Associated Papers
Novel SIM1 Variants Expanding the Spectrum of SIM1-Related Obesity.
Mohammed I et al.
International Journal of Molecular Sciences, 2026
Genetic etiology and clinical features of non-syndromic pediatric obesity in the Chinese population: a large cohort study.
Hui H et al.
Bmc Pediatrics, 2025
Loss-of-function mutations in MRAP2 are pathogenic in hyperphagic obesity with hyperglycemia and hypertension.
Baron M et al.
Nature Medicine, 2019
31700171 (PubMed )
Supplement: EMS84473-supplement-Supplementary_Tables.pdf
Identification of two novel loss-of-function SIM1 mutations in two overweight children with developmental delay.
Montagne L et al.
Obesity (silver Spring, Md.), 2014
Characterization of human variants in obesity-related SIM1 protein identifies a hot-spot for dimerization with the partner protein ARNT2.
Sullivan AE et al.
The Biochemical Journal, 2014
Rare variants in single-minded 1 (SIM1) are associated with severe obesity.
Ramachandrappa S et al.
The Journal of Clinical Investigation, 2013
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