Preimplantation genetic testing for monogenic disorders (PGT-M) for monogenic nephropathy: a single-center retrospective cohort analysis
PGT-M is an effective means of preventing intergenerational inheritance of monogenic nephropathy. The absence of genetic abnormalities detected by prenatal diagnosis in healthy newborns without monogenic nephropathy also underscore its validity.
Authors
- Yuan Gao (ORCID: https://orcid.org/0000-0001-9290-4397)
- Kexin Cao (ORCID: https://orcid.org/0000-0002-1846-508X)
- Wei Zhou (ORCID: https://orcid.org/0000-0002-5461-3617)
- Peiwen Xu
- Junhao Yan (ORCID: https://orcid.org/0000-0002-7110-8698)
- Qian Zhang (ORCID: https://orcid.org/0000-0003-4311-967X)
- Xinyu Liu (ORCID: https://orcid.org/0000-0001-7495-442X)
- Jie Li (ORCID: https://orcid.org/0000-0002-1432-0705)
- Shuzhen Sun (ORCID: https://orcid.org/0000-0002-3004-8844)
- Yuping Niu
- Tianxiang Ni (ORCID: https://orcid.org/0000-0001-6184-2832)
Institutions
- Shandong University (CN)
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Shandong Mental Health Center (CN)
- Shandong Provincial Hospital (CN)
- Reproductive Medicine Institute (US)
- Shandong Maternal and Child Health Hospital (CN)
- Shandong Academy of Chinese Medicine (CN)
Publication Details
- Journal
- Clinical Kidney Journal
- Published
- 2024-11-18
- DOI
- https://doi.org/10.1093/ckj/sfae356
- Citations
- 2
- Primary Topic
- Renal and related cancers
- Type
- article
- Field-Weighted Citation Impact
- 0.47
Funders
- National Natural Science Foundation of China
- Natural Science Foundation of Shandong Province
- National Key Research and Development Program of China