Yiming Lin

发表

Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening

Yiming Lin, Wenjun Wang, Chunmei Lin, 2021, Orphanet Journal of Rare Diseases.

Expanded newborn screening for inherited metabolic disorders and genetic characteristics in a southern Chinese population.

Yiming Lin, Zhenzhu Zheng, Qingliu Fu, 2019, Clinica chimica acta; international journal of clinical chemistry.

Glutaric Acidemia type 1 with Atypical Acylcarnitine Profile During Newborn Screening

Yiming Lin, Wenjun Wang, Chunmei Lin, 2021 .

Increased primary carnitine deficiency detection through second-tier newborn genetic screening

Yiming Lin, Chunmei Lin, Qingliu Fu, 2021 .

Increased detection of primary carnitine deficiency through second-tier newborn genetic screening

Yiming Lin, Chunmei Lin, Qingliu Fu, 2021, Orphanet Journal of Rare Diseases.

Screening 3.4 million newborns for primary carnitine deficiency in Zhejiang Province, China.

Ting Zhang, Zhenzhen Hu, Xinwen Huang, 2020, Clinica chimica acta; international journal of clinical chemistry.

Newborn screening for primary carnitine deficiency in Quanzhou, China.

Caifeng Fu, Yiming Lin, Zhenzhu Zheng, 2020, Clinica chimica acta; international journal of clinical chemistry.

Combined primary carnitine deficiency with neonatal intrahepatic cholestasis caused by citrin deficiency in a Chinese newborn

Yiming Lin, Chunmei Lin, Zhenzhu Zheng, 2020, BMC Pediatrics.

A novel synonymous ABCA3 variant identified in a Chinese family with lethal neonatal respiratory failure

Yiming Lin, Weifeng Zhang, Zhiyong Liu, 2021, BMC medical genomics.

Three Novel and One Potential Hotspot CPT1A Variants in Chinese Patients With Carnitine Palmitoyltransferase 1A Deficiency

Yiming Lin, Chunmei Lin, Qingliu Fu, 2021, Frontiers in Pediatrics.

Mild clinical features of isolated methylmalonic acidemia associated with a novel variant in the MMAA gene in two Chinese siblings

Yiming Lin, Chunmei Lin, Zhenzhu Zheng, 2018, BMC medical genetics.

Newborn screening and genetic features of patients with hyperphenylalaninemia in a southern Chinese population.

Yiming Lin, Zhenzhu Zheng, Qingliu Fu, 2022, Clinica chimica acta; international journal of clinical chemistry.

Determination of methylmalonic acid, 2-methylcitric acid, and total homocysteine in dried blood spots by liquid chromatography–tandem mass spectrometry: A reliable follow-up method for propionylcarnitine-related disorders in newborn screening

Junjuan Wang, Zhenzhen Hu, Xinwen Huang, 2020, Journal of medical screening.

Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening

Yiming Lin, Zhenzhu Zheng, Qingliu Fu, 2021, Orphanet Journal of Rare Diseases.

Clinical, biochemical, and genetic analysis of a Chinese Han pedigree with holocarboxylase synthetase deficiency: a case report

Min⁃ying Zheng, Yiming Lin, Zhenzhu Zheng, 2020, BMC Medical Genetics.

Incorporating second-tier genetic screening for multiple acyl-CoA dehydrogenase deficiency.

Yiming Lin, Qingliu Fu, Weilin Peng, 2022, Clinica chimica acta; international journal of clinical chemistry.

A prenatal diagnosis and genetics study of five pedigrees in the Chinese population with Xp22.31 microduplication

Yiming Lin, Chunling Lv, Yuying Jiang, 2019, Molecular Cytogenetics.

Clinical and genetic analysis of five Chinese patients with urea cycle disorders

Yiming Lin, Wenjun Wang, Zhenzhu Zheng, 2020, Molecular genetics & genomic medicine.

Newborn screening for inborn errors of metabolism in a northern Chinese population

Yiming Lin, Genxian Liu, Xingying Liu, 2023, Journal of pediatric endocrinology & metabolism : JPEM.

Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, China

Yiming Lin, Chunmei Lin, Qingliu Fu, 2021, Journal of pediatric endocrinology & metabolism : JPEM.

Newborn screening for isovaleric acidemia in Quanzhou, China.

Yiming Lin, Zhenzhu Zheng, Qingliu Fu, 2020, Clinica chimica acta; international journal of clinical chemistry.

Biochemical, Clinical, and Genetic Characteristics of Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency in Chinese Patients by Newborn Screening

Hongzhi Gao, Yiming Lin, Chunmei Lin, 2019, Front. Genet..

Clinical, biochemical and genetic analysis of Chinese patients with isobutyryl-CoA dehydrogenase deficiency.

Yiming Lin, Chunmei Lin, Zhenzhu Zheng, 2018, Clinica chimica acta; international journal of clinical chemistry.

A novel compound heterozygous variant identified in GLDC gene in a Chinese family with non-ketotic hyperglycinemia

Wenjia Sun, Yiming Lin, Zhenzhu Zheng, 2018, BMC Medical Genetics.

Citrullinemia type I is associated with a novel splicing variant, c.773 + 4A > C, in ASS1: a case report and literature review

Hongzhi Gao, Yiming Lin, Qingliu Fu, 2019, BMC Medical Genetics.

The 46, XX Ovotesticular Disorder of Sex Development With Xq27.1q27.2 Duplication Involving the SOX3 Gene: A Rare Case Report and Literature Review

Chunnuan Chen, Jia Li, Yiming Lin, 2021, Frontiers in Pediatrics.

Biochemical, molecular, and clinical features of patients with glutaric acidemia type 1 identified through large-scale newborn screening in Zhejiang Province, China.

Xiaochun Zhu, Zhenzhen Hu, Yiming Lin, 2022, Clinica chimica acta; international journal of clinical chemistry.

C4OH is a potential newborn screening marker—a multicenter retrospective study of patients with beta-ketothiolase deficiency in China

Zhantao Yang, Y. Kong, T. Niu, 2021, Orphanet Journal of Rare Diseases.

C4OH is a Potential Screening Marker - A Multicenter Retrospective Study of Patients with Beta-Ketothiolase Deficiency in China

Yuanyuan Shen, Zhantao Yang, Y. Kong, 2020 .

Combining newborn metabolic and genetic screening for neonatal intrahepatic cholestasis caused by citrin deficiency

Chien-Hsing Lin, Zhenzhen Hu, Xinwen Huang, 2019, Journal of inherited metabolic disease.

Multiplex PCR-based next generation sequencing as a novel, targeted and accurate molecular approach for periprosthetic joint infection diagnosis

X. Fang, Chaofan Zhang, Zi-da Huang, 2023, Frontiers in Microbiology.

Newborn Screening for Spinal Muscular Atrophy in China Using DNA Mass Spectrometry

Chien-Hsing Lin, Zhenzhen Hu, Xinwen Huang, 2019, Front. Genet..

A novel compound heterozygous variant identified in GLDC gene in a Chinese family with non-ketotic hyperglycinemia

Wenjia Sun, Yiming Lin, Zhenzhu Zheng, 2018, BMC Medical Genetics.

Newborn screening for fatty acid oxidation disorders in a southern Chinese population

Yiming Lin, Chunmei Lin, Zhenzhu Zheng, 2023, Heliyon.