author-photo

Aijie Liu

Peking University

23

Papers

268

Citations

Citation Trend

Filter By

Papers (16) Sort By

Journal Conference Others

Muscle Magnetic Resonance Imaging in Patients with LAMA2-Related Muscular Dystrophy

2021 Neuromuscular Disorders
Show All
- Source
- Cite
- Save
Citations (0)
[A phenotypic and genetic study on ß-propeller protein-associated neurodegeneration].

2019 Chinese journal of pediatrics
Show All
- Source
- Cite
- Save
Citations (0)
Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45.

2018 Epilepsia
Show All
- Source
- Cite
- Save
Citations (35)
Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy

2018 Scientific Reports
Show All
- Source
- Cite
- Save
Citations (8)
Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort

2018 Journal of Human Genetics
Show All
- Source
- Cite
- Save
Citations (8)
Study of Pathogenic gene spectrum in benign familial infantile epilepsy

2017 Chinese Journal of Applied Clinical Pediatrics
Show All
- Source
- Cite
- Save
Citations (0)
Progress of protocadherin 19(PCDH19)gene related epilepsy

2017 Chinese Journal of Applied Clinical Pediatrics
- Aijie Liu
Show All
- Source
- Cite
- Save
Citations (0)
The clinical spectrum of female epilepsy patients with PCDH19 mutations in a Chinese population

2017 Clinical Genetics
Show All
- Source
- Cite
- Save
Citations (18)
Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort

2017 Scientific Reports
Show All
- Source
- Cite
- Save
Citations (31)
Clinical manifestations and prenatal diagnosis of congenital muscular dystrophy

2017 Chinese Journal of Perinatal Medicine
Show All
- Source
- Cite
- Save
Citations (0)