Publications by authors named "Qingliu Fu"

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Incorporating second-tier genetic screening for multiple acyl-CoA dehydrogenase deficiency.
Yiming Lin, Wenwei Zheng, Yanru Chen, Chenggang Huang, Qingliu Fu

Clin Chim Acta· December 2022

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Newborn screening and genetic features of patients with hyperphenylalaninemia in a southern Chinese population.
Yiming Lin, Weihua Lin, Run Su, Zhenzhu Zheng, Qingliu Fu

Clin Chim Acta· October 2022

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Correction to: Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening.
Yiming Lin, Bangbang Lin, Yanru Chen, Zhenzhu Zheng, Qingliu Fu

Orphanet J Rare Dis· January 2022

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Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening.
Yiming Lin, Bangbang Lin, Yanru Chen, Zhenzhu Zheng, Qingliu Fu

Orphanet J Rare Dis· December 2021

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Three Novel and One Potential Hotspot Variants in Chinese Patients With Carnitine Palmitoyltransferase 1A Deficiency.
Weifeng Zhang, Yanru Chen, Chunmei Lin, Weilin Peng, Qingliu Fu

Front Pediatr· November 2021

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Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening.
Yiming Lin, Wenjun Wang, Chunmei Lin, Zhenzhu Zheng, Qingliu Fu

Orphanet J Rare Dis· August 2021

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Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, China.
Yiming Lin, Weifeng Zhang, Zhixu Chen, Chunmei Lin, Weihua Lin, Qingliu Fu

J Pediatr Endocrinol Metab· May 2021

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Increased detection of primary carnitine deficiency through second-tier newborn genetic screening.
Yiming Lin, Weifeng Zhang, Chenggang Huang, Chunmei Lin, Weihua Lin, Qingliu Fu

Orphanet J Rare Dis· March 2021

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Newborn screening and genetic characteristics of patients with short- and very long-chain acyl-CoA dehydrogenase deficiencies.
Yiming Lin, Weifeng Zhang, Dongmei Chen, Chunmei Lin, Zhenzhu Zheng, Qingliu Fu

Clin Chim Acta· November 2020

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Newborn screening for isovaleric acidemia in Quanzhou, China.
Yiming Lin, Dongmei Chen, Weilin Peng, Kunyi Wang, Weihua Lin, Qingliu Fu

Clin Chim Acta· October 2020

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Combined primary carnitine deficiency with neonatal intrahepatic cholestasis caused by citrin deficiency in a Chinese newborn.
Yiming Lin, Weihua Lin, Yanru Chen, Chunmei Lin, Zhenzhu Zheng, Qingliu Fu

BMC Pediatr· October 2020

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Clinical and genetic analysis of five Chinese patients with urea cycle disorders.
Zhenzhu Zheng, Yiming Lin, Weihua Lin, Lin Zhu, Mengyi Jiang, Qingliu Fu

Mol Genet Genomic Med· July 2020

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Clinical, biochemical, and genetic analysis of a Chinese Han pedigree with holocarboxylase synthetase deficiency: a case report.
Zhenzhu Zheng, Gaopin Yuan, Minyan Zheng, Yiming Lin, Faming Zheng, Qingliu Fu

BMC Med Genet· July 2020

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[Characteristics of gene variants among patients with hyperphenylalaninemia from Quanzhou region of Fujian province].
Run Su, Lin Zhu, Yiming Lin, Jianhua Zhu, Faming Zheng, Qingliu Fu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· November 2019

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B
Biochemical, Clinical, and Genetic Characteristics of Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency in Chinese Patients by Newborn Screening.
Yiming Lin, Hongzhi Gao, Chunmei Lin, Yanru Chen, Shuang Zhou, Qingliu Fu

Front Genet· August 2019

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E
Expanded newborn screening for inherited metabolic disorders and genetic characteristics in a southern Chinese population.
Yiming Lin, Quanzhi Zheng, Tianwen Zheng, Zhenzhu Zheng, Weihua Lin, Qingliu Fu

Clin Chim Acta· July 2019

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C
Citrullinemia type I is associated with a novel splicing variant, c.773 + 4A > C, in ASS1: a case report and literature review.
Yiming Lin, Hongzhi Gao, Bin Lu, Shuang Zhou, Tianwen Zheng, Qingliu Fu

BMC Med Genet· June 2019

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Clinical, biochemical and genetic analysis of Chinese patients with isobutyryl-CoA dehydrogenase deficiency.
Yiming Lin, Weilin Peng, Mengyi Jiang, Chunmei Lin, Weihua Lin, Qingliu Fu

Clin Chim Acta· December 2018

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Mild clinical features of isolated methylmalonic acidemia associated with a novel variant in the MMAA gene in two Chinese siblings.
Yiming Lin, Chunmei Lin, Weihua Lin, Zhenzhu Zheng, Mingya Han, Qingliu Fu

BMC Med Genet· July 2018

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[Detection of GCDH mutations in five Chinese patients with glutaric acidemia type I].
Yiming Lin, Mingya Han, Zhenzhu Zheng, Weihua Lin, Ke Yu, Qingliu Fu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· February 2018

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A
A novel compound heterozygous variant identified in GLDC gene in a Chinese family with non-ketotic hyperglycinemia.
Yiming Lin, Zhenzhu Zheng, Wenjia Sun, Qingliu Fu

BMC Med Genet· January 2018

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[Mutational analysis of ASS1, ASL and SLC25A13 genes in six Chinese patients with citrullinemia].
Yiming Lin, Ke Yu, Lufeng Li, Zhenzhu Zheng, Weihua Lin, Qingliu Fu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· October 2017

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[Mutational analysis of SLC22A5 gene in eight patients with systemic primary carnitine deficiency].
Yiming Lin, Weihua Lin, Ke Yu, Faming Zheng, Zhenzhu Zheng, Qingliu Fu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· February 2017

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