Genetic testing in pediatric kidney transplant recipients to promote informed choice and improve individualized monitoring

Genetic diagnosis provides critical insights into the pathogenesis of kidney disease, optimizes clinical strategies concerning risk assessment of living donors, and enhances disease surveillance of recipients.

Authors

Institutions

Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2024-10-03
DOI
https://doi.org/10.1186/s13023-024-03379-4
Citations
3
Primary Topic
Renal Transplantation Outcomes and Treatments
Type
article
Field-Weighted Citation Impact
1.52

Funders

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article

Genetic testing in pediatric kidney transplant recipients to promote informed choice and improve individualized monitoring

Shicheng Xu, Jia Rao, Hongen Xu, Linan Xu et al.
3 citations
Orphanet Journal of Rare Diseases
Renal Transplantation Outcomes and Treatments
1.52
article

Genetic testing in pediatric kidney transplant recipients to promote informed choice and improve individualized monitoring

Shicheng Xu, Jia Rao, Hongen Xu, Linan Xu, Zhigang Wang, Guiwen Feng, Fang Ye, Yi Feng, Yonghua Feng, Lu Mao, Wenjun Shang, Jiancheng Guo, Na Zhao
article en
3 citations

Abstract

Genetic diagnosis provides critical insights into the pathogenesis of kidney disease, optimizes clinical strategies concerning risk assessment of living donors, and enhances disease surveillance of recipients.

Orphanet Journal of Rare DiseasesVol. 19(1)
National Kidney Foundation (US), Zhengzhou University (CN), Second Affiliated Hospital of Zhengzhou University (CN), First Affiliated Hospital of Zhengzhou University (CN), Children's Hospital of Fudan University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China, Science and Technology Innovation Plan Of Shanghai Science and Technology Commission
Openalex Percentile: Top 18%
Renal Transplantation Outcomes and Treatments
1.52
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Genetic testing in pediatric kidney transplant recipients to promote informed choice and improve individualized monitoring — Shicheng Xu, Jia Rao, et al. · Orphanet Journal of Rare Diseases (2024) | TGRS Research Map | TGRS