Yiming Lin

huaqiao university

H指数:15

被引数:652

个人简介

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教育背景

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工作经历

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Incorporating Next-Generation Sequencing in Newborn Screening for Organic Acidemias

将下一代测序技术应用于新生儿有机酸血症筛查

International Journal of Neonatal Screening

IF4

2026-03-210

OAAI

Pathogenic Analysis of Two SLC22A5 Variants That Alter RNA Splicing in Patients with Primary Carnitine Deficiency

原发性肉碱缺乏症患者中影响RNA剪接的两种SLC22A5变异的致病性分析

International Journal of Neonatal Screening

IF4

2026-03-170

A case of adult ileal duplication presenting with life-threatening bleeding: Diagnostic difficulties and literature review

成人回肠重复畸形并发危及生命出血的病例：诊断困难及文献综述

Asian Journal of Surgery

IF3.8

2025-11-200

OAAI

Clinical and genetic analysis of four Chinese patients with holocarboxylase synthetase deficiency and metabolic acidosis

四例全羧化酶合成酶缺乏合并代谢性酸中毒的中国患者的临床与遗传学分析

Orphanet Journal of Rare Diseases

IF3.5

2025-10-020

OAAI

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

HELIYON

IF3.6

2024-01-010

OAAI

Clinical and genetic analysis of 26 Chinese patients with neonatal intrahepatic cholestasis due to citrin deficiency

citrin缺陷所致新生儿肝内胆汁淤积症26例临床及基因分析

CLINICA CHIMICA ACTA

IF2.9

2024-01-013

PRE

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

CLINICA CHIMICA ACTA

IF2.9

2022-12-014

PRE

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

CLINICA CHIMICA ACTA

IF2.9

2022-10-015

PRE

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

CLINICA CHIMICA ACTA

IF2.9

2022-05-014

PRE

Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening (vol 16, 503, 2021)

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2022-01-240

OAAI

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

通过新生儿筛查确定的原发性肉碱缺乏症患者的生化和遗传特征

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2021-12-0415

OAAI

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

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2021-08-0310

OAAI

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

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2021-05-177

OAAI

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

通过第二级新生儿遗传筛查增加对原发性肉碱缺乏症的检测

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2021-03-2316

OAAI

Newborn screening for primary carnitine deficiency in Quanzhou, China

泉州地区新生儿原发性肉碱缺乏症筛查

CLINICA CHIMICA ACTA

IF2.9

2021-01-0110

PREAI

Newborn screening and genetic characteristics of patients with short- and very long-chain acyl-CoA dehydrogenase deficiencies

CLINICA CHIMICA ACTA

IF2.9

2020-11-015

PREAI

Newborn screening for isovaleric acidemia in Quanzhou, China

泉州地区新生儿异戊酸血症筛查

CLINICA CHIMICA ACTA

IF2.9

2020-10-018

PREAI

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

浙江省340万新生儿原发性肉碱缺乏症筛查

CLINICA CHIMICA ACTA

IF2.9

2020-08-0128

PREAI

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

CLINICA CHIMICA ACTA

IF2.9

2019-07-0159

PREAI

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

CLINICA CHIMICA ACTA

IF2.9

2018-12-0119

PREAI

Yiming Lin

个人简介

教育背景

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