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Author

Gaopin Yuan

Observed name: Yuan, Gaopin
ORCID: 0000-0002-5632-3883
Observed ORCID: 0000-0002-5632-3883
OpenAlex ID: A5066253867
Chinese familial central precocious puberty with hyperuricemia due to recurrent DLK1 mutation: Case report and review of the literature
2022 · Gaopin Yuan, Xiaohong Zhang, et al. · Molecular Genetics & Genomic Medicine · 16
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Clinical, biochemical, and genetic analysis of a Chinese Han pedigree with holocarboxylase synthetase deficiency: a case report
2020 · Zhenzhu Zheng, Gaopin Yuan, et al. · BMC Medical Genetics · 7
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Case report: A novel c.1842_1845dup mutation of ETFDH in two Chinese siblings with multiple acyl-CoA dehydrogenase deficiency
2023 · Gaopin Yuan, Xiaohong Zhang, et al. · Frontiers in Pediatrics · 2
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Clinical characteristics and molecular genetic analysis of ten cases of ornithine carbamoyltransferase deficiency in southeastern China
2024 · Gaopin Yuan, Zhiyong Liu, et al. · The Italian Journal of Pediatrics/Italian journal of pediatrics · 1
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The Viral Legacy in Diabetic Ketoacidosis: Impact of Concurrent Respiratory Viral Infections on Acute Severity and Long-Term Glycemic Control in Children With Newly Diagnosed Type 1 Diabetes
2026 · Tingli Chen, Xiaohong Zhang, et al. · Journal of Clinical Research in Pediatric Endocrinology
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Effect of Body Mass Index and Blood Lipid on peak Growth Hormone Response in Children with Short Stature
2023 · Xiaohong Zhang, Gaopin Yuan, et al. · Research Square
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Works count: 8
Citation count: 26
H-index: 2
I10-index: 1
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