Yaqing Guo

7 Kangfu Qian Street
Zhengzhou, 450052, China

Last Updated: 09/26/2026

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Found 11 publications

CPMOAD: comprehensive preeclampsia multi-omics analysis database.

CPMOAD: comprehensive preeclampsia multi-omics analysis database.

Journal: Journal of translational medicine

Published: August 30, 2025

Newborn screening, clinical characteristics and genetic variant analysis of Glutaric acidemia type I in Henan Province

Newborn screening, clinical characteristics and genetic variant analysis of Glutaric acidemia type I in Henan Province

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: August 05, 2025

Characterization and functional analysis of BRCA1 and BRCA2 variants in a cohort of 100 unselected patients undergoing germline screening.

Characterization and functional analysis of BRCA1 and BRCA2 variants in a cohort of 100 unselected patients undergoing germline screening.

Journal: Translational oncology

Published: April 09, 2025

Genetic analysis of isolated methylmalonic acidemia in Henan, China: c.1663G>A variant of MMUT prevalent in the Henan population.

Genetic analysis of isolated methylmalonic acidemia in Henan, China: c.1663G>A variant of MMUT prevalent in the Henan population.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: April 28, 2023

Analysis of GCH1 gene variant in a consanguineous Chinese pedigree affected with tetrahydrobiopterin deficiency

Analysis of GCH1 gene variant in a consanguineous Chinese pedigree affected with tetrahydrobiopterin deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: July 10, 2022

Allelic phenotype prediction of phenylketonuria based on the machine learning method.

Allelic phenotype prediction of phenylketonuria based on the machine learning method.

Journal: Human genomics

Published: July 09, 2022

Identification of phenylketonuria patient genotypes using single-gene full-length sequencing.

Identification of phenylketonuria patient genotypes using single-gene full-length sequencing.

Journal: Human genomics

Published: March 28, 2022

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy.

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy.

Journal: Human genomics

Published: December 02, 2019

Identification of a novel splicing mutation in the SLC25A13 gene from a patient with NICCD: a case report.

Identification of a novel splicing mutation in the SLC25A13 gene from a patient with NICCD: a case report.

Journal: BMC pediatrics

Published: May 31, 2019

Variant analysis of PEX11B gene from a family with peroxisome biogenesis disorder 14B by whole exome sequencing.

Variant analysis of PEX11B gene from a family with peroxisome biogenesis disorder 14B by whole exome sequencing.

Journal: Molecular genetics & genomic medicine

Published: February 26, 2019

Heteroatom-doped porous carbons derived from moxa floss of different storage years for supercapacitors.

Heteroatom-doped porous carbons derived from moxa floss of different storage years for supercapacitors.

Journal: RSC advances

Published: February 26, 2018

Showing 1-11 of 11

Last Updated: 09/26/2026