Jie-Yuan Jin

6PUBLICATIONS
9CO-AUTHORS
Proteomics and intermolecular interactions (excl. medical proteomics)Gene mappingImmunogenetics (incl. genetic immunology)Genetic immunologyAdolescent health
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Publications (6)

|Dec 09, 2023
Familial congenital heart disease caused by a frameshift variant in glyoxylate reductase 1 homolog (GLYR1).

C Liang, R Xiang, S-H Chang

|Apr 11, 2023
Late-onset hereditary spastic paraplegia associated with a genetic variant in interferon induced with helicase c domain 1 (IFIH1) gene.

S-Y Zhang, L Zhu, L-L Fan

|May 07, 2021
Whole-Exome Sequencing Identifies a Novel TRPM4 Mutation in a Chinese Family with Atrioventricular Block.

Yi Dong, Ran Du, Liang-Liang Fan

|Mar 22, 2021
A Novel COMP Mutated Allele Identified in a Chinese Family with Pseudoachondroplasia.

Bing-Bing Guo, Jie-Yuan Jin, Zhuang-Zhuang Yuan

|Jun 23, 2020
The Novel Compound Heterozygous Mutations of ECEL1 Identified in a Family with Distal Arthrogryposis Type 5D.

Jie-Yuan Jin, Dan-Yu Liu, Zi-Jun Jiao

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