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Lin Yang

5PUBLICATIONS

4CO-AUTHORS

NeurogeneticsNeonatologyDevelopmental genetics (incl. sex determination)Infant and child health

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Publications (5)

Sort by Publication Date:

|Oct 21, 2021

Use of medical exome sequencing for identification of underlying genetic defects in NICU: Experience in a cohort of 2303 neonates in China.

Lin Yang, Zejun Wei, Xiang Chen

|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

|Jul 27, 2020

Clinical features and underlying genetic causes in neonatal encephalopathy: A large cohort study.

Lin Yang, Xiang Chen, Xu Liu

|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

|Jun 01, 2019

Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.

Xiang Chen, Kai Yan, Yanyan Gao

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Frequent Collaborators

3 joint publications

Huijun Wang

2 joint publications

Yulan Lu

2 joint publications

Wenhao Zhou

1 joint publications

Wenhao Zhou

Frequent Collaborators

3 joint publications

Huijun Wang

2 joint publications

Yulan Lu

2 joint publications

Wenhao Zhou

1 joint publications

Wenhao Zhou

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