Huijun Wang

19PUBLICATIONS
14CO-AUTHORS
Infant and child healthNeonatologyGene mappingNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)
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Publications (19)

|Aug 29, 2024
Thirteen New Patients of PPP2R5D Gene Mutation and the Fine Profile of Genotype-Phenotype Correlation Unraveling the Pathogenic Mechanism Underlying Macrocephaly Phenotype.

Yinmo Jiang, Bingbing Wu, Xi Zhang

|Jul 19, 2022
Aetiology and outcomes of prolonged neonatal jaundice in tertiary centres: data from the China Neonatal Genome Project.

Tiantian Xiao, Jin Wang, Huijun Wang

|Jun 21, 2022
Hyaline fibromatosis syndrome with a novel 4.41-kb deletion in ANTXR2 gene: A case report and literature review.

Yunqian Zhu, Xiaonan Du, Li Sun

|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

|Apr 06, 2022
Intron retention by a novel intronic mutation in DKC1 gene caused recurrent still birth and early death in a Chinese family.

|Mar 02, 2022
Identification of Pathogenic Variants in RPGRIP1L with Meckel Syndrome and Preimplantation Genetic Testing in a Chinese Family.

Ping Zhang, Bingbing Wu, Yaqiong Wang

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Frequent Collaborators

6 joint publications

Wenhao Zhou

4 joint publications

Yulan Lu

3 joint publications

Lin Yang

2 joint publications

Sha Yu