melatonin in Smith-Magenis syndrome patients with RAI1 point mutations

(2011) Philip M. Boone et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Clan Genomics and the Complex Architecture of Human Disease

(2011) James R. Lupski et al.   CELL

Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndrome

(2010) Brooke Burns et al.   HUMAN MOLECULAR GENETICS

Review of disrupted sleep patterns in Smith-Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion

(2009) Eilis A. Boudreau et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Gonadectomy reveals sex differences in circadian rhythms and suprachiasmatic nucleus androgen receptors in mice

(2007) Eiko Iwahana et al.   HORMONES AND BEHAVIOR