Concepedia

Author

Zhiqiang Wang

Fujian Medical UniversityORCID

Also Known As

Z.‐Q. Wang, Zhi-Qiang Wang, Zhi-qiang Wang, ZhiQiang Wang, Zhiqiang Wang, Zhi‐qiang Wang

62

Publications

660

Citations

14

H-Index

30

Concepts

All Affiliations

Fujian Medical UniversityFirst Affiliated Hospital of Fujian Medical UniversityHuashan HospitalFudan UniversityPeking University
ZW

About

Zhiqiang Wang is an author at Fujian Medical University specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

8

8

257

2

Public Health

1

1

21

3

Biostatistics

1

1

21

4

Immunology

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1

16

5

Molecular Biology

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1

98

Zhiqiang Wang

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20

Publications

558

Citations

14

H-Index

YearCitations

Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A

Zhiqiang Wang, Xuejiao Chen, Shen-Xing Murong,

Journal of Molecular Medicine

2011

98

Single-molecule optical mapping enables quantitative measurement of D4Z4 repeats in facioscapulohumeral muscular dystrophy (FSHD)

Yi Dai, Pidong Li, Zhiqiang Wang,

Journal of Medical Genetics

2019

74

Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study

Zhiqiang Wang, Liangliang Qiu, Min-Ting Lin,

The Lancet Regional Health - Western Pacific

2021

38

1,2-Dichloroethane-induced toxic encephalopathy: A case series with morphological investigations

Shiyan Chen, Zhijian Zhang, Hong Lin,

Journal of the Neurological Sciences

2015

37

Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients

Danyu Song, Yi Dai, Xiaoyu Chen,

Clinical Genetics

2020

37

New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy

Lin Feng, Zhiqiang Wang, Min-Ting Lin,

Chinese Medical Journal

2015

32

Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency

Hong‐Xia Fu, Xinyi Liu, Zhiqiang Wang,

Neurological Sciences

2016

31

Clinical and genetic features of patients with facial‐sparing facioscapulohumeral muscular dystrophy

Junjie He, Xiaodan Lin, Fei Lin,

European Journal of Neurology

2017

28

Clinical and mutational characteristics of Duchenne muscular dystrophy patients based on a comprehensive database in South China

Danni Wang, Zhiqiang Wang, Lei Yan,

Neuromuscular Disorders

2017

26

FSHD in Chinese population

Zhi‐Ying Wu, Zhiqiang Wang, Shen-Xing Murong,

Neurology

2004

21

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