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Xiaoli Chen

7PUBLICATIONS

10CO-AUTHORS

Flight dynamicsNeurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)Neurogenetics

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Publications (7)

Sort by Publication Date:

|Jul 29, 2025

Alu-mediated FANCD2 exonic deletion contributes to Fanconi anaemia.

Shaofang Shangguan, Xinyuan Cui, Juanjuan Li

|Jul 30, 2024

A novel compound heterozygous mutation of UFC1 in a patient with neurodevelopmental disorder.

Ye Han, Yangyang Ge, Haoran Liu

|May 05, 2021

Confirming the contribution and genetic spectrum of de novo mutation in infantile spasms: Evidence from a Chinese cohort.

Liying Liu, Fang Liu, Qiuhong Wang

|Jan 06, 2021

CNV profiles of Chinese pediatric patients with developmental disorders.

Haiming Yuan, Shaofang Shangguan, Zhengchang Li

|Sep 02, 2020

Neurodevelopmental trajectory and modifiers of 16p11.2 microdeletion: A follow-up study of four Chinese children carriers.

Hua Xie, Fang Liu, Yu Zhang

|Sep 11, 2019

A rare case of acquired immunodeficiency associated with myelodysplastic syndrome.

Juanjuan Li, Junhui Li, Jianguo Li

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Frequent Collaborators

2 joint publications

Juanjuan Li

2 joint publications

Hua Xie

1 joint publications

Qian Chen

1 joint publications

Jian Wang

1 joint publications

Fang Liu

1 joint publications

Liping Zou

1 joint publications

Shaofang Shangguan

1 joint publications

Xinyuan Cui

1 joint publications

Niu Li

1 joint publications

Rong Liu

Frequent Collaborators

2 joint publications

Juanjuan Li

2 joint publications

Hua Xie

1 joint publications

Qian Chen

1 joint publications

Jian Wang

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