Yulan Lu
7PUBLICATIONS
14CO-AUTHORS
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Publications (7)
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|Apr 14, 2025
Balanced Translocation Disrupting JAG1 Identified by Optical Genomic Mapping in Suspected Alagille Syndrome.Yi-Qiong Zhang, Peng-Fei Gao, Jing-Min Yang
|Aug 01, 2023
The TRIM37 variants in Mulibrey nanism patients paralyze follicular helper T cell differentiation.Wangpeng Gu, Jia Zhang, Qing Li
|May 20, 2022
Genetic architecture in neonatal intensive care unit patients with congenital heart defects: a retrospective study from the China Neonatal Genomes Project.Huijun Wang, Feifan Xiao, Yanyan Qian
|Jan 27, 2021
Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project.Huijun Wang, Feifan Xiao, Xinran Dong
|Jan 27, 2021
Complete IFN-γR1 Deficiency in a Boy Due to UPD(6)mat with IFNGR1 Novel Splicing Variant.Ping Zhang, Wenjing Ying, Bingbing Wu
|May 16, 2020
Clinical utility of 24-h rapid trio-exome sequencing for critically ill infants.Huijun Wang, Yanyan Qian, Yulan Lu
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Frequent Collaborators
4 joint publications
Huijun Wang
3 joint publications
Wenhao Zhou
2 joint publications
Lin Yang
1 joint publications
Yi-Qiong Zhang
1 joint publications
Peng-Fei Gao
1 joint publications
Jing-Min Yang
1 joint publications
Jing Zhang
1 joint publications
Jian-She Wang
1 joint publications
Wenhao Zhou
1 joint publications
Qing Li
