Guanghua Liu

No. 18 Daoshan Road, Gulou District
Fuzhou, China

Last Updated: 09/26/2026

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Found 8 publications

Single-Cell Analysis Reveals the Role of the Neuropeptide Receptor FPR2 in Monocytes in Kawasaki Disease: A Bioinformatic Study.

Single-Cell Analysis Reveals the Role of the Neuropeptide Receptor FPR2 in Monocytes in Kawasaki Disease: A Bioinformatic Study.

Journal: Disease markers

Published: November 12, 2021

Correction: A machine learning approach to predict intravenous immunoglobulin resistance in Kawasaki disease patients: A study based on a Southeast China population.

Correction: A machine learning approach to predict intravenous immunoglobulin resistance in Kawasaki disease patients: A study based on a Southeast China population.

Journal: PloS one

Published: June 21, 2021

Knowledge Graphs of Kawasaki Disease.

Knowledge Graphs of Kawasaki Disease.

Journal: Health information science and systems

Published: October 02, 2020

Gene diagnosis and pedigree analysis of two Han ethnicity families with propionic acidemia in Fujian.

Gene diagnosis and pedigree analysis of two Han ethnicity families with propionic acidemia in Fujian.

Journal: Medicine

Published: July 20, 2020

Perinatal risk factors for congenital hypothyroidism: A retrospective cohort study performed at a tertiary hospital in China.

Perinatal risk factors for congenital hypothyroidism: A retrospective cohort study performed at a tertiary hospital in China.

Journal: Medicine

Published: June 27, 2020

Gene spectrum and clinical traits of 10 patients with primary carnitine deficiency.

Gene spectrum and clinical traits of 10 patients with primary carnitine deficiency.

Journal: Molecular genetics & genomic medicine

Published: June 09, 2020

Novel compound variants of the TMTC3 gene cause cobblestone lissencephaly-like syndrome: A case report.

Novel compound variants of the TMTC3 gene cause cobblestone lissencephaly-like syndrome: A case report.

Journal: Experimental and therapeutic medicine

Published: January 31, 2020

Systematic profiling of clinical missence mutation effects on the intermolecular interaction between human growth hormone and its receptor in isolated growth hormone deficiency.

Systematic profiling of clinical missence mutation effects on the intermolecular interaction between human growth hormone and its receptor in isolated growth hormone deficiency.

Journal: Journal of molecular graphics & modelling

Published: May 28, 2019

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Last Updated: 09/26/2026