Zhiying Wu

59PUBLICATIONS
86CO-AUTHORS
NeurogeneticsNeurology and neuromuscular diseasesGene mappingDynamics, vibration and vibration controlGene expression (incl. microarray and other genome-wide approaches)
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Publications (59)

|Sep 29, 2026
Large-scale genetic profiling of hereditary ataxias in China: implications for a stepwise molecular diagnostic strategy.

|Sep 11, 2026
PRRT2 as an auxiliary regulator of Nav channel slow inactivation.

|Sep 10, 2026
Non-coding repeat expansions within NOTCH2NLC and RFC1 genes contribute to unsolved inherited peripheral neuropathies.

|Jul 18, 2026
Genotype-phenotype relationship in a cohort of 131 Chinese patients with myotonic dystrophy type 1.

|May 07, 2026
ANXA11 suppression restores muscular function in the mdx mouse model of Duchenne muscular dystrophy (DMD).

|Mar 03, 2026
Heterozygous Loss-of-Function Variants of KCNJ10 Cause Paroxysmal Kinesigenic Dyskinesia.

Wan-Bing Sun, Jiao-Jiao Xu, Yu-Lan Chen

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Frequent Collaborators

6 joint publications

Hong-Fu Li

3 joint publications

Hai-Lin Dong

3 joint publications

Zhi-Qi Xiong

3 joint publications

Bin Lu