Associated Papers
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
The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals.
Cao Y et al.
Cell Research, 2020
32355288 (PubMed )
Supplement: 41422_2020_322_MOESM14_ESM.xlsx › S7
Mutations in the small heterodimer partner gene increase morbidity risk in Japanese type 2 diabetes patients.
Enya M et al.
Human Mutation, 2008
Mutations in the small heterodimer partner gene are associated with mild obesity in Japanese subjects.
Nishigori H et al.
Proceedings of the National Academy of Sciences of the United States of America, 2001
Gender-dependent penetrance of small heterodimer partner (SHP) gene deficiency in overweight/obese Chinese pedigrees.
Yang Z et al.
The Journal of International Medical Research, 0
Investigating genetic variants in early-onset obesity through exome sequencing: A retrospective cohort study.
Liu D et al.
Obesity Research & Clinical Practice, 0
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