Yulan Lu

7PUBLICATIONS
14CO-AUTHORS
Genetics not elsewhere classifiedMedical infection agents (incl. prions)NeurogeneticsNeonatologyGene expression (incl. microarray and other genome-wide approaches)
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Publications (7)

|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

|May 16, 2020
Clinical utility of 24-h rapid trio-exome sequencing for critically ill infants.

Huijun Wang, Yanyan Qian, Yulan Lu

|Feb 02, 2020
Clinical exome sequencing as the first-tier test for diagnosing developmental disorders covering both CNV and SNV: a Chinese cohort.

Xinran Dong, Bo Liu, Lin Yang

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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