List of works - Zhangyu Zou

A novel VRK1 mutation associated with recessive distal hereditary motor neuropathy.

scientific article

Clinical genetics of Alzheimer's disease

scientific article

Coexistence of Amyotrophic Lateral Sclerosis in the Proband of an X-Linked Charcot-Marie-Tooth Disease Type 1 Pedigree in China.

scientific article published in April 2018

De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China.

scientific article published on 6 October 2012

Familial flail leg ALS caused by PFN1 mutation

scientific article published on 10 August 2019

Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis.

scientific article published on 5 January 2017

Guillain-Barré syndrome in southern China: retrospective analysis of hospitalised patients from 14 provinces in the area south of the Huaihe River

scientific article

H46R SOD1 mutation is consistently associated with a relatively benign form of amyotrophic lateral sclerosis with slow progression.

scientific article published on 27 June 2016

Identification of a novel missense mutation in angiogenin in a Chinese amyotrophic lateral sclerosis cohort

scientific article published on 31 January 2012

Motor nerve conduction study and muscle strength in newly diagnosed POEMS syndrome

scientific article published on 01 January 2015

Mutations in FUS are the most frequent genetic cause in juvenile sporadic ALS patients of Chinese origin

scientific article published on 14 March 2016

Mutations in SOD1 and FUS caused juvenile-onset sporadic amyotrophic lateral sclerosis with aggressive progression

scientific article

Mutations in the profilin 1 gene are not common in amyotrophic lateral sclerosis of Chinese origin.

scientific article

Novel FUS mutation Y526F causing rapidly progressive familial amyotrophic lateral sclerosis

scientific article published on 28 July 2020

Novel mutation in optineurin causing aggressive ALS+/-frontotemporal dementia

scientific article published on 15 December 2019

Screening for C9orf72 repeat expansions in Chinese amyotrophic lateral sclerosis patients.

scientific article published on 20 December 2012

Screening of VCP mutations in Chinese amyotrophic lateral sclerosis patients ⬇️

scientific article published on October 24, 2012

Screening of the FUS gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin

scientific article published on 16 February 2012

Screening of the TARDBP gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin

scientific article published on 09 May 2012

Surgical treatment of pituitary apoplexy in association with hemispheric infarction.

scientific article published on 23 July 2015

The distinctive genetic architecture of ALS in mainland China

scientific article published on 30 October 2015

Toward precision medicine in amyotrophic lateral sclerosis

scientific article

List of works by Zhangyu Zou

A novel VRK1 mutation associated with recessive distal hereditary motor neuropathy.

Clinical genetics of Alzheimer's disease

Coexistence of Amyotrophic Lateral Sclerosis in the Proband of an X-Linked Charcot-Marie-Tooth Disease Type 1 Pedigree in China.

De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China.

Familial flail leg ALS caused by PFN1 mutation

Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis.

Guillain-Barré syndrome in southern China: retrospective analysis of hospitalised patients from 14 provinces in the area south of the Huaihe River

H46R SOD1 mutation is consistently associated with a relatively benign form of amyotrophic lateral sclerosis with slow progression.

Identification of a novel missense mutation in angiogenin in a Chinese amyotrophic lateral sclerosis cohort

Motor nerve conduction study and muscle strength in newly diagnosed POEMS syndrome

Mutations in FUS are the most frequent genetic cause in juvenile sporadic ALS patients of Chinese origin

Mutations in SOD1 and FUS caused juvenile-onset sporadic amyotrophic lateral sclerosis with aggressive progression

Mutations in the profilin 1 gene are not common in amyotrophic lateral sclerosis of Chinese origin.

Novel FUS mutation Y526F causing rapidly progressive familial amyotrophic lateral sclerosis

Novel mutation in optineurin causing aggressive ALS+/-frontotemporal dementia

Screening for C9orf72 repeat expansions in Chinese amyotrophic lateral sclerosis patients.

Screening of VCP mutations in Chinese amyotrophic lateral sclerosis patients ⬇️

Screening of the FUS gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin

Screening of the TARDBP gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin

Surgical treatment of pituitary apoplexy in association with hemispheric infarction.

The distinctive genetic architecture of ALS in mainland China

Toward precision medicine in amyotrophic lateral sclerosis