Yongjian Yue

No. 135 Xingang Xi Road
Guangzhou, 510275, China

Last Updated: 09/26/2026

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Found 15 publications

GP6 polymorphisms and venous thromboembolism: a Chinese case-control study with cross-population assessment.

GP6 polymorphisms and venous thromboembolism: a Chinese case-control study with cross-population assessment.

Journal: BMC cardiovascular disorders

Published: June 24, 2025

Diagnosis and follow-up of a PCDH19 epilepsy patient.

Diagnosis and follow-up of a PCDH19 epilepsy patient.

Journal: Psychiatric genetics

Published: November 25, 2024

Novel mutations in RSPH4A and TTN genes lead to primary ciliary dyskinesia-hereditary myopathy with early respiratory failure overlap syndrome.

Novel mutations in RSPH4A and TTN genes lead to primary ciliary dyskinesia-hereditary myopathy with early respiratory failure overlap syndrome.

Journal: Genes & diseases

Published: August 16, 2022

Pathogenic variants identified using whole-exome sequencing in Chinese patients with primary ciliary dyskinesia.

Pathogenic variants identified using whole-exome sequencing in Chinese patients with primary ciliary dyskinesia.

Journal: American journal of medical genetics. Part A

Published: January 14, 2022

Influence of roundness errors of bearing components on rotational accuracy of cylindrical roller bearings.

Influence of roundness errors of bearing components on rotational accuracy of cylindrical roller bearings.

Journal: Scientific reports

Published: August 22, 2021

Mutational Pattern in Multiple Pulmonary Nodules Are Associated With Early Stage Lung Adenocarcinoma.

Mutational Pattern in Multiple Pulmonary Nodules Are Associated With Early Stage Lung Adenocarcinoma.

Journal: Frontiers in oncology

Published: September 07, 2020

Identification of a distinct luminal subgroup diagnosing and stratifying early stage prostate cancer by tissue-based single-cell RNA sequencing.

Identification of a distinct luminal subgroup diagnosing and stratifying early stage prostate cancer by tissue-based single-cell RNA sequencing.

Journal: Molecular cancer

Published: July 10, 2020

Identification of Pathogenic Mutations and Investigation of the NOTCH Pathway Activation in Kartagener Syndrome.

Identification of Pathogenic Mutations and Investigation of the NOTCH Pathway Activation in Kartagener Syndrome.

Journal: Frontiers in genetics

Published: May 02, 2019

Association of SERPINC1 Gene Polymorphism (rs2227589) With Pulmonary Embolism Risk in a Chinese Population.

Association of SERPINC1 Gene Polymorphism (rs2227589) With Pulmonary Embolism Risk in a Chinese Population.

Journal: Frontiers in genetics

Published: January 29, 2019

Pathogenic variants of PROC gene caused type I activity deficiency in a familial Chinese venous thrombosis.

Pathogenic variants of PROC gene caused type I activity deficiency in a familial Chinese venous thrombosis.

Journal: Journal of cellular and molecular medicine

Published: December 06, 2018

iTRAQ-based proteomic analysis of human umbilical vein endothelial cells with platelet endothelial aggregation receptor-1 knockdown.

iTRAQ-based proteomic analysis of human umbilical vein endothelial cells with platelet endothelial aggregation receptor-1 knockdown.

Journal: Journal of cellular biochemistry

Published: November 13, 2018

A comprehensive immune repertoire study for patients with pulmonary tuberculosis.

A comprehensive immune repertoire study for patients with pulmonary tuberculosis.

Journal: Molecular genetics & genomic medicine

Published: August 16, 2018

Showing 1-12 of 15

Last Updated: 09/26/2026