Author

Pei Qian

Institutions: Xi’an Children’s Hospital, Xi'an Jiaotong University

Observed institutions: Xi’an Children’s Hospital, Xi'an Jiaotong University

ORCID: 0009-0002-8811-6018

Observed ORCID: 0009-0002-8811-6018

OpenAlex ID: A5095778154

A deep intronic splice variant of the COL4A5 gene in a Chinese family with X-linked Alport syndrome

2023 · Pei Qian, Ying Bao, et al. · Frontiers in Pediatrics · 9

Nephrotic syndrome as the first symptom in Alport syndrome children

2025 · Ying Bao, Pei Qian, et al. · Clinical Nephrology · 1

Genome sequencing based sequential diagnostic strategy improve diagnosed yield of pediatric genetic kidney disease: a national multicenter study

2026 · Chunyan Wang, Xiaoshan Tang, et al. · npj Genomic Medicine

Identification and pathogenicity analysis of a novel intronic COL4A5 variant in a Chinese family

2026 · Pei Qian, Hui-mei Huang, et al. · Frontiers in Medicine

A monocenter study on pediatric Alport syndrome featuring nephrotic syndrome as the primary manifestation

2024 · Pei Qian · Research Square

Works count: 5

Citation count: 10

H-index: 1

I10-index: