Hao Hu

5PUBLICATIONS
16CO-AUTHORS
Neurology and neuromuscular diseasesMedical infection agents (incl. prions)NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|Dec 13, 2022
Monoallelic <i>CRMP1</i> gene variants cause neurodevelopmental disorder.

Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker

|Jul 01, 2022
Reply: Is it time to rename hereditary cases of cerebral palsy?

Hao Hu, Kaishou Xu

|Jun 14, 2021
Hypomorphic and hypermorphic mouse models of Fsip2 indicate its dosage-dependent roles in sperm tail and acrosome formation.

Xiang Fang, Yaser Gamallat, Zhiheng Chen

|Jun 02, 2021
In-depth analysis reveals complex molecular aetiology in a cohort of idiopathic cerebral palsy.

Na Li, Pei Zhou, Hongmei Tang

|Apr 09, 2021
Zebrafish modeling mimics developmental phenotype of patients with RAPGEF1 mutation.

Na Li, Pei Zhou, Miaomiao Yang

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Frequent Collaborators

2 joint publications

Xiang Fang

1 joint publications

Ansar A Abbasi

1 joint publications

Pei Zhou

1 joint publications

Jozef Gecz