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Author

Qingliu Fu

Observed name: Fu, Qingliu
ORCID: 0000-0002-8383-5235
Observed ORCIDs: 0000-0002-8383-5235, 0000-0001-6346-0256
OpenAlex ID: A5046165044
Expanded newborn screening for inherited metabolic disorders and genetic characteristics in a southern Chinese population
2019 · Yiming Lin, Quanzhi Zheng, et al. · Clinica Chimica Acta · 84
Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening
2021 · Yiming Lin, Bangbang Lin, et al. · Orphanet Journal of Rare Diseases · 29
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Clinical, biochemical and genetic analysis of Chinese patients with isobutyryl-CoA dehydrogenase deficiency
2018 · Yiming Lin, Weilin Peng, et al. · Clinica Chimica Acta · 29
Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening
2021 · Yiming Lin, Wenjun Wang, et al. · Orphanet Journal of Rare Diseases · 22
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Increased detection of primary carnitine deficiency through second-tier newborn genetic screening
2021 · Yiming Lin, Weifeng Zhang, et al. · Orphanet Journal of Rare Diseases · 21
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Newborn screening for isovaleric acidemia in Quanzhou, China
2020 · Yiming Lin, Dongmei Chen, et al. · Clinica Chimica Acta · 15
Citrullinemia type I is associated with a novel splicing variant, c.773 + 4A > C, in ASS1: a case report and literature review
2019 · Yiming Lin, Hongzhi Gao, et al. · BMC Medical Genetics · 14
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Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, China
2021 · Yiming Lin, Weifeng Zhang, et al. · Journal of Pediatric Endocrinology and Metabolism · 13
Biochemical, Clinical, and Genetic Characteristics of Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency in Chinese Patients by Newborn Screening
2019 · Yiming Lin, Hongzhi Gao, et al. · Frontiers in Genetics · 13
Incorporating second-tier genetic screening for multiple acyl-CoA dehydrogenase deficiency
2022 · Yiming Lin, Wenwei Zheng, et al. · Clinica Chimica Acta · 9
A novel compound heterozygous variant identified in GLDC gene in a Chinese family with non-ketotic hyperglycinemia
2018 · Yiming Lin, Zhenzhu Zheng, et al. · BMC Medical Genetics · 9
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Newborn screening and genetic features of patients with hyperphenylalaninemia in a southern Chinese population
2022 · Yiming Lin, Weihua Lin, et al. · Clinica Chimica Acta · 8
Combined primary carnitine deficiency with neonatal intrahepatic cholestasis caused by citrin deficiency in a Chinese newborn
2020 · Yiming Lin, Weihua Lin, et al. · BMC Pediatrics · 8
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Mild clinical features of isolated methylmalonic acidemia associated with a novel variant in the MMAA gene in two Chinese siblings
2018 · Yiming Lin, Chunmei Lin, et al. · BMC Medical Genetics · 8
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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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Newborn screening and genetic characteristics of patients with short- and very long-chain acyl-CoA dehydrogenase deficiencies
2020 · Yiming Lin, Weifeng Zhang, et al. · Clinica Chimica Acta · 7
[Mutational analysis of ASS1, ASL and SLC25A13 genes in six Chinese patients with citrullinemia].
2017 · Yiming Lin, Ke Yu, et al. · PubMed · 6
[Mutational analysis of SLC22A5 gene in eight patients with systemic primary carnitine deficiency].
2017 · Yiming Lin, Weihua Lin, et al. · PubMed · 5
Clinical and genetic analysis of five Chinese patients with urea cycle disorders
2020 · Zhenzhu Zheng, Yiming Lin, et al. · Molecular Genetics & Genomic Medicine · 4
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[Detection of GCDH mutations in five Chinese patients with glutaric acidemia type I].
2018 · Yiming Lin, Mingya Han, et al. · PubMed · 3
Three Novel and One Potential Hotspot CPT1A Variants in Chinese Patients With Carnitine Palmitoyltransferase 1A Deficiency
2021 · Weifeng Zhang, Yanru Chen, et al. · Frontiers in Pediatrics · 1
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Correction to: Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening
2022 · Yiming Lin, Bangbang Lin, et al. · Orphanet Journal of Rare Diseases
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[Characteristics of gene variants among patients with hyperphenylalaninemia from Quanzhou region of Fujian province].
2019 · Run Su, Lin Zhu, et al. · PubMed
Works count: 42
Citation count: 315
H-index: 9
I10-index: 9
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