Author

Hou Qian

Institutions: Shenzhen University, Shenzhen Second People's Hospital

Observed institutions: Shenzhen University, Shenzhen University Health Science Center, Shenzhen Second People's Hospital

ORCID: 0000-0001-6627-8038

Observed ORCID: 0000-0001-6627-8038

OpenAlex ID: A5067918150

Prenatal diagnosis of a rare β‐thalassemia gene －90 (C>T) (HBB: c.‐140 C>T) mutation associated with deletional Hb H disease (‐‐SEA/‐α4.2)

2020 · Hou Qian, Jianlin Huang, et al. · Molecular Genetics & Genomic Medicine · 3

Identifying Diabetic Cardiomyopathy Biomarkers via Proteomic and Glycation Modification Analysis Using DIA and PRM

2026 · Lin Lin, Mingyu Hao, et al. · Journal of Proteome Research · 2

α‑thalassemia deletion [‑SEA(Southeast Asian)] and a compound heterozygote for the ChineseGγ+(Aγδβ)0/βCD17‑thalassemia mutation: A case report

2023 · Hou Qian, Weifeng Li, et al. · Molecular Medicine Reports · 1

A Precision Screening Framework for Thalassemia in a High-Mobility Population: Integrating 3D Phenotypic Mapping and Genotype-Specific Thresholds

2026 · Hou Qian, Weifeng Li, et al. · Research Square

Simultaneous quantification of fat- and water-soluble vitamins in serum by valve-mediated dual LC-MS/MS

2026 · Weifeng Li, Ka Luo, et al. · Journal of Pharmaceutical and Biomedical Analysis

Cloning and expression of cytochrome CYP6 gene from Phyllonorycter ringoniella.

2016 · Tian Tian, Xin Li, et al. · Journal of Northwest A&F University

Works count: 6

Citation count: 6

H-index: 2

I10-index: