Publications by authors named "Xin-Fu Lin"

Claim this Profile
A
A de novo INSR variant in Type A insulin resistance syndrome: familial investigation and genetic implications.
Xin Lin, Zi-Yan Xu, Li-Jun Xie, Juan Zhu, Hong-Ping Yu, Xin-Fu Lin

Gene· February 2026

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Correction to: Pedigree Analysis of Nonclassical Cholesteryl Ester Storage Disease with Dominant Inheritance in a LIPA I378T Heterozygous Carrier.
Jian-Hui Zhang, Ai-Ping Lin, Li Zhang, Dan-Dan Ruan, Mei-Zhu Gao, Xin-Fu Lin, Fan Lin, Xiao-Ling Zheng

Dig Dis Sci· March 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemia.
Kai-Ying He, Hong-Ping Yu, Jing Zou, Xiang Chen, Li Chen, Xin-Fu Lin

Clin Chim Acta· January 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Analysis of low-density lipoprotein receptor gene mutations in a family with familial hypercholesterolemia.
Ya-Nan Hu, Min Wu, Hong-Ping Yu, Qiu-Yan Wu, Ying Chen, Xin-Fu Lin, Fan Lin

PLoS One· October 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation.
Dan-Dan Ruan, Xing-Lin Ruan, Ruo-Li Wang, Xin-Fu Lin, Yan-Ping Zhang, Bin Lin, Fan Lin

Sci Rep· September 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel splicing mutation DNAH5 c.13,338 + 5G > C is involved in the pathogenesis of primary ciliary dyskinesia in a family with primary familial brain calcification.
Xiu-Juan Yao, Qian Chen, Hong-Ping Yu, Dan-Dan Ruan, Shi-Jie Li, Xin-Fu Lin

BMC Pulm Med· July 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
study of p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism.
Dan-Dan Ruan, Jing Zou, Li-Sheng Liao, Ming-Dong Ji, Ruo-Li Wang, Fan Lin, Xin-Fu Lin

Front Neurosci· July 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pedigree Analysis of Nonclassical Cholesteryl Ester Storage Disease with Dominant Inheritance in a LIPA I378T Heterozygous Carrier.
Jian-Hui Zhang, Ai-Ping Lin, Li Zhang, Dan-Dan Ruan, Mei-Zhu Gao, Xin-Fu Lin, Fan Lin, Xiao-Ling Zheng

Dig Dis Sci· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient: a case report.
Jian-Hui Zhang, Hui Chen, Dan-Dan Ruan, Ying Chen, Li Zhang, Xin-Fu Lin, Xiao-Ling Zheng

Ann Hematol· May 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation.
Dan-Dan Ruan, Xing-Lin Ruan, Ruo-Li Wang, Xin-Fu Lin, Yan-Ping Zhang, Bin Lin, Fan Lin

Sci Rep· April 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndrome.
Hong-Hong Pan, Dan-Dan Ruan, Min Wu, Ting Chen, Tao Lu, Xin-Fu Lin

J Med Genet· November 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritis.
Shi-Jie Li, Dan-Dan Ruan, Wei-Zhen Wu, Min Wu, Qiu-Yan Wu, Xin-Fu Lin

Pediatr Rheumatol Online J· October 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Han family with essential tremor caused by the P421L variant of the TENM4 gene in China.
Wu Chi, Min Wu, Han-Lu Wang, Qiu-Yan Wu, Yan-Ping Zhang, Xin-Fu Lin, Xing-Lin Ruan

Neurol Sci· June 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription.
Yu-Mian Gan, Yan-Ping Zhang, Dan-Dan Ruan, Jian-Bin Huang, Yao-Bin Zhu, Xin-Fu Lin

Cell Death Dis· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by Variant.
Ruo-Li Wang, Dan-Dan Ruan, Ya-Nan Hu, Yu-Mian Gan, Xin-Fu Lin

Front Pediatr· May 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family.
Wen Wei, Xiu-Fen Zheng, Dan-Dan Ruan, Yu-Mian Gan, Yan-Ping Zhang, Xin-Fu Lin

Neurol Sci· April 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A.
Yao-Bin Zhu, Jian-Hui Zhang, Yuan-Yuan Ji, Ya-Nan Hu, Han-Lu Wang, Xin-Fu Lin

Cardiol Res Pract· April 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical and Genetic Analysis of a Family With Sitosterolemia Caused by a Novel ATP-Binding Cassette Subfamily G Member 5 Compound Heterozygous Mutation.
Ming-Fang Shen, Ya-Nan Hu, Wei-Xiang Chen, Li-Sheng Liao, Min Wu, Xin-Fu Lin

Front Cardiovasc Med· April 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency.
Ya-Nan Hu, Yu-Mian Gan, Yan-Ping Zhang, Dan-Dan Ruan, Yao-Bin Zhu, Xin-Fu Lin

J Gene Med· February 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous Mutations.
Jian-Hui Zhang, Dan-Dan Ruan, Ya-Nan Hu, Xing-Lin Ruan, Yao-Bin Zhu, Xin-Fu Lin

Biomed Res Int· September 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1.
Yan-Ping Zhang, Bin Lin, Yuan-Yuan Ji, Ya-Nan Hu, Xin-Fu Lin, Sen-Lin Cai

Thromb J· September 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene.
Li Chen, Han-Lu Wang, Yao-Bin Zhu, Zhao Jin, Jian-Bin Huang, Xin-Fu Lin

Cell Death Dis· March 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic mutation of familial dilated cardiomyopathy based on next‑generation semiconductor sequencing.
Xin-Fu Lin, Jie-Wei Luo, Gui Liu, Yao-Bin Zhu, Zhao Jin, Xing Lin

Mol Med Rep· November 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis